Zhang K, Zhang F-J, Zhao W-J, Xing G-S, Bai X, Wang Y
Department of Laboratory, Tianjin Hospital, Tianjin, China.
Eur Rev Med Pharmacol Sci. 2014 Jun;18(11):1610-7.
This work aims to investigate the effects of parathyroid hormone-related peptide (PTHrP) (1-86) on osteogenic and adipogenic differentiation of human mesenchymal stem cells (hMSCs) and the related mechanisms.
hMSCs were isolated and cultured in vitro. They were divided into control group, osteogenesis group, adipogenesis group, osteogenesis+PTHrP group and adipogenesis+PTHrP group. The cell proliferation and differentiation, and expression levels of osteopontin (OPN) and lipoprotein lipase (LPL) mRNA were observed.
The proliferation rates of hMSCs in osteogenesis+PTHrP and adipogenesis+PTHrP group were significantly higher than that in control group, respectively (p < 0.01). The alkaline phosphatase (ALP)-positive osteoblasts firstly appeared in osteogenesis+PTHrP group, and Sudan IV-positive adipocytes firstly appeared in adipogenesis group. The expression level of OPN mRNA in osteogenesis+PTHrP group was significantly higher than that in osteogenesis group (p < 0.05), and that in adipogenesis+PTHrP group was also higher than adipogenesis group (p < 0.05). The expression level of LPL mRNA in osteogenesis+PTHrP group was significantly lower than that in osteogenesis group, and that in adipogenesis+PTHrP group was also lower than adipogenesis group (p < 0.05).
The osteogenesis and adipogenesis are related to each other during the induced differentiation of hMSCs. PTHrP (1-86) can promote the osteogenic differentiation and inhibits the adipogenic differentiation for hMSCs.
本研究旨在探讨甲状旁腺激素相关肽(PTHrP)(1 - 86)对人骨髓间充质干细胞(hMSCs)成骨和成脂分化的影响及其相关机制。
体外分离培养hMSCs。将其分为对照组、成骨组、成脂组、成骨+PTHrP组和成脂+PTHrP组。观察细胞增殖、分化情况以及骨桥蛋白(OPN)和脂蛋白脂肪酶(LPL)mRNA的表达水平。
成骨+PTHrP组和脂肪+PTHrP组hMSCs的增殖率分别显著高于对照组(p < 0.01)。碱性磷酸酶(ALP)阳性成骨细胞最早出现在成骨+PTHrP组,苏丹IV阳性脂肪细胞最早出现在成脂组。成骨+PTHrP组OPN mRNA表达水平显著高于成骨组(p < 0.05),成脂+PTHrP组也高于成脂组(p < 0.05)。成骨+PTHrP组LPL mRNA表达水平显著低于成骨组,成脂+PTHrP组也低于成脂组(p < 0.05)。
hMSCs诱导分化过程中成骨与成脂相互关联。PTHrP(1 - 86)可促进hMSCs的成骨分化并抑制其成脂分化。