Human osteogenic protein-1 induces osteogenic differentiation of adipose-derived stem cells harvested from mice

被引:46
作者
Al-Salleeh, Fahd [2 ]
Beatty, Mark W. [1 ,2 ]
Reinhardt, Richard A. [2 ,3 ]
Petro, Thomas M. [2 ]
Crouch, Larry [2 ]
机构
[1] Univ Nebraska, Dept Adult Restorat Dent, Med Ctr, Coll Dent, Lincoln, NE 68583 USA
[2] Univ Nebraska, Med Ctr, Coll Dent, Dept Oral Biol, Lincoln, NE 68583 USA
[3] Univ Nebraska, Med Ctr, Coll Dent, Dept Surg Specialties, Lincoln, NE 68583 USA
关键词
adipose-derived stem cells; osteogenic protein-1; osteogenic differentiation; calcification; osteopontin;
D O I
10.1016/j.archoralbio.2008.05.014
中图分类号
R78 [口腔科学];
学科分类号
1003 [口腔医学];
摘要
Objective: Osteogenic protein-1 (OP-1) has been shown to stimulate undifferentiated cells to produce mineralized tissue. Adipose tissue is a rich source of undifferentiated cells for tissue engineering purposes. The purpose of this study was to investigate the effect of OP-1 on osteogenic differentiation of adipose-derived stem cells and the production of bony tissue in vitro. Design: Adipose-derived stem cells (ADSCs) were isolated from inguinal fat pads of adult mice. Following cell expansion the cells were plated in 8-well chambered slides. The cells received one of four treatments: Group I cells were maintained in control medium, Group 2 cells were cultured in a common osteogenic medium, Group 3 cells were cultured in osteogenic medium supplemented with 250 ng/mL of OP-1, and Group 4 cells were cultured with 250 ng/mL of OP-1 added to control medium. Osteogenic differentiation of ADSCs was determined by estimating the number and size of mineralized nodules, and the amount of extracellular osteopontin secreted into cell culture medium. Mineralized nodule production was assessed at day 21 with von Kossa staining. Extracellular osteopontin release was measured after 8 and 21 days by enzyme-linked immunosorbant assay (ELISA). ANOVA/Tukey tests were used to identify differences among the four treatment groups for mineralized nodule production and osteopontin release (p < 0.05). Results: Deposition of calcified nodules and osteopontin secretion was significantly greater for cell cultures incubated with OP-1 (p <= 0.05). At day 21, no significant differences in osteopontin secretion were noted among groups incubated with osteogenic nutrients and/ or OP-1 (p > 0.05), which were significantly higher than the group incubated in cell growth medium only (p <= 0.05). No significant differences in osteopontin secretion were noted between 8 and 21 days for any group (p > 0.05). Linear regression analysis demonstrated a linear relationship was present between the presence of calcified nodules and the amount of osteopontin released (p < 0.05). Conclusions: OP-1 is a powerful inducer of osteogenic differentiation of adult adipose-derived stem cells. (c) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:928 / 936
页数:9
相关论文
共 37 条
[1]
HUMAN OSTEOGENIC PROTEIN-1 INDUCES BOTH CHONDROBLASTIC AND OSTEOBLASTIC DIFFERENTIATION OF OSTEOPROGENITOR CELLS DERIVED FROM NEWBORN RAT CALVARIA [J].
ASAHINA, I ;
SAMPATH, TK ;
NISHIMURA, I ;
HAUSCHKA, PV .
JOURNAL OF CELL BIOLOGY, 1993, 123 (04) :921-933
[2]
Proliferation and differentiation of osteoblasts and adipocytes in rat bone marrow stroma cell cultures: Effects of dexamethasone and calcitriol [J].
Atmani, H ;
Chappard, D ;
Basle, MF .
JOURNAL OF CELLULAR BIOCHEMISTRY, 2003, 89 (02) :364-372
[3]
MINERALIZED BONE NODULES FORMED INVITRO FROM ENZYMATICALLY RELEASED RAT CALVARIA CELL-POPULATIONS [J].
BELLOWS, CG ;
AUBIN, JE ;
HEERSCHE, JNM ;
ANTOSZ, ME .
CALCIFIED TISSUE INTERNATIONAL, 1986, 38 (03) :143-154
[4]
DETERMINATION OF THE CAPACITY FOR PROLIFERATION AND DIFFERENTIATION OF OSTEOPROGENITOR CELLS IN THE PRESENCE AND ABSENCE OF DEXAMETHASONE [J].
BELLOWS, CG ;
HEERSCHE, JNM ;
AUBIN, JE .
DEVELOPMENTAL BIOLOGY, 1990, 140 (01) :132-138
[5]
Born again bone: Tissue engineering for bone repair [J].
Braddock, M ;
Houston, P ;
Campbell, C ;
Ashcroft, P .
NEWS IN PHYSIOLOGICAL SCIENCES, 2001, 16 :208-213
[6]
Influence of osteogenic protein-1 (OP-1;BMP-7) and transforming growth factor-beta 1 on bone formation in vitro [J].
Cheifetz, S ;
Li, IWS ;
McCulloch, CAG ;
Sampath, K ;
Sodek, J .
CONNECTIVE TISSUE RESEARCH, 1996, 35 (1-4) :71-78
[7]
A quadripotential mesenchymal progenitor cell isolated from the marrow of an adult mouse [J].
Dennis, JE ;
Merriam, A ;
Awadallah, A ;
Yoo, JU ;
Johnstone, B ;
Caplan, AI .
JOURNAL OF BONE AND MINERAL RESEARCH, 1999, 14 (05) :700-709
[8]
Bone induction by BMP-2 transduced stem cells derived from human fat [J].
Dragoo, JL ;
Choi, JY ;
Lieberman, JR ;
Huang, J ;
Zuk, PA ;
Zhang, J ;
Hedrick, MH ;
Benhaim, P .
JOURNAL OF ORTHOPAEDIC RESEARCH, 2003, 21 (04) :622-629
[9]
Osf2/Cbfa1: A transcriptional activator of osteoblast differentiation [J].
Ducy, P ;
Zhang, R ;
Geoffroy, V ;
Ridall, AL ;
Karsenty, G .
CELL, 1997, 89 (05) :747-754
[10]
Differentiation of osteoblasts from mouse embryonic stem cells without generation of embryoid body [J].
Duplomb, Laurence ;
Dagouassat, Maylis ;
Jourdon, Philippe ;
Heymann, Dominique .
IN VITRO CELLULAR & DEVELOPMENTAL BIOLOGY-ANIMAL, 2007, 43 (01) :21-24