Retention of Multilineage Differentiation Potential of Mesenchymal Cells during Proliferation in Response to FGF

Biochemical and Biophysical Research Communications Volume 288 Issue 2 Page 413-419 published_at 2001-10-26
アクセス数 : 861
ダウンロード数 : 324

今月のアクセス数 : 6
今月のダウンロード数 : 8
File
BBRC_288_413.pdf 1.12 MB 種類 : fulltext
Title ( eng )
Retention of Multilineage Differentiation Potential of Mesenchymal Cells during Proliferation in Response to FGF
Creator
Tsutsumi Shinichi
Miyazaki Kazuko
Pan Haiou
Koike Chika
Yoshida Eri
Takagishi Kenji
Kato Yukio
Source Title
Biochemical and Biophysical Research Communications
Volume 288
Issue 2
Start Page 413
End Page 419
Abstract
Mesenchymal stem cells (MSC) that can differentiate to various connective tissue cells may be useful for autologous cell transplantation to defects of bone, cartilage, and tendon, if MSC can be expanded in vitro. However, a short life span of MSC and a reduction in their differentiation potential in culture have limited their clinical application. The purpose of this study is to identify a growth factor(s) involved in self-renewal of MSC and the maintenance of their multilineage differentiation potential. Fibroblast growth factor-2 (FGF-2) markedly increased the growth rate and the life span of rabbit, canine, and human bone marrow MSC in monolayer cultures. This effect of FGF-2 was more prominent in low-density cultures than in high-density cultures. In addition, all MSC expanded in vitro with FGF-2, but not without FGF-2, differentiated to chondrocytes in pellet cultures. The FGF(+) MSC also retained the osteogenic and adipogenic potential throughout many mitotic divisions. These findings suggest that FGFs play a crucial role in self-renewal of MSC.
Keywords
mesenchymal stem cell
FGF
multilineage differentiation potential
life span
NDC
Medical sciences [ 490 ]
Language
eng
Resource Type journal article
Publisher
Elsevier
Date of Issued 2001-10-26
Rights
Copyright (c) 2001 Academic Press
Publish Type Author’s Original
Access Rights open access
Source Identifier
[ISSN] 0006-291X
[DOI] 10.1006/bbrc.2001.5777
[NCID] AA00564395
[DOI] http://dx.doi.org/10.1006/bbrc.2001.5777