| Literature DB >> 33960573 |
Akitoshi Hara1,2, Katsuhiro Kato2, Toshikazu Ishihara1,2, Hiroki Kobayashi1, Naoya Asai3, Shinji Mii1, Yukihiro Shiraki1, Yuki Miyai1, Ryota Ando1, Yasuyuki Mizutani1, Tadashi Iida1, Mikito Takefuji2, Toyoaki Murohara2, Masahide Takahashi4, Atsushi Enomoto1.
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.Entities:
Keywords: Islr; Meflin; Mesenchymal stem cells; Mesenchymal stromal cells; immunoglobulin superfamily containing leucine-rich repeat; satellite cell
Year: 2021 PMID: 33960573 DOI: 10.1111/gtc.12855
Source DB: PubMed Journal: Genes Cells ISSN: 1356-9597 Impact factor: 1.891