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Apico-basal intercalations enable the integrity of curved epithelia

Abstract

Non-invasive force inference based on imaging data has significantly advanced our understanding of the mechanical cues driving morphogenesis. In 2D studies of confluent tissues, these methods allow for the computation of forces acting on cells by analyzing their geometrical features. Here, we present a novel approach for 3D force and energy inference in curved epithelia. Specifically, we focus on tubular epithelia, which form the foundation of many vital organs, including the lungs, kidneys, and vasculature. Our technique analyzes the average mechanical behavior of cells along their apico-basal axis and is based on an optimal parametrization of a vertex model aimed at obtaining effective tissue parameters. We apply our method to in silico data to investigate the mechanical consequences of different 3D cellular packing scenarios. Our results reveal that in squamous epithelia, prismatic cellular shapes are mechanically stable. However, in cubic/columnar tubes, prismatic shapes are incompatible with the adhesion required to maintain tissue integrity. In conclusion, this study indicates that in cubic/columnar epithelia, stability can only be achieved if cells undergo apico-basal intercalations and adopt an alternative shape: the scutoid.

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Apico-basal intercalations enable the integrity of curved epithelia

Author: Anbari, Samira; Gómez Gálvez, Pedro; Vicente Munuera, Pablo; Escudero Cuadrado, Luis María; Buceta, Javier
Publisher: Elsevier
Year: 2025
DOI: 10.1016/j.csbj.2025.03.011
Source: https://idus.us.es/bitstreams/22fd9bc0-d664-457c-8d52-9dc545266c08/download
Compu a ional and S uc u al Bio echnology Jou nal 27 (2025) 1204–1214
A ailable online 19 Ma ch 2025
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Resea ch A icle
Apico-basal in e cala ions enable he in eg i y o cu ed epi helia
Sami a Anba ia,1, Ped o Gómez-Gál ezb,c,e, ,g,1, Pablo Vicen e-Munue ad,,
Luis M. Escude oe, ,g, ,∗, Ja ie Buce ah, ,∗∗
aBiomedical Enginee ing Depa men , Johns Hopkins Uni e si y, Bal imo e, MD 21205, USA
bMRC Labo a o y o Molecula Biology, Camb idge Biomedical Campus, F ancis C ick A e., T umping on, Camb idge CB2 0QH, Camb idgeshi e, UK
cDepa men o Physiology, De elopmen and Neu oscience, Uni e si y o Camb idge, 4 Downing Pl., Camb idge CB2 3EL, Camb idgeshi e, UK
dLabo a o y o Molecula Cell Biology, Uni e si y College London, London, UK
eIns i u o de Biomedicina de Se illa (IBiS), Hospi al Uni e si a io Vi gen del Rocío/CSIC/Uni e sidad de Se illa, 41013 Se ille, Spain
Depa amen o de Biología Celula , Uni e sidad de Se illa, 41013 Se ille, Spain
gBiomedical Ne wo k Resea ch Cen e on Neu odegene a i e Diseases (CIBERNED), Mad id, Spain
hIns i u e o In eg a i e Sys ems Biology (I2SysBio), Theo e ical and Compu a ional Sys ems Biology P og am, CSIC-UV, Pa e na 46980, Spain
A B S T R A C T
Non-in asi e o ce in e ence based on imaging da a has significan ly ad anced ou unde s anding o he mechanical cues d i ing mo phogenesis. In 2D s udies o
confluen issues, hese me hods allow o he compu a ion o o ces ac ing on cells by analyzing hei geome ical ea u es. He e, we p esen a no el app oach o
3D o ce and ene gy in e ence in cu ed epi helia. Specifically, we ocus on ubula epi helia, which o m he ounda ion o many i al o gans, including he lungs,
kidneys, and ascula u e. Ou echnique analyzes he a e age mechanical beha io o cells along hei apico-basal axis and is based on an op imal pa ame iza ion o a
e ex model aimed a ob aining effec i e issue pa ame e s. We apply ou me hod o in silico da a o in es iga e he mechanical consequences o diffe en 3D cellula
packing scena ios. Ou esul s e eal ha in squamous epi helia, p isma ic cellula shapes a e mechanically s able. Howe e , in cubic/columna ubes, p isma ic
shapes a e incompa ible wi h he adhesion equi ed o main ain issue in eg i y. In conclusion, his s udy indica es ha in cubic/columna epi helia, s abili y can
only be achie ed i cells unde go apico-basal in e cala ions and adop an al e na i e shape: he scu oid.
1. In oduc ion
Du ing animal de elopmen , mul iple ac o s such as cell-cell in e -
ac ions, cell p oli e a ion, cell shape changes, and biophysical o ces
con ibu e o o gan o ma ion [1–3]. In confluen issues such as epi he-
lia, hese p ocesses de e mine cell packing p ope ies, and hei analysis
has significan ly ad anced ou unde s anding o mo phogenesis [4,5].
T adi ionally, mos s udies ha e been conduc ed in wo dimensions (2D)
by analyzing he apical su aces o monolaye epi helia. Howe e , ecen
esea ch has unde sco ed he need o in es iga e 3D cellula packing and
mo phology [6]. In his con ex , epi helial cells a e ypically classified
by hei wid h- o-heigh aspec a io as squamous (“fla ”), cuboidal, o
columna (“ all”) cells [7,8]. No ably, he ole o diffe en 3D cell ge-
ome ies, in conjunc ion wi h hei packing p ope ies, in main aining
issue in eg i y emains insufficien ly explo ed.
The impo ance o accu a ely analyzing 3D cell-cell con ac s has
been highligh ed by ecen s udies on a ious biological p ocesses, in-
*Co esponding au ho a : Ins i u o de Biomedicina de Se illa (IBiS), Hospi al Uni e si a io Vi gen del Rocío/CSIC/Uni e sidad de Se illa, 41013 Se ille, Spain.
** Co esponding au ho a : Ins i u e o In eg a i e Sys ems Biology (I2SysBio), CSIC-UV, 46980 Pa e na, Spain.
E-mail add esses: [email p o ec ed] (L.M. Escude o), [email p o ec ed] (J. Buce a).
1Equally con ibu ed.
cluding he g ow h o mouse emb yonic lung explan s [9], he ea ly
de elopmen o C. elegans [10] and ascidians [11], and he cellula
and mechanical basis o sel -o ganiza ion in cu ed issues wi hin a
confined geome y [12]. A majo b eak h ough in unde s anding ep-
i helial 3D packing and mo phogenesis came wi h he disco e y o a
no el geome ical shape, he scu oid, which plays a key ole in epi helial
mo phogenesis [6,13–20]. Scu oids, cha ac e ized by apico-basal in e -
cala ions o cells, acili a e epi helial packing when issues a e subjec ed
o cu a u e [14] and a e conside ed a gene al biophysical phenomenon
[21]. Addi ionally, scu oids ha e been shown o modula e local p essu e
inc eases due o cell di ision [22]. This cell shape has been iden i-
fied in epi helial issues ac oss a ious me azoans, including mammals
[6,19,22]. Howe e , key open ques ions emain: (1) how do apico-basal
in e cala ions con ibu e o he mechanical s abili y and in eg i y o an
epi helium? and (2) can a cu ed issue main ain i s in eg i y wi h-
ou scu oids? Expe imen ally add essing hese ques ions by emo ing
o modi ying apico-basal in e cala ions is cu en ly un easible. Thus, a
h ps://doi.o g/10.1016/j.csbj.2025.03.011
Recei ed 8 Janua y 2025; Recei ed in e ised o m 6 Ma ch 2025; Accep ed 8 Ma ch 2025
Compu a ional and S uc u al Bio echnology Jou nal 27 (2025) 1204–1214
1205
S. Anba i, P. Gómez-Gál ez, P. Vicen e-Munue a e al.
compu a ional app oach is equi ed o in e mechanical o ces in di -
e en 3D cellula packing configu a ions. Specifically, a me hodology
is needed o fi s simula e epi helial issues subjec ed o cu a u e and
composed o cuboidal/columna cells wi h ei he p isma ic o scu oidal
packing configu a ions, and second, o de elop a o ce/ene gy in e ence
echnique o analyze and pa ame e ize he esul s o hese simula ions.
