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体内邻近标记法可识别斑马鱼心脏再生过程中的心肌细胞蛋白质网络。

In vivo proximity labeling identifies cardiomyocyte protein networks during zebrafish heart regeneration.

作者信息

Pronobis Mira I, Zheng Susan, Singh Sumeet Pal, Goldman Joseph A, Poss Kenneth D

机构信息

Department of Cell Biology, Duke University Medical Center, Durham, United States.

Regeneration Next, Duke University, Durham, United States.

出版信息

Elife. 2021 Mar 25;10:e66079. doi: 10.7554/eLife.66079.

Abstract

Strategies have not been available until recently to uncover interacting protein networks specific to key cell types, their subcellular compartments, and their major regulators during complex in vivo events. Here, we apply BioID2 proximity labeling to capture protein networks acting within cardiomyocytes during a key model of innate heart regeneration in zebrafish. Transgenic zebrafish expressing a promiscuous BirA2 localized to the entire myocardial cell or membrane compartment were generated, each identifying distinct proteomes in adult cardiomyocytes that became altered during regeneration. BioID2 profiling for interactors with ErbB2, a co-receptor for the cardiomyocyte mitogen Nrg1, implicated Rho A as a target of ErbB2 signaling in cardiomyocytes. Blockade of Rho A during heart regeneration, or during cardiogenic stimulation by the mitogenic influences Nrg1, Vegfaa, or vitamin D, disrupted muscle creation. Our findings reveal proximity labeling as a useful resource to interrogate cell proteomes and signaling networks during tissue regeneration in zebrafish.

摘要

直到最近,在复杂的体内事件中,还没有可用的策略来揭示特定于关键细胞类型、其亚细胞区室及其主要调节因子的相互作用蛋白网络。在这里,我们应用BioID2邻近标记来捕获斑马鱼先天性心脏再生关键模型中在心肌细胞内起作用的蛋白质网络。我们生成了表达定位于整个心肌细胞或膜区室的混杂BirA2的转基因斑马鱼,每一种都识别出成年心肌细胞中在再生过程中发生改变的不同蛋白质组。对心肌细胞有丝分裂原Nrg1的共受体ErbB2的相互作用蛋白进行BioID2分析,表明Rho A是心肌细胞中ErbB2信号传导的一个靶点。在心脏再生期间,或在有丝分裂影响Nrg1、Vegfaa或维生素D引起的心脏发生刺激期间,阻断Rho A会破坏肌肉生成。我们的研究结果表明,邻近标记是在斑马鱼组织再生过程中探究细胞蛋白质组和信号网络的有用资源。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/50e1/8034980/42ad5e4b411b/elife-66079-fig1-figsupp1.jpg

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