Astudillo Pablo, Ríos Susana, Pastenes Luis, Pino Ana María, Rodríguez J Pablo
Laboratorio de Biología Celular, Instituto de Nutrición y Tecnología de los Alimentos (INTA), Universidad de Chile, Santiago, Chile.
J Cell Biochem. 2008 Mar 1;103(4):1054-65. doi: 10.1002/jcb.21516.
The bone marrow contains mesenchymal stem cells (MSCs) that differentiate to the osteogenic and adipogenic lineages. The fact that the decrease in bone volume of age-related osteoporosis is accompanied by an increase in marrow adipose tissue implies the importance that the adipogenic process may have in bone loss. We previously observed that MSCs from control and osteoporotic women showed differences in their capacity to differentiate into the osteogenic and adipogenic pathways. In vitro studies indicate that bone marrow stromal cells are responsive to leptin, which increases their proliferation, differentiation to osteoblasts, and the number of mineralized nodules, but inhibits their differentiation to adipocytes. The aim of the present report was to study the direct effect of leptin on control and osteoporotic MSCs analyzing whether the protective effect of leptin against osteoporosis could be expressed by inhibition of adipocyte differentiation. MSCs from control, and osteoporotic donors were subjected to adipogenic conditions, in the absence or in the presence of 62.5 nM leptin. The number of adipocytes, the content of PPARgamma protein, and mRNA, and leptin mRNA were measured by flow cytometry, Western blot, and RT-PCR, respectively. Results indicate that control and osteoporotic MSCs differ in their adipogenic potential as shown by expression of active PPARgamma protein. Leptin exerted an antiadipogenic effect only on control MSCs increasing the proportion of inactive phosphorylated PPARgamma protein. Finally, results obtained during adipogenesis of osteoporotic cells suggest that this process is abnormal not only because of increased adipocyte number, but because of impaired leptin cells response.
骨髓中含有间充质干细胞(MSC),这些细胞可分化为成骨和成脂谱系。与年龄相关的骨质疏松症患者骨量减少的同时骨髓脂肪组织增加,这一事实表明成脂过程可能在骨质流失中具有重要作用。我们之前观察到,来自对照女性和骨质疏松症女性的间充质干细胞在分化为成骨和成脂途径的能力上存在差异。体外研究表明,骨髓基质细胞对瘦素敏感,瘦素可增加其增殖、向成骨细胞的分化以及矿化结节的数量,但会抑制其向脂肪细胞的分化。本报告的目的是研究瘦素对对照和骨质疏松症间充质干细胞的直接作用,分析瘦素对骨质疏松症的保护作用是否可通过抑制脂肪细胞分化来体现。将来自对照和骨质疏松症供体的间充质干细胞置于成脂条件下,分别在不存在或存在62.5 nM瘦素的情况下培养。分别通过流式细胞术、蛋白质印迹法和逆转录聚合酶链反应测定脂肪细胞数量、PPARγ蛋白含量、mRNA以及瘦素mRNA。结果表明,如活性PPARγ蛋白的表达所示,对照和骨质疏松症间充质干细胞在成脂潜能上存在差异。瘦素仅对对照间充质干细胞发挥抗成脂作用,增加非活性磷酸化PPARγ蛋白的比例。最后,骨质疏松症细胞成脂过程中获得的结果表明,这一过程异常不仅是因为脂肪细胞数量增加,还因为瘦素细胞反应受损。