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一种新的基因陷阱系揭示了富含半胱氨酸和甘氨酸蛋白 3 在斑马鱼心脏发育和再生中的动态模式和关键作用。

A novel gene-trap line reveals the dynamic patterns and essential roles of cysteine and glycine-rich protein 3 in zebrafish heart development and regeneration.

机构信息

TaiKang Medical School (School of Basic Medical Sciences), Wuhan University, Wuhan, 430071, China.

School of Life Sciences, Fudan University, Shanghai, 200433, China.

出版信息

Cell Mol Life Sci. 2024 Mar 31;81(1):158. doi: 10.1007/s00018-024-05189-0.

DOI:10.1007/s00018-024-05189-0
PMID:38556571
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10982097/
Abstract

Mutations in cysteine and glycine-rich protein 3 (CSRP3)/muscle LIM protein (MLP), a key regulator of striated muscle function, have been linked to hypertrophic cardiomyopathy (HCM) and dilated cardiomyopathy (DCM) in patients. However, the roles of CSRP3 in heart development and regeneration are not completely understood. In this study, we characterized a novel zebrafish gene-trap line, gSAIzGFFM218A, which harbors an insertion in the csrp3 genomic locus, heterozygous fish served as a csrp3 expression reporter line and homozygous fish served as a csrp3 mutant line. We discovered that csrp3 is specifically expressed in larval ventricular cardiomyocytes (CMs) and that csrp3 deficiency leads to excessive trabeculation, a common feature of CSRP3-related HCM and DCM. We further revealed that csrp3 expression increased in response to different cardiac injuries and was regulated by several signaling pathways vital for heart regeneration. Csrp3 deficiency impeded zebrafish heart regeneration by impairing CM dedifferentiation, hindering sarcomere reassembly, and reducing CM proliferation while aggravating apoptosis. Csrp3 overexpression promoted CM proliferation after injury and ameliorated the impairment of ventricle regeneration caused by pharmacological inhibition of multiple signaling pathways. Our study highlights the critical role of Csrp3 in both zebrafish heart development and regeneration, and provides a valuable animal model for further functional exploration that will shed light on the molecular pathogenesis of CSRP3-related human cardiac diseases.

摘要

突变胱氨酸和甘氨酸丰富蛋白 3(CSRP3)/肌肉 LIM 蛋白(MLP),一种横纹肌功能的关键调节因子,与肥厚型心肌病(HCM)和扩张型心肌病(DCM)患者有关。然而,CSRP3 在心脏发育和再生中的作用还不完全清楚。在这项研究中,我们对一种新型的斑马鱼基因捕获系 gSAIzGFFM218A 进行了特征描述,该系在 csrp3 基因组位点插入了一个基因,杂合子鱼作为 csrp3 表达报告线,纯合子鱼作为 csrp3 突变体线。我们发现 csrp3 特异性地在幼鱼心室心肌细胞(CMs)中表达,csrp3 缺失导致过度的小梁化,这是 CSRP3 相关 HCM 和 DCM 的一个共同特征。我们进一步揭示了 csrp3 的表达在受到不同心脏损伤后会增加,并受到几种对心脏再生至关重要的信号通路的调节。Csrp3 缺失通过损害 CM 去分化、阻碍肌节重排、减少 CM 增殖和加重细胞凋亡来阻碍斑马鱼心脏再生。Csrp3 过表达在损伤后促进 CM 增殖,并改善多种信号通路药物抑制引起的心室再生损伤。我们的研究强调了 Csrp3 在斑马鱼心脏发育和再生中的关键作用,并提供了一个有价值的动物模型,用于进一步的功能探索,这将为 CSRP3 相关人类心脏疾病的分子发病机制提供启示。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/08b1/11073095/459a8d1852cc/18_2024_5189_Fig7_HTML.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/08b1/11073095/459a8d1852cc/18_2024_5189_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/08b1/11073095/b02fe8b5e5ca/18_2024_5189_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/08b1/11073095/b5be3a0090ff/18_2024_5189_Fig2_HTML.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/08b1/11073095/459a8d1852cc/18_2024_5189_Fig7_HTML.jpg

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