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论文摘要

原发性痛风患者外周血单个核细胞PYCARD基因及其转录剪接体的表达变化

Changes in Expression of PYCARD Gene and Its Transcript Variant mRNA in Peripheral Blood MononuclearCells of Patients with Primary Gout

作者:党万太, 谢文光, 蔡燕等

Author:DANG Wan-tai, XIE Wen-guang, CAI Yan.et al

收稿日期:          年卷(期)页码:2015,46(1):16-21

期刊名称:四川大学学报(医学版)

Journal Name:JOURNAL OF SICHUAN UNIVERSITY (MEDICAL SCIENCE EDITION)

关键字:原发性痛风 PYCARD 基因 剪接体

Key words:Primary gout PYCARD Gene Transcript variant

基金项目:

中文摘要

目的 了解凋亡相关斑点样蛋白(PYCARD)基因及其转录剪接体-1、-2(PYCARD-1、-2)在原发性痛风(PG)患者外周血单个核细胞(PBMCs)中的表达水平及作用。方法 采用半定量聚合酶链反应(RT-PCR)法检测95例PG患者〔原发性痛风急性期(APPG)44例、原发性痛风非急性期(NAPPG)51例〕和87例健康对照PBMCs中PYCARD基因及其PYCARD-1、-2 mRNA表达水平;Western blot法检测PG患者和健康对照PBMCs的PYCARD、核因子-κB(p105/p50)〔NF-κB(p105/p50)〕蛋白表达水平;检测APPG、NAPPG患者与健康对照血尿酸及部分血常规指标,并分析PYCARD基因及其PYCARD-1、-2 mRNA表达与各指标的相关性。结果 APPG与NAPPG患者PYCARD基因及其PYCARD-1、-2 mRNA相对表达量均高于健康对照组(PPYCARD、2x mRNA和2y mRNA的相对表达量高于健康对照和APPG患者组(PP均<0.05〕;相关性分析显示NAPPG组PYCARD-2 mRNA表达与嗜中性粒细胞绝对值呈正相关(r=0.3785,PPYCARD基因及其转录剪接体mRNA表达以及PYCARD蛋白表达均异常,提示在PG患者的炎症反应中PYCARD基因及其转录剪接体可能发挥重要的调控作用。

英文摘要

Objective To determine the expression level and role of PYCARD 〔PYRIN-PAAD-DAPIN domain (PYD) and a C-terminal caspase recruitment domain (CARD), PYCARD〕 gene and its transcript variant mRNA in peripheral blood mononuclear cells (PBMCs) of patients with primary gout (PG). Methods PYCARDgene and its transcript variant mRNA were measured using reverse transcription-polymerase chain reaction (RT-PCR) in PBMCs. The expression of PYCARDgene and PYCARD-1,-2 mRNA in PBMCs was compared between the patients with acute phase PG (APPG) (n=44), non-acute phase PG (NAPPG) (n=51) and healthy controls (HC) (n=87). PYCARD and NF-κB (p105/p50) protein expressions were measured using Western blot in the PBMCs of participants in the PG and HC groups. Routine blood tests and blood uric acid test were undertaken in all participants. Differences in the indicators were examined among the three groups. Correlations between the expression of PYCARDgene and PYCARD-1,-2 mRNA and other indicators were analyzed. Results The expression level of PYCARDgene, PYCARD-1,-2 mRNA was significantly higher in the APPG and NAPPG group than in the HC group(P PYCARDgene transcript variant 2x mRNA and 2y mRNA in the HC and APPG groups (P P PYCARD-2mRNA and granulocyte were positively correlated in the NAPPG group. Conclusion Abnormal expression of PYCARD gene and its transcript variant and PYCARD protein in PG patients suggests that PYCARDgene and its transcript variant may play an important role in regulating the inflammatory response of PG patients.

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