FGF-2 suppresses cellular senescence of human mesenchymal stem cells by down-regulation of TGF-β2

被引:123
作者
Ito, Tomomi
Sawada, Rumi
Fujiwara, Yoko
Seyama, Yousuke
Tsuchiya, Toshie
机构
[1] Natl Inst Hlth Sci, Div Med Devices, Setagaya Ku, Tokyo 1588501, Japan
[2] Ochanomizu Univ, Grad Sch Humanities & Sci, Bunkyo Ku, Tokyo 1128610, Japan
关键词
human mesenchymal stem cells; FGF-2; TGF-beta; cellular senescence; cyclin-dependent kinase inhibitors; RB;
D O I
10.1016/j.bbrc.2007.05.067
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Human mesenchymal stem cells (hMSCs) are able to both self-replicate and differentiate into a variety of cell types. Fibroblast growth factor-2 (FGF-2) stimulates the growth of hMSCs in vitro, but its mechanisms have not been clarified yet. In this study, we investigated whether cellular senescence was involved in the stimulation of hMSCs growth by FGF-2 and the expression levels of transforming growth factor-beta 1 and beta 2 (TGF-beta s). Because hMSCs were induced cellular senescence due to long-term culture, FGF-2 decreased the percentage of senescent cells and suppressed GI cell growth arrest through the suppression of p21(CiP1), p53, and p16(INK4a), mRNA expression levels. Furthermore, the levels of TGF-beta s mRNA expression in hMSCs were increased by long-term culture, but FGF-2 suppressed the increase of TGF-beta 2 mRNA expression due to long-term culture. These results suggest that FGF-2 suppresses the hMSCs cellular senescence dependent on the length of culture through down-regulation of TGF-beta 2 expression. (C) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:108 / 114
页数:7
相关论文
共 38 条
[1]
Reversal of human cellular senescence:: roles of the p53 and p16 pathways [J].
Beauséjour, CM ;
Krtolica, A ;
Galimi, F ;
Narita, M ;
Lowe, SW ;
Yaswen, P ;
Campisi, J .
EMBO JOURNAL, 2003, 22 (16) :4212-4222
[2]
Ex vivo enrichment of mesenchymal cell progenitors by fibroblast growth factor 2 [J].
Bianchi, G ;
Banfi, A ;
Mastrogiacomo, M ;
Notaro, R ;
Luzzatto, L ;
Cancedda, R ;
Quarto, R .
EXPERIMENTAL CELL RESEARCH, 2003, 287 (01) :98-105
[3]
Mesenchymal stem cells: building blocks for molecular medicine in the 21st century [J].
Caplan, AI ;
Bruder, SP .
TRENDS IN MOLECULAR MEDICINE, 2001, 7 (06) :259-264
[4]
CHARLES JS, 1999, GENE DEV, V13, P1501
[5]
Measurements of hydrogen peroxide induced premature senescence:: Senescence-associated β-galactosidase and DNA synthesis index in human diploid fibroblasts with down-regulated p53 or Rb [J].
Chen, QM ;
Tu, VC ;
Liu, JP .
BIOGERONTOLOGY, 2000, 1 (04) :335-339
[6]
Darwin JP, 1997, SCIENCE, V276, P71
[7]
A BIOMARKER THAT IDENTIFIES SENESCENT HUMAN-CELLS IN CULTURE AND IN AGING SKIN IN-VIVO [J].
DIMRI, GP ;
LEE, XH ;
BASILE, G ;
ACOSTA, M ;
SCOTT, C ;
ROSKELLEY, C ;
MEDRANO, EE ;
LINSKENS, M ;
RUBELJ, I ;
PEREIRASMITH, O ;
PEACOCKE, M ;
CAMPISI, J .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (20) :9363-9367
[8]
WAF1, A POTENTIAL MEDIATOR OF P53 TUMOR SUPPRESSION [J].
ELDEIRY, WS ;
TOKINO, T ;
VELCULESCU, VE ;
LEVY, DB ;
PARSONS, R ;
TRENT, JM ;
LIN, D ;
MERCER, WE ;
KINZLER, KW ;
VOGELSTEIN, B .
CELL, 1993, 75 (04) :817-825
[9]
In vivo cardiovasculogenesis by direct injection of isolated adult mesenchymal stem cells [J].
Gojo, S ;
Gojo, N ;
Takeda, Y ;
Mori, T ;
Abe, H ;
Kyo, S ;
Hata, J ;
Umezawa, A .
EXPERIMENTAL CELL RESEARCH, 2003, 288 (01) :51-59
[10]
TGF beta-induced growth inhibition in primary fibroblasts requires the retinoblastoma protein [J].
Herrera, RE ;
Makela, TP ;
Weinberg, RA .
MOLECULAR BIOLOGY OF THE CELL, 1996, 7 (09) :1335-1342