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1. 重庆医科大学基础医学院生物信息学教研室,重庆,400016
2. 重庆医科大学基础医学院细胞生物学及遗传学教研室,重庆,400016
3. 重庆医科大学第一附属医院感染科,重庆,400016
4. 重庆医科大学实验教学中心,重庆,400331
纸质出版日期:2014,
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彭 睿, 周 吉, 李天驹, 等. miR-451调控早期糖尿病肾病小鼠肾小球肥大的机制[J]. 重庆医科大学学报, 2014,38(11):1584-1589.
Peng Rui, Zhou Ji, Li Tianju, et al. Involvement of miR-451 in the regulation of glomerular hypertrophy in db/db mouse with diabetic nephropathy at early stage[J]. Journal of Chongqing Medical University, 2014,38(11):1584-1589.
彭 睿, 周 吉, 李天驹, 等. miR-451调控早期糖尿病肾病小鼠肾小球肥大的机制[J]. 重庆医科大学学报, 2014,38(11):1584-1589. DOI:
Peng Rui, Zhou Ji, Li Tianju, et al. Involvement of miR-451 in the regulation of glomerular hypertrophy in db/db mouse with diabetic nephropathy at early stage[J]. Journal of Chongqing Medical University, 2014,38(11):1584-1589. DOI:
目的:观察miR-451对早期糖尿病肾病(diabetic nephropathy,DN)db/db小鼠肾脏形态学影响,探讨miR-451在DN发病机制中的作用。方法:采用24只7周龄雄性db/db小鼠和8只正常对照db/m小鼠依次分为未处理组、空质粒组、miR-451组及对照组。腹腔注射法进行质粒注射处理2周后,光镜下观察肾小球形态学变化,实时荧光定量PCR(real-time PCR)检测肾脏组织miR-451的表达水平,Western blot和激光共聚焦检测肾脏组织中miR-451的靶基因酪氨酸-3单氧化酶/色氨酸单氧化酶活化蛋白(tyrosine3-monooxy-genase/tryptophan 5-monooxygenase activation protein,Ywhaz)及其相关的丝裂原激活蛋白激酶(mitogen-activated protein kinase,MAPK)途径中p38丝裂原激活的蛋白激酶(p38MAPK)及其上游激酶MKK3(MAPK kinase 3)的表达水平。结果:7周龄db/db小鼠未处理组相比对照组出现高血糖且尿白蛋白排泄率(urinary albumin excretion rate,UAE)增加,提示进入早期DN阶段,给予30 mg/(kg?d)质粒注射实验2周。光镜观察和肾小球直径测量发现,miR-451处理组肾小球形态减小(P=0.000)。Real-time PCR检测显示miR-451组小鼠肾脏组织中miR-451的表达水平增高1.79倍(P=0.002),West-ern blot和激光共聚焦结果显示,miR-451组较未处理组和空质粒组肾脏组织Ywhaz的表达受到下调,同时p38MAPK及上游激酶MKK3蛋白表达水平减少(P均=0.000)。结论:miR-451可能通过直接靶向Ywhaz基因,调控MAPK途径中关键蛋白p38MAPK、MKK3的表达,从而抑制肾小球肥大,在DN发病机制中可能起着重要的作用。
Objective:To observe the effect of miR-451 on glomerular morphological changes in diabetic nephmpathy(DN) of type 2 diabetic db/db mice and to explore the role of miR-451 in pathogenesis of early DN. Methods:Thirty-two 7-week-old db/db and normal db/m male mice were divided into miR-451 group,empty plasmid group,untreated group and normal control group. After in-traperitoneal injection of plasmid for two weeks,the glomerular morphological changes were observed under the light microscope. Also,the expression of miR-451 was tested by real-time PCR and the tyrosine3-monooxy-genase/tryptophan 5-monooxygenase activation protein(Ywhaz),p38MAPK and MAPK kinase 3(MKK3) protein levels were examined by Western blot and immunofluorescence. Results:Elevation of urinary albumin excretion rate(UAE) was shown in the untreated group of 7-week-old db/db mice,suggesting that the 7-week-old db/db mice had the features similar to the diabetic nephropathy at early stage. Then plasmid injection ex-periment was executed on mice for two weeks. Real-time RT-PCR results showed that miR-451 was 1.79 folds high in miR-451 group than in empty plasmid group(P=0.002). Also,glo-meruli acreage was smaller in miR-451-treated group than in the empty plasmid and untreated groups(P=0.000). Moreover,Western blot and immunofluorescence results demonstrated that Ywhaz,p38MAPK and MKK3 proteins were reduced in miR-451 group(P=0.000). Conclusion:miR-451 can repress glomerular hypertrophy by targeting Ywhaz gene and affecting MAPK signal pathway. Therefore,miR-451 might play an important role in the pathogenesis of DN.
糖尿病肾病微小RNA酪氨酸-3单氧化酶/色氨酸单氧化酶活化蛋白p38丝裂原激活的蛋白激酶
diabetic nephropathymicroRNAtyrosine3-monooxy-genase/tryptophan 5-monooxygenase activation proteinp38 mito-gen-activated protein kinase
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