麻疯病人皮肤病变中CXCL8和CXCL10趋化因子的表达及分析

K. Rawat, M. Chahar, P. Reddy, N. Srivastava, U. Gupta, M. Natrajan, V. Katoch, K. Katoch, D. Chauhan
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引用次数: 3

摘要

本研究的重点是分析CXCL8和CXCL10趋化因子基因的表达谱,并探讨这些趋化因子在麻风晚期感染人皮肤病变样本中的作用。本研究收集麻风患者皮肤活检样本(n=35),其中BL-LL=12, BB=14, BT=8,健康志愿者(n=3)。所有活检标本在RNALater中进行mRNA表达研究,10%缓冲福尔马林(BF)进行组织病理学分析。从收集的样品中分离总RNA,制备cDNA。通过q-PCR和原位RT-PCR检测CXCL8和CXCL10趋化因子基因mRNA表达水平,定位麻风支原体感染组织中CXCL8和CXCL10趋化因子的存在。CXCL8 mRNA在麻风(BL-LL)皮肤样本中的表达明显高于BB类麻风;而在BT病例中则记录了下调。CXCL10 mRNA在麻风(BL-LL)病例中的表达高于其他麻风(BT、BB)病例。在组织病理学检查中,BL-LL型麻风患者的浸润率最高达59.38%,原位RT-PCR证实组织切片中存在趋化因子基因。有趣的是,趋化因子CXCL-10和CXCL-8在BL-LL组中表达升高。该研究主张CXCL10和cxcl8可能在麻风型(BL-LL)麻风中发挥作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Expression and Analysis of CXCL8 and CXCL10 Chemokines in Human SkinLesions Infected with M.leprae
This study is focused to analyze the expression profile of CXCL8 and CXCL10 chemokines genes and to address the contribution of these chemokines in late phase of M.leprae infection in human skin lesion samples. In this study skin biopsy samples from leprosy patients (n=35) were collected including BL-LL=12, BB=14, BT=8 and healthy volunteers (n=3). All the biopsy samples were collected in RNALater for mRNA expression study as well as 10% buffered formalin (BF) for histopathologic analysis. Total RNA was isolated from collected samples and cDNA was prepared. Level of mRNA expression of CXCL8 and CXCL10 chemokine genes was measured via q-PCR and insitu RT-PCR to locate the presence of CXCL8 and CXCL10 chemokines inside M. leprae infected tissue. The mRNA expression of CXCL8 was found relatively elevated in lepromatous (BL-LL) skin samples significantly as compared to BB category of leprosy; whereas in BT cases down-regulation was recorded. CXCL10 mRNA expression was found elevated in lepromatous (BL-LL) cases than other cases (BT, BB) of leprosy samples. In histopathological examination, 59.38% maximum infiltration was observed in BL-LL cases of leprosy and in-situ RT-PCR confirmed the presence of chemokines genes in tissue sections. Interestingly, chemokines CXCL-10 and CXCL-8 showed elevated expression in BL-LL category. The study advocated that CXCL10 and CXCL-8 possibly may have a role in lepromatous (BL-LL) form of leprosy.
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