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一项利用转录组学、蛋白质组学和微小RNA分析对天然羟基磷灰石诱导间充质干细胞成骨分化的综合研究。

An integrated study of natural hydroxyapatite-induced osteogenic differentiation of mesenchymal stem cells using transcriptomics, proteomics and microRNA analyses.

作者信息

Zhang Zhiwei, Wang Jiandan, Lü Xiaoying

机构信息

State Key Laboratory of Bioelectronics, School of Biological Science and Medical Engineering, Southeast University, Nanjing, 210096, People's Republic of China.

出版信息

Biomed Mater. 2014 Aug;9(4):045005. doi: 10.1088/1748-6041/9/4/045005. Epub 2014 Jun 19.

Abstract

This work combined transcriptomics, proteomics, and microRNA (miRNA) analyses to elucidate the mechanism of natural hydroxyapatite (NHA)-induced osteogenic differentiation of mesenchymal stem cells (MSCs). First, NHA powder was obtained from pig bones and fabricated into disc-shaped samples. Subsequently, the proliferation and osteogenic differentiation of MSCs cultured on NHA were investigated. Then, proteomics was employed to detect the protein expression profiles of MSCs cultured on NHA, and the effect of NHA on MSCs was analyzed through an integrated pathway analysis (including proteomics and previous transcriptomics data) in which specific NHA-induced differentiation pathways were analyzed. The pathway nodes with expression data at both the mRNA and protein levels (mRNA-protein pairs) were filtered in differentiation-related pathways. miRNAs corresponding to these target mRNA-protein pairs were predicted, screened and tested, and the regulatory effects of miRNAs on mRNA-protein pairs were analyzed. Finally, the NHA-induced osteogenic pathways were verified. The results of an MTT assay and alkaline phosphatase (ALP) staining showed that the cell proliferation rate decreased and the osteogenic performance improved in the presence of NHA. By integrating transcriptomics and proteomics, the genes and proteins involved in 89 pathways were shown to be differentially expressed. Among them, 5 differentiation-associated pathways, in which 9 miRNAs and 8 regulated-target mRNA-protein zby inhibiting the target mRNA-protein pair HSPA8 in the MAPK signaling pathway, and miR-26a and miR-26b might inhibit adipogenic differentiation by repressing the target mRNA-protein pair HMGA1 in the adipogenesis pathway. A verification experiment for the osteogenic pathway indicated that the ERK1/2 or JNK MAPK pathways might play an important role in NHA-induced osteogenic differentiation. In conclusion, NHA affected MSCs at both the transcriptional and translational levels, and MSC osteogenic differentiation eventually occurred through the MAPK and adipogenesis pathways, in which miRNAs and target mRNAs/proteins participated cooperatively.

摘要

本研究结合转录组学、蛋白质组学和微小RNA(miRNA)分析,以阐明天然羟基磷灰石(NHA)诱导间充质干细胞(MSCs)成骨分化的机制。首先,从猪骨中获取NHA粉末,并制成圆盘状样品。随后,研究了在NHA上培养的MSCs的增殖和成骨分化情况。接着,采用蛋白质组学检测在NHA上培养的MSCs的蛋白质表达谱,并通过综合通路分析(包括蛋白质组学和先前的转录组学数据)分析NHA对MSCs的影响,其中分析了特定的NHA诱导分化通路。在分化相关通路中筛选出在mRNA和蛋白质水平均有表达数据的通路节点(mRNA-蛋白质对)。预测、筛选并测试了与这些靶mRNA-蛋白质对相对应的miRNAs,并分析了miRNAs对mRNA-蛋白质对的调控作用。最后,验证了NHA诱导的成骨通路。MTT法和碱性磷酸酶(ALP)染色结果表明,在NHA存在的情况下,细胞增殖率降低而成骨性能提高。通过整合转录组学和蛋白质组学,发现89条通路中的基因和蛋白质存在差异表达。其中,5条与分化相关的通路中,有9个miRNAs和8个调控靶mRNA-蛋白质对,通过抑制丝裂原活化蛋白激酶(MAPK)信号通路中的靶mRNA-蛋白质对热休克蛋白家族A成员8(HSPA8),miR-26a和miR-26b可能通过抑制脂肪生成通路中的靶mRNA-蛋白质对高迁移率族蛋白A1(HMGA1)来抑制脂肪生成分化。成骨通路的验证实验表明,细胞外信号调节激酶1/2(ERK1/2)或应激活化蛋白激酶(JNK)MAPK通路可能在NHA诱导的成骨分化中起重要作用。总之,NHA在转录和翻译水平上影响MSCs,MSCs的成骨分化最终通过MAPK和脂肪生成通路发生,其中miRNAs与靶mRNA/蛋白质协同参与。

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