Osteo-maturation of adipose-derived stem cells required the combined action of vitamin D3, β-glycerophosphate, and ascorbic acid

被引:30
作者
Gupta, Anurag
Leong, David Tai
Bai, Hui Fen
Singh, Shiv Brat
Lim, Thiam-Chye
Hutmacher, Dietmar Werner
机构
[1] Queensland Univ Technol, Inst Hlth & Biomed Innovat, Brisbane, Qld 4059, Australia
[2] Indian Inst Technol, Sch Med Sci & Technol, Kharagpur 721302, W Bengal, India
[3] Natl Univ Singapore, Dept Biol Sci, Singapore 117548, Singapore
[4] Natl Univ Singapore, Div Bioengn, Singapore 117548, Singapore
[5] Indian Inst Technol, Fac Sch Med Sci & Technol, Dept Mat & Met Engn, Kharagpur 721302, W Bengal, India
[6] Natl Univ Singapore Hosp, Div Plast Surg, Singapore 117548, Singapore
[7] Natl Univ Singapore, Dept Orthoped Surg, Singapore 117548, Singapore
[8] Queensland Univ Technol, Inst Hlth & Biomed Innovat, Brisbane, Qld, Australia
关键词
adipose-derived stem cells; vitamin D3; Osteoblasts; differentiation; induction;
D O I
10.1016/j.bbrc.2007.07.112
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
This study investigated the effects of various components [vitamin D3 (VD3), beta-glycerophosphate (BGP), and ascorbic acid (AA)] on the potential of human adipose-derived progenitor cells (ADPCs) to transdifferentiate into osteoblast-like cells. ADPCs were induced under four different supplement groups: (1) VD3 + BGP + AA, (2) VD3 alone, (3) BGP + AA, and (4) no VD3, BGP or AA. Mineralization studies and presence of bone matrix-related proteins by immunostaining showed that the Group I ADPCs showed their ability to undergo osteoblastic differentiation. Further evaluation was made by estimation of levels of RUNX-2 and TAZ genes. Group I ADPCs showed the consistent expression of RUNX-2 and TAZ levels over the study period of 28 days. The study showed good correlation among various parameters evaluated to conclude that ADPCs could be an alternative source for generating osteoblast-like cells. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:17 / 24
页数:8
相关论文
共 19 条
[1]   CRYSTALS IN CALCIFIED EPIPHYSEAL CARTILAGE AND CORTICAL BONE OF THE RAT [J].
ARSENAULT, AL ;
GRYNPAS, MD .
CALCIFIED TISSUE INTERNATIONAL, 1988, 43 (04) :219-225
[2]   OSTEOCALCIN INDUCES CHEMOTAXIS, SECRETION OF MATRIX PROTEINS, AND CALCIUM-MEDIATED INTRACELLULAR SIGNALING IN HUMAN OSTEOCLAST-LIKE CELLS [J].
CHENU, C ;
COLUCCI, S ;
GRANO, M ;
ZIGRINO, P ;
BARATTOLO, R ;
ZAMBONIN, G ;
BALDINI, N ;
VERGNAUD, P ;
DELMAS, PD ;
ZALLONE, AZ .
JOURNAL OF CELL BIOLOGY, 1994, 127 (04) :1149-1158
[3]   1,25-(OH)2-vitamin D3 suppresses the bone-related Runx2/Cbfa1 gene promoter [J].
Drissi, H ;
Pouliot, A ;
Koolloos, C ;
Stein, JL ;
Lian, JB ;
Stein, GS ;
van Wijnen, AJ .
EXPERIMENTAL CELL RESEARCH, 2002, 274 (02) :323-333
[4]   Increased bone formation in osteocalcin-deficient mice [J].
Ducy, P ;
Desbois, C ;
Boyce, B ;
Pinero, G ;
Story, B ;
Dunstan, C ;
Smith, E ;
Bonadio, J ;
Goldstein, S ;
Gundberg, C ;
Bradley, A ;
Karsenty, G .
NATURE, 1996, 382 (6590) :448-452
[5]  
DUEY P, 1997, CELL, V89, P747
[6]   The function of adipocytes in the bone marrow stroma: An update [J].
Gimble, JM ;
Robinson, CE ;
Wu, X ;
Kelly, KA .
BONE, 1996, 19 (05) :421-428
[7]   Strategies for directing the differentiation of stem cells into the osteogenic lineage in vitro [J].
Heng, BC ;
Cao, T ;
Stanton, LW ;
Robson, P ;
Olsen, B .
JOURNAL OF BONE AND MINERAL RESEARCH, 2004, 19 (09) :1379-1394
[8]   TAZ, a transcriptional modulator of mesenchymal stem cell differentiation [J].
Hong, JH ;
Hwang, ES ;
McManus, MT ;
Amsterdam, A ;
Tian, Y ;
Kalmukova, R ;
Mueller, E ;
Benjamin, T ;
Spiegelman, BM ;
Sharp, PA ;
Hopkins, N ;
Yaffe, MB .
SCIENCE, 2005, 309 (5737) :1074-1078
[9]   Collagen integrin receptors regulate early osteoblast differentiation induced by BMP-2 [J].
Jikko, A ;
Harris, SE ;
Chen, D ;
Mendrick, DL ;
Damsky, CH .
JOURNAL OF BONE AND MINERAL RESEARCH, 1999, 14 (07) :1075-1083
[10]   Osteogenesis versus chondrogenesis by BMP-2 and BMP-7 in adipose stem cells [J].
Knippenberg, M ;
Helder, MN ;
Doulabi, BZ ;
Wuisman, PIJM ;
Klein-Nulend, J .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2006, 342 (03) :902-908