Zhang Lan, Liu Yao-Zhong, Zeng Yong, Zhu Wei, Zhao Ying-Chun, Zhang Ji-Gang, Zhu Jia-Qiang, He Hao, Shen Hui, Tian Qing, Deng Fei-Yan, Papasian Christopher J, Deng Hong-Wen
Center for Bioinformatics and Genomics, Department of Biostatistics and Bioinformatics, School of Public Health and Tropical Medicine, Tulane University, New Orleans, LA, USA.
College of Life Sciences and Bioengineering, Beijing Jiaotong University, Beijing, P. R. China.
Proteomics. 2016 Jan;16(1):12-28. doi: 10.1002/pmic.201500005. Epub 2015 Dec 3.
Menopause is one of the crucial physiological events during the life of a woman. Transition of menopause status is accompanied by increased risks of various health problems such as osteoporosis. Peripheral blood monocytes can differentiate into osteoclasts and produce cytokines important for osteoclast activity. With quantitative proteomics LC-nano-ESI-MS(E) (where MS(E) is elevated-energy MS), we performed protein expression profiling of peripheral blood monocytes in 42 postmenopausal women with discordant bone mineral density (BMD) levels. Traditional comparative analysis showed proteins encoded by four genes (LOC654188, PPIA, TAGLN2, YWHAB) and three genes (LMNB1, ANXA2P2, ANXA2) were significantly down- and upregulated, respectively, in extremely low- versus high-BMD subjects. To study functionally orchestrating groups of detected proteins in the form of networks, we performed weighted gene coexpression network analysis and gene set enrichment analysis. Weighted gene coexpression network analysis showed that the module including the annexin gene family was most significantly correlated with low BMD, and the lipid-binding related GO terms were enriched in this identified module. Gene set enrichment analysis revealed that two significantly enriched gene sets may be involved in postmenopausal BMD variation by regulating pro-inflammatory cytokines activities. To gain more insights into the proteomics data generated, we performed integrative analyses of the datasets available to us at the genome (DNA level), transcriptome (RNA level), and proteome levels jointly.
绝经是女性生命中的关键生理事件之一。绝经状态的转变伴随着各种健康问题风险的增加,如骨质疏松症。外周血单核细胞可分化为破骨细胞并产生对破骨细胞活性重要的细胞因子。我们采用定量蛋白质组学液相色谱 - 纳升电喷雾串联质谱法(其中 MS(E) 为高能质谱),对42名骨密度(BMD)水平不一致的绝经后女性的外周血单核细胞进行了蛋白质表达谱分析。传统的比较分析表明,在极低BMD与高BMD受试者中,四个基因(LOC654188、PPIA、TAGLN2、YWHAB)编码的蛋白质显著下调,三个基因(LMNB1、ANXA2P2、ANXA2)编码的蛋白质显著上调。为了以网络形式研究检测到的蛋白质的功能协调组,我们进行了加权基因共表达网络分析和基因集富集分析。加权基因共表达网络分析表明,包含膜联蛋白基因家族的模块与低BMD最显著相关,并且在该识别模块中富集了脂质结合相关的基因本体术语。基因集富集分析显示,两个显著富集的基因集可能通过调节促炎细胞因子活性参与绝经后BMD的变化。为了更深入了解所生成的蛋白质组学数据,我们对可获得的基因组(DNA水平)、转录组(RNA水平)和蛋白质组水平的数据集进行了联合综合分析。