A phosphodiesterase inhibitor, pentoxifylline, enhances the bone morphogenetic protein-4 (BMP-4)-dependent differentiation of osteoprogenitor cells

被引:37
|
作者
Tsutsumimoto, T [1 ]
Wakabayashi, S [1 ]
Kinoshita, T [1 ]
Horiuchi, H [1 ]
Takaoka, K [1 ]
机构
[1] Shinshu Univ, Sch Med, Dept Orthopaed Surg, Nagano, Japan
关键词
phosphodiesterase inhibitor; pentoxifylline; bone morphopenetic protein (BMP); cyclic adenosine monophosphate (cAMP); osteoprogenitor cells; osteogenic differentiation;
D O I
10.1016/S8756-3282(02)00839-6
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Bone morphogenetic protein-4 (BMP-4), a member of the transforming growth factor-beta superfamily is capable of initiating differentiation of uncommitted mesenchymal cells into a chondro/osteogenic pathway. This Study reports the effects of pentoxifylline (PT-X), a nonspecific inhibitor of phosphodiesterases (PDEs), that causes elevation of the intracellular cyclic adenosine monophosphate (cAMP) level on the BMP4-induced chondro/osteogenic diffierentiation of a mesenchymal cell line. C3H10T1/2; a bone marrow stromal cell line ST2; and an osteoblastic cell fine, MC3T3-E1. It was found that PTX enhanced BMP-4-induced chondro/osteogenic differentiation in C3H10T1/2 and ST2 cells. Similar effects were observed when adding dibutyryl-cAMP and forskolin. These results indicate that cAMP may potentiate the action of BMP-4 on osteoprogenitor cells, highlighting, the possibility that PDE inhibitors could be used as therapeutic agents to enhance bone formation through this effect. (C) 2002 by Elsevier Science Inc. All rights reserved.
引用
收藏
页码:396 / 401
页数:6
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