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  3. Neuropilin 1 mediates epicardial activation and revascularization in the regenerating zebrafish heart
 

Neuropilin 1 mediates epicardial activation and revascularization in the regenerating zebrafish heart

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BORIS DOI
10.7892/boris.135529
Date of Publication
2019
Publication Type
Article
Division/Institute

Institut für Anatomie...

Author
Lowe, Vanessa
Wisniewski, Laura
Sayers, Jacob
Evans, Ian
Frankel, Paul
Mercader Huber, Nadia Isabelorcid-logo
Institut für Anatomie
Institut für Anatomie, Entwicklungsbiologie und Regeneration
Zachary, Ian C.
Pellet-Many, Caroline
Subject(s)

600 - Technology::610...

500 - Science::570 - ...

Series
Development
ISSN or ISBN (if monograph)
0950-1991
Publisher
Company of Biologists Limited
Language
English
Publisher DOI
10.1242/dev.174482
PubMed ID
31167777
Description
Unlike adult mammals, zebrafish can regenerate their heart. A key mechanism for regeneration is the activation of the epicardium, leading to the establishment of a supporting scaffold for new cardiomyocytes, angiogenesis and cytokine secretion. Neuropilins are co-receptors that mediate signaling of kinase receptors for cytokines with crucial roles in zebrafish heart regeneration. We investigated the role of neuropilins in response to cardiac injury and heart regeneration. All four neuropilin isoforms (nrp1a, nrp1b, nrp2a and nrp2b) were upregulated by the activated epicardium and an nrp1a-knockout mutant showed a significant delay in heart regeneration and displayed persistent collagen deposition. The regenerating hearts of nrp1a mutants were less vascularized, and epicardial-derived cell migration and re-expression of the developmental gene wt1b was impaired. Moreover, cryoinjury-induced activation and migration of epicardial cells in heart explants were reduced in nrp1a mutants. These results identify a key role for Nrp1 in zebrafish heart regeneration, mediated through epicardial activation, migration and revascularization.
Handle
https://boris-portal.unibe.ch/handle/20.500.12422/183629
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dev174482.full.pdftextAdobe PDF14.3 MBAttribution (CC BY 4.0)publishedOpen
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