期刊文献+

银屑病患者骨髓CD34^+细胞定向分化的T细胞对角质形成细胞增殖的影响 被引量:5

Influence of T cells differentiated from bone marrow-derived CD34^+ cells of psoriatic patients on keratinocyte proliferation in vitro
下载PDF
导出
摘要 目的:探讨家族史阳性的银屑病患者骨髓CD34+细胞体外定向分化的T细胞对表皮角质形成细胞(KC)增殖调控蛋白表达的影响。方法:将银屑病患者骨髓CD34+细胞体外定向分化的T细胞经链球菌超抗原活化后与KC共培养,分别采用免疫组化法及ELISA法检测KCC-myc、bcl-xL、p53及Ki67蛋白表达及培养上清白介素(IL)-8、干扰素(IFN)-γ水平。结果:①受银屑病患者CD34+细胞定向分化T细胞作用的KCC-myc及Ki67蛋白表达与自然增殖组及正常人CD34+细胞定向分化的T细胞作用组相比显著增强(P<0.05),而bcl-xL及p53蛋白表达3组间的差异无统计学意义(P>0.05);②受正常人CD34+细胞定向分化T细胞作用的KCC-myc、bcl-xL、p53及Ki67蛋白表达与自然增殖组比较差异亦无统计学意义(P>0.05);③银屑病CD34+细胞定向分化的T细胞作用组培养上清IL-8及IFN-γ水平显著高于正常对照组(P<0.01)。结论:银屑病患者骨髓造血细胞定向分化的T细胞可影响KC增殖状态,显示类似银屑病外周血T细胞的活性特点。 Objective: To explore the effect of T cells differentiated from bone marrow-derived CD34^+ cells of psoriatic patients on keratinocytes. Methods: Keratinocytes (KCs) from foreskin were cultured with or without T cells, differentiated from bone marrow-derived CD34^+ hematopoietic cells from psoriatic patients with family history or normal controls and activated by streptococcal superantigen (SAg). C-myc, bcl-xL, p53 and Ki67 proteins on KCs were determined by immunohistochemistry and IL-8 and IFN-γ levels in the culture supematant were detected by enzyme linked immunosorbent assay (ELISA). Results: C-myc, bcl-xL, p53 and Ki67 proteins were expressed at low density and proportion in KCs cultured with the T cells from normal controls and did not show significant difference with those without any T cell stimulation. However, C-myc and I(367 protein expression was greatly increased after KCs were cultured with T cells differentiated from bone marrow CD34^+ cells of psoriatic patients with higher IL-8 and IFN-γ levels in supematant. Conclusions; T cells derived from hematopoietic cells of psoriatic patients with family history are abnormal in their functions similar to psoriatic circulating T cells since they can influence proliferation of, keratinocytes probably by secreting cytokines.
出处 《临床皮肤科杂志》 CAS CSCD 北大核心 2008年第6期348-350,共3页 Journal of Clinical Dermatology
基金 国家自然科学基金(30771940) 山西省自然科学基金(20031110) 太原市科技局基金(0503044)资助项目
关键词 银屑病 骨髓 CD34^+细胞 T细胞 角质形成细胞 psoriasis bone marrow CD34^+ cells T cells keratinocytes
  • 相关文献

参考文献12

  • 1李新华,张开明,康玉英.银屑病患者T细胞对表皮c-myc、bcl-2及p53蛋白表达影响的实验研究[J].中华皮肤科杂志,2004,37(3):147-149. 被引量:24
  • 2Li X, Fan X, Zhang K, et al. Influence of psoriatic peripheral blood CD4T and CD8T lymphocytes on C-myc, Bcl-xL and Ki67 gene expression in keratinocytes[J]. Eur J Dermatol, 2007, 17(5): 392-396.
  • 3Zhang K, Zhang R, Li X, et al. The mRNA expression and promoter methylation status of the p16 gene in colony-forming cells with high proliferative potential in patients with psoriasis[J]. Clin Exp Dermatol, 2007, 32(6): 702-708.
  • 4张开明,李新华.骨髓,银屑病的发病“中枢”?[J].中国皮肤性病学杂志,2004,18(8):501-503. 被引量:32
  • 5尹国华,李新华,张开明,刘玉峰.银屑病患者骨髓CD34^+细胞体外定向分化的T细胞活性研究[J].中华皮肤科杂志,2006,39(3):124-127. 被引量:35
  • 6Austin LM, Ozawa M, Kikuchi T, et al. The majority of epidermal T cells in Psoriasis vulgaris lesions can produce type 1 cytokines, interferon-gamma, interleukin-2, and tumor necrosis factor-alpha, defining TC1 (cytotoxic T lymphocyte) and TH1 effector populations: a type 1 differentiation bias is also measured in circulating blood T cells in psoriatic patients[J]. J Invest Dermatol, 1999, 113(5): 752-759.
  • 7Nickoloff BJ. The immunologic and genetic basis of psorlasis[J]. Arch Dermatel, 1999, 135(9): 1104-1110.
  • 8Bowcock AM. The genetics of psoriasis and autoimmunity[J]. Annu Rev Genomics Hum Genet, 2005, 6: 93-122.
  • 9Barker JN, Mitra RS, Griffiths CE, et al. Keratinocytes as initiators of inflammation[J]. Lancet, 1991, 337(8735): 211-214.
  • 10Elder .JT, Klein SB, Tavakkol A, et al. Growth factor and protooncogene expression in psoriasis[J]. J Invest Dermatol, 1990, 95 (5): 7S-9S.

二级参考文献37

  • 1张开明,李新华.骨髓,银屑病的发病“中枢”?[J].中国皮肤性病学杂志,2004,18(8):501-503. 被引量:32
  • 2李新华,康玉英,张开明.SAg作用的银屑病T细胞对表皮c-myc bcl-2及P53蛋白的影响[J].中国皮肤性病学杂志,2004,18(11):654-656. 被引量:4
  • 3王刚,刘玉峰.银屑病患者外周血单一核细胞对自身角朊细胞的促生长作用[J].中华皮肤科杂志,1996,29(2):111-112. 被引量:3
  • 4普雄明.p53蛋白在一些皮肤病理组织中的检测及应用[J].国外医学(皮肤性病学分册),1996,22(1):13-15. 被引量:2
  • 5Nickoloff BJ,Wrone-Smith T,Bonish B,et al. Response of murine and normal human skin to injection of allogeneic blood-derived psoriatic immunocytes: detection of T cells expressing receptors typically present on natural killer cells, including CD94, CD158,
  • 6Bata-Csorgo Z,Hammerberg C,Voorhees JJ,et al. Intralesional Tlymphocyte activation as a mediator of psoriatic epidermal hyperplasia. J Invest Dermatol, 1995, 105( 1 Suppl): 89S-94S.
  • 7Soini Y,Kamel D, Paakko P, et al. Aberrant accumulation of p53 associates with Ki67 and mitotic count in benign skin lesions. Br J Dermatol, 1994, 131: 514-520.
  • 8Moles JP,Theillet C, Basset-Seguin N, et al.Mutation of the tumor suppressor gene TP53 is not detected in psoriatic skin. J Invest Dermatol, 1993, 101: 100-102.
  • 9Kastelan M,Massari LP,Pasic A,et al.New trends in the im munopathogenesis of psoriasis.Acta Dermatovenerol Croat,2004,12:26-29.
  • 10Makino S,Fukuda K,Miyoshi S,et al.Cardiomyocytes can be generated from marrow stromal cells in vitro.J Clin Invest,1999,103:697-705.

共引文献58

同被引文献59

引证文献5

二级引证文献17

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