Cargando…
A connexin/ifi30 pathway bridges HSCs with their niche to dampen oxidative stress
Reactive oxygen species (ROS) represent a by-product of metabolism and their excess is toxic for hematopoietic stem and progenitor cells (HSPCs). During embryogenesis, a small number of HSPCs are produced from the hemogenic endothelium, before they colonize a transient organ where they expand, for e...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8302694/ https://www.ncbi.nlm.nih.gov/pubmed/34301940 http://dx.doi.org/10.1038/s41467-021-24831-0 |
_version_ | 1783726927339585536 |
---|---|
author | Cacialli, Pietro Mahony, Christopher B. Petzold, Tim Bordignon, Patrizia Rougemont, Anne-Laure Bertrand, Julien Y. |
author_facet | Cacialli, Pietro Mahony, Christopher B. Petzold, Tim Bordignon, Patrizia Rougemont, Anne-Laure Bertrand, Julien Y. |
author_sort | Cacialli, Pietro |
collection | PubMed |
description | Reactive oxygen species (ROS) represent a by-product of metabolism and their excess is toxic for hematopoietic stem and progenitor cells (HSPCs). During embryogenesis, a small number of HSPCs are produced from the hemogenic endothelium, before they colonize a transient organ where they expand, for example the fetal liver in mammals. In this study, we use zebrafish to understand the molecular mechanisms that are important in the caudal hematopoietic tissue (equivalent to the mammalian fetal liver) to promote HSPC expansion. High levels of ROS are deleterious for HSPCs in this niche, however this is rescued by addition of antioxidants. We show that Cx41.8 is important to lower ROS levels in HSPCs. We also demonstrate a new role for ifi30, known to be involved in the immune response. In the hematopoietic niche, Ifi30 can recycle oxidized glutathione to allow HSPCs to dampen their levels of ROS, a role that could be conserved in human fetal liver. |
format | Online Article Text |
id | pubmed-8302694 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-83026942021-08-12 A connexin/ifi30 pathway bridges HSCs with their niche to dampen oxidative stress Cacialli, Pietro Mahony, Christopher B. Petzold, Tim Bordignon, Patrizia Rougemont, Anne-Laure Bertrand, Julien Y. Nat Commun Article Reactive oxygen species (ROS) represent a by-product of metabolism and their excess is toxic for hematopoietic stem and progenitor cells (HSPCs). During embryogenesis, a small number of HSPCs are produced from the hemogenic endothelium, before they colonize a transient organ where they expand, for example the fetal liver in mammals. In this study, we use zebrafish to understand the molecular mechanisms that are important in the caudal hematopoietic tissue (equivalent to the mammalian fetal liver) to promote HSPC expansion. High levels of ROS are deleterious for HSPCs in this niche, however this is rescued by addition of antioxidants. We show that Cx41.8 is important to lower ROS levels in HSPCs. We also demonstrate a new role for ifi30, known to be involved in the immune response. In the hematopoietic niche, Ifi30 can recycle oxidized glutathione to allow HSPCs to dampen their levels of ROS, a role that could be conserved in human fetal liver. Nature Publishing Group UK 2021-07-23 /pmc/articles/PMC8302694/ /pubmed/34301940 http://dx.doi.org/10.1038/s41467-021-24831-0 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Cacialli, Pietro Mahony, Christopher B. Petzold, Tim Bordignon, Patrizia Rougemont, Anne-Laure Bertrand, Julien Y. A connexin/ifi30 pathway bridges HSCs with their niche to dampen oxidative stress |
title | A connexin/ifi30 pathway bridges HSCs with their niche to dampen oxidative stress |
title_full | A connexin/ifi30 pathway bridges HSCs with their niche to dampen oxidative stress |
title_fullStr | A connexin/ifi30 pathway bridges HSCs with their niche to dampen oxidative stress |
title_full_unstemmed | A connexin/ifi30 pathway bridges HSCs with their niche to dampen oxidative stress |
title_short | A connexin/ifi30 pathway bridges HSCs with their niche to dampen oxidative stress |
title_sort | connexin/ifi30 pathway bridges hscs with their niche to dampen oxidative stress |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8302694/ https://www.ncbi.nlm.nih.gov/pubmed/34301940 http://dx.doi.org/10.1038/s41467-021-24831-0 |
work_keys_str_mv | AT caciallipietro aconnexinifi30pathwaybridgeshscswiththeirnichetodampenoxidativestress AT mahonychristopherb aconnexinifi30pathwaybridgeshscswiththeirnichetodampenoxidativestress AT petzoldtim aconnexinifi30pathwaybridgeshscswiththeirnichetodampenoxidativestress AT bordignonpatrizia aconnexinifi30pathwaybridgeshscswiththeirnichetodampenoxidativestress AT rougemontannelaure aconnexinifi30pathwaybridgeshscswiththeirnichetodampenoxidativestress AT bertrandjulieny aconnexinifi30pathwaybridgeshscswiththeirnichetodampenoxidativestress AT caciallipietro connexinifi30pathwaybridgeshscswiththeirnichetodampenoxidativestress AT mahonychristopherb connexinifi30pathwaybridgeshscswiththeirnichetodampenoxidativestress AT petzoldtim connexinifi30pathwaybridgeshscswiththeirnichetodampenoxidativestress AT bordignonpatrizia connexinifi30pathwaybridgeshscswiththeirnichetodampenoxidativestress AT rougemontannelaure connexinifi30pathwaybridgeshscswiththeirnichetodampenoxidativestress AT bertrandjulieny connexinifi30pathwaybridgeshscswiththeirnichetodampenoxidativestress |