期刊文献+

结缔组织生长因子在瘢痕疙瘩中表达的研究 被引量:17

A Preliminary Study on the Expression of Connective Tissue Growth Factor in Keloids
原文传递
导出
摘要 目的探讨结缔组织生长因子(CTGF)在瘢痕疙瘩发病中的作用。方法应用半定量逆转录聚合酶链反应技术检测30例瘢痕疙瘩患者皮损及对应邻近未受累皮肤中CTGFmRNA的表达,并以15例正常人皮肤组织作为对照。同时应用SP免疫组化技术对5例瘢痕疙瘩组织和5例正常人皮肤标本进行了检测。结果CTGFmRNA在瘢痕疙瘩及其边缘正常皮肤中的表达均明显高于正常人对照,差异有显著性(P<0.01)。瘢痕疙瘩CTGF的表达高低与病程无相关性(P>0.05)。免疫组化研究证实CTGF在瘢痕疙瘩中呈强表达,而在正常人皮肤中无表达。在瘢痕疙瘩组织边缘,CTGF表达呈现由强至弱的过渡现象。结论CTGF在瘢痕疙瘩中持续高度表达,提示其与瘢痕疙瘩的慢性纤维化有关。CTGF可能成为临床治疗瘢痕疙瘩的一个有力靶位。 Objective To investigate the role of connective tissue growth factor(CTGF)in the pathogenesis of keloid.Methods The expression of CTGF mRNA was detected with semiquantitative RT-PCR technique in keloid tissue and adjacent uninvolved skin from30patients.The expression of CTGF pro-tein was determined by SP immunohistochemistry in5keloid tissues and5normal skin samples.Results Compared with normal controls,the mean levels of CTGF mRNA expression were significantly increased in both keloid lesions and adjacent uninvolved skin(P<0.01).There was no correlation between CTGF mR-NA expression and the course of keloids(P>0.05).In immunohistochemistry study,CTGF protein was strongly expressed in keloid tissue,whereas it was not expressed in normal skin.Transitional phenomenon was observed from strong to weak expression of CTGF protein at the edge of keloid tissue.Conclusion These findings suggest that CTGF may be related to the development of persistent fibrotic tissue formation in keloids.CTGF may be a new potential target for the therapeutic intervention of keloids.
出处 《中华皮肤科杂志》 CAS CSCD 北大核心 2003年第7期380-383,共4页 Chinese Journal of Dermatology
  • 相关文献

参考文献9

  • 1Border WA, Noble NA. Transforming growth factor beta in tissue fibrosis. N Engl J Med, 1994, 331: 1286-1292.
  • 2Takehara K. Growth regulation of skin fibroblasts. J Dermatol Sci,2000, 24(Suppl 1 ): S70-77.
  • 3Igarashi A, Nashiro K, Kikuchi K, et al. Connective tissue growth factor gene expression in tissue sections from localized scleroderma,keloid, and other fibrotic skin disorders. J Invest Dermatol, 1996,106: 729-733.
  • 4Darzi MA, Chowdri NA, Kaul SK, et al. Evaluation of various methods of treating keloids and hypertrophic scars: a 10-year follow-up study. Br J Plast Surg, 1992, 45: 374-379.
  • 5Yamamoto S, Kitadai Y, Tsuchida A, et al. Expression of plateletderived endothelial cell growth factor/thymidine phosphorylase in human gallbladder lesions. Eur J Cancer, 2000, 36: 257-263.
  • 6Igarashi A, Nashiro K, Kikuchi K, et al. Significant correlation between connective tissue growth factor gene expression and skin sclerosis in tissue sections from patients with systemic sclerosis. J Invest Dermatol, 1995, 105: 280-284.
  • 7Mori T, Kawara S, Shinozaki M, et al. Role and interaction of connective tissue growth factor with transforming growth factor-beta in persistent fibrosis: A mouse fibrosis model. J Cell Physiol, 1999,181: 153-159.
  • 8Chiou S, Yoo J, Loh KC, et al. Identification of rat mammary tumor-1 gene (RMT-1), which is highly expressed in rat mammary tumors. Cancer Lett, 2001, 174: 45-55.
  • 9陈晓栋,张国成.促纤维化细胞因子与瘢痕疙瘩[J].国外医学(皮肤性病学分册),2002,28(1):31-34. 被引量:30

二级参考文献25

  • 1Border WA, Noble NA. Transforming growth factor beta in tissue fibrosis.N Engl J Med, 1994,331 (19): 1286-1292.
  • 2Shah M, Foreman DM, Ferguson MW. Neutralisation of TGF-beta 1 and TGF-beta 2 or exogenous addition of TGF-beta 3 to cutaneous rat wounds reduces scarring. J Cell Sci,1995,108 ( Pt 3):985-1002.
  • 3Wu L, Siddiqui A, Morris DE, et al. Transforming growth factor beta 3(TGF beta 3) accelerates wound healing without alteration of scar prominence. Histologic and competitive reverse-transcription-polymerase chain reaction studies. Arch Surg, 1997,132(7) :753-760.
  • 4Lee TY, Chin GS, Kim WJ, et al. Expression of transforming growth factor beta 1, 2, and 3 proteins in keloids. Ann Plast Surg, 1999 ,43(2): 179-184.
  • 5Smith P, Mosiello G, Deluca L, et al. TGF-beta2 activates proliferative scar fibroblasts. J Surg Res, 1999,82(2):319-323.
  • 6Bettinger DA, Yager DR, Diegelmann RF, et al. The effect of TGF-beta on keloid fibroblast proliferation and collagen synthesis. Plast Reconstr Surg, 1996,98(5):827-833.
  • 7Schmid P, Itin P, Cherry G, et al. Enhanced expression of transforming growth factor-beta type Ⅰ and type Ⅱ receptors in wound granulation tissue and hypertrophic scar. Am J Pathol, 1998 , 152(2) :485-493.
  • 8Meyer-Ingold W, Eichner W. Platelet-derived growth factor. Cell Biol Int,1995,19(5): 389-398.
  • 9Tan EM, Qin H, Kennedy SH, et al. Platelet-derived growth factors-AA and -BB regulate collagen and collagenase gene expression differentially in human fibroblasts. Biochem J, 1995,310 ( Pt 2) :585-588.
  • 10Haisa M, Okochi H, Grotendorst GR. Elevated levels of PDGF alpha receptors in keloid fibroblasts contribute to an enhanced response to PDGF.J Invest Dermatol, 1994,103(4) :560-563.

共引文献29

同被引文献211

引证文献17

二级引证文献78

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