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人腹主动脉瘤中自然杀伤细胞细胞毒性途径的免疫组织化学分析

Immunohistochemical analysis of the natural killer cell cytotoxicity pathway in human abdominal aortic aneurysms.

作者信息

Hinterseher Irene, Schworer Charles M, Lillvis John H, Stahl Elizabeth, Erdman Robert, Gatalica Zoran, Tromp Gerard, Kuivaniemi Helena

机构信息

Department of General, Visceral, Vascular and Thoracic Surgery, Charité Universitätsmedizin, Campus Mitte, 10117 Berlin, Germany.

Sigfried and Janet Weis Center for Research, Geisinger Health System, Danville, PA 17822, USA.

出版信息

Int J Mol Sci. 2015 May 18;16(5):11196-212. doi: 10.3390/ijms160511196.

Abstract

Our previous analysis using genome-wide microarray expression data revealed extreme overrepresentation of immune related genes belonging the Natural Killer (NK) Cell Mediated Cytotoxicity pathway (hsa04650) in human abdominal aortic aneurysm (AAA). We followed up the microarray studies by immunohistochemical analyses using antibodies against nine members of the NK pathway (VAV1, VAV3, PLCG1, PLCG2, HCST, TYROBP, PTK2B, TNFA, and GZMB) and aortic tissue samples from AAA repair operations (n = 6) and control aortae (n = 8) from age-, sex- and ethnicity-matched donors from autopsies. The results confirmed the microarray results. Two different members of the NK pathway, HCST and GRZB, which act at different steps in the NK-pathway, were actively transcribed and translated into proteins in the same cells in the AAA tissue demonstrated by double staining. Furthermore, double staining with antibodies against CD68 or CD8 together with HCST, TYROBP, PTK2B or PLCG2 revealed that CD68 and CD8 positive cells expressed proteins of the NK-pathway but were not the only inflammatory cells involved in the NK-pathway in the AAA tissue. The results provide strong evidence that the NK Cell Mediated Cytotoxicity Pathway is activated in human AAA and valuable insight for future studies to dissect the pathogenesis of human AAA.

摘要

我们之前利用全基因组微阵列表达数据进行的分析显示,在人类腹主动脉瘤(AAA)中,属于自然杀伤(NK)细胞介导的细胞毒性途径(hsa04650)的免疫相关基因极度富集。我们通过免疫组织化学分析对微阵列研究进行了跟进,使用针对NK途径的九个成员(VAV1、VAV3、PLCG1、PLCG2、HCST、TYROBP、PTK2B、TNFA和GZMB)的抗体,以及来自AAA修复手术的主动脉组织样本(n = 6)和来自尸检的年龄、性别和种族匹配供体的对照主动脉(n = 8)。结果证实了微阵列结果。通过双重染色证明,NK途径中在不同步骤起作用的两个不同成员HCST和GRZB,在AAA组织的同一细胞中被积极转录并翻译成蛋白质。此外,用抗CD68或CD8抗体与HCST、TYROBP、PTK2B或PLCG2进行双重染色显示,CD68和CD8阳性细胞表达NK途径的蛋白质,但不是AAA组织中参与NK途径的唯一炎症细胞。这些结果提供了强有力的证据,表明NK细胞介导的细胞毒性途径在人类AAA中被激活,并为未来研究剖析人类AAA的发病机制提供了有价值的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/08dd/4463696/a53adee0db1a/ijms-16-11196-g001.jpg

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