期刊文献+

5,7,4′-三羟基异黄酮对增生性瘢痕成纤维细胞增殖细胞核抗原表达及细胞周期的影响

Effects of genistein on PCNA expression and cell cycle in human hypertrophic scar fibroblasts in vitro
原文传递
导出
摘要 目的观察5,7,4′-三羟基异黄酮(genistein)对增生性瘢痕成纤维细胞增殖细胞核抗原(proliferating cell nuclear antigen,PCNA)及细胞周期的影响,探讨5,7,4′-三羟基异黄酮抑制增生性瘢痕成纤维细胞增殖的机制。方法分离培养人增生性瘢痕成纤维细胞,分别加入25、50、100μmol/L浓度的5,7,4′-三羟基异黄酮共培养48h,免疫细胞化学法观察成纤维细胞PCNA蛋白的表达,流式细胞术检测细胞周期的变化。结果各组5,7,4′-三羟基异黄酮作用后细胞PCNA的表达均降低(P〈0.05),50μmol/L及100μmol/L浓度组的抑制作用最为显著(P〈0.01);随药物浓度的增加,G0~G1期细胞比例逐渐下降,G2~M期细胞比例增加,表明细胞分裂受到抑制;100μmol/L组的S期细胞数量比例也有增加,并于G1期前出现亚二倍体凋亡峰。结论5,7,4′-三羟基异黄酮可通过影响细胞分裂与DNA合成抑制瘢痕增生。 Objective To observe the effects of genistein on PCNA expression and cell cycle in fibroblasts derived from human hypertrophic scar in order to explore the mechanism of its inhibition on hypertrophic scar (HS) fibroblast proliferation. Methods The human hypertrophic scar fibroblasts were cultured in vitro. Genistein with various concentrations (25, 50, 100 μmol/L) was co-cultured in the medium for 48 hours. The expression of PCNA was detected with immunocytochemical staining method and the cell cycle was measured with flow cytometry. Results Genistein could significantly decrease PCNA expression in HS fibroblasts, especially when its concentration at 50 μmol/L or 100 μmol/L. The cell percentage of G0 - G1 phase decreased with drug's concentration, and G2 -M percentage increased conversely, implying the suspension of mitosis. In 100 μmol/L group, most cells blocked at S phase and a hypodiploid apoptosis peak could be observed ahead of G1 phase. Conclusion Genistein can inhibit the proliferation of human hypertrophic scar by blocking cell division as well as decreasing DNA synthesis.
出处 《中华医学美学美容杂志》 2008年第3期159-162,共4页 Chinese Journal of Medical Aesthetics and Cosmetology
关键词 增生性瘢痕 成纤维细胞 增殖细胞核抗原 细胞周期 5 7 4′-三羟基异黄酮 Hypertrophic scar Fibroblasts Proliferating cell nuclear antigen Cell cycle Genistein
  • 相关文献

参考文献6

二级参考文献20

  • 1丁乂,俞莉章,李鸣,刘漓波,钟华.人肾颗粒细胞癌细胞系(GRC-1)的建立及其生物学特性[J].中华泌尿外科杂志,1995,16(1):3-6. 被引量:17
  • 2[2]POLKOWSKI K,MAZUREK A P.Biological properties of genistein.A review of in vitro and in vivo data[J].Acta Pol Pharm,2000,57(2):135-155. 被引量:1
  • 3[3]SARKAR F H,LI Y.Mechanism of cancer chemoprevention by soy isoflavone genistein[J].Cancer Metastasis Rev,2002,21(3-4):265-280. 被引量:1
  • 4[4]NEUGARTEN J,ACHARYA A,LEI J,et al.Selective estrogen receptor modulators suppress mesangial cell collagen synthesis[J].Am J Physiol Renal Physiol,2000,279(2):309-318. 被引量:1
  • 5[5]QI L H,KANG L P,ZHANG J P,et al.Antifibrotic effects of genistein and quercetin in vitro[J].YAO XUE XUE BAO,2001,36(9):648-651. 被引量:1
  • 6[6]BRASS D M,HOYLE G W,POOVEY H G,et al.Reduced tumor necrosis factor-alpha and transforming growth factor-beta1 expression in the lungs of inbred mice that fail to develop fibroproliferative lesions consequent to asbestos exposure[J].Am J Pathol,1999,154(3):853-862. 被引量:1
  • 7[7]FOTSIS T,PEPPER M,ADLERCREUTZ H,et al.Genistein,a dietary-derived inhibitor of in vitro angiogenesis[J].Proc Natl Acad Sci USA,1993,90(7):2690-2694. 被引量:1
  • 8[8]HELDIN C H,MIYAZONO K,ten DIJKE P,et al.TGF-beta signalling from cell membrane to nucleus through SMAD proteins,[J] Nature,1997,390(6659):465-471. 被引量:1
  • 9[10]KANG L P,QI L H,ZHANG J P,et al.Effect of genistein and quercetin on proliferation,collagen synthesis,and type I procollagen mRNA levels of rat hepatic stellate cells[J].Acta Pharmacol Sin,2001,22(9):793-796. 被引量:1
  • 10Roqhow R. The role of extracellular matrix in past inflammatorty wound healing and fibresis[J]. J FASEB, 1999,8:823. 被引量:1

共引文献14

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部