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基于 β-连环蛋白结构域的探针在体内血管形态发生过程中突出了血管内皮的成熟。

A β-catenin chromobody-based probe highlights endothelial maturation during vascular morphogenesis in vivo.

机构信息

Department of Developmental Genetics, Max Planck Institute for Heart and Lung Research, 61231 Bad Nauheim, Germany.

Pharmaceutical Biotechnology, University of Tübingen, 72076 Tübingen, Germany.

出版信息

Development. 2024 Jun 1;151(11). doi: 10.1242/dev.202122. Epub 2024 Jun 7.

DOI:10.1242/dev.202122
PMID:38847494
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11190570/
Abstract

Visualization of protein dynamics is a crucial step in understanding cellular processes. Chromobodies, fluorescently labelled single-domain antibodies, have emerged as versatile probes for live cell imaging of endogenous proteins. However, how these chromobodies behave in vivo and how accurately they monitor tissue changes remain poorly explored. Here, we generated an endothelial-specific β-catenin chromobody-derived probe and analyzed its expression pattern during cardiovascular development in zebrafish. Using high-resolution confocal imaging, we show that the chromobody signal correlates with the localization of β-catenin in the nucleus and at cell-cell junctions, and thereby can be used to assess endothelial maturation. Loss of Cadherin 5 strongly affects the localization of the chromobody at the cell membrane, confirming the cadherin-based adherens junction role of β-catenin. Furthermore, using a genetic model to block blood flow, we observed that cell junctions are compromised in most endothelial cells but not in the endocardium, highlighting the heterogeneous response of the endothelium to the lack of blood flow. Overall, our data further expand the use of chromobodies for in vivo applications and illustrate their potential to monitor tissue morphogenesis at high resolution.

摘要

蛋白质动力学的可视化是理解细胞过程的关键步骤。荧光标记的单域抗体——染色质体已成为活细胞内源性蛋白质成像的多功能探针。然而,这些染色质体在体内的行为以及它们监测组织变化的准确性仍未得到充分探索。在这里,我们生成了一个内皮特异性β-catenin 染色质体衍生探针,并分析了它在斑马鱼心血管发育过程中的表达模式。使用高分辨率共聚焦成像,我们表明染色质体信号与β-catenin 在核内和细胞-细胞连接处的定位相关,因此可用于评估内皮细胞成熟度。Cadherin 5 的缺失强烈影响染色质体在细胞膜上的定位,证实了β-catenin 基于钙黏蛋白的黏着连接的作用。此外,使用一种阻断血流的遗传模型,我们观察到大多数内皮细胞的细胞连接受损,但心内膜不受影响,这突出表明内皮对血流缺失的反应具有异质性。总的来说,我们的数据进一步扩展了染色质体在体内应用的用途,并说明了它们在高分辨率监测组织形态发生方面的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5242/11190570/79ba292495c1/develop-151-202122-g4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5242/11190570/465eb731b5ba/develop-151-202122-g1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5242/11190570/0481fcf9c966/develop-151-202122-g2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5242/11190570/2b0314b57473/develop-151-202122-g3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5242/11190570/79ba292495c1/develop-151-202122-g4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5242/11190570/465eb731b5ba/develop-151-202122-g1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5242/11190570/0481fcf9c966/develop-151-202122-g2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5242/11190570/2b0314b57473/develop-151-202122-g3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5242/11190570/79ba292495c1/develop-151-202122-g4.jpg

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Apelin signaling dependent endocardial protrusions promote cardiac trabeculation in zebrafish.Apelin 信号依赖性心内膜突起促进斑马鱼心脏小梁化。
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