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生长因子对间皮细胞增殖及合成细胞外基质的影响 被引量:1

Effect of growth factors on proliferation and extracellular matrix biosynthesis by human peritoneal mesothelial cells
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摘要 目的 探讨血小板源生长因子bb(PDGFbb) 、转化生长因子β(TGFβ) 对人腹膜间皮细胞(HPMC)增殖及合成细胞外基质(ECM) 的影响。方法 建立HPMC体外培养体系。3HTdR 掺入法测定细胞增殖;放射免疫法检测细胞上清中Ⅲ型前胶原( ⅢPC) 。结果 PDGFbb 促进、但TGFβ抑制HPMC增殖,均呈剂量依赖性( P< 0-01) 。2 者均能刺激HPMC 产生ⅢPC( P< 0-01)。结论 CAPD相关性腹膜炎时腹腔中高浓度的PDGFbb 、TGFβ能调节间皮层的修复和重塑,刺激其合成分泌ECM,后者可能是腹膜炎(PI)反复发生最终导致腹膜硬化的重要机制之一。 Objective To examine the effect of PDGF bb and TGF β on the proliferation and extracellular matrix(ECM) biosynthesis by human peritoneal mesothelial cells (HPMC).Methods In vitro HPMC culture system was established. Cell proliferation was assessed by 3 H TdR incorporation and type Ⅲ precollagen (ⅢPC) in supernatants was quantitated by radioimmunoassay. Results PDGF bb stimulated, but TGF β inhibited the proliferation of HPMC in dose dependent manner (P<0 01). Both growth factors induced significant increases in ⅢPC production by HPMC (P<0 01).Conclusion During peritonitis complicated with CAPD, enhanced PDGF bb and TGF β in the peritoneal cavity may regulate the repairing and remodeling of mesothelium, and accelerate the synthesis of ECM by HPMC, which might potentially contribute to the pro fibrotic process in CAPD.
机构地区 南方医院肾内科
出处 《中华肾脏病杂志》 CAS CSCD 北大核心 1999年第6期358-360,共3页 Chinese Journal of Nephrology
基金 国家自然科学基金!( 基金号:39470337)
关键词 腹膜 间皮细胞增殖 细胞外基质 生长因子 Peritoneum Mesothelial cells Proliferation Extracellular matrix Growth factor
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同被引文献15

  • 1侯凡凡,臧燕,张训,杨铁城.高浓度葡萄糖对人腹膜间皮细胞生长和基质合成的影响[J].中华内科杂志,1995,34(5):326-329. 被引量:8
  • 2臧燕,侯凡凡,杨铁成,杨满球.高浓度葡萄糖对人腹膜间皮细胞的损伤作用及对其增殖的影响[J].中华肾脏病杂志,1995,11(4):230-232. 被引量:7
  • 3张凯,李继承,陈一芳,徐萍,李华.腹膜透析液对小鼠腹膜间皮细胞超微结构影响的比较研究[J].肾脏病与透析肾移植杂志,1996,5(1):20-21. 被引量:2
  • 4Krediet RT, Ho-Dac-Pannekeet MM, Struijk DG. Preservation of peritoneal membrane function [ J]. Kidney Int, 1996,50[ Suppl 56 ] : S62-68.
  • 5Fischereder M, Luckow B, Sitter T, et al. Immortalization and characterization of human peritoneal mesothelial cells[ J]. Kidney Int, 1997,51(6) :2001-2012.
  • 6Ho-dac-Pannekeet MM, Hiralall JK, Struijk DG, et al. Longituctinal follow-up of CAI25 in peritoneal effluent[ J]. Kidney, Int, 1997,51 ( 3 ) :888-893.
  • 7Carozzi S, Nasini MG, Santoni O, et al. Peritoneal macrophage anti lymphocyte cytoplasmic Ca^2 + :effects on peritoneal immune defense mechanisms and ultrafiltration capacity in CAPD[J]. Peri Dial Int, 1997,17(51) :29-32.
  • 8Breborowicz A, Rodela H, Oreopoulos DG. Toxicity of osmotic solutes on human mesothelial cells in vitro[ J]. Kidney Int, 1992,41 (5):1280-1284.
  • 9Brown BR, Rodgers GM, Hoidal JR, et al. Human mesothelial cells express components of both the fibrinolytic and procoagulant pathways[J] . Am Rev Respir Dis, 1991,143(4) : A766.
  • 10Yamamoto T, Izumotani T, Otoshi T. et al. Morphological studies of mesothelial cells in CAPD effluent and their elinieal signifieance[J]. Am J Kidney Dis, 1998,32(2) :946-952.

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