期刊文献+

圆盘状受体1在瘢痕疙瘩中的作用 被引量:2

Role of discoidin domain receptor 1 in keloid
下载PDF
导出
摘要 目的:观察圆盘状受体1在瘢痕疙瘩不同部位的表达情况,进一步分析其在瘢痕疙瘩形成和发展中的作用。方法:选择2005-02/06在解放军第二军医大学附属长海医院门诊就诊的3例瘢痕疙瘩患者,均知情同意。瘢痕疙瘩事先均未进行任何治疗,将瘢痕疙瘩分为中央凹陷的老化部、隆起明显的增生部、表面潮红的浸润部及正常皮肤部。体外培养成纤维细胞,通过WESTBLOT实验检测瘢痕疙瘩不同部位圆盘状受体1、p53、基质金属蛋白酶表达情况,应用流式细胞仪检测细胞凋亡率。结果:①WESTBLOT实验检测结果:圆盘状受体1的表达以增生部、浸润部最明显,而老化部次之,正常皮肤部表达最弱。p53表达以老化部、增生部、浸润部为显著,正常皮肤部表达不显著。基质金属蛋白酶在老化部、增生部、浸润部表达强于正常皮肤部,而浸润部较老化部表达更强。②瘢痕疙瘩不同部位细胞凋亡率比较:正常皮肤部细胞凋亡率显著高于老化部及增生部[(10.1±3.5)%,(6.2±1.8)%,(5.1±3.7)%(P<0.05)],其中浸润部(4.6±3.4)%与正常皮肤部相比,差异具有极其显著性意义(P<0.01)。结论:在瘢痕疙瘩中表现出圆盘状受体1高表达及成纤维细胞低凋亡的特性,圆盘状受体1强表达区也有p53强表达,以上作用可保护细胞,防止细胞凋亡,而且有利于瘢痕疙瘩的浸润。 AIM: To observe the expressions of diseoidin domain receptor 1 (DDR1) in different parts of keloid and further explore its role in formation and progression of keloid. METHODS: Totally 3 keloid patients in Affiliated Changhai Hospital of Second Milirary Medical University of Chinese PLA from February to June 2006 were selected and all subjects knew and agreed with items. Untreated keloids were divided into several parts: ageing part with central foveas, proliferative part with obvious eminence, infiltrating part with flush surface and normal skin part. Samples were cultured in vitro into fibroblasts. Expressions of DDR1, p53 and matrix metalloproteinase (MMP) in different parts of keloid were detected with West blot method and apoptotic rate was determined by flow cytometry. RESULTS: ① Results of determination in West blot experiment: expressions of DDR1 were most significant in proliferative part and infiltrating part, then was the ageing part that in normal skin part was the weakest. Expressions of p53 were the most remarkable in ageing part, proliferative part and infiltrating part, while that in normal skin part was not marked. Expressions of MMP in ageing part, proliferative part and infiltrating part were stronger than that in normal skin part and that in infiltrating part was stronger than that in ageing part. ②Comparison of apoptotic rate in different parts of keloid: that in normal skin part was significantly higher than that in ageing part and proliferative part of keloid [(10.1±3.5)%,(6.2±1.8)%,(5.1±3.7)%, P〈 0.05]. There were remarkable significances in comparison between infiltrating part [(4.6±3.4)%] and normal skin part (P 〈 0.01). CONCLUSION: There are expressions of DDR1 and low apoptotic characteristics of fibroblast in keloid and there are expression of p53 in strong expressive area of DDR1, which may protect fibroblast from apoptosis and is beneficial to infiltration of keloid.
出处 《中国临床康复》 CSCD 北大核心 2006年第16期89-91,共3页 Chinese Journal of Clinical Rehabilitation
  • 相关文献

