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Clarification of mural cell coverage of vascular endothelial cells by live imaging of zebrafish
Author(s) -
Koji Ando,
Shigetomo Fukuhara,
Nanae Izumi,
Hiroyuki Nakajima,
Hajime Fukui,
Robert N. Kelsh,
Naoki Mochizuki
Publication year - 2016
Publication title -
development
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.754
H-Index - 325
eISSN - 1477-9129
pISSN - 0950-1991
DOI - 10.1242/dev.132654
Subject(s) - biology , lateral plate mesoderm , neural crest , zebrafish , mural cell , mesoderm , anatomy , microbiology and biotechnology , live cell imaging , vascular smooth muscle , cell , smooth muscle , embryo , endocrinology , embryonic stem cell , genetics , gene
Mural cells (MCs) consisting of vascular smooth muscle cells and pericytes cover the endothelial cells (ECs) to regulate vascular stability and homeostasis. Here, we clarified the mechanism by which MCs develop and cover ECs by generating transgenic zebrafish lines that allow live imaging of MCs and by lineage tracing in vivo To cover cranial vessels, MCs derived from either neural crest cells or mesoderm emerged around the preformed EC tubes, proliferated and migrated along EC tubes. During their migration, the MCs moved forward by extending their processes along the inter-EC junctions, suggesting a role for inter-EC junctions as a scaffold for MC migration. In the trunk vasculature, MCs derived from mesoderm covered the ventral side of the dorsal aorta (DA), but not the posterior cardinal vein. Furthermore, the MCs migrating from the DA or emerging around intersegmental vessels (ISVs) preferentially covered arterial ISVs rather than venous ISVs, indicating that MCs mostly cover arteries during vascular development. Thus, live imaging and lineage tracing enabled us to clarify precisely how MCs cover the EC tubes and to identify the origins of MCs.

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