Contribution of PDGFRα lineage cells in adult mouse hematopoiesis.


Journal

Biochemical and biophysical research communications
ISSN: 1090-2104
Titre abrégé: Biochem Biophys Res Commun
Pays: United States
ID NLM: 0372516

Informations de publication

Date de publication:
01 01 2021
Historique:
received: 26 11 2020
accepted: 27 11 2020
pubmed: 15 12 2020
medline: 10 4 2021
entrez: 14 12 2020
Statut: ppublish

Résumé

Platelet-derived growth factor receptor alpha (PDGFRα) is a dominant marker of mesodermal mesenchymal cells in mice. Previous studies demonstrated that PDGFRα-positive (PDGFRα+) mesodermal cells develop not only into mesenchymal cells but also into a subset of total hematopoietic cells (HCs) in the limited period during mouse embryogenesis. However, the precise characteristics of the PDGFRα lineage positive (PDGFRα Lin+) HCs in adult mouse hematopoiesis are largely unknown. In this study, we systematically evaluated the characteristics of PDGFRα Lin+ HCs in the bone marrow and peripheral blood using PDGFRα-CRE; ROSA

Identifiants

pubmed: 33309273
pii: S0006-291X(20)32158-6
doi: 10.1016/j.bbrc.2020.11.114
pii:
doi:

Substances chimiques

Receptor, Platelet-Derived Growth Factor alpha EC 2.7.10.1

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

186-192

Informations de copyright

Copyright © 2020 The Authors. Published by Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: Conflicts of interest K.T. is a scientific founder of and received research funding from StemRIM. K.T. and T.S. are stockholders of StemRIM. T.K., Y.O., S.Y., M.N., E.T., R.Y., and E.W. are employees of StemRIM. A.M declares no conflict of interest in this study.

Auteurs

Asaka Miura (A)

Department of Stem Cell Therapy Science, Graduate School of Medicine, Osaka University, Suita, 565-0871, Japan.

Takashi Shimbo (T)

Department of Stem Cell Therapy Science, Graduate School of Medicine, Osaka University, Suita, 565-0871, Japan; StemRIM Institute of Regeneration-Inducing Medicine, Osaka University, Suita, 565-0871, Japan.

Tomomi Kitayama (T)

Department of Stem Cell Therapy Science, Graduate School of Medicine, Osaka University, Suita, 565-0871, Japan; StemRIM Co., Ltd., Ibaraki, Osaka, 567-0085, Japan.

Yuya Ouchi (Y)

Department of Stem Cell Therapy Science, Graduate School of Medicine, Osaka University, Suita, 565-0871, Japan; StemRIM Co., Ltd., Ibaraki, Osaka, 567-0085, Japan.

Sho Yamazaki (S)

Department of Stem Cell Therapy Science, Graduate School of Medicine, Osaka University, Suita, 565-0871, Japan; StemRIM Co., Ltd., Ibaraki, Osaka, 567-0085, Japan.

Mami Nishida (M)

Department of Stem Cell Therapy Science, Graduate School of Medicine, Osaka University, Suita, 565-0871, Japan; StemRIM Co., Ltd., Ibaraki, Osaka, 567-0085, Japan.

Eiichi Takaki (E)

Department of Stem Cell Therapy Science, Graduate School of Medicine, Osaka University, Suita, 565-0871, Japan; StemRIM Co., Ltd., Ibaraki, Osaka, 567-0085, Japan.

Ryoma Yamamoto (R)

Department of Stem Cell Therapy Science, Graduate School of Medicine, Osaka University, Suita, 565-0871, Japan; StemRIM Co., Ltd., Ibaraki, Osaka, 567-0085, Japan.

Edward Wijaya (E)

Department of Stem Cell Therapy Science, Graduate School of Medicine, Osaka University, Suita, 565-0871, Japan; StemRIM Co., Ltd., Ibaraki, Osaka, 567-0085, Japan.

Katsuto Tamai (K)

Department of Stem Cell Therapy Science, Graduate School of Medicine, Osaka University, Suita, 565-0871, Japan. Electronic address: tamai@gts.med.osaka-u.ac.jp.

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Classifications MeSH