The blood flow-klf6a-tagln2 axis drives vessel pruning in zebrafish by regulating endothelial cell rearrangement and actin cytoskeleton dynamics.

Recent studies have focused on capillary pruning in various organs and species. However, the way in which large-diameter vessels are pruned remains unclear. Here we show that pruning of the zebrafish caudal vein (CV) from ventral capillaries of the CV plexus in different transgenic embryos is driven...

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Main Authors: Lin Wen, Tao Zhang, Jinxuan Wang, Xuepu Jin, Muhammad Abdul Rouf, Desha Luo, Yuan Zhu, Daoxi Lei, Hans Gregersen, Yeqi Wang, Guixue Wang
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2021-07-01
Series:PLoS Genetics
Online Access:https://doi.org/10.1371/journal.pgen.1009690
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spelling doaj-216f3b91cf2b4236b9887c22b36649892021-08-04T04:31:22ZengPublic Library of Science (PLoS)PLoS Genetics1553-73901553-74042021-07-01177e100969010.1371/journal.pgen.1009690The blood flow-klf6a-tagln2 axis drives vessel pruning in zebrafish by regulating endothelial cell rearrangement and actin cytoskeleton dynamics.Lin WenTao ZhangJinxuan WangXuepu JinMuhammad Abdul RoufDesha LuoYuan ZhuDaoxi LeiHans GregersenYeqi WangGuixue WangRecent studies have focused on capillary pruning in various organs and species. However, the way in which large-diameter vessels are pruned remains unclear. Here we show that pruning of the zebrafish caudal vein (CV) from ventral capillaries of the CV plexus in different transgenic embryos is driven by endothelial cell (EC) rearrangement, which involves EC nucleus migration, junction remodeling, and actin cytoskeleton remodeling. Further observation reveals a growing difference in blood flow velocity between the two vessels in CV pruning in zebrafish embryos. With this model, we identify the critical role of Kruppel-like factor 6a (klf6a) in CV pruning. Disruption of klf6a functioning impairs CV pruning in zebrafish. klf6a is required for EC nucleus migration, junction remodeling, and actin cytoskeleton dynamics in zebrafish embryos. Moreover, actin-related protein transgelin 2 (tagln2) is a direct downstream target of klf6a in CV pruning in zebrafish embryos. Together these results demonstrate that the klf6a-tagln2 axis regulates CV pruning by promoting EC rearrangement.https://doi.org/10.1371/journal.pgen.1009690
collection DOAJ
language English
format Article
sources DOAJ
author Lin Wen
Tao Zhang
Jinxuan Wang
Xuepu Jin
Muhammad Abdul Rouf
Desha Luo
Yuan Zhu
Daoxi Lei
Hans Gregersen
Yeqi Wang
Guixue Wang
spellingShingle Lin Wen
Tao Zhang
Jinxuan Wang
Xuepu Jin
Muhammad Abdul Rouf
Desha Luo
Yuan Zhu
Daoxi Lei
Hans Gregersen
Yeqi Wang
Guixue Wang
The blood flow-klf6a-tagln2 axis drives vessel pruning in zebrafish by regulating endothelial cell rearrangement and actin cytoskeleton dynamics.
PLoS Genetics
author_facet Lin Wen
Tao Zhang
Jinxuan Wang
Xuepu Jin
Muhammad Abdul Rouf
Desha Luo
Yuan Zhu
Daoxi Lei
Hans Gregersen
Yeqi Wang
Guixue Wang
author_sort Lin Wen
title The blood flow-klf6a-tagln2 axis drives vessel pruning in zebrafish by regulating endothelial cell rearrangement and actin cytoskeleton dynamics.
title_short The blood flow-klf6a-tagln2 axis drives vessel pruning in zebrafish by regulating endothelial cell rearrangement and actin cytoskeleton dynamics.
title_full The blood flow-klf6a-tagln2 axis drives vessel pruning in zebrafish by regulating endothelial cell rearrangement and actin cytoskeleton dynamics.
title_fullStr The blood flow-klf6a-tagln2 axis drives vessel pruning in zebrafish by regulating endothelial cell rearrangement and actin cytoskeleton dynamics.
title_full_unstemmed The blood flow-klf6a-tagln2 axis drives vessel pruning in zebrafish by regulating endothelial cell rearrangement and actin cytoskeleton dynamics.
title_sort blood flow-klf6a-tagln2 axis drives vessel pruning in zebrafish by regulating endothelial cell rearrangement and actin cytoskeleton dynamics.
publisher Public Library of Science (PLoS)
series PLoS Genetics
issn 1553-7390
1553-7404
publishDate 2021-07-01
description Recent studies have focused on capillary pruning in various organs and species. However, the way in which large-diameter vessels are pruned remains unclear. Here we show that pruning of the zebrafish caudal vein (CV) from ventral capillaries of the CV plexus in different transgenic embryos is driven by endothelial cell (EC) rearrangement, which involves EC nucleus migration, junction remodeling, and actin cytoskeleton remodeling. Further observation reveals a growing difference in blood flow velocity between the two vessels in CV pruning in zebrafish embryos. With this model, we identify the critical role of Kruppel-like factor 6a (klf6a) in CV pruning. Disruption of klf6a functioning impairs CV pruning in zebrafish. klf6a is required for EC nucleus migration, junction remodeling, and actin cytoskeleton dynamics in zebrafish embryos. Moreover, actin-related protein transgelin 2 (tagln2) is a direct downstream target of klf6a in CV pruning in zebrafish embryos. Together these results demonstrate that the klf6a-tagln2 axis regulates CV pruning by promoting EC rearrangement.
url https://doi.org/10.1371/journal.pgen.1009690
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