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基质金属蛋白酶与基质金属蛋白酶抑制剂在光老化中作用的研究进展 被引量:6

Roles of matrix metalloproteinase and tissue inhibitors of metalloproteinases in photoaging
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摘要 紫外线照射会给人体的皮肤造成有害影响,其中,光老化是目前公认的长期暴露于紫外线照射所造成的主要危害之一。紫外线照射导致了基质金属蛋白酶家族的表达增加,其可降解真皮中的胶原及其他细胞外基质蛋白。大量的皮肤正常结缔组织结构的破坏损害了皮肤的功能并引起皮肤的老化。基质金属蛋白酶抑制剂是基质金属蛋白酶家族特异性的内源性抑制剂,并参与调控其在机体组织中的活性变化。二者之间的平衡在皮肤光老化的发生与发展中占有举足轻重的地位。 Ultraviolet (UV) irradiation has harmful effects on human skin. Photoaging is currently considered as a primary harmful effect of chronic solar UV exposure. UV irradiation can induce increased expression of certain members of the matrix metalloproteinase (MMP) family, which in turn degrade dermal collagen and other extracellular matrix (ECM) proteins, then lead to the disruption of normal architecture of skin connective tissue followed by the impairment of skin function and aging of skin. Tissue inhibitors of metalloproteinases (TIMPs) are considered as the specific endogenous inhibitor of matrix metalloproteinases (MMPs), and participate in the regulation of MMP activity. The balance between MMPs and TIMPs plays an important role in the occurrence and development of skin aging.
出处 《国际皮肤性病学杂志》 2012年第3期163-166,共4页 International Journal of Dermatology and Venereology
关键词 光老化 基质金属蛋白酶 基质金属蛋白酶抑制剂 Photoaging Matrix metalloproteinase Tissue inhibitors of metalloproteinases
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  • 1宋秀祖,夏济平,毕志刚.Effects of (-)-epigallocatechin-3-gallate on expression of matrix metalloproteinase-1 and tissue inhibitor of metalloproteinase-1 in fibroblasts irradiated with ultraviolet A[J].Chinese Medical Journal,2004,17(12):1838-1841. 被引量:8
  • 2李世泰,俞宝田,谢勇,冯景春,李红春,王宝明,方凯,王玉琪,闫岩.PUVA/UVB治疗银屑病60例疗效观察[J].中华皮肤科杂志,1996,29(2):128-129. 被引量:9
  • 3Fisher G J, Datta SC, Talwar HS, et al. Molecular basis of suninduced premature skin ageing and retinoid antagonism. Nature,1996, 379(6563): 335-339.
  • 4Bayramgtirler D, Ozkara SK, Apaydin R, et al. Heat shock proteins 60 and 70 expression of cutaneous lichen planus: comparison with normal skin and psoriasis vulgaris. J Cutan Pathol, 2004, 31(9): 586-594.
  • 5Garcia RL, Coltrera MD, Gown AM. Analysis of proliferative grade using anti-PCNA/cyclin monoclonal antibodies in fixed, embedded tissues. Comparison with flow cytometric analysis. Am J Pathol, 1989, 134(4): 733-739.
  • 6Shingleton WD, Hodges D J, Brick P, et al. Collagenase: a key enzyme in collagen turnover. Biochem Cell Biol, 1996, 74(6): 759-775.
  • 7Chung JH, Seo JY, Choi HR, et al. Modulation of skin collagen metabolism in aged and photoaged human skin in vivo. J Invest Dermatol, 2001, 117(5):1218-1224.
  • 8Hase T, Shinta K, Murase T, et al. Histological increase in inflammatory infiltrate in sun-exposed skin of female subjects: the possible involvement of matrix metalloproteinase-1 produced by inflammatory infiltrate on collagen degradation. Br J Dermatol, 2000, 142(2): 267-273.
  • 9Nova D, Le Griel C, Holvoet S, et al. Comparative studies on the secretion and activation of MMPs in two reconstructed human skin models using HaCaT- and HaCaT-ras-transfected cell lines. Clin Exp Metastasis, 2003, 20(8 ): 675-683.
  • 10Wertz K, Seifert N, Hunziker PB, et al. Beta-carotene inhibits UVA-induced matrix metalloprotease 1 and 10 expression in keratinocytes by a singlet oxygen-dependent mechanism. Free Radic Biol Med, 2004, 37(5): 654-670.

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