目的探讨糖尿病肾小球细胞烟酰胺磷酸核糖转移酶(Nampt)与骨形态发生蛋白7(BMP7)表达的关系及烟酰胺单核苷酸(NMN)缓解糖尿病肾小球细胞炎症纤维化的作用机制。方法 (1)动物实验:C57/BL6自发性糖尿病小鼠和C57/BL6野生型小鼠,均采取普通饲料喂养,当自发性糖尿病小鼠血糖〉(34.2±1.9)mmol·L-1并出现明显肾组织损伤时,取肾组织进行病理切片,免疫共聚焦法检测肾小球细胞Nampt、核转录因子κB p65(NF-κB p65)、沉默调节蛋白1(SIRT1)和BMP7的表达。(2)细胞实验:葡萄糖200 mmol·L-1培养大鼠肾小球系膜HBZY-1细胞,在不同时间(24,48和72 h)以及不同浓度NMN(50,100和200μmol·L-1)处理24 h时后,免疫印迹法检测Nampt和BMP7的表达;葡萄糖200 mmol·L-1处理HBZY-1细胞96 h,免疫荧光法检测NF-κB p65和α-平滑肌肌动蛋白(α-SMA)的表达;应用NMN 100μmol·L-1和Nampt特异抑制剂FK866 10μmol·L-1作用HBZY-1细胞24 h后,免疫印迹法检测HBZY-1细胞Nampt,BMP7和NF-κB p65表达。结果 (1)动物实验:自发性糖尿病小鼠肾小球明显萎缩,肾小球细胞Nampt和NF-κB p65的荧光强度比野生型小鼠明显升高(P〈0.05),而BMP7和SIRT1的荧光强度显著降低(P〈0.01)。(2)细胞实验:Western蛋白印迹检测显示,葡萄糖200 mmol·L-1培养48和72 h,HBZY-1细胞Nampt表达增加(P〈0.01),BMP7表达下降(P〈0.01,P〈0.05)。葡萄糖200 mmol·L-1条件下加NMN 50,100和200μmol·L-1作用24 h,各组BMP7表达均增加(P〈0.01);免疫荧光结果显示,与细胞对照组比较,葡萄糖200 mmol·L-1处理HBZY-1细胞,NF-κB p65和α-SMA的荧光强度升高(P〈0.01);NMN干预后,与葡萄糖200 mmol·L-1处理组比,Nampt和NF-κB p65表达降低(P〈0.01),BMP7表达增加(P〈0.01);加FK866后,Nampt表达降低(P〈0.01),NF-κB p65表达下降,BMP7表达虽然有上升趋势,但其表达增高没有NMN组明显。结论严重糖?
OBJECTIVE To investigate the mechanism of nicotinamide mononucleotide(NMN) on inflammation and fibrosis between endogenous nicotinamide phosphoribosyltransferase(NAMPT) and bone morphogenetic protein 7(BMP-7) in diabetic glomerular cells. METHODS(1) In vivo, spontaneous diabetic C57/BL6 mice and wild C57/BL6 mice were divided into two groups. When blood glucose was above(34.2±1.9) mmol·L-1, renal histology of diabetic mice became obvious. The protein expressions of Nampt and nuclear transcription factors-kappa B p65(NF-κB p65), silent mating type information regulation 2 homolog 1(SIRT1) and BMP7 were analyzed by lengths of immunofluorescence.(2) In vitro, rats′glomerular cells HBZY-1 were incubated with glucose 200 mmol·L-1for different lengths of time(0,24,48 and 72 h) and at different concentrations of NMN(0,50,100 and 200 μmol·L-1). The protein levels of Nampt and BMP7 were detected by Western blotting and the protein expressions of NF-κB p65 and α-SMA were measured by immunofluorescence assay. The protein levels of Nampt, BMP7 and NF-κB p65 were detected by Western blotting after HBZY-1 cells were treated with NMN 100 μmol·L-1and FK86610 μmol·L-1for 24 h. RESULTS(1) In vivo, the glomeruli of diabetic C57/BL6 mice showed obvious atrophy. Fluorescence intensity of Nampt was increased(P〈0.05), but that of BMP7 and SIRT1 in renal glomeruli cells was decreased compared with the wild type(P〈0.01).(2) In vitro, HBZY-1 cells were cultured in glucose 200 mmol·L-1for 48 and 72 h. The protein expression of NAMPT was increased, but that of BMP7 was decreased(P〈0.05, P〈0.01). Expressions of NF-κB p65 and α-SMA were increased(P〈0.01) by immunofluorescence. The expression of BMP7 was increased after treatment with glucose200 mmol · L-1, followed by NMN 50, 100 and 200 μmol · L-1for 24 h(P〈0.01). The expressions of NAMPT and NF-κB p65 were decreased(P〈0.01). The expressions of Nampt and NF-κB p65 in glucose 5.6 mmol?