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通过质膜蛋白质组学分析揭示树突状细胞亚群之间病原体识别分子的差异表达。

Differential expression of pathogen-recognition molecules between dendritic cell subsets revealed by plasma membrane proteomic analysis.

机构信息

Immunology Division, The Walter and Eliza Hall Institute of Medical Research, 1G Royal Parade, Parkville, Victoria 3050, Australia.

出版信息

Mol Immunol. 2010 May;47(9):1765-73. doi: 10.1016/j.molimm.2010.02.028. Epub 2010 Mar 29.

Abstract

Dendritic cells (DC) are comprised of several subsets with distinct functions, differing in their capacity to respond to pathogen products. To gain novel insights into their pathogen specificity, we compared the protein composition of the plasma membrane of CD8+ and CD8- DC, directly isolated from mouse spleens. Differences in protein expression were determined using semi-quantitative high-resolution mass spectrometry of label-free plasma membrane-enriched fractions. Our comparative proteomic analysis detected over 1500 proteins, revealing broad differences in expression of pathogen receptors, adhesion molecules and T-cell regulatory molecules. Many of these findings were validated using flow cytometry and Western Blot analysis of integral and luminal surface-associated membrane proteins. This analysis provides major advantages over genomic approaches as it directly measures protein expression at a particular location. Our study highlights the diversity of surface protein expression amongst components of the DC network.

摘要

树突状细胞(DC)由具有不同功能的几个亚群组成,它们对病原体产物的反应能力存在差异。为了深入了解其病原体特异性,我们直接从小鼠脾脏中分离 CD8+和 CD8- DC,比较了它们的质膜蛋白组成。使用无标记质膜富集部分的半定量高分辨率质谱来确定蛋白质表达的差异。我们的比较蛋白质组学分析检测到超过 1500 种蛋白质,揭示了病原体受体、粘附分子和 T 细胞调节分子表达的广泛差异。使用流式细胞术和全细胞和腔表面相关膜蛋白的 Western Blot 分析验证了其中许多发现。与基因组方法相比,这种分析具有很大的优势,因为它直接测量特定位置的蛋白质表达。我们的研究强调了 DC 网络成分表面蛋白表达的多样性。

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