Back to Search Start Over

Piezo1-Regulated Mechanotransduction Controls Flow-Activated Lymphatic Expansion.

Authors :
Choi, Dongwon
Choi, Dongwon
Park, Eunkyung
Yu, Roy P
Cooper, Michael N
Cho, Il-Taeg
Choi, Joshua
Yu, James
Zhao, Luping
Yum, Ji-Eun Irene
Yu, Jin Suh
Nakashima, Brandon
Lee, Sunju
Seong, Young Jin
Jiao, Wan
Koh, Chester J
Baluk, Peter
McDonald, Donald M
Saraswathy, Sindhu
Lee, Jong Y
Jeon, Noo Li
Zhang, Zhenqian
Huang, Alex S
Zhou, Bin
Wong, Alex K
Hong, Young-Kwon
Choi, Dongwon
Choi, Dongwon
Park, Eunkyung
Yu, Roy P
Cooper, Michael N
Cho, Il-Taeg
Choi, Joshua
Yu, James
Zhao, Luping
Yum, Ji-Eun Irene
Yu, Jin Suh
Nakashima, Brandon
Lee, Sunju
Seong, Young Jin
Jiao, Wan
Koh, Chester J
Baluk, Peter
McDonald, Donald M
Saraswathy, Sindhu
Lee, Jong Y
Jeon, Noo Li
Zhang, Zhenqian
Huang, Alex S
Zhou, Bin
Wong, Alex K
Hong, Young-Kwon
Source :
Circulation research; vol 131, iss 2, e2-e21; 0009-7330
Publication Year :
2022

Abstract

BackgroundMutations in PIEZO1 (Piezo type mechanosensitive ion channel component 1) cause human lymphatic malformations. We have previously uncovered an ORAI1 (ORAI calcium release-activated calcium modulator 1)-mediated mechanotransduction pathway that triggers lymphatic sprouting through Notch downregulation in response to fluid flow. However, the identity of its upstream mechanosensor remains unknown. This study aimed to identify and characterize the molecular sensor that translates the flow-mediated external signal to the Orai1-regulated lymphatic expansion.MethodsVarious mutant mouse models, cellular, biochemical, and molecular biology tools, and a mouse tail lymphedema model were employed to elucidate the role of Piezo1 in flow-induced lymphatic growth and regeneration.ResultsPiezo1 was found to be abundantly expressed in lymphatic endothelial cells. Piezo1 knockdown in cultured lymphatic endothelial cells inhibited the laminar flow-induced calcium influx and abrogated the flow-mediated regulation of the Orai1 downstream genes, such as KLF2 (Krüppel-like factor 2), DTX1 (Deltex E3 ubiquitin ligase 1), DTX3L (Deltex E3 ubiquitin ligase 3L,) and NOTCH1 (Notch receptor 1), which are involved in lymphatic sprouting. Conversely, stimulation of Piezo1 activated the Orai1-regulated mechanotransduction in the absence of fluid flow. Piezo1-mediated mechanotransduction was significantly blocked by Orai1 inhibition, establishing the epistatic relationship between Piezo1 and Orai1. Lymphatic-specific conditional Piezo1 knockout largely phenocopied sprouting defects shown in Orai1- or Klf2- knockout lymphatics during embryo development. Postnatal deletion of Piezo1 induced lymphatic regression in adults. Ectopic Dtx3L expression rescued the lymphatic defects caused by Piezo1 knockout, affirming that the Piezo1 promotes lymphatic sprouting through Notch downregulation. Consistently, transgenic Piezo1 expression or pharmacological Piezo1 activation enhanced lymphatic sprouti

Details

Database :
OAIster
Journal :
Circulation research; vol 131, iss 2, e2-e21; 0009-7330
Notes :
application/pdf, Circulation research vol 131, iss 2, e2-e21 0009-7330
Publication Type :
Electronic Resource
Accession number :
edsoai.on1391550156
Document Type :
Electronic Resource