A wide ange o expe imen al echniques a e a ailable o mea-
su e o es ima e o ces in cells and issues, including lase abla ion
[23–27], unc ionalized d ople s [28–30], op ical and magne ic weez-
e s [31–34], molecula senso s [35], and ac ion mic oscopy [36],
among o he s [37]. Al e na i ely, in epi helial monolaye s, in e ence
me hods p o ide non-in asi e means o es ima ing o ces using imag-
ing da a [38–46]. These echniques le e age he ac ha he apical
su aces o cells in hese issues exhibi polygonal-like shapes, allowing
hei geome ical ea u es o be co ela ed wi h mechanical equilib ium
condi ions. This polygonal-like packing cha ac e is ic led o he de el-
opmen o he e ex model, which aims o desc ibe he o ces ac ing
on epi helial cells in bo h 2D and 3D en i onmen s [47–51]. In a 3D
con ex , only ecen ly ha e some s udies a emp ed o quan i y o ces
( ensions and p essu es) using Young’s o mula [52,53]. No ably, o
da e, no o ce in e ence s udy has e alua ed he impac o epi helial
cell shape on he mechanical s abili y o issues.
He e, we implemen a no el app oach o 3D o ce in e ence o exam-
ine he ole o cellula shapes and hei packing in epi helial issues. Con-
en ional in e ence me hods ely on o ce balance wi hou inco po a ing
assump ions abou cell mechanics, such as elas ici y o adhesion. In con-
as , ou app oach assumes he alidi y o he e ex model’s desc ip-
ion o cellula mechanics and in e s he pa ame e alues ha sa is y
o ce balance. Fu he mo e, we employ a s a is ical me hod ha quan i-
fies he a e age cell beha io in e ms o ene gy and o ce componen s,
p o iding insigh s in o he ele ance o 3D cellula shapes. Specifically,
we aim o de e mine he biophysical pa ame e s ha bes desc ibe he
mechanical p ope ies and s abili y o issues depending on packing con-
figu a ions. We es ou in e ence me hod on simula ed ubula issues.
These epi helia o m he ounda ion o many i al o gans, including
he lungs, kidneys, and ascula u e, and ha e been shown o exhibi
he highes p e alence o scu oidal cells due o cu a u e effec s com-
pa ed o o he epi helial geome ies [14] (see Discussion). We gene -
a ed ubula epi helia h ough a compu a ional geome y app oach ha
p oduces wo possible cellula shapes: scu oidal shapes, which exhibi
apico-basal in e cala ions, and p isma ic-like shapes, whe e apico-basal
in e cala ions a e absen . Addi ionally, we compa e hese wo scena -
ios in diffe en issue ypes by employing compu a ional ubula models
composed o ei he squamous o cuboidal/columna cells. The biophysi-
cal pa ame iza ion o hese models e eals ha issue in eg i y depends
on a balance be ween packing a chi ec u e and he wid h- o-heigh as-
pec a io o cells. Ou findings sugges ha he adhesi e p ope ies
cha ac e is ic o epi helia equi e he p esence o apico-basal in e ca-
la ions o s abilize ubula s uc u es composed o cuboidal/columna
cells. In o he wo ds, he physical p ope ies o epi helial issues p e en
he exis ence o cuboidal/columna epi helial ubes composed solely o
p isma ic-like shapes.
2. Me hods
2.1. Ve ex model: o ce balance
Ou o ce in e ence me hodology is based on a pa ame iza ion o
he e ex model [54] and assumes he s anda d ene gy unc ional o
each o he e exes, 𝑖, ha define he polygonal-like shape o a cell a
a gi en plana su ace:
𝐸𝑖=∑
𝛼
𝐾𝛼
2 (𝐴𝛼−𝐴0
𝛼(𝑡))2+∑
𝛼
Γ𝛼
2
𝐿2
𝛼+∑
⟨𝑖𝑗⟩
Λ𝑖𝑗𝑙𝑖𝑗
=𝐸elas ic
𝑖+𝐸con ac .
𝑖+𝐸adh.
𝑖
(1)
whe e he sums indexed by 𝛼and ⟨𝑖𝑗⟩ un, espec i ely, o e he cells,
𝛼, and he e exes, 𝑗, ha sha e e ex 𝑖. The fi s e m, 𝐸elas ic
𝑖=
∑𝛼
𝐾𝛼
2 (𝐴𝛼−𝐴0
𝛼(𝑡))2accoun s o he elas ic ene gy o cells (𝐾𝛼be-
ing p opo ional o he Young modulus) due o he diffe ence be ween
he ac ual cell a ea, 𝐴𝛼, and he a ge a ea 𝐴0
𝛼(𝑡). The second e m,
𝐸con ac .
𝑖=∑𝛼
Γ𝛼
2
𝐿2
𝛼, models con ibu ions om he ension associa ed
o he con ac ion ac i i y o he ac omyosin co ical ing, 𝐿𝛼being he
cell pe ime e . Finally, he hi d e m, 𝐸adh.
𝑖=∑⟨𝑖𝑗⟩Λ𝑖𝑗𝑙𝑖𝑗 , ep esen s
he line ension (adhesion o ce), wi h 𝑙𝑖𝑗 being he leng h o he edge
connec ing neighbo ing e exes 𝑖and 𝑗.
By neglec ing ine ia (low Reynolds numbe ) and including dissipa-
ion, he ollowing o ce balance equa ion holds,
𝟎=−∇𝐸𝑖−𝛾
𝐫𝑖
whe e 𝐫𝑖is he posi ion ec o o e ex 𝑖and 𝛾is he coefficien ha
de e mines he cha ac e is ic ime scale linked o he dissipa ion o he
mechanical ene gy, 𝑡𝑐=𝛾∕(𝐾𝛼𝐴0
𝛼). Fu he , i he cha ac e is ic ime
scale o cell a ea changes, ei he due o g ow h o mechanical inpu s, is
slow compa ed o 𝑡𝑐(o equi alen ly i he issue is a a s eady s a e),
he balance o he conse a i e o ces a each cell e ex de e mines he
equilib ium condi ion:
𝟎≃−∇𝐸𝑖=𝐅elas ic
𝑖+𝐅con ac .
𝑖+𝐅adh.
𝑖(2)
In he Euclidian plane, he a ea, 𝐴𝛼, and he pe ime e , 𝐿𝛼, o a
polygon (i.e., cell 𝛼) wi h 𝑛clockwise-o de ed e exes a e gi en by:
𝐴𝛼=−1
2
𝑛
∑
𝑘=1 (𝑥𝛼
𝑘𝑦𝛼
𝑘+1 −𝑥𝛼
𝑘+1𝑦𝛼
𝑘)
𝐿𝛼=
𝑛
∑
𝑘=1
𝑙𝛼
𝑘,𝑘+1 =
𝑛
∑
𝑘=1 √(𝑥𝛼
𝑘+1 −𝑥𝛼
𝑘)2
+(𝑦𝛼
𝑘+1 −𝑦𝛼
𝑘)2
whe e 𝐫𝛼
𝑖=(𝑥𝛼
𝑖,𝑦𝛼
𝑖) ep esen s he Ca esian coo dina es o e ex 𝑖o
cell 𝛼, and he ollowing pe iodic bounda y condi ions o he polygon
ha desc ibe a cell apply: 𝐫𝛼
𝑛+1 =𝐫𝛼
1and 𝐫𝛼
0=𝐫𝛼
𝑛. Thus, he diffe en
o ce e ms in Eq. (2) ead,
𝐅elas ic
𝑖=− 𝜕
𝜕𝐫𝑖∑
𝛼
𝐾𝛼
2 (𝐴𝛼−𝐴0
𝛼(𝑡))2
=1
2∑
𝛼
𝐾𝛼(𝐴𝛼−𝐴0
𝛼(𝑡))(𝑦𝛼
𝑖+1 −𝑦𝛼
𝑖−1,𝑥𝛼
𝑖−1 −𝑥𝛼
𝑖+1)
𝐅con ac .
