scholarly journals Cell-Polarity Dynamics Controls the Mechanism of Lumen Formation in Epithelial Morphogenesis

2008 ◽  
Vol 18 (8) ◽  
pp. 630
Author(s):  
Fernando Martín-Belmonte ◽  
Wei Yu ◽  
Alejo E. Rodríguez-Fraticelli ◽  
Andrew J. Ewald ◽  
Zena Werb ◽  
...  
2008 ◽  
Vol 18 (7) ◽  
pp. 507-513 ◽  
Author(s):  
Fernando Martín-Belmonte ◽  
Wei Yu ◽  
Alejo E. Rodríguez-Fraticelli ◽  
Andrew Ewald ◽  
Zena Werb ◽  
...  

2008 ◽  
Vol 18 (13) ◽  
pp. 1016
Author(s):  
Fernando Martín-Belmonte ◽  
Wei Yu ◽  
Alejo E. Rodríguez-Fraticelli ◽  
Andrew J. Ewald ◽  
Zena Werb ◽  
...  

2008 ◽  
Vol 295 (2) ◽  
pp. C545-C556 ◽  
Author(s):  
Marion Desclozeaux ◽  
Juliana Venturato ◽  
Fiona G. Wylie ◽  
Jason G. Kay ◽  
Shannon R. Joseph ◽  
...  

The correct targeting and trafficking of the adherens junction protein epithelial cadherin (E-cadherin) is a major determinant for the acquisition of epithelial cell polarity and for the maintenance of epithelial integrity. The compartments and trafficking components required to sort and transport E-cadherin to the basolateral cell surface remain to be fully defined. On the basis of previous data, we know that E-cadherin is trafficked via the recycling endosome (RE) in nonpolarized and newly polarized cells. Here we explore the role of the RE throughout epithelial morphogenesis in MDCK monolayers and cysts. Time-lapse microscopy in live cells, altering RE function biochemically, and expressing a dominant-negative form of Rab11 (DN-Rab11), each showed that the RE is always requisite for E-cadherin sorting and trafficking. The RE remained important for E-cadherin trafficking in MDCK cells from a nonpolarized state through to fully formed, polarized epithelial monolayers. During the development of epithelial cysts, DN-Rab11 disrupted E-cadherin targeting and trafficking, the subapical localization of pERM and actin, and cyst lumen formation. This final effect demonstrated an early and critical interdependence of Rab11 and the RE for E-cadherin targeting, apical membrane formation, and cell polarity in cysts.


2015 ◽  
Vol 212 (1) ◽  
pp. 113-124 ◽  
Author(s):  
Nduka O. Enemchukwu ◽  
Ricardo Cruz-Acuña ◽  
Tom Bongiorno ◽  
Christopher T. Johnson ◽  
José R. García ◽  
...  

Epithelial cells cultured within collagen and laminin gels proliferate to form hollow and polarized spherical structures, recapitulating the formation of a rudimentary epithelial organ. However, the contributions of extracellular matrix (ECM) biochemical and biophysical properties to morphogenesis are poorly understood because of uncontrolled presentation of multiple adhesive ligands, limited control over mechanical properties, and lot-to-lot compositional variability in these natural ECMs. We engineered synthetic ECM-mimetic hydrogels with independent control over adhesive ligand density, mechanical properties, and proteolytic degradation to study the impact of ECM properties on epithelial morphogenesis. Normal cyst growth, polarization, and lumen formation were restricted to a narrow range of ECM elasticity, whereas abnormal morphogenesis was observed at lower and higher elastic moduli. Adhesive ligand density dramatically regulated apicobasal polarity and lumenogenesis independently of cell proliferation. Finally, a threshold level of ECM protease degradability was required for apicobasal polarity and lumen formation. This synthetic ECM technology provides new insights into how cells transduce ECM properties into complex morphogenetic behaviors.


2008 ◽  
Vol 20 (2) ◽  
pp. 227-234 ◽  
Author(s):  
Fernando Martin-Belmonte ◽  
Keith Mostov

Cell Cycle ◽  
2008 ◽  
Vol 7 (1) ◽  
pp. 57-62 ◽  
Author(s):  
Arnaud A. Mailleux ◽  
Michael Overholtzer ◽  
Joan S. Brugge

2012 ◽  
Vol 23 (15) ◽  
pp. 2845-2855 ◽  
Author(s):  
Kazunori Senga ◽  
Keith E. Mostov ◽  
Toshihiro Mitaka ◽  
Atsushi Miyajima ◽  
Naoki Tanimizu

During development, epithelial progenitors establish intercellular junctions, including tight junctions (TJs), and form three-dimensional (3D) tissue structures, which are often associated with luminal structures. Here we identify grainyhead-like 2 (Grhl2) as a transcription factor that regulates the size of luminal space surrounded by polarized epithelial cells. We show that HPPL, a liver progenitor cell line, transfected with Grhl2 cDNA forms remarkably larger cysts than the control cells in 3D cultures. We find that Grhl2 up-regulates claudin (Cldn) 3 and Cldn4, and their functions are necessary for the formation of large cysts. Overexpression of Cldn3 alone induces the cyst expansion. In contrast, expression of Cldn4 alone does not induce expansion, as it is not localized at TJs. Of interest, Rab25, another Grhl2 target, not only increases the Cldn4 protein, but also enhances its localization at TJs. Taken together, the results indicate that Grhl2 regulates epithelial morphogenesis through transcriptional up-regulation of Cldn3 and Cldn4, as well as of Rab25, which increases the Cldn4 protein and its localization at TJs. The results reveal a molecular network regulating epithelial lumen formation organized by Grhl2.


2002 ◽  
Vol 158 (5) ◽  
pp. 941-951 ◽  
Author(s):  
Emmanuelle Médina ◽  
Janice Williams ◽  
Elizabeth Klipfell ◽  
Daniela Zarnescu ◽  
Graham Thomas ◽  
...  

The apical transmembrane protein Crumbs is necessary for both cell polarization and the assembly of the zonula adherens (ZA) in Drosophila epithelia. The apical spectrin-based membrane skeleton (SBMS) is a protein network that is essential for epithelial morphogenesis and ZA integrity, and exhibits close colocalization with Crumbs and the ZA in fly epithelia. These observations suggest that Crumbs may stabilize the ZA by recruiting the SBMS to the junctional region. Consistent with this hypothesis, we report that Crumbs is necessary for the organization of the apical SBMS in embryos and Schneider 2 cells, whereas the localization of Crumbs is not affected in karst mutants that eliminate the apical SBMS. Our data indicate that it is specifically the 4.1 protein/ezrin/radixin/moesin (FERM) domain binding consensus, and in particular, an arginine at position 7 in the cytoplasmic tail of Crumbs that is essential to efficiently recruit both the apical SBMS and the FERM domain protein, DMoesin. Crumbs, Discs lost, βHeavy-spectrin, and DMoesin are all coimmunoprecipitated from embryos, confirming the existence of a multimolecular complex. We propose that Crumbs stabilizes the apical SBMS via DMoesin and actin, leading to reinforcement of the ZA and effectively coupling epithelial morphogenesis and cell polarity.


2010 ◽  
Vol 18 (1) ◽  
pp. 39-51 ◽  
Author(s):  
Ann C. Zovein ◽  
Alfonso Luque ◽  
Kirsten A. Turlo ◽  
Jennifer J. Hofmann ◽  
Kathleen M. Yee ◽  
...  

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