参考文献8

  • 1Nemoto T,Ohashi K,Akashi T,et al.Overexpression of protein tyrosine in human esophageal cancer.Pathobiology 1997;65(4):195-204.
  • 2Vogel W,Gish GD,Alves F,et al.The discoidin domain receptor tyrosine kinase are activated by collagen.Mol Cell 1997;1(1):13-23.
  • 3陈伟,付小兵,孙同柱,孙晓庆,赵志力,盛志勇.增生性瘢痕组织中p53和c-myc蛋白含量的变化及其对瘢痕内细胞凋亡发生的影响[J].中国危重病急救医学,2002,14(2):100-103. 被引量:6
  • 4段红杰,高建华,沈光裕.瘢痕疙瘩成纤维细胞P53基因突变检测[J].中国临床康复,2002,6(22):3358-3359. 被引量:10
  • 5Lee SW,Fang L,Igarashi M,et al.Sustained activation of Ras/Raf/mitogenactivated protein kinase cascade by the tumor suppressor p53.Proc Natl Acad Sci USA 2000;97(15):8302-5.
  • 6Ongusaha PP,Kim JL,Fang L,et al.p53 induction and activation of DDR1 kinase counteract p53-mediated apoptosis and influence p53 regulation through a positive feedback loop.EMBO J 2003;22(6):1289-301.
  • 7Mohan RR,Mohan RR,Wilson SE.Discoidin Domain Receptor(DDR)1 and 2:Collagen-activated tyrosine kinase receptors in the cornea.Exp Eye Res 2001;72(1):87-92.
  • 8Faraci E,Eck M,Gerstmayer B,et al.An extracellular matrix-specific microarray allowed the identification of target genes downstream of discoidin domain receptors.Matrix Biol 2003;22(4):373-81.

二级参考文献8

  • 1[1]EHRLICH HP,DESMULIERE A,DIGEIMAN RF,et al. Morphological and immunochemical differences between keloid and hypertrophic scars[J].Am J Pathol,1994,145:105-113.
  • 2[2]HIROKI N,SHUN J,YOSHIHARU M.Proliferating activity of dermal fibroblasts in keloids and hypertrophic scars[J]. Acta Derm Venereol,1995,75:102-104.
  • 3[3]LAN A,NICOLA J,BROWN,et al.Apoptosis, necrosis, and proliferation possible implications in the etiology of keloids[J].Am J Path,1996,5:1441-1447.
  • 4[4]LANE DP.P53 guardian of the genome[J].Nature, 1992, 358:15-16.
  • 5[5]YONISH RE,GRUNWALD D,WILDER S,et al.P53 mediate cell death: relationship to cell cycle control[J].Mol Cell Biol,1993,13:1415-1420.
  • 6庄贤韩.c-Myc介导的细胞凋亡途径[J].国外医学(分子生物学分册),1999,21(4):214-217. 被引量:9
  • 7付小兵,杨银辉,孙同柱,蒋礼先,盛志勇.缺血再灌注诱导bcl2基因表达及其对肠道细胞凋亡的影响[J].中国危重病急救医学,1999,11(8):459-461. 被引量:17
  • 8秦军志,周树夏,刘荫秋.颌面部火器伤损伤组织中C-myc原癌基因的表达[J].中国危重病急救医学,2000,12(8):485-487. 被引量:1

共引文献14

同被引文献26

  • 1郑素军,任红,王升启.反义寡核苷酸研究进展[J].国外医学(临床生物化学与检验学分册),2004,25(6):506-509. 被引量:2
  • 2莫济贤,罗少军,梁杰,张刚.瘢痕疙瘩形成机制的研究进展[J].医学综述,2006,12(12):705-706. 被引量:4
  • 3吴乃虎.基因工程原理[M].北京:科学出版社,2001.389.
  • 4Vogel W.Discoidin domain receptors:structural relations and functional implications.FASEB J 1999;Suppl:S77-82
  • 5Vogel W,Gish GD,Alves F,et al.The discoidin domain receptor tyrosine kinase are activated by collagen.Mol Cell 1997;1:13
  • 6Shrivastave A,Radziekewski C,Campbell E,et al.An orphan receptor tyrosine kinase family whose members serve as nonintegrin collagen receptors.Mol Cell 1997;1:25
  • 7Chin GS,Liu W,Steinbrech D,et al.Cellular signaling by tyrosine phosphorylation in keloid and normal human dermal fibroblasts.Plast Reconstr Surg 2000;106(7):1532-40
  • 8Bock O,Yu H,Zitron S,et al.Studies of transforming growth factors beta 1-3 and their receptors Ⅰ and Ⅱ in fibroblast of keloids and hypertrophic scars.Acta Derm Venereol 2005; 85(3):216-220
  • 9Chin GS,Lee S,Hsu M,et al.Discoidin domain receptors and their ligand,collagen,are temporally regulated in fetal rat fibroblasts in vitro.Plast Reconstr Surg 2001;107(3):769-76
  • 10Faraci E,Eck M,Gerstmayer B,et al.An extracellular matrix-specific microarray allowed the identification of target genes downstream of discoidin domain receptors.Matrix Biol 2003;22(4):373-381

引证文献2

二级引证文献5

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