Cargando…

Dysregulated Hematopoietic Stem and Progenitor Cell Activity Promotes Interleukin-23-Driven Chronic Intestinal Inflammation

In interleukin-23 (IL-23)-dependent colitis, there is excessive accumulation of short-lived neutrophils and inflammatory monocytes in the intestine. It is unknown whether this reflects changes in mature cell populations or whether the IL-23-driven colitogenic T cell program regulates upstream hemato...

Descripción completa

Detalles Bibliográficos
Autores principales: Griseri, Thibault, McKenzie, Brent S., Schiering, Chris, Powrie, Fiona
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cell Press 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3664922/
https://www.ncbi.nlm.nih.gov/pubmed/23200826
http://dx.doi.org/10.1016/j.immuni.2012.08.025
_version_ 1782271185061412864
author Griseri, Thibault
McKenzie, Brent S.
Schiering, Chris
Powrie, Fiona
author_facet Griseri, Thibault
McKenzie, Brent S.
Schiering, Chris
Powrie, Fiona
author_sort Griseri, Thibault
collection PubMed
description In interleukin-23 (IL-23)-dependent colitis, there is excessive accumulation of short-lived neutrophils and inflammatory monocytes in the intestine. It is unknown whether this reflects changes in mature cell populations or whether the IL-23-driven colitogenic T cell program regulates upstream hematopoietic stem and progenitor cells (HSPC). Here we have shown dysregulation of hematopoiesis in colitis mediated by inflammatory cytokines. First, there was an interferon-gamma-dependent accumulation of proliferating hematopoietic stem cells in the bone marrow and spleen. Second, there was a strong skew toward granulocyte-monocyte progenitor (GMP) production at the expense of erythroid and lymphoid progenitors. Extramedullary hematopoiesis was also evident, and granulocyte macrophage-colony stimulating factor (GM-CSF) blockade reduced the accumulation of splenic and colonic GMPs, resulting in amelioration of colitis. Importantly, transfer of GMPs exacerbated colitis. These data identify HSPCs as a major target of the IL-23-driven inflammatory axis suggesting therapeutic strategies for the treatment of inflammatory bowel disease.
format Online
Article
Text
id pubmed-3664922
institution National Center for Biotechnology Information
language English
publishDate 2012
publisher Cell Press
record_format MEDLINE/PubMed
spelling pubmed-36649222013-05-28 Dysregulated Hematopoietic Stem and Progenitor Cell Activity Promotes Interleukin-23-Driven Chronic Intestinal Inflammation Griseri, Thibault McKenzie, Brent S. Schiering, Chris Powrie, Fiona Immunity Article In interleukin-23 (IL-23)-dependent colitis, there is excessive accumulation of short-lived neutrophils and inflammatory monocytes in the intestine. It is unknown whether this reflects changes in mature cell populations or whether the IL-23-driven colitogenic T cell program regulates upstream hematopoietic stem and progenitor cells (HSPC). Here we have shown dysregulation of hematopoiesis in colitis mediated by inflammatory cytokines. First, there was an interferon-gamma-dependent accumulation of proliferating hematopoietic stem cells in the bone marrow and spleen. Second, there was a strong skew toward granulocyte-monocyte progenitor (GMP) production at the expense of erythroid and lymphoid progenitors. Extramedullary hematopoiesis was also evident, and granulocyte macrophage-colony stimulating factor (GM-CSF) blockade reduced the accumulation of splenic and colonic GMPs, resulting in amelioration of colitis. Importantly, transfer of GMPs exacerbated colitis. These data identify HSPCs as a major target of the IL-23-driven inflammatory axis suggesting therapeutic strategies for the treatment of inflammatory bowel disease. Cell Press 2012-12-14 /pmc/articles/PMC3664922/ /pubmed/23200826 http://dx.doi.org/10.1016/j.immuni.2012.08.025 Text en © 2012 ELL & Excerpta Medica. https://creativecommons.org/licenses/by/3.0/ Open Access under CC BY 3.0 (https://creativecommons.org/licenses/by/3.0/) license
spellingShingle Article
Griseri, Thibault
McKenzie, Brent S.
Schiering, Chris
Powrie, Fiona
Dysregulated Hematopoietic Stem and Progenitor Cell Activity Promotes Interleukin-23-Driven Chronic Intestinal Inflammation
title Dysregulated Hematopoietic Stem and Progenitor Cell Activity Promotes Interleukin-23-Driven Chronic Intestinal Inflammation
title_full Dysregulated Hematopoietic Stem and Progenitor Cell Activity Promotes Interleukin-23-Driven Chronic Intestinal Inflammation
title_fullStr Dysregulated Hematopoietic Stem and Progenitor Cell Activity Promotes Interleukin-23-Driven Chronic Intestinal Inflammation
title_full_unstemmed Dysregulated Hematopoietic Stem and Progenitor Cell Activity Promotes Interleukin-23-Driven Chronic Intestinal Inflammation
title_short Dysregulated Hematopoietic Stem and Progenitor Cell Activity Promotes Interleukin-23-Driven Chronic Intestinal Inflammation
title_sort dysregulated hematopoietic stem and progenitor cell activity promotes interleukin-23-driven chronic intestinal inflammation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3664922/
https://www.ncbi.nlm.nih.gov/pubmed/23200826
http://dx.doi.org/10.1016/j.immuni.2012.08.025
work_keys_str_mv AT griserithibault dysregulatedhematopoieticstemandprogenitorcellactivitypromotesinterleukin23drivenchronicintestinalinflammation
AT mckenziebrents dysregulatedhematopoieticstemandprogenitorcellactivitypromotesinterleukin23drivenchronicintestinalinflammation
AT schieringchris dysregulatedhematopoieticstemandprogenitorcellactivitypromotesinterleukin23drivenchronicintestinalinflammation
AT powriefiona dysregulatedhematopoieticstemandprogenitorcellactivitypromotesinterleukin23drivenchronicintestinalinflammation