1,25(OH)2vitamin D3 inhibits cell proliferation by promoting cell cycle arrest without inducing apoptosis and modifies cell morphology of mesenchymal multipotent cells

被引:71
作者
Artaza, Jorge N. [1 ,2 ]
Sirad, Fara
Ferrini, Monica G. [2 ]
Norris, Keith C. [2 ]
机构
[1] Charles R Drew Univ Med & Sci, Dept Internal Med, Div Endocrinol, Los Angeles, CA 90059 USA
[2] Univ Calif Los Angeles, David Geffen Sch Med, Dept Med, Los Angeles, CA 90095 USA
基金
美国国家卫生研究院;
关键词
VDR; PCNA; Rho; Wrch-1; Bcl-2; Survivin; VITAMIN-D; ANDROGEN RECEPTOR; STEM-CELLS; DIFFERENTIATION; EXPRESSION; RHO; TRANSCRIPTION; ADIPOGENESIS; MYOGENESIS; PHENOTYPE;
D O I
10.1016/j.jsbmb.2010.01.001
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The vitamin D receptor (VDR) and its ligand 1,25D play an important role in regulating cell growth and cell fate. We examined the effect of 1,25D on cell morphology, cell proliferation, cell cycle progression and apoptosis on mesenchymal multipotent cells. Multipotent cells were treated with and without 1,25D in a time- and dose-dependent manner. Changes in cell morphology were evaluated by a green fluorescence fluorocrome. Cell proliferation was determined by the Formazan assay and PCNA antigen expression. The expression of genes related to the cell cycle was analyzed by DNA microarrays, (RTPCR)-P-2 arrays and western blots. Apoptosis was evaluated by TUNEL assay, and the expression of pro- and anti-apoptotic related genes by (RTPCR)-P-2 arrays and western blots. 1,25D inhibited cell proliferation, induced cell cycle arrest, and promoted accumulation of cells in G0/G1 phase without inducing apoptosis. An increase in cell size was associated with a decrease in the GTPase Rho and the atypical Rho family GTPase Rhou/Wrch-1 expression without inducing Wnt-1 expression. Survivin expression was also increased and may represent a novel 1,25D-mediated pathway regulating tissue injury and fibrosis. The data provide a mechanistic explanation for the anti-proliferative and anti-apoptotic properties of 1,25D in mesenchymal multipotent cells. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:73 / 83
页数:11
相关论文
共 49 条
[1]   Myostatin inhibits myogenesis and promotes adipogenesis in C3H 10T(1/2) mesenchymal multipotent cells [J].
Artaza, JN ;
Bhasin, S ;
Magee, TR ;
Reisz-Porszasz, S ;
Shen, RQ ;
Groome, NP ;
Fareez, MM ;
Gonzalez-Cadavid, NF .
ENDOCRINOLOGY, 2005, 146 (08) :3547-3557
[2]   Myostatin promotes a fibrotic phenotypic switch in multipotent C3H 10T1/2 cells without affecting their differentiation into myofibroblasts [J].
Artaza, Jorge N. ;
Singh, Rajan ;
Ferrini, Monica G. ;
Braga, Melissa ;
Tsao, James ;
Gonzalez-Cadavid, Nestor F. .
JOURNAL OF ENDOCRINOLOGY, 2008, 196 (02) :235-249
[3]   Alterations in myostatin expression are associated with changes in cardiac left ventricular mass but not ejection fraction in the mouse [J].
Artaza, Jorge N. ;
Reisz-Porszasz, Suzanne ;
Dow, Joan S. ;
Kloner, Robert A. ;
Tsao, James ;
Bhasin, Shalender ;
Gonzalez-Cadavid, Nestor F. .
JOURNAL OF ENDOCRINOLOGY, 2007, 194 (01) :63-76
[4]   Vitamin D reduces the expression of collagen and key profibrotic factors by inducing an antifibrotic phenotype in mesenchymal multipotent cells [J].
Artaza, Jorge N. ;
Norris, Keith C. .
JOURNAL OF ENDOCRINOLOGY, 2009, 200 (02) :207-221
[5]   Muscle satellite cells are multipotential stem cells that exhibit myogenic, osteogenic, and adipogenic differentiation [J].
Asakura, A ;
Komaki, M ;
Rudnicki, MA .
DIFFERENTIATION, 2001, 68 (4-5) :245-253
[6]   Stem cells in adult skeletal muscle [J].
Asakura, A .
TRENDS IN CARDIOVASCULAR MEDICINE, 2003, 13 (03) :123-128
[7]  
Atkinson BL, 1997, J CELL BIOCHEM, V65, P325, DOI 10.1002/(SICI)1097-4644(19970601)65:3<325::AID-JCB3>3.3.CO
[8]  
2-G
[9]   MODULATION OF CELL-PROLIFERATION AND CELL-CYCLE, AND INHIBITION OF CYTOKINESIS BY 1,25-DIHYDROXYVITAMIN-D3 IN C3H/10T1/2 FIBROBLASTS [J].
BRACKMAN, D ;
LILLEHAUG, JR ;
AKSNES, L ;
AARSKOG, D .
JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 1993, 46 (02) :155-162
[10]   The Transforming Rho Family GTPase Wrch-1 Disrupts Epithelial Cell Tight Junctions and Epithelial Morphogenesis [J].
Brady, Donita C. ;
Alan, Jamie K. ;
Madigan, James P. ;
Fanning, Alan S. ;
Cox, Adrienne D. .
MOLECULAR AND CELLULAR BIOLOGY, 2009, 29 (04) :1035-1049