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Wnt/β-连环蛋白信号通路以细胞自主方式发挥作用,促进斑马鱼心脏中的心肌细胞再生。

Wnt/β-catenin signaling acts cell-autonomously to promote cardiomyocyte regeneration in the zebrafish heart.

作者信息

Bertozzi Alberto, Wu Chi-Chung, Hans Stefan, Brand Michael, Weidinger Gilbert

机构信息

Institute of Biochemistry and Molecular Biology, Ulm University, Albert-Einstein-Allee 11, 89081, Ulm, Germany.

Institute of Biochemistry and Molecular Biology, Ulm University, Albert-Einstein-Allee 11, 89081, Ulm, Germany; Max Planck Institute for Heart and Lung Research, Department of Developmental Genetics, Ludwigstrasse 43, 61231, Bad Nauheim, Germany.

出版信息

Dev Biol. 2022 Jan;481:226-237. doi: 10.1016/j.ydbio.2021.11.001. Epub 2021 Nov 6.

Abstract

Zebrafish can achieve scar-free healing of heart injuries, and robustly replace all cardiomyocytes lost to injury via dedifferentiation and proliferation of mature cardiomyocytes. Previous studies suggested that Wnt/β-catenin signaling is active in the injured zebrafish heart, where it induces fibrosis and prevents cardiomyocyte cell cycling. Here, via targeting the destruction complex of the Wnt/β-catenin pathway with pharmacological and genetic tools, we demonstrate that Wnt/β-catenin activity is required for cardiomyocyte proliferation and dedifferentiation, as well as for maturation of the scar during regeneration. Using cardiomyocyte-specific conditional inhibition of the pathway, we show that Wnt/β-catenin signaling acts cell-autonomously to promote cardiomyocyte proliferation. Our results stand in contrast to previous reports and rather support a model in which Wnt/β-catenin signaling plays a positive role during heart regeneration in zebrafish.

摘要

斑马鱼能够实现心脏损伤的无瘢痕愈合,并通过成熟心肌细胞的去分化和增殖有力地替代因损伤而丢失的所有心肌细胞。先前的研究表明,Wnt/β-连环蛋白信号通路在受伤的斑马鱼心脏中活跃,在那里它会诱导纤维化并阻止心肌细胞的细胞周期。在这里,通过使用药理学和遗传学工具靶向Wnt/β-连环蛋白通路的破坏复合物,我们证明Wnt/β-连环蛋白活性对于心肌细胞增殖、去分化以及再生过程中瘢痕的成熟是必需的。通过对该通路进行心肌细胞特异性条件性抑制,我们表明Wnt/β-连环蛋白信号通路以细胞自主的方式促进心肌细胞增殖。我们的结果与先前的报道相反,而是支持一种模型,即Wnt/β-连环蛋白信号通路在斑马鱼心脏再生过程中起积极作用。

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