𝑖=− 𝜕
𝜕𝐫𝑖∑
𝛼
Γ𝛼
2
𝐿2
𝛼
=−∑
𝛼
Γ𝛼𝐿𝛼(𝑥𝛼
𝑖−𝑥𝛼
𝑖−1
𝑙𝛼
𝑖−1,𝑖
+
𝑥𝛼
𝑖−𝑥𝛼
𝑖+1
𝑙𝛼
𝑖,𝑖+1
,𝑦𝛼
𝑖−𝑦𝛼
𝑖−1
𝑙𝛼
𝑖−1,𝑖
+
𝑦𝛼
𝑖−𝑦𝛼
𝑖+1
𝑙𝛼
𝑖,𝑖+1 )
𝐅adh.
𝑖=− 𝜕
𝜕𝐫𝑖∑
⟨𝑖𝑗⟩
Λ𝑖𝑗𝑙𝑖𝑗
=−∑
⟨𝑖𝑗⟩
Λ𝑖𝑗 (𝑥𝑗−𝑥𝑖
𝑙𝑖𝑗
,𝑦𝑗−𝑦𝑖
𝑙𝑖𝑗 )
2.2. Geome ical decomposi ion o o ces: es ima ion o no mal and shea
s esses
In o de o p o ide an in ui i e in e p e a ion o he di ec ionali y
o he o ces, we implemen a geome ical decomposi ion ha es ima es
no mal and shea s esses. Since o ces in a e ex model a e applied
a cell e exes, he no mal and pe pendicula di ec ions a e no well-
defined. To add ess his, we define mock no mal and shea o ces based
on he angle o med by he edges adjacen o a e ex (Fig. 1A). Fo
a gi en o ce ype applied o a e ex 𝑖, 𝐅𝑖=(𝐹𝑖,𝑥,𝐹𝑖,𝑦), we compu e
he no mal and shea componen s, 𝐅′
𝑖=(𝐹𝑖,n,𝐹𝑖,s)by using he ge-
ome ic o a ional ans o ma ion 𝐅′
𝑖=𝑅𝜃𝐅𝑖whe e 𝜃is defined as a
Compu a ional and S uc u al Bio echnology Jou nal 27 (2025) 1204–1214
1206
S. Anba i, P. Gómez-Gál ez, P. Vicen e-Munue a e al.
Fig. 1. A: No mal and shea o ces. To es ima e he no mal and shea componen s o a o ce 𝐅𝑖ac ing upon e ex 𝑖, we implemen a geome ical decomposi ion
ha defines he no mal di ec ion along he bisec o o he angle 𝛼 o med by he adjacen edges 𝐫𝑖+1 −𝐫𝑖and 𝐫𝑖−1 −𝐫𝑖(a o a ion o an angle 𝜃wi h espec o he
ex e nal coo dina e sys em). B: Simula ion o Vo onoi and us a ubes. (Le ) Side iew o a ube. F om he apical (inne ) adius, 𝑅𝑎, o he basal (ou e ) adius,
𝑅𝑏, he simula ion app oach is based on he adial p ojec ion o geome ical ea u es o he cells (a ow). (Righ ) In Vo onoi ubes, he cell seeds a e p ojec ed, while
in us a ubes, he cell e exes a e p ojec ed (see ex ). C: Simula ion Examples. In ou in silico expe imen s we conside ubes ha mimic squamous (𝑠𝑏≃1.5)
and cuboidal/columna (𝑠𝑏=4) cells ha pack ollowing ei he a us a-like (Le ) o a scu oidal-like (Righ ) geome y. The g een and ed ci cles indica e he apical
(inne ) and basal (ou e ) adii, espec i ely. The shapes and packing o highligh ed cells (whi e con ou s in ubes) a e shown a diffe en apico-basal coo dina es
( om bo om o op, 𝑠=1,2,4). Since each ealiza ion o us a and Vo onoi ubes was gene a ed om he same ini ial cell dis ibu ion a he apical su ace, 𝑠=1
(apical su ace), he cells ha e iden ical shapes in bo h cases. No ice ha in Vo onoi ubes, a he apical su ace, he ed and yellow cells a e nea es neighbo s while
he g een and blue cells a e no , whe eas a he basal su ace, he nea es -neighbo ela ionship is e e sed (blue and g een cells become nea es neighbo s while
ed and yellow a e no ). In us a ubes, he neighbo ing ela ionships among cells emain unchanged along he apico-basal axis as in e cala ions a e p ecluded. D:
Quan ifica ion o cellula packing. 3D his og ams o cells neighbo s, 𝑃(𝑛𝑎,𝑛𝑏), o Vo onoi (𝑠𝑏=1.5, Cen e ; 𝑠𝑏=4, Righ ) and us a (Le ) ubes, sample size o
10 ubes. The absence o apico-basal in e cala ions in us a ubes esul s in iden ical polygonal dis ibu ions a he apical and basal su aces. In Vo onoi ubes, as he
su ace a io inc eases, he dis ibu ion widens, indica ing an inc ease in he numbe o apico-basal in e cala ions (scu oid-like cell shapes). E: Tubula geome y:
o ce in e ence. Gi en an epi helial ube o leng h 𝐿and apical and basal adii 𝑅𝑎and 𝑅𝑏, ou omog aphic app oach o o ce in e ence assumes equilib ium is
achie ed a each su ace o cons an adius be ween 𝑅𝑎 o 𝑅𝑏. F: Elas ic null-s ess plane. In a plana epi helial monolaye cells acqui e a p ism-like shape wi h
a cha ac e is ic a ea in each plane om apical o basal 𝐴0(g ey mesh). When he issue is subjec ed o bending ( ubula geome y) he cells de o m and acqui e a
us um-like shape. Cell olume conse a ion implies ha cells a e unde comp ession in he apical plane and unde ension in he basal plane. The elas ic null-s ess
plane is defined by he alue o he apico-basal coo dina e o which he a ea in ha plane is 𝐴0.
unc ion o he bisec o o he angle o med by he edges (𝐫𝛼
𝑖+1 −𝐫𝛼
𝑖)
and
(𝐫𝛼
𝑖−1 −𝐫𝛼
𝑖)o e ex 𝑖:
(𝐹𝑖,n
𝐹𝑖,s)=[𝑐𝑜𝑠(𝜃)𝑠𝑖𝑛(𝜃)
−𝑠𝑖𝑛(𝜃)𝑐𝑜𝑠(𝜃)](𝐹𝑖,𝑥
𝐹𝑖,𝑦)(3)
Finally, he magni ude o he no mal/shea o ces ac ing on each cell
is calcula ed by a e aging he magni udes o he no mal/shea o ces
applied o all i s e exes, 𝑀, such ha 𝐹n=1
𝑀∑𝑀
𝑖=1 𝐹𝑖,nand 𝐹s=
1
𝑀∑𝑀
𝑖=1 𝐹𝑖,s. The a e age cellula no mal and shea o ces a e hen com-
pu ed by a e aging o e all cells, 𝑁: ⟨𝐹𝑛⟩=1
𝑁∑𝐹nand ⟨𝐹𝑠⟩=1
𝑁∑𝐹𝑠.
2.3. Simula ions o Vo onoi and us a ubula models
An in-house Ma lab code was used o model ubula epi helia ol-
lowing wo diffe en app oaches ha lead o dis inc cellula packing
configu a ions: Vo onoi and us a ubes. Vo onoi ubes we e gene a ed
ollowing a simila app oach as desc ibed in [14]. The inne (apical) su -
ace o he ubes (i.e., hollow cylinde s) was popula ed wi h a numbe o
seeds (i.e., poin s) andomly dis ibu ed. Subsequen ly, he Vo onoi al-
go i hm was applied o he seeds o gene a e he co esponding Vo onoi
cells. To mimic he ac ual apical o ganiza ion o epi helial ubes (see
[6,15]), he Lloyd algo i hm was i e a i ely applied 7 imes [55]. The
Lloyd algo i hm upda es he loca ion o he Vo onoi seeds by eloca -
ing hem o he cen e o mass o each Vo onoi cell; subsequen ly, he
Vo onoi algo i hm is eapplied o he upda ed Vo onoi seeds, esul ing
in a mo e homogeneous Vo onoi essella ion in e ms o cellula size.
Once he 2D Vo onoi cells o he apical su ace we e gene a ed, he
3D cellula shape was buil as ollows. The ou e (basal) su ace o he
ubes was gene a ed wi h a adius 𝑅𝑏=𝑠𝑏𝑅𝑎and he Vo onoi cell seeds
we e adially p ojec ed om he inne o he ou e su ace (Fig. 1B).
