scholarly journals Dynamics of cell polarity in tissue morphogenesis: a comparative view from Drosophila and Ciona

F1000Research ◽  
2016 ◽  
Vol 5 ◽  
pp. 1084 ◽  
Author(s):  
Michael T. Veeman ◽  
Jocelyn A. McDonald

Tissues in developing embryos exhibit complex and dynamic rearrangements that shape forming organs, limbs, and body axes. Directed migration, mediolateral intercalation, lumen formation, and other rearrangements influence the topology and topography of developing tissues. These collective cell behaviors are distinct phenomena but all involve the fine-grained control of cell polarity. Here we review recent findings in the dynamics of polarized cell behavior in both the Drosophila ovarian border cells and the Ciona notochord. These studies reveal the remarkable reorganization of cell polarity during organ formation and underscore conserved mechanisms of developmental cell polarity including the Par/atypical protein kinase C (aPKC) and planar cell polarity pathways. These two very different model systems demonstrate important commonalities but also key differences in how cell polarity is controlled in tissue morphogenesis. Together, these systems raise important, broader questions on how the developmental control of cell polarity contributes to morphogenesis of diverse tissues across the metazoa.

2006 ◽  
Vol 11 (4) ◽  
pp. 459-470 ◽  
Author(s):  
J. Todd Blankenship ◽  
Stephanie T. Backovic ◽  
Justina S.P. Sanny ◽  
Ori Weitz ◽  
Jennifer A. Zallen

2007 ◽  
Vol 306 (1) ◽  
pp. 305
Author(s):  
James T. Blankenship ◽  
Justina Sanny ◽  
Ori Weitz ◽  
Jennifer Zallen

2011 ◽  
Vol 21 (1) ◽  
pp. 120-133 ◽  
Author(s):  
Ryan S. Gray ◽  
Isabelle Roszko ◽  
Lilianna Solnica-Krezel

eLife ◽  
2020 ◽  
Vol 9 ◽  
Author(s):  
Margot LK Williams ◽  
Lilianna Solnica-Krezel

During vertebrate gastrulation, convergence and extension (C and E) of the primary anteroposterior (AP) embryonic axis is driven by polarized mediolateral (ML) cell intercalations and is influenced by AP axial patterning. Nodal signaling is essential for patterning of the AP axis while planar cell polarity (PCP) signaling polarizes cells with respect to this axis, but how these two signaling systems interact during C and E is unclear. We find that the neuroectoderm of Nodal-deficient zebrafish gastrulae exhibits reduced C and E cell behaviors, which require Nodal signaling in both cell- and non-autonomous fashions. PCP signaling is partially active in Nodal-deficient embryos and its inhibition exacerbates their C and E defects. Within otherwise naïve zebrafish blastoderm explants, however, Nodal induces C and E in a largely PCP-dependent manner, arguing that Nodal acts both upstream of and in parallel with PCP during gastrulation to regulate embryonic axis extension cooperatively.


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