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Meflin defines mesenchymal stem cells and/or their early progenitors with multilineage differentiation capacity.

Authors :
Hara, Akitoshi
Kato, Katsuhiro
Ishihara, Toshikazu
Kobayashi, Hiroki
Asai, Naoya
Mii, Shinji
Shiraki, Yukihiro
Miyai, Yuki
Ando, Ryota
Mizutani, Yasuyuki
Iida, Tadashi
Takefuji, Mikito
Murohara, Toyoaki
Takahashi, Masahide
Enomoto, Atsushi
Source :
Genes to Cells. Jul2021, Vol. 26 Issue 7, p495-512. 18p.
Publication Year :
2021

Abstract

Mesenchymal stem cells (MSCs) are the likely precursors of multiple lines of mesenchymal cells. The existence of bona fide MSCs with self‐renewal capacity and differentiation potential into all mesenchymal lineages, however, has been unclear because of the lack of MSC‐specific marker(s) that are not expressed by the terminally differentiated progeny. Meflin, a glycosylphosphatidylinositol‐anchored protein, is an MSC marker candidate that is specifically expressed in rare stromal cells in all tissues. Our previous report showed that Meflin expression becomes down‐regulated in bone marrow‐derived MSCs cultured on plastic, making it difficult to examine the self‐renewal and differentiation of Meflin‐positive cells at the single‐cell level. Here, we traced the lineage of Meflin‐positive cells in postnatal and adult mice, showing that those cells differentiated into white and brown adipocytes, osteocytes, chondrocytes and skeletal myocytes. Interestingly, cells derived from Meflin‐positive cells formed clusters of differentiated cells, implying the in situ proliferation of Meflin‐positive cells or their lineage‐committed progenitors. These results, taken together with previous findings that Meflin expression in cultured MSCs was lost upon their multilineage differentiation, suggest that Meflin is a useful potential marker to localize MSCs and/or their immature progenitors in multiple tissues. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
13569597
Volume :
26
Issue :
7
Database :
Academic Search Index
Journal :
Genes to Cells
Publication Type :
Academic Journal
Accession number :
151330041
Full Text :
https://doi.org/10.1111/gtc.12855