维甲酸对再生斑马鱼鳍关节形成过程中连接蛋白43表达的影响。

IF 1.6 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Bioelectricity Pub Date : 2023-09-01 Epub Date: 2023-09-12 DOI:10.1089/bioe.2023.0018
Alexander W Seaver, Noah S Weaver, M Kathryn Iovine
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引用次数: 0

摘要

背景:再生的斑马鱼鳍骨架由多条骨鳍组成,每条骨鳍由交替的骨段和鳍鳍关节组成。这种模式由间隙连接蛋白连接蛋白43(Cx43)调节,它为骨骼前体细胞(SPC)提供指导线索。Cx43升高有利于成骨细胞分化,不利于关节形成细胞分化。本文的目的是测试视黄酸(RA)是否有助于调节cx43的表达。材料和方法:使用原位杂交来监测基因表达,并测量鳍鱼节段的长度来监测对SPC分化和关节形成的影响,评估抑制RA合成酶Adh1a2的功能研究。结果:Aldh12a2敲低导致cx43的表达减少,evx1的表达增加,evx1是关节形成所需的基因。此外,Aldh12a2功能的抑制导致短鳍射线段。我们还发现了aldh1a2和cx43之间协同作用的证据,表明这些基因在调节关节形成的共同分子途径中发挥作用。结论:RA的作用是促进cx43在再生鳍中的表达,以调节关节的形成和骨鳍段的长度。我们认为RA信号传导必须与其他调节cx43转录的途径协调。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Retinoic Acid Influences connexin43 Expression During Joint Formation in the Regenerating Zebrafish Fin.

Background: The regenerating zebrafish fin skeleton is comprised of multiple bony fin rays, each made of alternating bony segments and fin ray joints. This pattern is regulated by the gap junction protein Connexin43 (Cx43), which provides instructional cues to skeletal precursor cells (SPCs). Elevated Cx43 favors osteoblast differentiation and disfavors joint forming cell differentiation. The goal of this article is to test if retinoic acid (RA) contributes to the regulation of cx43 expression.

Materials and methods: Functional studies inhibiting the RA-synthesizing enzyme Adh1a2 were evaluated using in situ hybridization to monitor gene expression and with measurements of the length of fin ray segments to monitor impacts on SPC differentiation and joint formation.

Results: Aldh1a2-knockdown leads to reduced expression of cx43 and increased expression of evx1, a gene required for joint formation. Additionally, inhibition of Aldh1a2 function leads to short fin ray segments. We also find evidence for synergy between aldh1a2 and cx43, suggesting that these genes function in a common molecular pathway to regulate joint formation.

Conclusions: The role of RA is to promote cx43 expression in the regenerating fin to regulate joint formation and the length of bony fin ray segments. We suggest that RA signaling must coordinate with additional pathways that also regulate cx43 transcription.

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来源期刊
Bioelectricity
Bioelectricity Multiple-
CiteScore
3.40
自引率
4.30%
发文量
33
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