کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
5532020 1401826 2016 11 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
The hyaloid vasculature facilitates basement membrane breakdown during choroid fissure closure in the zebrafish eye
ترجمه فارسی عنوان
ویسکوزیته هیالوئید تخریب غشاء زیرزمین را در طی بسته شدن شکاف کوروئید در چشم زبرافیش تسهیل می کند
موضوعات مرتبط
علوم زیستی و بیوفناوری بیوشیمی، ژنتیک و زیست شناسی مولکولی بیولوژی سلول
چکیده انگلیسی


• Utilizing zebrafish as a model to identify the cellular and molecular underpinnings of choroid fissure closure.
• Choroid fissure closure can be segregated into three stages: optic cup growth/morphogenesis, basement membrane breakdown, and fusion.
• The hyaloid vasculature and/or the POM-derived endothelial cells that give rise the hyaloid vasculature contribute to basement membrane breakdown during CF closure.

A critical aspect of vertebrate eye development is closure of the choroid fissure (CF). Defects in CF closure result in colobomas, which are a significant cause of childhood blindness worldwide. Despite the growing number of mutated loci associated with colobomas, we have a limited understanding of the cell biological underpinnings of CF closure. Here, we utilize the zebrafish embryo to identify key phases of CF closure and regulators of the process. Utilizing Laminin-111 as a marker for the basement membrane (BM) lining the CF, we determine the spatial and temporal patterns of BM breakdown in the CF, a prerequisite for CF closure. Similarly, utilizing a combination of in vivo time-lapse imaging, β-catenin immunohistochemistry and F-actin staining, we determine that tissue fusion, which serves to close the fissure, follows BM breakdown closely. Periocular mesenchyme (POM)-derived endothelial cells, which migrate through the CF to give rise to the hyaloid vasculature, possess distinct actin foci that correlate with regions of BM breakdown. Disruption of talin1, which encodes a regulator of the actin cytoskeleton, results in colobomas and these correlate with structural defects in the hyaloid vasculature and defects in BM breakdown. cloche mutants, which entirely lack a hyaloid vasculature, also possess defects in BM breakdown in the CF. Taken together, these data support a model in which the hyaloid vasculature and/or the POM-derived endothelial cells that give rise to the hyaloid vasculature contribute to BM breakdown during CF closure.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Developmental Biology - Volume 419, Issue 2, 15 November 2016, Pages 262–272