Cell adhesion marker expression dynamics during fusion of the optic fissure

IF 1 4区 生物学 Q4 DEVELOPMENTAL BIOLOGY Gene Expression Patterns Pub Date : 2023-10-14 DOI:10.1016/j.gep.2023.119344
Holly Hardy, Joe Rainger
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引用次数: 0

Abstract

Tissue fusion is a critical process that is repeated in multiple contexts during embryonic development and shares common attributes to processes such as wound healing and metastasis. Ocular coloboma is a developmental eye disorder that presents as a physical gap in the ventral eye, and is a major cause of childhood blindness. Coloboma results from fusion failure between opposing ventral retinal epithelia, but there are major knowledge gaps in our understanding of this process at the molecular and cell behavioural levels. Here we catalogue the expression of cell adhesion proteins: N-cadherin, E-cadherin, R-cadherin, ZO-1, and the EMT transcriptional activator and cadherin regulator SNAI2, in the developing chicken embryonic eye. We find that fusion pioneer cells at the edges of the fusing optic fissure have unique and dynamic expression profiles for N-cad, E-cad and ZO-1, and that these are temporally preceded by expression of SNAI2. This highlights the unique properties of these cells and indicates that regulation of cell adhesion factors may be a critical process in optic fissure closure.

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视裂融合过程中细胞粘附标记物的表达动态。
组织融合是胚胎发育过程中在多种情况下重复的一个关键过程,与伤口愈合和转移等过程有着共同的特点。眼部缺损是一种发育性眼部疾病,表现为腹侧眼睛的物理间隙,是儿童失明的主要原因。睑板是由相对的腹侧视网膜上皮融合失败引起的,但在分子和细胞行为水平上,我们对这一过程的理解存在重大知识差距。在这里,我们对细胞粘附蛋白的表达进行了分类:N-钙粘蛋白、E-钙粘蛋白和R-钙粘蛋白,ZO-1,以及EMT转录激活剂和钙粘蛋白调节因子SNAI2,在发育中的鸡胚胎眼中。我们发现,融合视裂边缘的融合先驱细胞具有独特的N-cad、E-cad和ZO-1的动态表达谱,并且这些表达在时间上先于SNAI2的表达。这突出了这些细胞的独特特性,并表明细胞粘附因子的调节可能是视裂闭合的关键过程。
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来源期刊
Gene Expression Patterns
Gene Expression Patterns 生物-发育生物学
CiteScore
2.30
自引率
0.00%
发文量
42
审稿时长
35 days
期刊介绍: Gene Expression Patterns is devoted to the rapid publication of high quality studies of gene expression in development. Studies using cell culture are also suitable if clearly relevant to development, e.g., analysis of key regulatory genes or of gene sets in the maintenance or differentiation of stem cells. Key areas of interest include: -In-situ studies such as expression patterns of important or interesting genes at all levels, including transcription and protein expression -Temporal studies of large gene sets during development -Transgenic studies to study cell lineage in tissue formation
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