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不同培养基血清体积分数对RANKL依赖的RAW264.7细胞分化为破骨细胞影响的蛋白质组学研究

Proteomic study of different culture medium serum volume fractions on RANKL-dependent RAW264.7 cells differentiating into osteoclasts.

作者信息

Xiong Qi, Zhang Lihai, Xin Lingli, Gao Yanpan, Peng Ye, Tang Peifu, Ge Wei

机构信息

Department of Orthopedics, General Hospital of Chinese PLA, Fuxing Road 28# Haidian district, Beijing, 100853 China.

Department of Obstetrics and Gynecology, The Second Artillery General Hospital of Chinese PLA, Xinjiekouwai Street 16# Xicheng district, Beijing, 100088 China.

出版信息

Proteome Sci. 2015 May 2;13:16. doi: 10.1186/s12953-015-0073-6. eCollection 2015.

Abstract

BACKGROUND

Cultivation of osteoclasts is a basic tool for investigating osteolytic bone diseases. Fetal bovine serum (FBS) is the standard supplement used for in vitro cell culture medium. Typically, the serum volume fraction used for osteoclast cultivation is 10%. In this study, we investigated the use of a low serum (1% FBS) model for culturing osteoclasts.

RESULTS

To confirm the validity of this model for use in osteoclast research, we compared the capacity for osteoclastogenesis and bone resorption of RANKL-induced RAW 264.7 cells cultured in medium supplemented with 10% FBS and 1% FBS. Osteoclasts were successfully generated in medium supplemented with 1% FBS, and exhibited prolonged longevity and similar bone resorbing ability to those generated in medium supplemented with 10% FBS, although the osteoclasts were smaller in size. Proteomics and bioinformatics analyses were performed to assess the suitability of osteoclasts formed in low serum-containing medium for use in research focusing on osteoclast differentiation and function. Our study demonstrated that a total of 100 proteins were differentially expressed in cells cultured in medium containing 1% FBS, of which 29 proteins were upregulated, and 71 proteins were downregulated. Bioinformatics analysis showed that the electron transport chain and oxidative phosphorylation pathways were downregulated obviously; however, the osteoclast signaling pathway was unaffected. The data have been deposited to the ProteomeXchange with identifier PXD001935.

CONCLUSION

Our study provides clear evidence of the validity of the low serum model for use in studying RANKL-dependent osteoclasts differentiation and bone resorption with the advantage of prolonged survival time.

摘要

背景

破骨细胞培养是研究溶骨性骨疾病的基本手段。胎牛血清(FBS)是体外细胞培养基常用的标准补充剂。通常,用于破骨细胞培养的血清体积分数为10%。在本研究中,我们探讨了使用低血清(1%FBS)模型培养破骨细胞。

结果

为了证实该模型用于破骨细胞研究的有效性,我们比较了在补充10%FBS和1%FBS的培养基中培养的RANKL诱导的RAW 264.7细胞的破骨细胞生成能力和骨吸收能力。在补充1%FBS的培养基中成功生成了破骨细胞,尽管其尺寸较小,但与在补充10%FBS的培养基中生成的破骨细胞相比,具有更长的寿命和相似的骨吸收能力。进行了蛋白质组学和生物信息学分析,以评估在低血清培养基中形成的破骨细胞用于破骨细胞分化和功能研究的适用性。我们的研究表明,在含有1%FBS的培养基中培养的细胞共有100种蛋白质表达存在差异,其中29种蛋白质上调,71种蛋白质下调。生物信息学分析表明,电子传递链和氧化磷酸化途径明显下调;然而,破骨细胞信号通路未受影响。数据已提交至ProteomeXchange,标识符为PXD001935。

结论

我们的研究提供了明确证据,证明低血清模型可有效用于研究RANKL依赖的破骨细胞分化和骨吸收,且具有延长存活时间的优势。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c326/4427947/2d80206dfbd9/12953_2015_73_Fig1_HTML.jpg

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