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人髓样细胞触发性受体-1在急性胆管炎的表达及意义 被引量:4

Expression and significance of human triggering receptor on myeloid cells-1 in acute cholangitis
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摘要 目的观察人髓样细胞触发性受体(TREM)-1在急性胆管炎患者中表达的规律及其临床意义,探讨TREM-1在急性胆管炎中与肿瘤坏死因子(TNF)-α,CRP的相关性。方法分别收集34例急性胆管炎患者(AC),24例急性重症胆管炎(ACST)患者和60例正常人外周血白细胞,以半定量逆转录一聚合酶链反应(RT-PCR)检测中性粒细胞中TREM-1的mRNA表达;免疫细胞化学检测TREM-1的蛋白表达。结果对照组TREM-1的mRNA半定量比值为0.458±0.043。AC和ACST组治疗前分别为0.809±0.044、0.981±0.089,术后24h为0.785±0.077、0.954±0.072,48h为0.565±0.009、0.719±0.047,ACST的TREM-1表达水平明显高于AC(P〈0.05)。免疫细胞化学镜下观察结果与RT-PCR结果一致。TREM-1与TNF-α,CRP表达水平高度正相关(r1=0.719,r2=0.701,P〈0.01)。结论人TREM-1在急性胆管炎发病初表达增高,与TNF-α,CRP表达高度正相关。提示TREM-1在急性胆管炎的发生发展中起重要作用。 Objective To investigate the expression of human triggering receptor on myeloid cells-1 (TREM-1) and its regularity or clinical significance in patients with acute cholangitis,and discuss the relationship of TREM-1 ,TNF-α and CRP in acute cholangitis. Methods Peripheral blood of 24 patients with ACST,34 patients with AC and 60 health adults were collected respectively. TREM-I mRNA and protein was delected by semi-quantitative RT-PCR and immunocytochemistry respectively. Results The values of TREM-1/β-actin in control group was 0. ,158 ± 0. 043, while those in AC and ACST group were 0. 809 ± 0.044 and 0.981±0.089 before therapy,and 0. 785 ± 0. 077,0.954± 0.072 at 24 h,0. 565 ± 0. 009,0. 719 ±0.047 at 48 h, respectively. The level of TREM-1 express in ACST was higher than in AC ( P 〈 0.05 ). Immunocytochemistry revealed the results similar to those of RT-PCR. TREM-1 expression was closely related with TNF-α,CRP expression (r1 = 0. 719 ,r2 = 0. 701 ,P 〈 0.01 ). Conclusion Expression of human TREM-1 was up-regulated obviously in patients with AC and ACST in the early stage,indicating that TREM-1 might play an important role in the development of acute cholangitis.
出处 《中华实验外科杂志》 CAS CSCD 北大核心 2008年第10期1245-1247,共3页 Chinese Journal of Experimental Surgery
基金 国家自然科学基金资助项目(30471696,30500473)
关键词 胆管炎 髓样细胞触发性受体-1 肿瘤坏死因子 Acute cholangiiis Triggering receptor expressed on myeloid cells-1 TNF-α
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参考文献9

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共引文献16

同被引文献54

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