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作 者:秦伟[1] 钟翔[1] 张颖娟[1] 谭淳予[2] 杨立川[1] 樊均明[1]
机构地区:[1]四川大学华西医院肾内科,成都610041 [2]四川大学华西医院风湿免疫科,成都610041
出 处:《中华肾脏病杂志》2008年第6期377-381,共5页Chinese Journal of Nephrology
基 金:四川省中医药管理局科学研究基金(2004A63);四川省人事厅人才基金(06SXS-13)
摘 要:目的探讨IgA肾病(IgAN)患者核心181,3半乳糖基转移酶伴侣蛋白(Cosmc)表达低下的原因,到底是基因突变还是外源性抑制。方法40例IgAN患者、16例非IgAN。肾小球。肾炎患者、21例健康对照被纳入本研究。直接测序方法测定Cosmc基因外显子区域的核酸序列。免疫磁珠分离IgAN患者、非IgAN肾小球肾炎患者和健康对照者外周血B淋巴细胞,并分别在RPMI-1640及RPMI—1640+脂多糖(LPS)中培养72h。实时荧光RT—PCR方法测定Cosmc基因的mRNA表达水平。结果(1)IgAN患者Cosmc基因外显子区域没有共同突变位点,仅在2例患者中发现2处错义突变和2处无意义突变,而且这些突变并不影响患者Cosmc基因的表达:(2)IgAN患者外周血B淋巴细胞的基础Cosmc基因表达显著降低,为健康对照组的31%。(3)经RPMI-1640培养后,IgAN患者Cosmc基因的表达水平升高至基础值的219%。RPMI—1640+LPS组Cosmc基因的上调受到明显抑制。(4)健康对照Cosmc基因的表达不受RPMI-1640和LPS的影响。结论IgAN患者外周血B淋巴细胞Cosmc基因表达低下可能与基因突变无关,而是受外源性抑制因素影响所致.Objective To clarify whether the Cosmc gene down-regulation in lgA nephropathy (IgAN) patients is resulted from genetic disorders or external suppressions. Methods Forty IgAN patients, 16 non-IgAN glomemlonephritis patients and 21 healthy controls were enrolled in the study. Genomic DNA was extracted and then Cosmc gene was amplified and sequenced. Peripheral B lymphocytes were isolated and cultured with RPMI-1640 alone or plus lipopolysaccharide (LPS). The Cosnw mRNA expression levels at baseline, after RPMl-1640 culture or RPMI-1640+LPS treatment were measured respectively by real-time RT-PCR. Results (1) Only 2 missense mutations and 2 silent mutations were detected in coding frame region of Cosmc gene in 2 IgAN patients. (2) The baseline Cosmc gene expression level was significantly lower in IgAN patients (31% of that in healthy controls) than that in healthy controls. (3) Relative quantification PCR indicated that Cosmc mRNA expression level was significantly increased (219% of baseline) after RPMI-1640 culture, and treatment of LPS could strongly inhibit this effect. (4) The Cosmc gene expression of healthy control was not affected by RPMI-1640 or LPS. Conclusion It is not genetic disorders but external suppression to cause the down-regulatlon of Cosmc gene mRNA expression in IgAN.
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