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肥厚性疤痕成纤维细胞的基因芯片分析 被引量:2

Analysis of Hypertrophic Scar Fibroblasts Expression Fingerprint Using cDNA Microarray
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摘要 用基因芯片分析肥厚性疤痕与正常皮肤成纤维细胞在静息及TGF beta3刺激下的表达谱的改变 .正常成纤维细胞在TGF beta3刺激前后的表达谱与肥厚性疤痕成纤维细胞在TGF beta3刺激前的表达谱正相关 (r=0 .76 0 37) ,刺激后 2种成纤维细胞的表达差异与肥厚性疤痕成纤维细胞TGF beta3刺激前后的表达谱差异正相关 (r =0 .82 6 76 2 ) .构成以上差异的基因有 6 2 0条 ,涉及细胞骨架蛋白、细胞周期蛋白、细胞因子、受体、转录因子及糖、蛋白质和核酸代谢的酶类 ;未发现胶原蛋白Ⅰ ,Ⅲ的表达水平的改变 .结果提示 :1.肥厚性疤痕成纤维细胞在静息状态下表现出与正常细胞受TGF beta3刺激后相似的反应 ,其可能处于一种应激状态 ;2 .TGF beta3刺激后 2种细胞的反应差异与肥厚性疤痕细胞的异常反应相关 ,TGF beta3的作用背景可能是肥厚性疤痕的分子病理学基础之一 ;3 .基因表达变化涉及细胞因子、细胞周期调控、凋亡等 ,其具备疾病遗传异质性的分子基础 ;4.胶原表达无明显上升 ,提示在肥厚性疤痕发病中 ,胶原纤维及细胞外基质堆积有复杂的分子生物学基础 . The expression fingerprint of HS fibroblasts was analyzed by cDNA microarray, using mRNA derived from multiple tissues as a contrast. The expression fingerprint of HS fibroblasts was similar to that of normal fibroblast post stimulated by TGF beta3. The expression pattern between the HS and the normal fibroblasts post stimulated was correlated to expression pattern between HS fibroblasts prior and post stimulated by TGF beta3. The expression of 620 genes related to cell cycle, cytokine, oncoprotein and apoptosis was up regulated or down regulated at least 3 times. However, the expression of type Ⅰ and Ⅲ collagen was not changed. The results suggest: (1)The HS fibroblast was in a stress status; (2) Over expression of collagen type Ⅰ and Ⅲ was not necessary for HS formation.
出处 《复旦学报(自然科学版)》 CAS CSCD 北大核心 2000年第6期634-638,644,共6页 Journal of Fudan University:Natural Science
基金 上海现代生物与新药产业发展基金资助项目!(98431912 1)
关键词 肥厚性疤痛 CDNA基因芯片 成纤维细胞 表达谱 转化生长因子Β3 hypertrophic scar(HS) cDNA microarray fibroblast expression fingerprint TGF beta3
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参考文献5

  • 1周宗祥,徐坚,等.RBM13 cDNA的克隆及其表达谱分析[J].复旦学报(自然科学版),2000,39(6):583-587. 被引量:19
  • 2Lee N J,Laryngoscope,2000年,110卷,616页
  • 3周宗祥,复旦学报,2000年,39卷,6期,583页
  • 4Lin R Y,Ann Surg,1995年,222卷,146154页
  • 5Ghahary A,Mol Cell Biochem,1995年,148卷,25页

二级参考文献7

  • 1[1] Brud C G, Dreyfuss G. Conserved structures and diversity of functions of RNA-binding proteins[J]. Science, 1994, 265: 615-621.
  • 2[2] Chernova O B, Chernov M V, Agarwal M L, et al. The role of p53 in regulating genomic stability when DNA and RNA synthesis are inhibited[J]. Trends Biochem Sci, 1995, 20(10): 431-434.
  • 3[3] Dreyfuss G, Matunis M J, Pinol-Roma S, et al. hnRNP proteins and the biogenesis of mRNA[J]. Annu Rev Biochem, 1993, 62: 289-321.
  • 4[4] Karsch-Mizrachi I, Haynes S R. The Rb97D gene encodes a potential RNA-binding protein required for spermatogenesis in Drosophila[J]. Nucleic Acids Res, 1993, 21(9): 2229-2235.
  • 5[5] Baker BS. Sex in flies: The splice of life[J]. Nature, 1989, 340(6234): 521-524.
  • 6[6] Matunis E L, Kelley R, Dreyfuss G. Essential role for a heterogeneous nuclear ribonucleoprotein (hnRNP) in oogenesis: Hrp40 is absent from the germ line in the dorsoventral mutant squid[J]. Proc Natl Acad Sci USA, 1994, 91(7): 2781-2784.
  • 7[7] Chambers J C, Kenan D, Martin B J, et al. Genomic structure and amino acid sequence domains of the human La autoantigen[J]. J Biol Chem, 1988, 263(34): 18043-18051.

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  • 1SHUKLA A,RASIK AM,JAIN GK,et al.In vitro andinvivowound healing activity of asiaticoside isolated from Centalla asiatica [J].J Ethnopharmacol,1999,65(1):1-11.
  • 2CHOMCZYNSKI P,SACCHI N.Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction[J].Anal Biochem,1987,162,156-159.
  • 3EISENMB,SPEL.LMAN PT,BROWN PO,et al.Cluster analysis and display of genome-wide expression patterns [J].Proc Natl Acad Sci USA,1998,95(25):14 863-14 868.
  • 4中华人民共和国卫生部药典委员会.中华人民共和国药典(3 一部)[M].广州:广东科技出版社,化学工业出版社,1995.253.
  • 5MAQUART FX,BELLON G,GILLERY P,et al.Stimulation of collagen synthesisinfibroblast cultures by atriterpene extractedfrom Centalla asiatica[J].ConnectTissueRes,1990,24(2):107-120.
  • 6MAQUART FX,CHASTANG F,SIMEON A,et al.Triterpenes from Centalla asiatica stimulate extracellular matrix accumulation in rat experimental wounds[J].Eur J Dermatol,1999,9(4):289-296.
  • 7韦多,葛绳德,陈玉林,苏波,戴方平.烧伤创面组织TGFβ和其Ⅰ型、Ⅱ型受体的基因表达研究[J].中国病理生理杂志,1997,13(5):456-460. 被引量:1
  • 8杨银辉,付小兵,王亚平,孙同柱,许明火,盛志勇.定量PCR技术检测增生性瘢痕组织纤维连接蛋白的基因表达[J].中华整形烧伤外科杂志,1998,14(6):404-406. 被引量:8
  • 9刘凯,钱云良,范志宏.转化生长因子β与组织创伤修复综述[J].中国修复重建外科杂志,1999,13(5):283-285. 被引量:8
  • 10耿智敏,向国安,刘效恭,韩庆,王康敏,刘青光,潘承恩.犬胆肠吻合愈合过程的组织学观察[J].西安医科大学学报,2000,21(5):446-448. 被引量:6

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