New factors controlling the balance between osteoblastogenesis and adipogenesis

被引:113
作者
Abdallah, Basem M. [1 ,2 ]
Kassem, Moustapha [1 ,2 ,3 ]
机构
[1] Odense Univ Hosp, Endocrine Res Lab KMEB, Dept Endocrinol & Metab, DK-5000 Odense C, Denmark
[2] Univ So Denmark, Odense, Denmark
[3] King Saud Univ, Stem Cell Unit, Riyadh, Saudi Arabia
关键词
DIk1; Pref-1; sFRP-1; Osteoblast; Adipocyte; MESENCHYMAL STEM-CELLS; PREADIPOCYTE FACTOR-I; MATERNAL UNIPARENTAL DISOMY; NECROSIS-FACTOR-ALPHA; ADIPOCYTE DIFFERENTIATION; BONE-FORMATION; STROMAL CELLS; CHROMOSOME; 14; PROTEIN DLK; MARROW;
D O I
10.1016/j.bone.2011.06.030
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
The majority of conditions associated with bone loss, including aging, are accompanied by increased marrow adiposity possibly due to shifting of the balance between osteoblast and adipocyte differentiation in bone marrow stromal (skeletal) stem cells (MSC). In order to study the relationship between osteoblastogenesis and adipogenesis in bone marrow, we have characterized cellular models of multipotent MSC as well as pre-osteoblastic and pre-adipocytic cell populations. Using these models, we identified two secreted factors in the bone marrow microenviroment: secreted frizzled-related protein 1 (sFRP-1) and delta-likel (preadipocyte factor 1) (Dlk1/Pref-1). Both exert regulatory effects on osteoblastogenesis and adipogenesis. Our studies suggest a model for lineage fate determination of MSC that is regulated through secreted factors in the bone marrow microenvironment that mediate a cross-talk between lineage committed cell populations in addition to controlling differentiation choices of multipotent MSC. This article is part of a Special Issue entitled: Interactions Between Bone, Adipose Tissue and Metabolism. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:540 / 545
页数:6
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