ZFIN ID: ZDB-PUB-140928-4
Spatial pattern of cell geometry and cell-division orientation in zebrafish lens epithelium
Mochizuki, T., Suzuki, S., Masai, I.
Date: 2014
Source: Biology Open 3(10): 982-94 (Journal)
Registered Authors: Masai, Ichiro, Mochizuki, Toshiaki
Keywords: E-cadherin, cell division, cell proliferation, lens, zebrafish
MeSH Terms: none
PubMed: 25260917 Full text @ Biol. Open
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ABSTRACT
Cell proliferation is a key regulator of tissue morphogenesis. We examined cell proliferation and cell division in zebrafish lens epithelium by visualizing cell-cycle phases and nuclear positions, using fluorescent-labeled geminin and histone proteins. Proliferation was low in the anterior region of lens epithelium and higher in the marginal zone anterior to the equator, suggesting that the proliferation zone, called the germinative zone, is formed in zebrafish lens. Interestingly, cell-division orientation was biased longitudinally in the anterior region, shifted from longitudinal to circumferential along the anterior-posterior axis of lens sphere, and was biased circumferentially in the peripheral region. These data suggest that cell-division orientation is spatially regulated in zebrafish lens epithelium. The Hertwig rule indicates that cells tend to divide along their long axes. Orientation of long axes and cell division were biased similarly in zebrafish lens epithelium, suggesting that cell geometry correlates with cell-division orientation. A cell adhesion molecule, E-cadherin, is expressed in lens epithelium. In a zebrafish e-cadherin mutant, the long axes and cell-division orientation were shifted more longitudinally. These data suggest that E-cadherin is required for the spatial pattern of cell geometry and cell-division orientation in zebrafish lens epithelium.
ADDITIONAL INFORMATIONNo data available