Wnt signalling mediates the cross-talk between bone marrow derived pre-adipocytic and pre-osteoblastic cell populations

被引:87
作者
Taipaleenmaki, Hanna [1 ,2 ]
Abdallah, Basem M. [1 ]
AlDahmash, Abdullah [3 ]
Saamanen, Anna-Marja [2 ]
Kassem, Moustapha [1 ,3 ]
机构
[1] Odense Univ Hosp, Dept Endocrinol & Metab, Endocrine Res Lab KMEB, DK-5000 Odense, Denmark
[2] Univ Turku, Dept Med Biochem & Genet, Turku, Finland
[3] King Saud Univ, Stem Cell Unit, Riyadh, Saudi Arabia
基金
英国医学研究理事会;
关键词
Mesenchymal stromal cell; Adipocyte; Osteoblast; Wnt signaling; sFRP-1; FRIZZLED-RELATED PROTEIN-1; MESENCHYMAL STEM-CELLS; RECEPTOR TYROSINE KINASE; STROMAL CELLS; IN-VITRO; CHONDROCYTE DIFFERENTIATION; PROGENITOR CELLS; GENE-EXPRESSION; TRABECULAR BONE; ADIPOSE-TISSUE;
D O I
10.1016/j.yexcr.2010.12.015
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The mechanisms underlying the inverse relationship between osteogenic and adipogenic differentiation of bone marrow stromal cells (MSC) are not known in detail. We have previously established two cell lines from mouse bone marrow that are committed to either osteogenic (osteoblasts and chondrocytes) (mMSC(Bone)) or adipogenic (mMSC(Adipo)) lineage. To identify the molecular mechanism determining the lineage commitment, we compared the basal gene expression profile of mMSC(Bone) versus mMSC(Adipo) using Affymetrix GeneChip (R) MG430A 2.0 Array. Gene annotation analysis based on biological function revealed an over-representation of skeletal development genes in mMSC(Bone) while genes related to lipid metabolism and immune response were highly expressed in mMSC(Adipo). In addition, there was a significant up-regulation of canonical Wnt signalling genes in mMSC(Bone) compared to mMSC(Adipo) (p < 0.006). Dual-luciferase assay and expression analysis of genes related to Wnt signalling demonstrated significant activation of Wnt signalling pathway in mMSC(Bone) compared to mMSC(Adipo). Reduced Wnt activity in mMSC(Adipo) was associated with increased expression of the Wnt inhibitor, secreted frizzled-related protein 1 (sFRP-1) at both mRNA and protein levels in mMSC(Adipo). Interestingly, conditioned medium (CM) collected from mMSC(Adipo) (mMSC-CMAdipo) inhibited osteoblast differentiation of mMSC, while depletion of sFRP-1 protein from mMSC-CMAdipo abolished its inhibitory effect on osteoblast differentiation. Furthermore, treatment of mMSC with recombinant sFRP-1 resulted in a dose-dependent inhibition of osteoblast and stimulation of adipocyte differentiation. In conclusion, crosstalk exists between different populations of MSC in the bone marrow, and Wnt signalling functions as a molecular switch that determines the balance between osteoblastogenesis and adipogenesis. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:745 / 756
页数:12
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