ヤマト マサユキ
Yamato Masayuki
大和 雅之 所属 医学研究科 医学研究科 (医学部医学科をご参照ください) 職種 教授 |
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論文種別 | 原著 |
言語種別 | 英語 |
査読の有無 | 査読あり |
表題 | CD61 enriches long-term repopulating hematopoietic stem cells. |
掲載誌名 | 正式名:Biochemical and biophysical research communications 略 称:Biochem Biophys Res Commun ISSNコード:(1090-2104)0006-291X(Linking) |
掲載区分 | 国外 |
出版社 | Elsevier |
巻・号・頁 | 365(1),pp.176-182 |
著者・共著者 | Umemoto Terumasa†, Yamato Masayuki, Shiratsuchi Yoshiko, Terasawa Masao, Yang Joseph, Nishida Kohji, Kobayashi Yoshiro, Okano Teruo* |
担当区分 | 2nd著者 |
発行年月 | 2008/01 |
概要 | Among the subsets that define hematopoietic stem cells (HSCs), CD34- c-kit+ Sca-1+ lineage marker- (CD34-KSL) cells are regarded as one of the populations that have the highest enrichment of HSCs in adult mouse bone marrow. Here, we demonstrate that long-term repopulating hematopoietic stem cells (LTR-HSCs) have high expression of CD61 (integrin beta3) within the CD34-KSL population. Approximately 60% of CD34-KSL cells showed high expression of CD61. CD61HighCD34-KSL populations also exhibited significantly greater properties of HSC, such as expression of HSC markers, the side population (SP) phenotype, and ability for long-term repopulation. In both SP cells and non-SP (NSP) cells, CD61HighCD34-KSL cells also contained significantly more LTR-HSCs than CD61Low/-CD34-KSL cells. Our results indicate that CD61 is exploitable for HSC enrichment as a supportive positive cell surface marker. |
DOI | 10.1016/j.bbrc.2007.10.168 |
PMID | 17983596 |