A each in e media e adius, 𝑅∈[𝑅𝑎,𝑅𝑏], he in e sec ion o he adial
p ojec ions wi h he adial su ace (su ace wi h cons an adius) defines
he loca ion o he Vo onoi seeds, and he esul ing Vo onoi essella ion
ende s he shape o he cells a ha su ace. Fo a gi en seed, he se
o 2D Vo onoi cells ac oss all adial su aces, om 𝑅𝑎 o 𝑅𝑏, defines he
3D cellula shape (Fig. 1B).
Fo us a ubes, we p oceed as p e iously desc ibed o define he
apical shape o he cells. Howe e , ins ead o p ojec ing he cell seeds,
we p ojec ed he cell e exes (Fig. 1B). Thus, he cell shape o a gi en
cell in a pa icula adial su ace is desc ibed by he in e sec ion o he
p ojec ed e exes. To c ea e he 3D shape o an indi idual cell, we
p oceed as p e iously desc ibed: combining he se o 2D cells ac oss
all adial su aces, om 𝑅𝑎 o 𝑅𝑏. Fig. 1C shows examples o ubula
epi helia simula ed using hese al e na i e app oaches. Ou esul s a e
ypically based on he analysis o 10 ealiza ions o each ubula config-
u a ion wi h 𝑁= 200 cells and he ollowing p ope ies: 𝑠𝑏=𝑅𝑏∕𝑅𝑎=
1.46875 ≃ 1.5( e e ed o as squamous cells), 𝑠𝑏=4 ( e e ed o as
cuboidal/columna cells), see also Table 1.
The exis ence and effec o apico-basal in e cala ions in Vo onoi
ubes is shown by he 3D his og am o cell neighbo s in Fig. 1D, i.e.,
Compu a ional and S uc u al Bio echnology Jou nal 27 (2025) 1204–1214
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Table 1
Cellula packing p ope ies in us a and Vo onoi ubes. A e age numbe
o neighbo s (in-plane polygonal o de , ⟨𝑛⟩), s anda d de ia ion (𝜎𝑛), and coe -
ficien o a ia ion (𝐶𝑉 ) in he apical and basal su aces o us a and Vo onoi
ubes. Apico-basal in e cala ions lead o g ea e diso de in he polygonal dis-
ibu ion o cuboidal/columna cells.
F us a ubes Vo onoi ubes
Apical /Basal Apical (𝑠=1) Basal (𝑠≃1.5) Basal (𝑠=4)
⟨𝑛⟩6.0 6.0 6.0 6.0
𝜎𝑛0.8 0.8 0.8 1
𝐶𝑉 =𝜎𝑛
⟨𝑛⟩0.13 0.13 0.13 0.17
he p obabili y 𝑃(𝑛𝑎,𝑛𝑏)o cells ha ing 𝑛𝑎neighbo s in he apical
su ace and 𝑛𝑏neighbo s in he basal su ace [15]. In us a ubes,
𝑃(𝑛𝑎,𝑛𝑏)=𝑃(𝑛𝑎)𝛿𝑛𝑏,𝑛𝑎=𝑃(𝑛𝑏)𝛿𝑛𝑎,𝑛𝑏(𝛿𝑖,𝑗 being he K onecke del a).
Tha is, he his og am only con ains en ies along he diagonal since
he e a e no changes in he nea es -neighbo ela ionship om apical o
basal. Howe e , in Vo onoi ubes, he en ies o he 3D his og am ou -
side he diagonal indica e apico-basal in e cala ions: some cells ei he
gained o los neighbo s be ween he apical and basal su aces.
2.4. Dimensionless uni s
In e ms o he cha ac e is ic leng h scale based on he cellula size,
𝑙𝑐=√⟨𝛼𝑎⟩, whe e ⟨𝛼𝑎⟩is he a e age a ea o cells a he apical
su ace (⟨𝛼𝑎⟩=⟨𝛼0⟩when conside ing only 2D cellula packing,
as in con ol simula ions; see Appendix), and he cha ac e is ic elax-
a ion/dissipa ion ime o he mechanical ene gy, 𝑡𝑐=𝛾∕(𝐾𝛼⟨𝑎
𝛼⟩), we
implemen a dimensionless o m o Eq. (1).
Using hese defini ions, he dimensionless elas ic pa ame e is se as

𝐾𝛼=1, while he adhesion and con ac ili y pa ame e s a e gi en by

Λ𝑖𝑗 =Λ𝑖𝑗∕(𝐾𝛼⟨𝛼𝑎⟩3∕2)and

Γ𝛼=Γ
𝛼∕(𝐾𝛼⟨𝑎
𝛼⟩), espec i ely.
Fu he mo e, when applying he omog aphic app oach owa d o ce
in e ence (see below), he dimensionless a ge cell a ea in he elas ic
null-s ess su ace (see below) is gi en by

𝛼0=𝛼0∕⟨𝛼𝑎⟩. Thus,
we pe o m an addi ional change o uni s such ha


𝛼0=1 (i.e.,
𝑙′
𝑐=√
𝛼0), leading o


𝐾𝛼 =1
,


Λ𝑖𝑗 =
Λ𝑖𝑗∕(
𝐴0
𝛼
3∕2), and


Γ𝛼=
Γ𝛼∕
𝐴0
𝛼.
Fo he sake o simplici y, we assume ha all quan i ies a e exp essed
in dimensionless uni s and omi he single and double o e -ha symbols.
2.5. Linea p og amming: omog aphic o ce in e ence
Dis ega ding bounda y effec s, in a issue comp ising 𝑁cells, he
equilib ium condi ion, Eq. (2), p o ides 2×2𝑁scala equa ions (on
a e age, each cell has six e exes sha ed by h ee cells) a any gi en
ime. Rega ding he numbe o unknowns, in a issue composed o cells
o he same ype (i.e., wi h supposedly iden ical mechanical p ope ies),
he numbe is jus ou (𝐴0, 𝐾, Γ, and Λ). Mo eo e , hese pa ame e s
can be educed o h ee (see Dimensionless uni s abo e), making he
sys em o equa ions in Eq. (2) o e de e mined and sol able.
Gi en ha he esul ing o ce balance equa ions desc ibed by Eq. (2)
a e linea in he unknowns (i.e., he pa ame e s Λ, Γ, e c.), we sol e
he o e de e mined sys em using a linea p og amming op imiza-
ion app oach and employ an 𝑙1-minimiza ion me hod [56]. The 𝑙1-
minimiza ion aims o find he minimum 𝑙1-no m solu ion o a linea
sys em 𝔸𝐗=𝔹, whe e 𝐗∈ℝ𝑚(i.e., 𝑚unknowns), 𝔹∈ℝ𝑝(𝑚<𝑝,
whe e 𝑝 ep esen s he o al numbe o e exes), and 𝔸∈ℝ𝑝×𝑚[57].
In ou s udy, we implemen he “L1-No m Minimiza ion” unc ion and
he “simplex” algo i hm in Wol am Ma hema ica [58] o de e mine he
op imal alues o he unknowns.
The omog aphic o ce in e ence app oach o 3D ubula issues
(Fig. 1E) assumes equilib ium a e e y alue o he apico-basal coo -
dina e (i.e., adial su ace) and sol es Eq. (2) simul aneously o all su -
aces, om 𝑅𝑎 o 𝑅𝑏. The adhesion pa ame e (ene gy pe uni leng h)
and 𝐴0( a ge cell a ea in he elas ic null-s ess plane, see below) a e
assumed o be he same o all alues along he apico-basal coo dina e,
while he con ac ili y pa ame e , Γ, is allowed o a y along he apico-
basal axis.
Thus, in a 3D con ex , he numbe o equa ions and unknowns a e
gi en by 2×2𝑁×𝑁su aces and 2+𝑁su aces (i.e., 𝐴0+Λ+𝑁su aces ×Γ),
espec i ely, whe e 𝑁su aces is he numbe o apico-basal su aces (i.e.,
adial “slices”) conside ed.
