Scube2 Modulates Coronary Vessel Formation During Cardiac Growth and Regeneration in Zebrafish.

IF 8.8 1区 医学 Q1 HEMATOLOGY
Ke-Hsuan Wei, Ann Nee Lee, Kaushik Chowdhury, Muhammad Abdul Rouf, An-Ju Chu, Yu-Jen Hung, Ku-Chi Tsao, Yan-Ting Chen, Yuh-Charn Lin, Edita Bakūnaitė, Yao-Ming Chang, Darius Balciunas, Rubén Marín-Juez, Ruey-Bing Yang, Shih-Lei Ben Lai
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引用次数: 0

Abstract

Background: Coronary vessel formation is essential for cardiac growth and regeneration, yet the extracellular mechanisms coordinating coronary vascular remodeling remain incompletely understood. Scube2 (signal peptide-CUB [complement C1r/C1s, Uegf, Bmp1 (bone morphogenetic protein 1)]-EGF domain-containing protein 2) has been implicated in developmental vascular signaling, but its role in coronary vessel formation and cardiac regeneration has not been established.

Methods: We investigated Scube2 function using zebrafish genetic loss-of-function mutants, inducible global and epicardial-specific dominant-negative models, cryoinjury-induced cardiac regeneration, confocal and ultrastructural imaging, bulk RNA sequencing, and biochemical analyses to examine signaling mechanisms.

Results: Scube2 was expressed in the epicardium under homeostatic conditions and was rapidly induced in epicardial-derived cells following cardiac injury. Loss of Scube2 impaired developmental coronary vessel formation and caused myocardial ultrastructural abnormalities. Following injury, Scube2 deficiency resulted in defective revascularization, reduced mural cell association, decreased endothelial and cardiomyocyte proliferation, persistent fibrosis, and impaired cardiac regeneration. Temporal and epicardial-specific inhibition of Scube2 recapitulated these regenerative defects. Transcriptomic analyses identified dysregulation of VEGF (vascular endothelial growth factor) and PDGF (platelet-derived growth factor) signaling pathways, accompanied by reduced endothelial proliferation and prolonged inflammatory responses. Mechanistically, SCUBE2 interacted with PDGF-B (PDGF subunit B) and PDGFRβ (PDGF receptor β) and enhanced PDGFRβ activation, supporting a role in endothelial-mural cell communication during vascular remodeling.

Conclusions: Scube2 is a critical regulator of coronary vessel formation and regenerative revascularization in zebrafish. By promoting PDGF-dependent endothelial-mural cell interactions, Scube2 coordinates vascular remodeling that supports myocardial regeneration. These findings identify Scube2 as a previously unrecognized regulator of coronary vascularization and suggest extracellular modulation of PDGF signaling as a potential therapeutic strategy to enhance cardiac repair after ischemic injury.

Scube2在斑马鱼心脏生长和再生过程中调节冠状血管形成。
背景:冠状血管的形成对心脏生长和再生至关重要,但协调冠状血管重构的细胞外机制仍不完全清楚。Scube2(信号肽- cub[补体C1r/C1s, Uegf, Bmp1]-EGF结构域含蛋白2)与发育血管信号传导有关,但其在冠状血管形成和心脏再生中的作用尚未确定。方法:我们使用斑马鱼基因功能缺失突变体、可诱导的全局和心外膜特异性显性阴性模型、低温损伤诱导的心脏再生、共聚焦和超微结构成像、大量RNA测序和生化分析来研究Scube2的功能,以研究信号传导机制。结果:在稳态条件下,Scube2在心外膜中表达,并在心脏损伤后的心外膜源性细胞中被快速诱导。Scube2缺失损害了发育中的冠状血管形成并引起心肌超微结构异常。损伤后,Scube2缺乏导致血管重建缺陷、壁细胞关联减少、内皮细胞和心肌细胞增殖减少、持续纤维化和心脏再生受损。Scube2的时间和心外膜特异性抑制再现了这些再生缺陷。转录组学分析发现VEGF(血管内皮生长因子)和PDGF(血小板衍生生长因子)信号通路失调,伴有内皮细胞增殖减少和炎症反应延长。在机制上,SCUBE2与PDGF-B (PDGF亚基B)和PDGFRβ (PDGF受体β)相互作用,增强PDGFRβ活化,支持血管重构过程中内皮-壁细胞通讯的作用。结论:Scube2是斑马鱼冠状血管形成和再生血管重建的关键调节因子。通过促进pdgf依赖性内皮-壁细胞相互作用,Scube2协调血管重塑,支持心肌再生。这些发现确定了Scube2是一种以前未被识别的冠状动脉血管形成调节因子,并提示PDGF信号的细胞外调节是一种潜在的治疗策略,可以增强缺血性损伤后的心脏修复。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
15.60
自引率
2.30%
发文量
337
审稿时长
2-4 weeks
期刊介绍: The journal "Arteriosclerosis, Thrombosis, and Vascular Biology" (ATVB) is a scientific publication that focuses on the fields of vascular biology, atherosclerosis, and thrombosis. It is a peer-reviewed journal that publishes original research articles, reviews, and other scholarly content related to these areas. The journal is published by the American Heart Association (AHA) and the American Stroke Association (ASA). The journal was published bi-monthly until January 1992, after which it transitioned to a monthly publication schedule. The journal is aimed at a professional audience, including academic cardiologists, vascular biologists, physiologists, pharmacologists and hematologists.
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