脂肪生成
间充质干细胞
脂肪细胞
成骨细胞
生物
细胞分化
骨髓
碱性磷酸酶
祖细胞
干细胞
细胞生物学
内分泌学
内科学
化学
脂肪组织
免疫学
生物化学
体外
医学
酶
基因
作者
Zhuo Chen,Min Chang,Yan Peng,Li Zhao,Yurui Zhan,Lijing Wang,Rui Wang
标识
DOI:10.1016/j.regpep.2007.01.003
摘要
Cumulative evidence indicates that bone marrow mesenchymal stem cells (MSCs) are multipotent cells capable of differentiating to osteogenic and adipogenic lineages when stimulated under appropriate conditions. Whether OGP(10–14) directly regulates the progenitor cells differentiating into osteoblasts or adipocytes remains unknown. In the present study, we investigated the roles of OGP(10–14) in differentiation along these separate lineages using rat bone marrow MSCs. Our results showed that OGP(10–14) promoted osteogenic differentiation of the stem cells and concurrently inhibited adipocyte formation. OGP(10–14) increased alkaline phosphatase (ALP) activity and mineralized nodule formation, and stimulated osteoblast-specific mRNA expression of core-binding factor 1 (cbfa1). In contrast, OGP(10–14) decreased adipocyte numbers and inhibited adipocyte-specific mRNA expression of peroxisome proliferator-activated receptor-γ 2 (PPARγ2). These observations suggest that commitment of MSCs into osteogenic or adipogenic lineages is regulated by OGP(10–14).
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