Please use this identifier to cite or link to this item:
Title: Androgens stimulate erythropoiesis through the DNA binding activity of the androgen receptor in non-hematopoietic cells.
Austin Authors: McManus, Julie F;Nguyen, Nhu-Y N;Davey, Rachel A;MacLean, Helen E;Pomilio, Giovanna;McCormack, Matthew P;Chiu, Wan Sze;Wei, Andrew H;Zajac, Jeffrey D ;Curtis, David J
Affiliation: Human Molecular Pathology, Alfred Pathology Service, Alfred Health, Melbourne, Australia
Cartherics Pty Ltd, Melbourne, Australia
Hudson Institute of Medical Research, Melbourne, Australia
Australian Centre for Blood Diseases, Central Clinical School, Monash University, Melbourne, Australia
Department of Clinical Haematology, Alfred Health, Melbourne, Australia
Department of Medicine, Austin Health, The University of Melbourne, Heidelberg, Victoria, Australia
Issue Date: Sep-2020 2020-04-20
Publication information: European journal of haematology 2020; 105(3): 247-254
Abstract: Androgens function through DNA and non-DNA binding-dependant signalling of the androgen receptor (AR). How androgens promote erythropoiesis is not fully understood. To identify the androgen signalling pathway, we treated male mice lacking the second zinc finger of the DNA binding domain of the AR (AR∆ZF2 ) with non-aromatizable 5α-dihydrotestosterone (5α-DHT), or aromatizable testosterone. To distinguish direct hematopoietic and non-hematopoietic mechanisms we performed bone marrow reconstitution experiments. In wild-type mice, 5α-DHT had greater erythroid activity than testosterone, which can be aromatized to estradiol. The erythroid response in wild-type mice following 5α-DHT treatment was associated with increased serum erythropoietin (EPO) and its downstream target erythroferrone, and hepcidin suppression. 5α-DHT had no erythroid activity in AR∆ZF2 mice, proving the importance of DNA binding by the AR. Paradoxically testosterone, but not 5α-DHT, suppressed EPO levels in AR∆ZF2 mice, suggesting testosterone following aromatization may oppose the erythroid-stimulating effects of androgens. Female wild-type mice reconstituted with AR∆ZF2 bone marrow cells remained responsive to 5α-DHT. In contrast, AR∆ZF2 mice reconstituted with female wild-type bone marrow cells showed no response to 5α-DHT. Erythroid promoting effects of androgens are mediated through DNA binding-dependent actions of the AR in non-hematopoietic cells, including stimulating EPO expression.
DOI: 10.1111/ejh.13431
ORCID: 0000-0001-5121-0209
Journal: European journal of haematology
PubMed URL: 32311143
Type: Journal Article
Subjects: DNA binding actions
androgen receptor signalling
genetically modified androgen receptor mouse model
non-hematopoietic cells
Appears in Collections:Journal articles

Show full item record

Page view(s)

checked on Jan 30, 2023

Google ScholarTM


Items in AHRO are protected by copyright, with all rights reserved, unless otherwise indicated.