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高浓度葡萄糖损伤人腹膜间皮细胞分子机制的研究 被引量:1

The study on molecular mechanism of high-glucose-inducing injury to human peritoneal mesothelial cells
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摘要 目的:探讨高浓度葡萄糖损伤人腹膜间皮细胞的机制。方法:(1)人腹膜间皮细胞分别经含1.5%、2.5%、4.25%葡萄糖的M199培养基培养48小时后,检测间皮细胞线粒体膜电位(Ψ)、凋亡率、caspase-3活性、bax和bcl-2基因mRNA表达;(2)分别用0.1μmol/L和0.01μmol/L环孢素A(CsA)与4.25%葡萄糖共同作用人腹膜间皮细胞,检测细胞凋亡率和caspase-3活性。结果:(1)随着葡萄糖浓度增加,Ψ丧失的细胞百分率、bax mRNA表达量、caspase-3活性、凋亡率增加(P<0.05),而bcl-2 mRNA表达量减少;(2)随着葡萄糖浓度增加,bax mRNA的表达量与Ψ丧失的间皮细胞百分率呈显著正相关(P<0.01);bcl-2 mRNA的表达量与Ψ丧失的间皮细胞百分率呈显著负相关(P<0.01),Ψ丧失的间皮细胞百分率与间皮细胞凋亡率、caspase-3活性呈显著正相关(P<0.01);(3)0.1μmol/LCsA组间皮细胞凋亡率和caspase-3活性显著低于高糖对照组(P<0.05)。结论:(1)高糖可能通过上调bax基因表达和下调bcl-2基因表达,诱导人腹膜间皮细胞线粒体活化、caspase-3活化和凋亡。(2)高糖诱导人腹膜间皮细胞caspase-3活化和凋亡可能依赖于线粒体活化。 Objective: To investigate mechanism of high-glucose-inducing injury to human peritoneal mesothelial cells. Methods: (1)The mesothelial cells were exposed to culture medium containing different concentrations of glucose (1.5%,2.5%,4.25%) for 48 hourso Then mitochondrial membrane potential (Ψ) , the apoptotic rate, caspase-3 activity, the level of bax mRNA and bcl-2 mRNA expression were measured. (2) The mesothelial cells were exposed to 4.25% glucose culture medium containing different concentrations of cyclosporin A (0.01, 0.1μmol/L) for 24 hours. Then the apoptotic rate and caspase-3 activity were measured. Results: (1) The level of bax mRNA expression of mesothelial cells, the percentage of mesothelial cells with loss of Ψ, caspase-3 activity of mesothelial cells, the apoptotic rate of mesothelial cells rose as glucose concentration increased, but the level of bcl-2 mRNA expression was decreased as glucose concentration increased (P〈0.01). (2) There was significantly positive correlation among the level of bax mRNA expression, the percentage of mesothelial cells with loss of Ψ, caspase-3 activity and the apoptotic rate . (3) Apoptotic rate and caspase-3 activity was significantly lower in 0.1μmol/L CsA group than that in control. Conclusion: (1) High-glucose could induce loss of Ψ, apoptosis and caspase-3 activation of human peritoneal mesothelial cells by up-regulatlng expression of bax and down-regulating expression of bcl-2. (2)High-glucose could induce Caspase-3 activation in progression of high-glucose-inducing apoptosis of human peritoneal mesothelial cells by mitochondria activation.
出处 《交通医学》 2008年第1期21-24,共4页 Medical Journal of Communications
关键词 葡萄糖 腹膜间皮细胞 线粒体 凋亡 glucose peritoneal mesothelial cells mitochondrion apoptosis
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参考文献10

  • 1邵维斌,钱家麒.高浓度葡萄糖诱导人腹膜间皮细胞凋亡[J].肾脏病与透析肾移植杂志,2003,12(1):58-59. 被引量:4
  • 2Podesta F, Romeo G, Liu WH, et al. Bax is increased in the retina of diabetic subjects and is associated with pericyte apoptosis in vivo and in vitro[J]. Am J Pathol, 2000,156:1025. 被引量:1
  • 3Moley KH, Chi MM, Knudson CM, et al. Hyperglycemia induces apoptosis in pre-implantation embryos through cell death effector pathways[J]. Nat Med, 1998,4:1421. 被引量:1
  • 4邵维斌,钱家麒.从网膜组织法培养人腹膜间皮细胞[J].肾脏病与透析肾移植杂志,2001,10(1):92-94. 被引量:13
  • 5Vander Heiden MG, Chandel NS, Willianson FK, et al. Belxl regulates the membrane potential and volume homeostasis of mitochondrial[J]. Cell, 1997,91 (5) :627-637. 被引量:1
  • 6Nagy JA. Peritoneal membrane morphology and function[J]. Kidney Int, 1996,50(Suppl 56):S2-S 11. 被引量:1
  • 7Zheng ZH, Ye RG, Bergstrom J,et al. Effect of dialysate composition on apoptosis and proliferation of HPMC and protein expression of Fas and C-myc Perit[J]. Dial Int,2000,20 (Suppl 1): S17. 被引量:1
  • 8Gotolib L, Shostak A, Waysrot V. High glucouse induces a hypertrophric,senecent mesothelial cell phenotype after long in vivo exposure[J]. Nephron, 1999,82 (2): 164-173. 被引量:1
  • 9Danial NN, Korsmeyer SJ. Cell death: critical control points [J]. Cell ,2004, 116(2):205-219. 被引量:1
  • 10Rosse T, Olivier R, Monney L, et al. Bcl-2 prolongs cell survival after Bax-induced release of cytochrome C [J]. Nature, 1998,391:496-499. 被引量:1

二级参考文献12

  • 1鄂征.组织培养和分子细胞学技术[M].北京:北京出版社(第二版),1997.438-439. 被引量:38
  • 2鄂征,组织培养和分子细胞学技术,1997年,56页 被引量:1
  • 3Wu Y J,Cell,1982年,31卷,693页 被引量:1
  • 4Gotloib L, Waisbrut U, Shostak A et al. Acute and long-term changes observed in inprints of mouse mesothelium exposed to glucose enriched,lactated, buffered dialysis solution. Nephron, 1995,70:466 被引量:1
  • 5Baumgartner-Parzer SM, Wagner LW, Pettermann M et al. High-glucosetriggered apoptosis in cultured ondothelial cells. Diabetes, 1995,44:1323 被引量:1
  • 6Zheng ZH, Ye RG, Bergstrom J et al. Effect of dialysate composition on apoptosis and proliferation of HPMC and protein expression of Fas and Cmyc. Adv Perit Dial,2000,16:31 被引量:1
  • 7Yang AH, Chen JY, Lin YP et al. Peritoneal dialysis solution induces apoptosis of mesothalial cells. Kidney Int, 1997,51:1280 被引量:1
  • 8Nagy JA. Peritoneal membrane morphology and function. Kidney Int,1996,50(Suppl 56) :S2 被引量:1
  • 9Krediet RT. The peritoneal membrane in chronic peritoneal dialysis. Kidney Int, 1999,55:341 被引量:1
  • 10Pollock CA,Ibels LS,Eckstein RP et al.Peritoneal morphology on maintenance dialysis. Am J Nephrol, 1989,9:198 被引量:1

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