首页|瞬时感受电位通道6在同型半胱氨酸诱导的小鼠肾脏足细胞自噬中的作用

瞬时感受电位通道6在同型半胱氨酸诱导的小鼠肾脏足细胞自噬中的作用

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目的 探讨在同型半胱氨酸(Hcy)作用下瞬时感受电位通道6(TRPC6)对小鼠肾脏足细胞自噬的调控作用。方法 将小鼠肾脏足细胞分为对照组与Hcy组(40、60、80、100 μmol/L的Hcy刺激48 h),采用qRT-PCR检测TRPC6 mRNA水平,筛选出Hcy的最佳浓度后,后续均以此浓度进行实验。采用Western blotting检测自噬相关蛋白LC3 Ⅱ、p62,以及足细胞结构蛋白Nephrin、Podocin的表达水平;采用qRT-PCR、Western blotting及免疫荧光检测两组TRPC6 mRNA及蛋白的表达水平。转染过表达或干扰TRPC6的细胞分别设置为:(1)对照组(不做处理)、TRPC6过表达阴性对照组、TRPC6过表达组;(2)对照组(不做处理)、TRPC6干扰阴性对照组和TRPC6干扰组(si-1、si-2、si-3),并采用qRT-PCR检测TRPC6表达水平。再将过表达或干扰TRPC6后的细胞分别设置为:(1)对照组(不做处理)、Hcy组(加入80 μmol/L Hcy)、TRPC6过表达对照+Hcy组、TRPC6过表达+Hcy组;(2)对照组(不做处理)、Hcy组、TRPC6干扰对照+Hcy组、TRPC6干扰+Hcy组,并采用Western blotting检测p62、LC3 Ⅱ、TRPC6蛋白的表达水平。结果 qRT-PCR检测结果显示,与对照组比较,TRPC6 mRNA表达水平随Hcy浓度增加而升高,其中80 μmol/L Hcy干预后的表达水平最高,因此将80 μmol/L作为Hcy的最佳干预浓度。此时,自噬相关蛋白LC3 Ⅱ的表达水平升高、p62表达水平降低(P<0。05)。Western blotting检测结果显示,与对照组比较,Hcy组中足细胞相关蛋白Nephrin、Podocin的表达水平明显降低(P<0。05)。qRT-PCR检测结果显示,与对照组比较,Hcy组中TRPC6 mRNA表达水平明显升高(P<0。05);与TRPC6过表达阴性对照组比较,TRPC6过表达组的TRPC6 mRNA及蛋白表达水平均明显升高(P<0。05);与TRPC6干扰阴性对照组比较,TRPC6干扰组的TRPC6 mRNA及蛋白表达水平均明显降低(P<0。05)。Western blotting检测结果显示,与TRPC6过表达对照组相比,TRPC6过表达+Hcy组中自噬相关蛋白LC3 Ⅱ表达水平明显升高,p62表达水平明显降低(P<0。05);与TRPC6干扰对照+Hcy组相比,TRPC6干扰+Hcy组中自噬相关蛋白LC3 Ⅱ表达水平明显降低,p62表达水平明显升高(P<0。05)。结论 Hcy可诱导小鼠肾脏足细胞自噬,抑制TRPC6的表达可明显减轻足细胞的自噬性损伤。
Role of transient receptor potential channel 6 in homocysteine-induced podocyte autophagy of mouse kidney
Objective To explore the regulatory role of transient receptor potential channel 6(TRPC6)on podocyte autophagy under the influence of homocysteine(Hcy)in mouse kidney.Methods Mouse renal podocytes were divided into control group and Hcy groups(stimulated by Hcy at 40,60,80 and 100 μmol/L for 48 h).The level of TRPC6 mRNA was assessed using quantitative reverse transcription polymerase chain reaction(qRT-PCR)to identify the optimal Hcy concentration for subsequent experiments.Western blotting was employed to evaluate the expression levels of autophagy-related proteins LC3 Ⅱ and p62,as well as the expression levels of podocyte structural proteins Nephrin and Podocin.The expression levels of TRPC6 mRNA and protein in both groups were determined using qRT-PCR,Western blotting and immunofluorescence.Transfections of cells with TRPC6 overexpression or interference were set as follows:(1)control group(untreated),negative control group of TRPC6 overexpression,and TRPC6 overexpression group;(2)control group(untreated),negative control group of TRPC6 interference,and TRPC6 interference group(si-1,si-2,si-3).The expression level of TRPC6 was detected using qRT-PCR.The cells after overexpressing or interfering of TRPC6 were further set as follows:(1)control group(untreated),Hcy group(80 μmol/L Hcy added),TRPC6 overexpression control+Hcy group,TRPC6 overexpression+Hcy group;(2)control group(untreated),Hcy group,TRPC6 interference control+Hcy group,and TRPC6 interference+Hcy group.The expression levels of p62,LC3 Ⅱ,and TRPC6 proteins were detected using Western blotting.Results qRT-PCR detection results showed that compared with control group,the expression level of TRPC6 mRNA in Hcy group increased with the increase of Hcy concentration,with the highest expression level observed at 80 μmol/L Hcy.Therefore,80 μmol/L Hcy was selected as the optimal concentration for intervention.At this time,the expression level of autophagy-related protein LC3 Ⅱ increased,and the expression level of p62 decreased(P<0.05).Western blotting results showed that compared with control group,the expression levels of podocyte-related proteins Nephrin and Podocin in Hcy group were significantly decreased(P<0.05).qRT-PCR results showed that compared with control group,the expression level of TRPC6 mRNA in Hcy group was significantly increased(P<0.05).Compared with negative control group for TRPC6 overexpression,both mRNA and protein expression levels of TRPC6 in TRPC6 overexpression group were significantly higher(P<0.05).Compared with negative control group for TRPC6 interference,both mRNA and protein expression levels of TRPC6 in TRPC6 interference group were significantly decreased(P<0.05).Western blotting results showed that compared with negative control group for TRPC6 overexpression,the expression level of autophagy-related protein LC3 Ⅱ in TRPC6 overexpression+Hcy group was significantly increased,and the expression level of p62 was significantly decreased(P<0.05).Compared with TRPC6 negative control+Hcy group for TRPC6 interference+Hcy,the expression level of autophagy-related protein LC3 Ⅱ in TRPC6 interference+Hcy group was significantly decreased,and the expression level of p62 was significantly increased(P<0.05).Conclusion Hcy can induce autophagy of renal podocytes.Inhibiting the expression of TRPC6 can significantly reduce the autophagy damage to podocytes.

podocyte autophagyhomocysteinetransient receptor potential channel 6

卢冠军、汪乐新、赵静、刘超、熊建团、焦运、杨安宁、姜怡邓、田宇佳、徐遥琴、石青、刘莉、张亚兰、白志刚、李淑娟

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宁夏医科大学总医院泌尿外科,宁夏银川 750004

宁夏医科大学第一临床医学院,宁夏银川 750004

国家卫生健康委员会代谢性心血管疾病研究重点实验室,宁夏银川 750004

绍兴复康护理院,浙江绍兴 312000

宁夏回族自治区人民医院检验科,宁夏银川 750004

宁夏医科大学总医院急诊科,宁夏银川 750004

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足细胞自噬 同型半胱氨酸 瞬时感受电位通道6

2024

解放军医学杂志
人民军医出版社

解放军医学杂志

CSTPCD北大核心
影响因子:1.644
ISSN:0577-7402
年,卷(期):2024.49(12)