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Citrullination regulates wound responses and tissue regeneration in zebrafish

Calcium is an important early signal in wound healing, yet how these early signals promote regeneration remains unclear. Peptidylarginine deiminases (PADs), a family of calcium-dependent enzymes, catalyze citrullination, a post-translational modification that alters protein function and has been imp...

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Autores principales: Golenberg, Netta, Squirrell, Jayne M., Bennin, David A., Rindy, Julie, Pistono, Paige E., Eliceiri, Kevin W., Shelef, Miriam A., Kang, Junsu, Huttenlocher, Anna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Rockefeller University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7147109/
https://www.ncbi.nlm.nih.gov/pubmed/32328635
http://dx.doi.org/10.1083/jcb.201908164
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author Golenberg, Netta
Squirrell, Jayne M.
Bennin, David A.
Rindy, Julie
Pistono, Paige E.
Eliceiri, Kevin W.
Shelef, Miriam A.
Kang, Junsu
Huttenlocher, Anna
author_facet Golenberg, Netta
Squirrell, Jayne M.
Bennin, David A.
Rindy, Julie
Pistono, Paige E.
Eliceiri, Kevin W.
Shelef, Miriam A.
Kang, Junsu
Huttenlocher, Anna
author_sort Golenberg, Netta
collection PubMed
description Calcium is an important early signal in wound healing, yet how these early signals promote regeneration remains unclear. Peptidylarginine deiminases (PADs), a family of calcium-dependent enzymes, catalyze citrullination, a post-translational modification that alters protein function and has been implicated in autoimmune diseases. We generated a mutation in the single zebrafish ancestral pad gene, padi2, that results in a loss of detectable calcium-dependent citrullination. The mutants exhibit impaired resolution of inflammation and regeneration after caudal fin transection. We identified a new subpopulation of cells displaying citrullinated histones within the notochord bead following tissue injury. Citrullination of histones in this region was absent, and wound-induced proliferation was perturbed in Padi2-deficient larvae. Taken together, our results show that Padi2 is required for the citrullination of histones within a group of cells in the notochord bead and for promoting wound-induced proliferation required for efficient regeneration. These findings identify Padi2 as a potential intermediary between early calcium signaling and subsequent tissue regeneration.
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spelling pubmed-71471092020-10-06 Citrullination regulates wound responses and tissue regeneration in zebrafish Golenberg, Netta Squirrell, Jayne M. Bennin, David A. Rindy, Julie Pistono, Paige E. Eliceiri, Kevin W. Shelef, Miriam A. Kang, Junsu Huttenlocher, Anna J Cell Biol Report Calcium is an important early signal in wound healing, yet how these early signals promote regeneration remains unclear. Peptidylarginine deiminases (PADs), a family of calcium-dependent enzymes, catalyze citrullination, a post-translational modification that alters protein function and has been implicated in autoimmune diseases. We generated a mutation in the single zebrafish ancestral pad gene, padi2, that results in a loss of detectable calcium-dependent citrullination. The mutants exhibit impaired resolution of inflammation and regeneration after caudal fin transection. We identified a new subpopulation of cells displaying citrullinated histones within the notochord bead following tissue injury. Citrullination of histones in this region was absent, and wound-induced proliferation was perturbed in Padi2-deficient larvae. Taken together, our results show that Padi2 is required for the citrullination of histones within a group of cells in the notochord bead and for promoting wound-induced proliferation required for efficient regeneration. These findings identify Padi2 as a potential intermediary between early calcium signaling and subsequent tissue regeneration. Rockefeller University Press 2020-03-04 /pmc/articles/PMC7147109/ /pubmed/32328635 http://dx.doi.org/10.1083/jcb.201908164 Text en © 2020 Golenberg et al. http://www.rupress.org/terms/https://creativecommons.org/licenses/by-nc-sa/4.0/This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms/). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 International license, as described at https://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Report
Golenberg, Netta
Squirrell, Jayne M.
Bennin, David A.
Rindy, Julie
Pistono, Paige E.
Eliceiri, Kevin W.
Shelef, Miriam A.
Kang, Junsu
Huttenlocher, Anna
Citrullination regulates wound responses and tissue regeneration in zebrafish
title Citrullination regulates wound responses and tissue regeneration in zebrafish
title_full Citrullination regulates wound responses and tissue regeneration in zebrafish
title_fullStr Citrullination regulates wound responses and tissue regeneration in zebrafish
title_full_unstemmed Citrullination regulates wound responses and tissue regeneration in zebrafish
title_short Citrullination regulates wound responses and tissue regeneration in zebrafish
title_sort citrullination regulates wound responses and tissue regeneration in zebrafish
topic Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7147109/
https://www.ncbi.nlm.nih.gov/pubmed/32328635
http://dx.doi.org/10.1083/jcb.201908164
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