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白癜风患者皮损NF—E2相关因子2的表达 被引量:2

Expression of NF-E 2 related factor in vitiligo lesions
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摘要 目的分析白癜风患者皮损处Nrf 2表达水平。方法采用AEC免疫组化法检测4例表皮移植的寻常型白癜风患者皮损处Nrf 2的表达,蛋白印迹分析表皮移植的8例寻常型白癜风患者皮损组织和其正常供皮处组织细胞核和细胞质中Nrf 2的表达水平,并进行统计学差异分析。结果与白癜风患者正常供皮处组织相比,皮损处Nrf 2的表达多数集中在角质形成细胞的胞质中,细胞核中表达量非常低。蛋白印迹结果表明,白癜风患者皮损处核蛋白中Nrf 2表达水平(0.10±0.03)显著低于正常部位(0.26±0.03,P〈0.01),胞质蛋白中皮损处Nrf 2表达水平(0.61±0.03)与正常部位(0.60±0.02)差异无统计学意义(P〉0.05)。结论白癜风患者皮损处存在Nrf 2核转位异常。 Objective To investigate the level of NF-E2 related factor 2 (Nrf 2) in vitiligo lesions. Methods Tissue samples were obtained by press suction blisters at lesional and donor sites of 12 patients with vitiligo who were managed with epidermal transplantation. Four lesional samples from the patients were subjected to primary culture and the level of Nrf 2 was detected by AEC immunohistochemistry after 48 hours of culture. Western blotting was utilized to further detect the level of cytoplasmic and nuclear Nrf 2 in tissue samples from the other 8 patients with vitiligo. Results Immunohistochemistry revealed that Nrf 2 was predominantly expressed in cytoplasm, rather than nuclei, of keratinocytes in vitiligo lesions compared with the normal skin of patients. The level of nuclear Nrf 2 was significantly lower in lesions than that in normal skin (0.10 ± 0.03 vs 0.26 ±0.03, P 〈 0.01 ) of the patients. In contrast, there was no significant difference in the level of cytoplasmic Nrf 2 between lesional and normal skin (0.61 ± 0.03 vs 0.60 ± 0.02, P 〉 0.05) of patients. Conclusion These results reveal an abnormality of nuclear translocation of Nrf 2 in vitiligo lesions.
出处 《中华皮肤科杂志》 CAS CSCD 北大核心 2008年第5期324-326,共3页 Chinese Journal of Dermatology
关键词 白癜风 患者 氧化性应激 NF—E2相关因子2 Vitiligo Oxidative stress NF-E2-related factor 2
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  • 1Yildirim M, Baysal V, Inaloz HS, et al. The role of oxidants and antioxidants in generalized vitiligo at tissue level. J Eur Acad Dermatol Venereol, 2004, 18 (6): 683-686.
  • 2Hazneci E, Karabulut AB, Ozturk C, et al. A comparative study of superoxide dismutase, catalase, and glutathione peroxidase activities and nitrate levels in vitiligo patients. Int J Dermatol, 2005, 44(8): 636-640.
  • 3Beazley WD, Gaze D, Panske A, et al. Serum selenium levels and blood glutathione peroxidase activities in vitiligo. Br J Dermatol, 1999, 141(2): 301-303.
  • 4Jiménez-Cervantes C, Marti nez-Esparza M, Pérez C, et al. Inhibition of melanogenesis in response to oxidative stress: transient downregulation of melanocyte differentiation markers and possible involvement of microphthalmia transcription factor. J Cell Sci, 2001, 114(Pt 12): 2335-2344.
  • 5Agrawal D, Shajil EM, Marfatia YS, et al. Study on the antioxidant status of vitiligo patients of different age groups in Baroda. Pigment Cell Res, 2004, 17(3): 289-294.
  • 6Boisseau-Garsaud AM, Garsaud P, Lejoly-Boisseau H, et al. Increase in total blood antioxidant status and selenium levels in black patients with active vitiligo. Int J Dermatol, 2002, 41 (10): 640-642.

同被引文献17

  • 1李煌元,石年.Keap1-Nrf2/ARE通路在分子毒理学中的研究进展[J].国外医学(卫生学分册),2006,33(3):129-135. 被引量:11
  • 2Ines D, Sonia B, Riadh BM, et al. A comparative study of oxidant-antioxidant status in stable and active vitiligo patients. Arch Dermatol Res, 2006, 298(4): 147-152.
  • 3Wu TY, Khor TO, Saw CL, et al. Anti-inflammatory/anti- oxidative stress activities and differential regulation of Nrf2- mediated genes by non-polar fractions of tea Chusanthemum zawadskii and licorice Glycyrrhiza uralensis. AAPS J, 2011, 13 (1): 1-13.
  • 4Natarajan VT, Singh A, Kumar AA, et al. Transcriptional upregulation of Nrf2-dependent phase II detoxifieation genes in the involved epidermis of vitiligo vulgaris. J Invest Derraatol, 2010, 130( 12): 2781-2789.
  • 5Tian FF, Zhang FF, Lai XD, et al. Nrf2-mediated protection against UVA radiation in human skin keratinocytes. Biosci Trends, 2011, 5( 1 ): 23-29.
  • 6hoh K, Tong KI, Yamamoto M. Molecular mechanism activating Nrf2-Keapl pathway in regulation of adaptive response to eleetrophiles. Free Radic Biol Med, 2004, 36( 10): 1208-1213.
  • 7Gao X, Talalay P. Induction of phase 2 genes by sulforaphane protects retinal pigment epithelial cells against photooxidative damage. Proc Natl Acad Sci U S A, 2004, 101 (28): 10446- 10451.
  • 8Nakaso K, Nakamura C, Sato H, et al. Novel cytoprotective mechanism of anti-parkinsonian drug deprenyl: PI3K and Nrf2- derived induction of antioxidative proteins. Biochem Biophys Res Commun, 2006, 339(3): 915-922.
  • 9Pawson T. Dynamic control of signaling by modular adaptor proteins. Curr Opin Cell Biol, 2007, 19(2): 112-116.
  • 10关翠萍,尉晓冬,陈惠英,章莉,周妙妮,许爱娥.白癜风患者皮损处核因子E2p45相关因子2核转位异常[J].中华医学杂志,2008,88(34):2403-2406. 被引量:6

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