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Comprehensive proteomic datasets for studying adipocyte-macrophage cell-cell communication

机译:全面的蛋白质组学数据集,用于研究脂肪细胞-巨噬细胞-细胞间的通讯

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摘要

Cellular communication is a fundamental process in biology. The interaction of adipocytes with macrophages is a key event in the development of common diseases such as type 2 diabetes. We applied an established bilayer cell coculture system and comprehensive MS detection to analyse on a proteome-wide scale the paracrine interaction of murine adipocytes and macrophages. Altogether, we identified 4486 proteins with at least two unique peptides, of which 2392 proteins were informative for 3T3-L1 adipocytes and 2957 proteins for RAW 264.7 macrophages. Further, we observed over 12000 phosphorylation sites, of which we could assign 3200 informative phosphopeptides with a single phosphosite for adipocytes and 4514 for macrophages. Using protein set enrichment and phosphosite analyses, we deciphered regulatory protein pathways involved in cellular stress and inflammation, which can contribute to metabolic impairment of cells including insulin resistance and other disorders. The generated datasets provide a holistic, molecular pathway-centric view on the interplay of adipocytes and macrophages in disease processes and a resource for further studies.
机译:细胞通讯是生物学的基本过程。脂肪细胞与巨噬细胞的相互作用是常见疾病(如2型糖尿病)发展中的关键事件。我们应用已建立的双层细胞共培养系统和全面的质谱检测技术,在蛋白质组范围内分析了小鼠脂肪细胞和巨噬细胞的旁分泌相互作用。我们总共鉴定了4486个蛋白质,其中至少有两个独特的肽,其中2392个蛋白质对3T3-L1脂肪细胞有用,而2957个蛋白质对RAW 264.7巨噬细胞有用。此外,我们观察到超过12000个磷酸化位点,其中我们可以为3200个信息性磷酸肽分配一个脂肪细胞单个磷酸化位点和4514个巨噬细胞磷酸化位点。使用蛋白质集富集和磷酸位点分析,我们破译了参与细胞应激和炎症的调控蛋白途径,这可能导致细胞的代谢受损,包括胰岛素抵抗和其他疾病。生成的数据集提供了疾病过程中脂肪细胞和巨噬细胞相互作用的整体,以分子途径为中心的视图,并提供了进一步研究的资源。

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