Cargando…

A novel association between relaxin receptor polymorphism and hematopoietic stem cell yield after mobilization

Mobilization of hematopoietic stem cells (HSCs) from the bone marrow to the peripheral blood is a complex mechanism that involves adhesive and chemotactic interactions of HSCs as well as their bone marrow microenvironment. In addition to a number of non-genetic factors, genetic susceptibilities also...

Descripción completa

Detalles Bibliográficos
Autores principales: Shin, Saeam, Kim, Juwon, Kim-Wanner, Soo-Zin, Bönig, Halvard, Cho, Sung Ran, Kim, Sinyoung, Choi, Jong Rak, Lee, Kyung-A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5493337/
https://www.ncbi.nlm.nih.gov/pubmed/28666004
http://dx.doi.org/10.1371/journal.pone.0179986
_version_ 1783247484681715712
author Shin, Saeam
Kim, Juwon
Kim-Wanner, Soo-Zin
Bönig, Halvard
Cho, Sung Ran
Kim, Sinyoung
Choi, Jong Rak
Lee, Kyung-A
author_facet Shin, Saeam
Kim, Juwon
Kim-Wanner, Soo-Zin
Bönig, Halvard
Cho, Sung Ran
Kim, Sinyoung
Choi, Jong Rak
Lee, Kyung-A
author_sort Shin, Saeam
collection PubMed
description Mobilization of hematopoietic stem cells (HSCs) from the bone marrow to the peripheral blood is a complex mechanism that involves adhesive and chemotactic interactions of HSCs as well as their bone marrow microenvironment. In addition to a number of non-genetic factors, genetic susceptibilities also contribute to the mobilization outcome. Identification of genetic factors associated with HSC yield is important to better understand the mechanism behind HSC mobilization. In the present study, we enrolled 148 Korean participants (56 healthy donors and 92 patients) undergoing HSC mobilization for allogeneic or autologous HSC transplantation. Among a total of 53 polymorphisms in 33 candidate genes, one polymorphism (rs11264422) in relaxin/insulin-like family peptide receptor 4 (RXFP4) gene was significantly associated with a higher HSC yield after mobilization in Koreans. However, in a set of 101 Europeans, no association was found between circulating CD34+ cell counts and rs11264422 genotype. Therefore, we suggest that the ethnic differences in subjects’ genetic background may be related to HSC mobilization. In conclusion, the relaxin—relaxin receptor axis may play an important role in HSC mobilization. We believe that the results of the current study could provide new insights for therapies that use relaxin and HSC populations, as well as a better understanding of HSC regulation and mobilization at the molecular level.
format Online
Article
Text
id pubmed-5493337
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-54933372017-07-18 A novel association between relaxin receptor polymorphism and hematopoietic stem cell yield after mobilization Shin, Saeam Kim, Juwon Kim-Wanner, Soo-Zin Bönig, Halvard Cho, Sung Ran Kim, Sinyoung Choi, Jong Rak Lee, Kyung-A PLoS One Research Article Mobilization of hematopoietic stem cells (HSCs) from the bone marrow to the peripheral blood is a complex mechanism that involves adhesive and chemotactic interactions of HSCs as well as their bone marrow microenvironment. In addition to a number of non-genetic factors, genetic susceptibilities also contribute to the mobilization outcome. Identification of genetic factors associated with HSC yield is important to better understand the mechanism behind HSC mobilization. In the present study, we enrolled 148 Korean participants (56 healthy donors and 92 patients) undergoing HSC mobilization for allogeneic or autologous HSC transplantation. Among a total of 53 polymorphisms in 33 candidate genes, one polymorphism (rs11264422) in relaxin/insulin-like family peptide receptor 4 (RXFP4) gene was significantly associated with a higher HSC yield after mobilization in Koreans. However, in a set of 101 Europeans, no association was found between circulating CD34+ cell counts and rs11264422 genotype. Therefore, we suggest that the ethnic differences in subjects’ genetic background may be related to HSC mobilization. In conclusion, the relaxin—relaxin receptor axis may play an important role in HSC mobilization. We believe that the results of the current study could provide new insights for therapies that use relaxin and HSC populations, as well as a better understanding of HSC regulation and mobilization at the molecular level. Public Library of Science 2017-06-30 /pmc/articles/PMC5493337/ /pubmed/28666004 http://dx.doi.org/10.1371/journal.pone.0179986 Text en © 2017 Shin et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Shin, Saeam
Kim, Juwon
Kim-Wanner, Soo-Zin
Bönig, Halvard
Cho, Sung Ran
Kim, Sinyoung
Choi, Jong Rak
Lee, Kyung-A
A novel association between relaxin receptor polymorphism and hematopoietic stem cell yield after mobilization
title A novel association between relaxin receptor polymorphism and hematopoietic stem cell yield after mobilization
title_full A novel association between relaxin receptor polymorphism and hematopoietic stem cell yield after mobilization
title_fullStr A novel association between relaxin receptor polymorphism and hematopoietic stem cell yield after mobilization
title_full_unstemmed A novel association between relaxin receptor polymorphism and hematopoietic stem cell yield after mobilization
title_short A novel association between relaxin receptor polymorphism and hematopoietic stem cell yield after mobilization
title_sort novel association between relaxin receptor polymorphism and hematopoietic stem cell yield after mobilization
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5493337/
https://www.ncbi.nlm.nih.gov/pubmed/28666004
http://dx.doi.org/10.1371/journal.pone.0179986
work_keys_str_mv AT shinsaeam anovelassociationbetweenrelaxinreceptorpolymorphismandhematopoieticstemcellyieldaftermobilization
AT kimjuwon anovelassociationbetweenrelaxinreceptorpolymorphismandhematopoieticstemcellyieldaftermobilization
AT kimwannersoozin anovelassociationbetweenrelaxinreceptorpolymorphismandhematopoieticstemcellyieldaftermobilization
AT bonighalvard anovelassociationbetweenrelaxinreceptorpolymorphismandhematopoieticstemcellyieldaftermobilization
AT chosungran anovelassociationbetweenrelaxinreceptorpolymorphismandhematopoieticstemcellyieldaftermobilization
AT kimsinyoung anovelassociationbetweenrelaxinreceptorpolymorphismandhematopoieticstemcellyieldaftermobilization
AT choijongrak anovelassociationbetweenrelaxinreceptorpolymorphismandhematopoieticstemcellyieldaftermobilization
AT leekyunga anovelassociationbetweenrelaxinreceptorpolymorphismandhematopoieticstemcellyieldaftermobilization
AT shinsaeam novelassociationbetweenrelaxinreceptorpolymorphismandhematopoieticstemcellyieldaftermobilization
AT kimjuwon novelassociationbetweenrelaxinreceptorpolymorphismandhematopoieticstemcellyieldaftermobilization
AT kimwannersoozin novelassociationbetweenrelaxinreceptorpolymorphismandhematopoieticstemcellyieldaftermobilization
AT bonighalvard novelassociationbetweenrelaxinreceptorpolymorphismandhematopoieticstemcellyieldaftermobilization
AT chosungran novelassociationbetweenrelaxinreceptorpolymorphismandhematopoieticstemcellyieldaftermobilization
AT kimsinyoung novelassociationbetweenrelaxinreceptorpolymorphismandhematopoieticstemcellyieldaftermobilization
AT choijongrak novelassociationbetweenrelaxinreceptorpolymorphismandhematopoieticstemcellyieldaftermobilization
AT leekyunga novelassociationbetweenrelaxinreceptorpolymorphismandhematopoieticstemcellyieldaftermobilization