Autogenous regulation of a network of bone morphogenetic proteins (BMPs) mediates the osteogenic differentiation in murine marrow stromal cells

被引:91
作者
Edgar, Cory M. [1 ]
Chakravarthy, Vinay [1 ]
Barnes, George [1 ]
Kakar, Sanjeev [1 ]
Gerstenfeld, Louis C. [1 ]
Einhorn, Thomas A. [1 ]
机构
[1] Boston Univ, Med Ctr, Dept Orthopaed Surg, Orthopaed Res Lab, Boston, MA 02118 USA
关键词
marrow stromal stem cells; bone morphogenctic proteins; BMP; osteoinduction; noggin;
D O I
10.1016/j.bone.2007.01.001
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The expression patterns of (bone morphogenetic proteins) BMPs during fracture repair and pre-natal bone development suggest that these processes are regulated through the coordinated actions of multiple BMPs. Marine bone marrow stromal cells (MSCs) in culture provide a well recognized ex vivo system of mesenchymal stem cell differentiation in which the effects of BMPs can be examined. Studies were performed to determine if MSC differentiation is dependent on the endogenous expression of multiple BMPs and to characterize their interactions. MSCs were harvested from the bone marrow of tibiae and femora of 8 to 10-week-old male C57/136 mice and prepared by standard methods. Osteogenic differentiation was assessed by histological assays, alkaline phosphatase enzyme activity and assays for the expression of multiple mRNAs for BMPs and osteogenic development. The role of autogenously expressed BMPs in controlling the osteogenic differentiation of marrow stromal cells in vitro was assessed in both gain-of-function and loss-of-function experiments. Gain of function experiments were carried out in the presence of exogenously added BMP-2 or -7 and loss-of-function experiments were carried out by BMP antagonism with noggin and BMP-2 antibody blockade. Osteogenic differentiation was concurrent with and proportional to increases in the expression of BMPs-2, -3, -4, -5, -6 and -8A. BMP antagonism with either noggin or BMP-2 antibody blockade inhibited osteogenic differentiation by 50% to 80%, respectively, and reduced the expression of endogenous levels of BMPs-2, -3, -5 and -8A. In contrast, antagonism induced the expression of BMP-4 and -6. The addition of rhBMP-2 or -7 enhanced osteogenic differentiation and produced a reciprocal expression profile in the endogenous BMPs expression as compared to BMP antagonism. BMP antagonism could be rescued through the competitive addition of rhBMP-2. These studies demonstrated that osteogenic differentiation was regulated by a complex network of multiple BMPs that showed selective increased and decreased expression during differentiation. They further demonstrated that BMP-2 was a central regulator in this network. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:1389 / 1398
页数:10
相关论文
共 34 条
[11]   Overexpression of BMP-2 and BMP-4 alters the size and shape of developing skeletal elements in the chick limb [J].
Duprez, D ;
Bella, EJD ;
Richardson, MK ;
Archer, CW ;
Wolpert, L ;
Brickell, PM ;
FrancisWest, PH .
MECHANISMS OF DEVELOPMENT, 1996, 57 (02) :145-157
[12]   A single percutaneous injection of recombinant human bone morphogenetic protein-2 accelerates fracture repair [J].
Einhorn, TA ;
Majeska, RJ ;
Mohaideen, A ;
Kagel, EM ;
Bouxsein, ML ;
Turek, TJ ;
Wozney, JM .
JOURNAL OF BONE AND JOINT SURGERY-AMERICAN VOLUME, 2003, 85A (08) :1425-1435
[13]   Osteogenic differentiation of human mesenchymal stem cells is regulated by bone morphogenetic protein-6 [J].
Friedman, Michael S. ;
Long, Michael W. ;
Hankenson, Kurt D. .
JOURNAL OF CELLULAR BIOCHEMISTRY, 2006, 98 (03) :538-554
[14]   BMP-3 is a novel inhibitor of both activin and BMP-4 signaling in Xenopus embryos [J].
Gamer, LW ;
Nove, J ;
Levin, M ;
Rosen, V .
DEVELOPMENTAL BIOLOGY, 2005, 285 (01) :156-168
[15]   Noggin arrests stromal cell differentiation in vitro [J].
Gazzerro, E ;
Du, Z ;
Devlin, RD ;
Rydziel, S ;
Priest, L ;
Economides, A ;
Canalis, E .
BONE, 2003, 32 (02) :111-119
[16]   Impaired fracture healing in the absence of TNF-α signaling:: The role of TNF-α in endochondral cartilage resorption [J].
Gerstenfeld, LC ;
Cho, TJ ;
Kon, T ;
Aizawa, T ;
Tsay, A ;
Fitch, J ;
Barnes, GL ;
Graves, DT ;
Einhorn, TA .
JOURNAL OF BONE AND MINERAL RESEARCH, 2003, 18 (09) :1584-1592
[17]   EXPRESSION OF DIFFERENTIATED FUNCTION BY MINERALIZING CULTURES OF CHICKEN OSTEOBLASTS [J].
GERSTENFELD, LC ;
CHIPMAN, SD ;
GLOWACKI, J ;
LIAN, JB .
DEVELOPMENTAL BIOLOGY, 1987, 122 (01) :49-60
[18]   Stage specific inhibition of osteoblast lineage differentiation by FGF2 and noggin [J].
Kalajzic, I ;
Kalajzic, Z ;
Hurley, MM ;
Lichtler, AC ;
Rowe, DW .
JOURNAL OF CELLULAR BIOCHEMISTRY, 2003, 88 (06) :1168-1176
[19]   Factors required for bone marrow stromal fibroblast colony formation in vitro [J].
Kuznetsov, SA ;
Friedenstein, AJ ;
Robey, PG .
BRITISH JOURNAL OF HAEMATOLOGY, 1997, 97 (03) :561-570
[20]   COLOCALIZATION OF BMP-7 AND BMP-2 RNAS SUGGESTS THAT THESE FACTORS COOPERATIVELY MEDIATE TISSUE INTERACTIONS DURING MURINE DEVELOPMENT [J].
LYONS, KM ;
HOGAN, BLM ;
ROBERTSON, EJ .
MECHANISMS OF DEVELOPMENT, 1995, 50 (01) :71-83