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PAD2-Mediated Citrullination Contributes to Efficient Oligodendrocyte Differentiation and Myelination
Citrullination, the deimination of peptidylarginine residues into peptidylcitrulline, has been implicated in the etiology of several diseases. In multiple sclerosis, citrullination is thought to be a major driver of pathology through hypercitrullination and destabilization of myelin. As such, inhibi...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cell Press
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6486480/ https://www.ncbi.nlm.nih.gov/pubmed/31018126 http://dx.doi.org/10.1016/j.celrep.2019.03.108 |
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author | Falcão, Ana Mendanha Meijer, Mandy Scaglione, Antonella Rinwa, Puneet Agirre, Eneritz Liang, Jialiang Larsen, Sara C. Heskol, Abeer Frawley, Rebecca Klingener, Michael Varas-Godoy, Manuel Raposo, Alexandre A.S.F. Ernfors, Patrik Castro, Diogo S. Nielsen, Michael L. Casaccia, Patrizia Castelo-Branco, Gonçalo |
author_facet | Falcão, Ana Mendanha Meijer, Mandy Scaglione, Antonella Rinwa, Puneet Agirre, Eneritz Liang, Jialiang Larsen, Sara C. Heskol, Abeer Frawley, Rebecca Klingener, Michael Varas-Godoy, Manuel Raposo, Alexandre A.S.F. Ernfors, Patrik Castro, Diogo S. Nielsen, Michael L. Casaccia, Patrizia Castelo-Branco, Gonçalo |
author_sort | Falcão, Ana Mendanha |
collection | PubMed |
description | Citrullination, the deimination of peptidylarginine residues into peptidylcitrulline, has been implicated in the etiology of several diseases. In multiple sclerosis, citrullination is thought to be a major driver of pathology through hypercitrullination and destabilization of myelin. As such, inhibition of citrullination has been suggested as a therapeutic strategy for MS. Here, in contrast, we show that citrullination by peptidylarginine deiminase 2 (PAD2) contributes to normal oligodendrocyte differentiation, myelination, and motor function. We identify several targets for PAD2, including myelin and chromatin-related proteins, implicating PAD2 in epigenomic regulation. Accordingly, we observe that PAD2 inhibition and its knockdown affect chromatin accessibility and prevent the upregulation of oligodendrocyte differentiation genes. Moreover, mice lacking PAD2 display motor dysfunction and a decreased number of myelinated axons in the corpus callosum. We conclude that citrullination contributes to proper oligodendrocyte lineage progression and myelination. |
format | Online Article Text |
id | pubmed-6486480 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-64864802019-05-02 PAD2-Mediated Citrullination Contributes to Efficient Oligodendrocyte Differentiation and Myelination Falcão, Ana Mendanha Meijer, Mandy Scaglione, Antonella Rinwa, Puneet Agirre, Eneritz Liang, Jialiang Larsen, Sara C. Heskol, Abeer Frawley, Rebecca Klingener, Michael Varas-Godoy, Manuel Raposo, Alexandre A.S.F. Ernfors, Patrik Castro, Diogo S. Nielsen, Michael L. Casaccia, Patrizia Castelo-Branco, Gonçalo Cell Rep Article Citrullination, the deimination of peptidylarginine residues into peptidylcitrulline, has been implicated in the etiology of several diseases. In multiple sclerosis, citrullination is thought to be a major driver of pathology through hypercitrullination and destabilization of myelin. As such, inhibition of citrullination has been suggested as a therapeutic strategy for MS. Here, in contrast, we show that citrullination by peptidylarginine deiminase 2 (PAD2) contributes to normal oligodendrocyte differentiation, myelination, and motor function. We identify several targets for PAD2, including myelin and chromatin-related proteins, implicating PAD2 in epigenomic regulation. Accordingly, we observe that PAD2 inhibition and its knockdown affect chromatin accessibility and prevent the upregulation of oligodendrocyte differentiation genes. Moreover, mice lacking PAD2 display motor dysfunction and a decreased number of myelinated axons in the corpus callosum. We conclude that citrullination contributes to proper oligodendrocyte lineage progression and myelination. Cell Press 2019-04-23 /pmc/articles/PMC6486480/ /pubmed/31018126 http://dx.doi.org/10.1016/j.celrep.2019.03.108 Text en © 2019 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Falcão, Ana Mendanha Meijer, Mandy Scaglione, Antonella Rinwa, Puneet Agirre, Eneritz Liang, Jialiang Larsen, Sara C. Heskol, Abeer Frawley, Rebecca Klingener, Michael Varas-Godoy, Manuel Raposo, Alexandre A.S.F. Ernfors, Patrik Castro, Diogo S. Nielsen, Michael L. Casaccia, Patrizia Castelo-Branco, Gonçalo PAD2-Mediated Citrullination Contributes to Efficient Oligodendrocyte Differentiation and Myelination |
title | PAD2-Mediated Citrullination Contributes to Efficient Oligodendrocyte Differentiation and Myelination |
title_full | PAD2-Mediated Citrullination Contributes to Efficient Oligodendrocyte Differentiation and Myelination |
title_fullStr | PAD2-Mediated Citrullination Contributes to Efficient Oligodendrocyte Differentiation and Myelination |
title_full_unstemmed | PAD2-Mediated Citrullination Contributes to Efficient Oligodendrocyte Differentiation and Myelination |
title_short | PAD2-Mediated Citrullination Contributes to Efficient Oligodendrocyte Differentiation and Myelination |
title_sort | pad2-mediated citrullination contributes to efficient oligodendrocyte differentiation and myelination |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6486480/ https://www.ncbi.nlm.nih.gov/pubmed/31018126 http://dx.doi.org/10.1016/j.celrep.2019.03.108 |
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