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细胞角蛋白和波形蛋白在皮肤淀粉样变淀粉样蛋白中表达的研究 被引量:4

Cytokeratins and vimentin expressions in the amyloids of lichen amyloidosis and macular amyloidosis
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摘要 目的:探讨皮肤淀粉样变淀粉样蛋白的生物学来源。方法:应用免疫组化染色技术检测4种角蛋白(cytokeratins,CKs)及波形蛋白在20例斑状或苔藓样型皮肤淀粉样变淀粉样蛋白中的表达情况。结果:①CK34βE12和CK5/6在20例标本的淀粉样蛋白团块中均呈阳性表达;而AE1/AE3、CK10/13和波形蛋白在淀粉样蛋白团块中均呈阴性表达;②淀粉样蛋白团块中波形蛋白表达阳性的成纤维细胞明显增生。结论:淀粉样蛋白主要来源于凋亡的表皮基底细胞而非真皮组织。 Objective: To discuss the biological origin of the amyloids in macular amyloidosis (MA) and lichen amyloidosis (LA). Methods: The immunohistochemical staining was used to investigate the expressions of cytokeratins (CKs) and vimentin in amyloid deposits of formalin-fixed and paraffin-embedded tissue specimens from 13 patients with LA and 7 with MA. Results: In amyloid deposits, only CK34βE12 and CK5/6 was positive in 20 biopsy specimens, and AE1/AE3, CK10/13 and vimentin were negative. Fibroblast cells which could express vimentin presented significant proliferation among the amyloids. Conclusion: The results confirm the hypothesis that the amyloid in lichen and macular amyloidosis mainly derived from basal keratinoeytes, not from dermal tissues.
出处 《临床皮肤科杂志》 CAS CSCD 北大核心 2010年第4期218-220,共3页 Journal of Clinical Dermatology
关键词 淀粉样变 皮肤 淀粉样蛋白 角蛋白 波形蛋白 免疫组化 amyloidosis, cutaneous amyloid cytokeratin vimentin immunohistochemistry
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参考文献10

  • 1Apaydin R,Gürbaz Y,Bayramgürler D,et al.Cytokeratin expression in lichen amyloidosus and maeular amyloidosis[J].J Eur Acad Dermatot Venereol,2004,18(3):305-309.
  • 2Chang YT,Liu HN,Wang WJ,et al.A study of cytokeratin profiles in localized cutaneous amyloids[J].Arch Dermatol Res,2004,296(2):83-88.
  • 3Ishii M,Kobayashi H,Chanoki M,et al.Possible formation of cutancous amyloid from degenerative collagen fibers.Ultrastructural collagen changes and the immunoreactivity of cutaneous amyloidosis employing anti-type Ⅰ,Ⅲ,Ⅳ,Ⅴ coUagen antibodies[J].Aeta Derm Venereol,1990,70(5):378-384.
  • 4谭燃景,郝进.原发性皮肤淀粉样变病的病因及发病机制[J].医学临床研究,2007,24(10):1799-1801. 被引量:7
  • 5袁锋(综述),王培光(审校),杨森(审校),张学军(审校).原发性皮肤淀粉样变研究进展[J].中国麻风皮肤病杂志,2008,24(12):981-983. 被引量:3
  • 6Chang YT,Wong CK,Chow KC,et al.Apoptosis in primary cutaneous Amyloidosis[J].Br J Dermatol,1999,140(2):210-215.
  • 7Hynes RO.Integrins:versatility,modulation,and signaling in cell adhesion[J].Cell,1992,69(1):11-25.
  • 8Hashimoto K,Ito K,Taniguchi Y,et al.Keratin in cutaneoug amyioidoses[J].Clin Dermatol,1990,8(2):55-65.
  • 9Ortiz-Romem PL,Ballestin-Carcaviila C,Lopez-Estebaranz JL,et al.Clinieopathologic and immunohistochemical studies on lichen arayloidosis and macular amyloidosis[J].Arch Dermatol,1994,130(12):1559-1560.
  • 10Apaydin R,Bilen N,Bayramgüer D,et al.Lichen amyloidosis,ankylesing spondylitis and aumimmune thyroiditis:coincidence or association[J].J Ear Acad Dermatol Vanereol,2000,14(2):135-137.

二级参考文献39

  • 1Chang YT, Liu HN, Wong CK, et al. Detection of Epstein- Barr virus in primary cutaneous amyloidosis. Br J Dermatol 1997; 136: 823 - 826.
  • 2Steciuk A, Dompmartin A, Troussard X, et al. Cutaneous amyloidosls and possible association with systemic amyloidosis. Int J Dermatol 2002;41 : 127 - 132.
  • 3Hazenberg BP, van Gameren II, Bijzet J, et al. Diagnostic and therapeutic approach of systemic amyloidosis. Neth J Med 2004; 62:121 - 128.
  • 4van Gameren II, Lokhorst H, Hazenberg BP, et al. Therapeutic options in systemic AL amyloidosis. Neth J Med 2004; 62: 106- 113.
  • 5Gertz MA. The classification and typing of amyloid deposits. Am J Clin Pathol 2004; 121:787 - 789.
  • 6Lee DD, Lin MW, Chen IC, et al. Genome - wide scan identifies a susceptibility locus for familial primary cutaneous amyloidosis on chromosome 5p13. 1 - q11.2. Br J Dermatol 2006; 155(6) : 1201 - 1208.
  • 7Lee DD, Huang JY, Wong CK, et al. Genetic heterogeneity of familial primary cutaneous amyloidosis: lack of evidence for linkage with the chromosome 10 pericentromeric region in Chinese families. J Invest Dermatol 1996; 107:30- 33.
  • 8Verga U, Fugazzola L, Cambiaghi S, et al. Frequent association between MEN 2A and cutaneous lichen amyloidosis. Clin Endocrinol 2003;59(2) : 156 - 161.
  • 9Lin MW, Lee DD, Lin CH, et al. Suggestive linkage of familial primary cutaneous amyloidosis to a locus on chromosome 1 q23. Br J Dermatol 2005 ; 152: 29 - 36.
  • 10Gazit E. Mechanisms of amyloid fibril self- assembly and inhibition. Model short peptides as a key research tool. FEBS J 2005; 272 : 5971 - 5978.

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