In he analyses p esen ed in his s udy o squamous and cuboidal/
columna issues, 𝑁su aces is 6and 7, espec i ely. As shown in he Ap-
pendix, ou con ol simula ions indica e ha he esul s emain obus
o diffe en alues o 𝑁su aces.
2.6. Elas ic null-s ess plane: ene gy as a unc ion o he apico-basal
coo dina e
Gi en an epi helial monolaye wi h 𝑁cells and issue dep h (i.e.,
cell heigh ) ℎ, i he issue is in a plana configu a ion (lacking ension-
comp ession s esses due o issue bending/cu a u e), hen he a e age
cell olume is ⟨𝑉⟩=⟨𝐴0⟩ℎ, whe e ⟨𝐴0⟩is he a ge a ea (Fig. 1F). On
he o he hand, i he same issue is shaped in o a ubula configu a ion,
wi h leng h 𝐿and apical and basal adii 𝑅𝑎and 𝑅𝑏, espec i ely, hen
he a e age cell olume is gi en by
⟨𝑉⟩=𝜋𝐿
𝑁(𝑅2
𝑏−𝑅2
𝑎).
I he cell heigh emains cons an , 𝑅𝑏−𝑅𝑎=ℎ, and he cell olume
is conse ed, i ollows ha
⟨𝐴0⟩=𝜋𝐿(𝑅𝑏+𝑅𝑎)
𝑁=𝑅𝑎𝜋𝐿(𝑠𝑏+1
)
𝑁=1
2⟨𝐴𝑎⟩(𝑠𝑏+1
),
whe e ⟨𝐴𝑎⟩is he cell apical a ea, and we define he dimensionless
apico-basal coo dina e 𝑠=𝑅∕𝑅𝑎, e e ed o as he su ace a io (𝑠𝑏=
𝑅𝑏∕𝑅𝑎).
The a e age elas ic ene gy o a gi en su ace a io eads:
⟨𝐸⟩𝐴=𝐾
2 ⟨(𝐴−𝐴0)2⟩=𝐸⟨𝐴⟩+𝐾
2
𝜎2
𝐴,
whe e 𝐸⟨𝐴⟩=𝐾
2 (⟨𝐴⟩−⟨𝐴0⟩)2is he elas ic ene gy o a cell wi h a e -
age a ea ⟨𝐴⟩, and 𝜎2
𝐴=⟨𝐴2⟩−⟨𝐴⟩2is he cellula a ea a iance. Cell
numbe conse a ion implies ha o a gi en su ace a io:
⟨𝐴⟩=2𝜋𝑅𝐿
𝑁=⟨𝐴𝑎⟩𝑠.
Consequen ly,
𝐸⟨𝐴⟩=𝐾⟨𝐴𝑎⟩2
2 (𝑠−1
2(𝑠𝑏+1
))2
.
The elas ic null-s ess plane, whe e 𝐸⟨𝐴⟩=0, is loca ed a :
𝑠∗=1
2(𝑠𝑏+1
)=⟨𝐴0⟩
⟨𝐴𝑎⟩.
F om he pe spec i e o plana elas ic de o ma ion, i 1≤𝑠<𝑠
∗, cells
a e unde comp ession, whe eas i 𝑠𝑏≥𝑠>𝑠
∗, cells a e unde ension.
Fu he mo e, since ⟨𝐿⟩∼⟨𝐴⟩1∕2 =(⟨𝐴𝑎⟩𝑠)1∕2, he a e age adhesion
and con ac ile ene gies, ⟨𝐸⟩𝐿and ⟨𝐸⟩𝐿2, espec i ely, scale as a unc-
ion o 𝑠as:
⟨𝐸⟩𝐿=𝐸⟨𝐿⟩=Λ⟨𝐿⟩∼Λ⟨𝐴𝑎⟩𝑠1∕2,
⟨𝐸⟩𝐿2=Γ
2
⟨𝐿2⟩=𝐸⟨𝐿2⟩+Γ
2
𝜎2
𝐿∼Γ
2
𝑠.
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Fig. 2. Con ac ili y in us a and Vo onoi ubes depending on he cellula
packing geome ies. Con ac ili y pa ame e as a unc ion o he su ace a io
(apico-basal coo dina e) as es ima ed by he in e ence me hod o us a (cyan)
and Vo onoi (yellow) geome ies in squamous (le ) and cuboidal/columna
( igh ) cells. The e o band accoun s o he s anda d de ia ion (10 samples).
3. Resul s
3.1. Fo ce in e ence e eals mechanical diffe ences be ween cell geome ies
We de eloped and implemen ed a o ce in e ence app oach based
on a e ex model pa ame iza ion (Me hods). Using con ol simula-
ions, we showed ha he p oposed in e ence me hodology is obus
o fini e-size and bounda y effec s and is also capable o cap u ing ime-
dependen mechanical pa ame e s accu a ely as long as hei empo al
a ia ion is slow compa ed o he ene gy dissipa ion ime scale (Ap-
pendix). We le e aged his la e ac o implemen a omog aphic ap-
p oach (i.e., plane by plane om he apical o he basal su ace) o 3D
o ce in e ence by exchanging he concep s o space and ime. This ool
was applied o in es iga e he mechanical cha ac e iza ion o epi helial
ubes based on hei cellula packing o ganiza ion and mo phological
p ope ies (Me hods). Specifically, we simula ed ubes composed o ei-
he cuboidal/columna o squamous epi helial cells and a ied hei
packing such ha apico-basal in e cala ions we e ei he allowed (scu-
oidal cell geome ies) o p ecluded ( us a cell geome ies).
We used dimensionless uni s such ha 𝐴0=1a he null-s ess plane
(𝑠∗=(𝑠𝑏+1)∕2) and assumed ha he pa ame e Λ(ene gy “cos ” pe
uni leng h) emains cons an along he apico-basal coo dina e, 𝑠(Me h-
ods). Howe e , we allowed he cell con ac ili y pa ame e o a y along
he apico-basal axis, i.e., Γ(𝑠). This assumes ha while cells adhe e o
each o he wi h he same “in ensi y,” co ical ac i i y may change as a
unc ion o he apico-basal coo dina e [59]. Fig. 2shows he es ima ed
con ac ili y pa ame e as a unc ion o he apico-basal coo dina e, 𝑠, o
us a and Vo onoi ubes using ei he squamous o cuboidal/columna
cells.
Fo a gi en ubula configu a ion (ei he squamous o cuboidal/colum-
na ), bo h cellula geome ies ( us a o Vo onoi) yielded simila con-
ac ili y alues and ends: Γdec eases as 𝑠inc eases (i.e., om apical
o basal) and app oaches ze o a he basal su ace. Howe e , diffe -
ences eme ged be ween ubula configu a ions, as cuboidal/columna
cells exhibi ed highe con ac ili y alues. In his ega d, we no e ha
he alue o ⟨
𝐴0
𝛼⟩diffe s be ween squamous and cuboidal/columna
cells (see Me hods, Dimensionless uni s):
⟨
𝐴0
𝛼⟩||||𝑠𝑏=4
⟨
𝐴0
𝛼⟩||||𝑠𝑏=1.5
≃2.
Consequen ly, using he same dimensionless uni s o cuboidal/colum-
na and squamous cells, he maximum con ac ili y pa ame e (apical
su ace) is app oxima ely ou imes la ge in cuboidal/columna cells
han in squamous cells.
Rega ding he line ension (adhesi eness), squamous cells displayed
simila alues o Vo onoi and us a geome ies:
ΛVo onoi =0.04 ± 0.01, Λ us a =0.03 ± 0.01.
Howe e , cuboidal/columna cells showed la ge diffe ences be ween
packing shapes:
ΛVo onoi =0.023 ± 0.009, Λ us a =0.0023 ± 0.002.
Fo he same dimensionless uni s, he adhesion pa ame e in Vo onoi
cuboidal/columna cells is ac ually la ge han in squamous cells (by
a ac o o ∼1.85), whe eas us a cuboidal/columna cells exhibi ed
significan ly lowe adhesion alues (∼0.185 o he alue obse ed in
squamous cells).
