Conditional deletion of Ahr alters gene expression profiles in hematopoietic stem cells.

The aryl hydrocarbon receptor (AHR) is a ligand activated bHLH transcription factor that belongs to the Per-Arnt-Sim (PAS) superfamily of proteins involved in mediating responses to cellular environment regulating normal physiological and developmental pathways. The AHR binds a broad range of natura...

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Main Authors: John A Bennett, Kameshwar P Singh, Stephen L Welle, Lisbeth A Boule, B Paige Lawrence, Thomas A Gasiewicz
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2018-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC6214519?pdf=render
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author John A Bennett
Kameshwar P Singh
Stephen L Welle
Lisbeth A Boule
B Paige Lawrence
Thomas A Gasiewicz
author_facet John A Bennett
Kameshwar P Singh
Stephen L Welle
Lisbeth A Boule
B Paige Lawrence
Thomas A Gasiewicz
author_sort John A Bennett
collection DOAJ
description The aryl hydrocarbon receptor (AHR) is a ligand activated bHLH transcription factor that belongs to the Per-Arnt-Sim (PAS) superfamily of proteins involved in mediating responses to cellular environment regulating normal physiological and developmental pathways. The AHR binds a broad range of naturally derived and synthetic compounds, and plays a major role in mediating effects of certain environmental chemicals. Although our understanding of the physiological roles of the AHR in the immune system is evolving, there is little known about its role in hematopoiesis and hematopoietic diseases. Prior studies demonstrated that AHR null (AHR-KO) mice have impaired hematopoietic stem cell (HSC) function; they develop myeloproliferative changes in peripheral blood cells, and alterations in hematopoietic stem and progenitor cell populations in the bone marrow. We hypothesized mice lacking AHR expression only within hematopoietic cells (AHRVav1 mice) would develop similar changes. However, we did not observe a complete phenocopy of AHR-KO and AHRVav1 animals at 2 or 18 months of age. To illuminate the signaling mechanisms underlying the alterations in hematopoiesis observed in these mice, we sorted a population of cells highly enriched for HSC function (LSK cells: CD34-CD48-CD150+) and performed microarray analyses. Ingenuity Pathway and Gene Set Enrichment Analyses revealed that that loss of AHR within HSCs alters several gene and signaling networks important for HSC function. Differences in gene expression networks among HSCs from AHR-KO and AHRVav1 mice suggest that AHR in bone marrow stromal cells also contributes to HSC function. In addition, numerous studies have suggested a role for AHR in both regulation of hematopoietic cells, and in the development of blood diseases. More work is needed to define what these signals are, and how they act upon HSCs.
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spelling doaj.art-beba980c23124282a5c3cf8304d128172022-12-21T23:20:15ZengPublic Library of Science (PLoS)PLoS ONE1932-62032018-01-011311e020640710.1371/journal.pone.0206407Conditional deletion of Ahr alters gene expression profiles in hematopoietic stem cells.John A BennettKameshwar P SinghStephen L WelleLisbeth A BouleB Paige LawrenceThomas A GasiewiczThe aryl hydrocarbon receptor (AHR) is a ligand activated bHLH transcription factor that belongs to the Per-Arnt-Sim (PAS) superfamily of proteins involved in mediating responses to cellular environment regulating normal physiological and developmental pathways. The AHR binds a broad range of naturally derived and synthetic compounds, and plays a major role in mediating effects of certain environmental chemicals. Although our understanding of the physiological roles of the AHR in the immune system is evolving, there is little known about its role in hematopoiesis and hematopoietic diseases. Prior studies demonstrated that AHR null (AHR-KO) mice have impaired hematopoietic stem cell (HSC) function; they develop myeloproliferative changes in peripheral blood cells, and alterations in hematopoietic stem and progenitor cell populations in the bone marrow. We hypothesized mice lacking AHR expression only within hematopoietic cells (AHRVav1 mice) would develop similar changes. However, we did not observe a complete phenocopy of AHR-KO and AHRVav1 animals at 2 or 18 months of age. To illuminate the signaling mechanisms underlying the alterations in hematopoiesis observed in these mice, we sorted a population of cells highly enriched for HSC function (LSK cells: CD34-CD48-CD150+) and performed microarray analyses. Ingenuity Pathway and Gene Set Enrichment Analyses revealed that that loss of AHR within HSCs alters several gene and signaling networks important for HSC function. Differences in gene expression networks among HSCs from AHR-KO and AHRVav1 mice suggest that AHR in bone marrow stromal cells also contributes to HSC function. In addition, numerous studies have suggested a role for AHR in both regulation of hematopoietic cells, and in the development of blood diseases. More work is needed to define what these signals are, and how they act upon HSCs.http://europepmc.org/articles/PMC6214519?pdf=render
spellingShingle John A Bennett
Kameshwar P Singh
Stephen L Welle
Lisbeth A Boule
B Paige Lawrence
Thomas A Gasiewicz
Conditional deletion of Ahr alters gene expression profiles in hematopoietic stem cells.
PLoS ONE
title Conditional deletion of Ahr alters gene expression profiles in hematopoietic stem cells.
title_full Conditional deletion of Ahr alters gene expression profiles in hematopoietic stem cells.
title_fullStr Conditional deletion of Ahr alters gene expression profiles in hematopoietic stem cells.
title_full_unstemmed Conditional deletion of Ahr alters gene expression profiles in hematopoietic stem cells.
title_short Conditional deletion of Ahr alters gene expression profiles in hematopoietic stem cells.
title_sort conditional deletion of ahr alters gene expression profiles in hematopoietic stem cells
url http://europepmc.org/articles/PMC6214519?pdf=render
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