破骨细胞
瘦素
化学
酸性磷酸酶
抗酒石酸酸性磷酸酶
激活剂(遗传学)
过氧化物酶体增殖物激活受体
受体
污渍
内科学
内分泌学
细胞生物学
分子生物学
生物化学
生物
酶
医学
基因
肥胖
作者
Zhenyu Wang,Yun Zhu,Xiaozhong Yang,Gang Yang,Weiwen Zhu,Tao Ma,Jian Zhang
出处
期刊:PubMed
日期:2015-02-01
卷期号:31 (2): 145-8
被引量:4
摘要
To investigate the effects of leptin on the differentiation of RAW264.7 cells into osteoclasts induced by soluble receptor activator of nuclear factor-κB ligand (sRANKL) and its possible mechanism.The effects of leptin on the differentiation from osteoclast precursor cells into osteoclasts were detected by tartrate-resistant acid phosphatase (TRAP) staining. The mRNA expressions of TRAP and peroxisome proliferator-activated receptor γ (PPARγ) in osteoclast precursor cells were measured by real-time quantitative PCR (qRT-PCR). The protein expressions of TRAP and PPARγ were detected by Western blotting.Compared with sRANKL treatment group, the differentiation from osteoclast precursor cells into osteoclasts was significantly inhibited in sRANKL combined with leptin treatment groups. Additionally, the mRNA and protein expressions of both TRAP and PPARγ significantly decreased in sRANKL combined with leptin treatment groups compared with the sRANKL treatment alone. Furthermore, the expression of PPARγ was reduced in a dose-dependent manner.Leptin could inhibit the differentiation of RAW264.7 cells into osteoclasts via inhibiting the expression of PPARγ.
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