In summa y, he in e ence me hod e ealed ha co ical ac i i y,
as cha ac e ized by he con ac ili y pa ame e , is simila in us a and
Vo onoi ubes bu significan ly g ea e in cuboidal/columna cells com-
pa ed o squamous cells. In con as , o he line ension pa ame e ,
scu oid- ee ( us a) cuboidal/columna cells exhibi ed mechanical s a-
bili y ha depended on ex emely low adhesion alues —an o de o
magni ude smalle han ei he Vo onoi o us a cells in squamous ubes
o Vo onoi cells in cuboidal/columna ubes.
3.2. Ene gy p ofiles e eal he ole played by apico-basal in e cala ions in
cuboidal/columna epi helia
Once he mechanical pa ame e s o he ubula models we e cali-
b a ed, we compu ed he a e age cellula ene gy p ofiles (Me hods),
Fig. 3. These p ofiles p o ide a “map” om he apical o he basal
su ace, ep esen ing he cha ac e is ic alues o diffe en ene gy com-
ponen s and illus a ing he effec o apico-basal in e cala ions (cellu-
la geome y) in squamous (Fig. 3A-B) and cuboidal/columna cells
(Fig. 3C-D).
Fo squamous cells, we ob ained simila ene gy p ofiles o us a and
Vo onoi geome ies. Tha is, in squamous epi helia, modi ying he cellu-
la geome y om us a o Vo onoi —and consequen ly al e ing cellula
connec i i y [15]— does no con e an ene ge ic ad an age. We p opose
ha his could explain why he scu oidal shape has no ye been epo ed
in squamous cells (Discussion). Addi ionally, he unc ional beha io o
he diffe en ene gy componen s aligns wi h he heo e ical expec a ions
(Me hods). In pa icula , he elas ic ene gy eaches a minimum a he
apico-basal coo dina e:
𝑠∗=1
2(𝑠𝑏+1)= ⟨𝐴0⟩
⟨𝐴𝑎⟩,
which defines he elas ic null-s ess plane.
Fo he cuboidal/columna ubula model, he unc ional beha io
o he ene gy componen s as a unc ion o 𝑠is also in ag eemen wi h
he heo e ical expec a ions. Howe e , we obse ed significan quan i a-
i e and quali a i e diffe ences be ween packing geome ies, o igina ing
om he dissimila alues o he line- ension pa ame e . In us a ge-
ome ies, elas ic ene gy domina es om he apical o he basal su ace,
whe eas in Vo onoi cells, adhesion becomes dominan a ound he elas-
ic null-s ess plane. Addi ionally, ega ding o al ene gy, he a e age
cellula ene gy is highe in Vo onoi han in us a ubes. Howe e , his
obse a ion mus be conside ed in he con ex o issue s uc u al s a-
bili y. The low adhesi eness equi ed o balance mechanical o ces in
us a-columna ubes is a guably incompa ible wi h he unc ionali y
o eal issues (Discussion).
3.3. Apico-basal in e cala ions buffe shea s esses in cuboidal/columna
epi helia
We u he analyzed he a e age cell o ce p ofile o elucida e how
apico-basal in e cala ions shape he s abili y o he ubes. To ha end,
we compu ed he diffe en o ce e ms exe ed by he cells and pe -
o med a decomposi ion in o no mal and shea s esses (Me hods),
Fig. 4. No mal o ces exe ed by cells exhibi ed wo egimes as a unc-
ion o he apico-basal coo dina e, 𝑠: ei he an expansi e (⟨𝐹𝑛⟩>0) o
comp essi e (⟨𝐹𝑛⟩<0) beha io . As expec ed, he ac i e cellula con-
ac ile o ce is always comp essi e (i.e., poin ing inwa d, ⟨𝐹𝑛⟩<0) and

Compu a ional and S uc u al Bio echnology Jou nal 27 (2025) 1204–1214
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S. Anba i, P. Gómez-Gál ez, P. Vicen e-Munue a e al.
Fig. 3. Ene gy in e ence in squamous and cuboidal/columna ubula models depending on he cell packing geome y. A-B: A e age ene gy pe cell as a
unc ion o he su ace a io (apico-basal coo dina e) (Le ) and indi idual cell ene gies a he apical, null-s ess, and basal su aces (Righ ) in ep esen a i e us a
(A) and Vo onoi (B) squamous ubes sha ing he same packing configu a ion a he apical su ace. In he le panels, he e o bands co espond o he s anda d
de ia ion (10 samples), and he g een, yellow, and ed iangles indica e he alues o 𝑠a he apical, null-s ess, and basal planes, espec i ely. Colo scales in he
igh panels ange om minimum (whi e) o maximum alues. C-D: Same in o ma ion as in A-B panels o ubes o med by cuboidal/columna cells. No ice ha in
us a ubes, he lack o apico-basal in e cala ions o ces cells o s e ch.
is mo e p onounced a he apical su ace. Addi ionally, since he line-
ension pa ame e is posi i e, Λ>0, he adhesion o ce a o s cellula
comp ession h oughou he apico-basal axis.
Rega ding diffe ences in no mal o ces be ween packing config-
u a ions o squamous (Fig. 4A-B) and cuboidal/columna epi helia
(Fig. 4C-D), he no mal o ce is domina ed by elas ic e ms (i.e., cell
olume conse a ion) in all cases. Howe e , in cuboidal/columna ep-
i helia, us a packing esul s in weake no mal o ces nea he basal
su ace compa ed o Vo onoi packing.
Fo shea s ess, we fi s no e ha i s sign does no ha e a pa icu-
la physical meaning (Me hods). In squamous epi helia, he diffe ences
be ween us a and Vo onoi packing a e minimal, simila o he case o
no mal s esses, and he elas ic componen domina es o e adhesion and
con ac ile o ces. Addi ionally, shea s esses a e a mos wo o de s o
magni ude smalle han no mal s esses. In con as , in cuboidal/colum-
na epi helia, he elas ic componen emains dominan , bu quan i a i e
diffe ences a ise depending on cellula packing.
In us a ubes, he maximum shea o ce (a he basal su ace) is ap-
p oxima ely h ee imes la ge han in Vo onoi ubes. This esul s om
inc eased cell s e ching in us a ubes compa ed o scu oidal cells (see
Fig. 3C-D). Consequen ly, he balance be ween shea and no mal o ces,
||⟨𝐹𝑠⟩∕⟨𝐹𝑛⟩||, is la ge in us a packing a he basal su ace, whe e shea
s esses each a maximum:
||⟨𝐹𝑠⟩∕⟨𝐹𝑛⟩|| us a ≃(101)×||⟨𝐹𝑠⟩∕⟨𝐹𝑛⟩||Vo onoi
Finally, es ima ion o he ne o ces exe ed a cell e exes (Fig. 4,
bo om ow) e eals ha o ce balance is achie ed independen ly o
cellula packing and geome y.
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S. Anba i, P. Gómez-Gál ez, P. Vicen e-Munue a e al.
Fig. 4. Fo ce in e ence in squamous and cuboidal/columna ubula models depending on he cell packing geome y. A/B: A e age no mal ( op) and shea
(middle) o ces pe cell as a unc ion o he su ace a io (apico-basal coo dina e) in us a (A) and Vo onoi (B) ubes. The e o bands co espond o he s anda d
de ia ion om 10 samples, and he g een, yellow, and ed iangles indica e he alues o 𝑠a he apical, null-s ess, and basal su aces, espec i ely. C/D: Same
esul s as in A and B o ubes ep esen ing cuboidal/columna epi helia. In all cases, he plo s in he bo om ow depic he dis ibu ion (PDF) o ne o ces exe ed
on all cell e exes, demons a ing ha o ce balance is achie ed, 𝐅=(𝐹𝑥,𝐹𝑦)≃𝟎, ega dless o cellula packing.
4. Discussion
He ein, we ha e in oduced a no el 3D o ce/ene gy in e ence ap-
p oach ha ocuses on wo main aspec s: ob aining he a e age cellula
beha io in issues and pa ame e izing a e ex model o de e mine he
effec i e biophysical pa ame e s o cells. Ou me hodology employs a o-
mog aphic app oach ha de e mines o ce equilib ium plane by plane
along he apico-basal axis. The pa ame iza ion, based on mapping o
he e ex model, allows us o elucida e elas ic, adhesi e, and con ac ile
o ce componen s. In his con ex , we exploi ed he ac ha he o ce
equilib ium condi ion is linea in hese o ce pa ame e s o implemen
a linea p og amming op imiza ion app oach.
While cells and issues a e inhe en ly 3D s uc u es, echnical di -
ficul ies in ob aining accu a e imaging da a ha e long hinde ed he
de elopmen o o ce in e ence me hods in 3D. Recen ad ances in mi-
c oscopy and machine-lea ning-assis ed segmen a ion [19] ha e signi -
ican ly p og essed he field o 3D o ce in e ence [60]. Howe e , all
cu en me hods s ill ace limi a ions. Recen app oaches assume he
emb yo as a “ oam” in equilib ium [52], wi h u he imp o emen s
achie able using simula ion-based in e ence [61]. S ill, hese me hods
p ima ily p o ide ela i e alues o cellula p essu e and su ace en-
sion.
Ou app oach assumes ha cell shape de o ma ion is d i en by in-
plane o ces while o ces along he apico-basal axis a e negligible. This
app oxima ion is well jus ified by he expec ed beha io o elas ic ma e-
ials. Howe e , applying ou me hodology o eal expe imen al ubula
epi helia equi es cau ion. The p oposed analysis elies on he assump-
ion ha when un olling he cylinde (see Fig. 1F), adial planes p ese e
e ex- e ex dis ances and cell a eas. I his condi ion is no me , o ce
es ima ion a cell e exes may in oduce a i ac s. Consequen ly, ou
me hodology is bes sui ed o compu a ional s udies, whe e i p o ides
insigh s in o a key biological p oblem: how apico-basal in e cala ions
con ibu e o he s abili y and in eg i y o ubula epi helia. Along hese
lines, while he me hodology could, in p inciple, be adap ed o o he
epi helial s uc u es, such as sphe ical o o al epi helia, doing so would
equi e subs an ial modifica ions. Specifically, defining o ce balance in
a ully enclosed 3D s uc u e a he e exes whe e apico-basal in e cala-
ions occu would necessi a e he de elopmen o a no el ene gy/ o ce
unc ional o cu ed su aces whe e s able scu oids de elop spon a-
neously —one ha , o he bes o ou knowledge, has no ye been ei he
p oposed o es ed in epi helial mechanics. O e all, while ou app oach
is heo e ically ex endable o o he epi helial geome ies, i is specifi-
cally op imized and well-sui ed o analyzing ubula epi helia.
Impo an ly, modeling is he only easible way o in es iga e ou
ques ions o in e es , as cu en expe imen al echniques canno selec-
i ely modi y issue packing a chi ec u es. Since hei disco e y, scu-
oids ha e been ecu en ly ound in cuboidal/columna epi helia ha
ha e been analyzed in 3D. Examples include issues in mice, zeb afish,
D osophila, cell cul u es, and o ganoids, suppo ing he gene ali y o his
packing shape. Howe e , o he bes o ou knowledge no s udy has e-
po ed he exis ence o scu oidal cell shapes in squamous epi helia. He e,
we explo ed he biophysical basis o his phenomenon by compa ing
ubula issues wi h wo diffe en su ace a ios, 𝑠𝑏≃1.5and 𝑠𝑏=4.
The logic unde lying his analysis is as ollows. I has been epo ed
ha a lowe alue o 𝑠𝑏co ela es wi h a educed numbe o scu oidal
cells [14], as he sho e heigh o hese cells limi s neighbo exchanges
along he apico-basal axis. This sugges s ha ubula epi helia wi h ei-
he us a o scu oidal cell packing can be ene ge ically compa ible and
main ain in eg i y a low alues o 𝑠𝑏. To simpli y, we use 𝑠𝑏≃1.5 ubes
as a model o squamous issue o p o ide a baseline o unde s anding
he esul s ob ained o 𝑠𝑏=4(cuboidal/columna model). Howe e , in
eal biological issues, squamous cells ypically exhibi e en lowe al-
ues o 𝑠𝑏. Indeed, ou simula ions e eal ha in 𝑠𝑏≃1.5Vo onoi ubes,
scu oids de elop in app oxima ely 35 ± 6% o cells. Taken oge he , ou
findings indica e ha in squamous issues subjec ed o cu a u e, us a
and scu oidal cell packing esul in simila ene gy and o ce p ofiles
(Figs. 3A-B and 4A-B). Thus, we p opose ha in eal issues, squamous
cells do no de i e any biophysical ad an age (ene ge ically speaking)
om emodeling hei mo phology in o a scu oidal shape.
Howe e , in cuboidal/columna issues, when apico-basal in e ca-
la ions a e supp essed (i.e., us a cell shapes), o ce equilib ium can
Compu a ional and S uc u al Bio echnology Jou nal 27 (2025) 1204–1214
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S. Anba i, P. Gómez-Gál ez, P. Vicen e-Munue a e al.
only be achie ed wi h ex emely low le els o cellula adhesion—
app oxima ely an o de o magni ude lowe han in sho squamous
cells. Such low adhesion is bo h un ealis ic and incompa ible wi h ep-
i helial in eg i y, whe e igh cell packing is essen ial. Fu he mo e, p e-
en ing apico-basal in e cala ions in cuboidal/columna cells dis up s
he balance be ween no mal and shea o ces, u he challenging issue
in eg i y. This imbalance is linked o basal su ace de o ma ion in us a
cells when 𝑠𝑏=4(Fig. 3C) bu is absen in squamous epi helia (𝑠𝑏≃1.5,
Fig. 3A). Con e sely, when apico-basal in e cala ions a e allowed in
cuboidal/columna issues, cellula adhesion alues a e highe han in
squamous cells, and he balance be ween shea and no mal o ces is
mo e compa ible wi h issue homeos asis, as no mal o ces clea ly dom-
ina e o e shea o ces (Fig. 4D).
In a b oade con ex , ecen s udies on 2D epi helial packing dynam-
ics ha e shown ha an inc ease in cell junc ion ension upon con ac ion
and a educ ion in ension upon ex ension can s abilize highe -o de
(e.g., ou - old) e ices [62]. Ex ending his o a 3D con ex , apico-basal
in e cala ions, es ablished by ou -cellula junc ions along he apico-
basal axis, may play a key ole in esol ing uns able cell geome ies
esul ing om cons ain s du ing issue packing while main aining is-
sue in eg i y, as demons a ed in ou s udy. Al hough ou wo k sheds
ligh on he ole o apico-basal in e cala ions in s a ic 3D epi helial
ubes, he mechanics unde lying cell dynamics du ing mo phogenesis—
while simul aneously accoun ing o s a iona y apico-basal in e cala-
ions and cell di ision— emain la gely unknown. Despi e ecen effo s
[20,22,63], u he esea ch is needed o elucida e he in e play be ween
mechanics and scu oid dynamics o be e unde s and complex p ocesses
such as issue g ow h and ea angemen , wound healing, cell ex usion,
and cell mig a ion.
CRediT au ho ship con ibu ion s a emen
Sami a Anba i: So wa e, Me hodology, In es iga ion. Ped o
Gómez-Gál ez: W i ing – e iew & edi ing, W i ing – o iginal d a ,
Visualiza ion, Valida ion, So wa e, Me hodology, In es iga ion. Pablo
Table 2
Pa ame e in e ence: fini e size effec s. G ound u h and es ima ed e ex
model pa ame e s alues as a unc ion o he a io 𝜌=𝑁𝑝∕𝑁.
Pa ame e G ound
T u h
𝜌=0.7𝜌=0.57 𝜌=0.51
(𝑁=20, 𝑁𝑝=14) (𝑁=30, 𝑁𝑝=17) (𝑁=45, 𝑁𝑝=23)
𝐴01.000 1.023 (𝛿=2.3%) 1.015 (𝛿=1.5%) 1.001 (𝛿=0.1%)
Λ 0.040 0.043 (𝛿=5.5%) 0.042 (𝛿=5%) 0.041 (𝛿=2.5%)
Γ 0.02 0.022 (𝛿= 10%) 0.021 (𝛿=5%) 0.020 (𝛿=0%)
Table 3
Pa ame e in e ence: diffe en ene gy egimes. G ound u h and es ima ed
e ex model pa ame e s alues in diffe en scena ios wi h espec o he domi-
nan ene ge ic con ibu ion.
Pa ame e Case A (elas ic dominan ) Case B (con ac ile dominan )
G ound T u h Es ima ion G ound T u h Es ima ion
𝐴02 2.001 (𝛿=0.05%) 1 1.002 (𝛿=0.2%)
Λ 0.04 0.041 (𝛿=2.5%) −0.02 −0.02 (𝛿=0%)
Γ 0.02 0.02 (𝛿=0%) 0.02 0.02 (𝛿=0%)
Fig. 5. In e ence o cell ene gy componen s: fini e-size effec s. A: Compa ison o cellula ene gies be ween es ima ed and g ound u h alues as a unc ion o
he a io 𝜌(𝑁and 𝑁𝑝a e indica ed in Table 2). Ci cles co espond o indi idual cells. A sp eading away om he diagonal indica es a misma ch be ween es ima ed
and g ound u h alues. B: Cell ene gy componen s in simula ed issues (colo code as in panel A); columns co esponds o he alues o 𝜌indica ed in panel A. The
scale ba s ange be ween he obse ed minimum and maximum o he ene gy alues in all cases.
Compu a ional and S uc u al Bio echnology Jou nal 27 (2025) 1204–1214
1212
S. Anba i, P. Gómez-Gál ez, P. Vicen e-Munue a e al.
Vicen e-Munue a: Visualiza ion, Me hodology. Luis M. Escude o:
W i ing – e iew & edi ing, W i ing – o iginal d a , Valida ion, Supe i-
sion, Funding acquisi ion, Concep ualiza ion. Ja ie Buce a: W i ing –
e iew & edi ing, W i ing – o iginal d a , Visualiza ion, Valida ion, Su-
pe ision, So wa e, Me hodology, In es iga ion, Funding acquisi ion,
Fo mal analysis, Concep ualiza ion.
Decla a ion o compe ing in e es
Decla e ha none o he au ho s: Ha e an undisclosed ela ionship
ha may pose a compe ing in e es ; Ha e an undisclosed unding sou ce
ha may pose a compe ing in e es .
Acknowledgemen s
This wo k was suppo ed by he Minis e io de Ciencia e Inno-
ación o Spain h ough g an s PID2019-103900GB-I00 AEI/10.13039/
501100011033 (L.M.E.), PID2022-137101NB-I00/AEI/10.13039/
501100011033/FEDER UE (L.M.E.), PID2022-137436NB-I00 (J.B.),
PID2019-105566GB-I00 (J.B.) and om he Li eHUB Resea ch Ne -
wo k h ough g an PIE-202120E047-ConexionesLi e (CSIC). P.G.-G.
has been unded by he Ma ga i a Salas p og am – Nex Gene a-
ion E.U. J.B. also ecei ed unding om he esea ch ne wo k
RED2022-134573-T unded by Minis e io de Ciencia e Inno ación
(MCIN/AEI/10.13039/501100011033) and by ‘ERDF: A way o mak-
ing Eu ope’, by he Eu opean Union. L.M.E. and J.B. ecei ed addi ional
suppo om he E.U. COST ac ion CA22153 ‘Eu opean Cu a u e and
Biology Ne wo k’ (Eu oCu oBioNe ).
Appendix A. Con ol simula ions
We an con ol simula ions using he e ex model o es he eli-
abili y o he o ce in e ence me hod. To ha end, we used he TiFoSi
package [64,65]. In addi ion o he pa ame e s ha desc ibe he cell me-
chanical p ope ies (i.e., he pa ame e s o be in e ed), we in oduced
some le el o s ochas ici y in he du a ion o he cell cycle o achie e di -
e en cellula sizes a a gi en ime. Thus, he du a ion o he cell cycle,
𝜏, is defined as,
𝜏=𝜖𝑡𝑑𝑒𝑡. +(1−𝜖)𝑡𝑠𝑡𝑜.
whe e 𝑡𝑑𝑒𝑡. is a de e minis ic ime scale ha accoun s o a mean cell
cycle du a ion and 𝑡𝑠𝑡𝑜. is a andom a iable ha accoun s o he a i-
abili y o cell cycle du a ion and ha is assumed o ollow an exponen ial
dis ibu ion:
𝜌(𝑡𝑠𝑡𝑜.)=𝑒−𝑡𝑠𝑡𝑜.
𝑡𝑑𝑒𝑡.
𝑡𝑑𝑒𝑡.
We se a alue o 𝜖=0.8 o he pa ame e ha weigh s he s ochas-
ici y o he cell-cycle du a ion (see [64,65] o de ails), and we se a
dimensionless a e age cell cycle du a ion o ⟨𝜏⟩=1.5⋅103(∼20hou s)
in all simula ions.
Con ol simula ions we e pe o med in wo s ages. Fi s , we allowed
cells o g ow and di ide un il he issue eached a gi en numbe o
cells, 𝑁. Du ing he second s age, we s opped cellula g ow h and ei-
he allowed he issue o mechanically elax o a s able configu a ion
o modula ed some mechanical p ope ies as a unc ion o ime o d i e
he sys em ou o equilib ium. Since cell e exes a he issue pe iphe y
a e sha ed by ei he one o wo cells, in con as o e exes in he issue
bulk ha a e sha ed by h ee cells, we fi s es ed he sensi i i y o ou
me hod o fini e-size (i.e., bounda y) effec s. To do so, we used he same
alues o he 𝐴0, Λ, and Γpa ame e s bu a ied he a io 𝜌=𝑁𝑝∕𝑁,
whe e 𝑁𝑝is he numbe o pe iphe al cells. Since 𝜌∼1∕
√𝑁, be e in-
e ence esul s a e expec ed as 𝑁inc eases (i.e., as 𝜌dec eases). The
esul s (Table 3) indica e ha as 𝜌app oaches ∼0.5, he obse ed e -
o , 𝛿, in he in e ed pa ame e s emains below 3% and s ays unde
10% e en in issues whe e bounda y effec s a e dominan (𝜌=0.7).
Once he pa ame e s 𝐴0, Λ, and Γwe e compu ed, we es ima ed in
each simula ion he ene gy componen s o each cell 𝑘:
𝐸elas ic
𝑘=1
2(𝐴𝑘−𝐴0)2
𝐸con ac .
𝑘=Γ
2
𝐿2
𝑘(A.1)
𝐸adh.
𝑘=Λ𝐿𝑘
Fig. 5shows ha con e gence o g ound u h alues is achie ed as 𝜌
app oaches ∼0.5.
We u he checked he obus ness o he in e ence me hod agains
he ela i e impo ance o diffe en ene gy con ibu ions. To ha end,
we pe o med con ol simula ions using diffe en pa ame e se s while
keeping 𝑁cons an . Table 3and Fig. 6show wo ep esen a i e cases
whe e Γis kep he same bu 𝐴0and Λchange such ha ei he he
con ac ile o he elas ic ene gy becomes he dominan ene ge ic con-
ibu ion (in con as o he simula ions shown in Fig. 5whe e he
adhesion ene gy is dominan ). The in e ence esul s emain in excellen
ag eemen wi h g ound u h alues ega dless o he dominan ene gy
componen .
Finally, we e alua e he eliabili y o he o ce in e ence app oach
when he mechanical pa ame e s a e modula ed in ime. In his ega d,
he ime scale o mechanical ene gy elaxa ion is 𝑡𝑟≃1(dimension-
less ime uni s). Thus, o ce equilib ium is eached a imes 𝑇≫1(i.e.,
𝑡𝑟∕𝑇≪1). This sugges s ha a dynamic modula ion o mechanical pa-
Fig. 6. In e ence o cell ene gy componen s: diffe en dominan con ibu-
ions. A/B: Elas ic/con ac ile ene gy dominan issues. In bo h cases 𝑁=45
and e ex model pa ame e s as shown in Table 3. In A ci cles co espond o in-
di idual cells. In B he colo code o cell ene gy componen s as in panel A and
he columns co esponds o he cases shown in panel A. The scale ba s ange be-
ween he obse ed minimum and maximum alues o he ene gy in all cases.
We no ice ha nega i e alues o he adhesion ene gy ob ained when Λ<0a e
because he alue o he line ension pa ame e is aken in o accoun in he cal-
cula ion o 𝐸adh. as s a ed in Eq. (A.1).