Matrix-degrading metalloproteinases in photoaging.

UV radiation from the sun impacts skin health adversely through complex, multiple molecular pathways. Premature skin aging (photoaging) is among the most widely appreciated harmful effects of chronic exposure to solar UV radiation. Extensive damage to the dermal connective tissue is a hallmark of photoaged skin. Disruption of the normal architecture of skin connective tissue impairs skin function and causes it to look aged. UV irradiation induces expression of certain members of the matrix metalloproteinase (MMP) family, which degrade collagen and other extracellular matrix proteins that comprise the dermal connective tissue. Although the critical role of MMPs in photoaging is undeniable, important questions remain. This article summarizes our current understanding of the role of MMPs in the photoaging process and presents new data that (1) describe the expression and regulation by UV irradiation of all members of the MMP family in human skin in vivo and (2) quantify the relative contributions of epidermis and dermis to the expression of UV irradiation-induced MMPs in human skin in vivo.Journal of Investigative Dermatology Symposium Proceedings (2009) 14, 20-24; doi:10.1038/jidsymp.2009.8.

[1]  K. Scharffetter-Kochanek,et al.  Ultraviolet-B irradiation and matrix metalloproteinases: from induction via signaling to initial events. , 2002, Annals of the New York Academy of Sciences.

[2]  M. Mayes,et al.  Effect of increased pigmentation on the antifibrotic response of human skin to UV-A1 phototherapy. , 2008, Archives of dermatology.

[3]  Z. Werb,et al.  New functions for the matrix metalloproteinases in cancer progression , 2002, Nature Reviews Cancer.

[4]  B. Wasylyk,et al.  The collagenase gene promoter contains a TPA and oncogene‐responsive unit encompassing the PEA3 and AP‐1 binding sites. , 1990, The EMBO journal.

[5]  H. Birkedal‐Hansen,et al.  An internal cysteine plays a role in the maintenance of the latency of human fibroblast collagenase. , 1991, Biochemistry.

[6]  J. Voorhees,et al.  Vascular tube formation on matrix metalloproteinase-1-damaged collagen , 2008, British Journal of Cancer.

[7]  Z. Werb,et al.  How matrix metalloproteinases regulate cell behavior. , 2001, Annual review of cell and developmental biology.

[8]  J. Krutmann,et al.  Photoaging of human skin , 2000, Photodermatology, photoimmunology & photomedicine.

[9]  J. Voorhees,et al.  c-Jun-dependent inhibition of cutaneous procollagen transcription following ultraviolet irradiation is reversed by all-trans retinoic acid. , 2000, The Journal of clinical investigation.

[10]  B. Fingleton,et al.  Matrix metalloproteinases: biologic activity and clinical implications. , 2000, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[11]  J. Voorhees,et al.  Ultraviolet irradiation increases matrix metalloproteinase-8 protein in human skin in vivo. , 2001, The Journal of investigative dermatology.

[12]  James Varani,et al.  Collagen degradation in aged/photodamaged skin in vivo and after exposure to matrix metalloproteinase-1 in vitro. , 2003, The Journal of investigative dermatology.

[13]  M. Kripke Immunological Unresponsiveness Induced by Ultraviolet Radiation , 1984, Immunological reviews.

[14]  J. Voorhees,et al.  Retinoic acid inhibits induction of c-Jun protein by ultraviolet radiation that occurs subsequent to activation of mitogen-activated protein kinase pathways in human skin in vivo. , 1998, The Journal of clinical investigation.

[15]  C. Overall Matrix metalloproteinase substrate binding domains, modules and exosites. Overview and experimental strategies. , 2001, Methods in molecular biology.

[16]  James T. Elder,et al.  Cellular, immunologic and biochemical characterization of topical retinoic acid-treated human skin. , 1991, The Journal of investigative dermatology.

[17]  M. Yaar,et al.  Ageing and photoageing of the skin: observations at the cellular and molecular level , 1992, The British journal of dermatology.

[18]  J. Voorhees,et al.  Ultraviolet irradiation alters transforming growth factor beta/smad pathway in human skin in vivo. , 2002, The Journal of investigative dermatology.

[19]  W. Parks,et al.  Activation and silencing of matrix metalloproteinases. , 2008, Seminars in cell & developmental biology.

[20]  James Varani,et al.  Mechanisms of photoaging and chronological skin aging. , 2002, Archives of dermatology.

[21]  J. Voorhees,et al.  Ultraviolet Irradiation Induces Smad7 via Induction of Transcription Factor AP-1 in Human Skin Fibroblasts* , 2005, Journal of Biological Chemistry.

[22]  A. Mauviel Cytokine regulation of metalloproteinase gene expression , 1993, Journal of cellular biochemistry.

[23]  C. López-Otín,et al.  The Role of the C-terminal Domain of Human Collagenase-3 (MMP-13) in the Activation of Procollagenase-3, Substrate Specificity, and Tissue Inhibitor of Metalloproteinase Interaction* , 1997, The Journal of Biological Chemistry.

[24]  E. Kerkelä,et al.  Matrix metalloproteinases in tumor progression: focus on basal and squamous cell skin cancer , 2003, Experimental dermatology.

[25]  M E Nimni,et al.  Collagen: structure, function, and metabolism in normal and fibrotic tissues. , 1983, Seminars in arthritis and rheumatism.

[26]  F. Bernerd,et al.  Matrix Metalloproteinase‐1 Production Observed After Solar‐Simulated Radiation Exposure is Assumed by Dermal Fibroblasts but Involves a Paracrine Activation Through Epidermal Keratinocytes ¶ , 2004, Photochemistry and photobiology.

[27]  C. Overall Matrix MetaIIoproteinase Substrate Binding Domains, Modules and Exosites , 2001 .

[28]  K. Scharffetter-Kochanek,et al.  Photoaging of the skin from phenotype to mechanisms , 2000, Experimental Gerontology.

[29]  J. Voorhees,et al.  Molecular basis of sun-induced premature skin ageing and retinoid antagonism , 1996, Nature.

[30]  A. Kligman,et al.  The nature of photoaging: its prevention and repair. , 1986, Photo-dermatology.

[31]  J. Voorhees,et al.  Solar ultraviolet irradiation reduces collagen in photoaged human skin by blocking transforming growth factor-beta type II receptor/Smad signaling. , 2004, The American journal of pathology.

[32]  H. Birkedal‐Hansen,et al.  Matrix metalloproteinases: a review. , 1993, Critical reviews in oral biology and medicine : an official publication of the American Association of Oral Biologists.

[33]  J. Voorhees,et al.  Pathophysiology of premature skin aging induced by ultraviolet light. , 1997, The New England journal of medicine.

[34]  J. Uitto,et al.  Molecular mechanisms of cutaneous aging: connective tissue alterations in the dermis. , 1998, The journal of investigative dermatology. Symposium proceedings.

[35]  F. Bernerd,et al.  Direct role of human dermal fibroblasts and indirect participation of epidermal keratinocytes in MMP-1 production after UV-B irradiation , 2001, Archives of Dermatological Research.

[36]  J. Voorhees,et al.  Inhibition of type I procollagen synthesis by damaged collagen in photoaged skin and by collagenase-degraded collagen in vitro. , 2001, The American journal of pathology.

[37]  J. Voorhees,et al.  Molecular mechanisms of photoaging and its prevention by retinoic acid: ultraviolet irradiation induces MAP kinase signal transduction cascades that induce Ap-1-regulated matrix metalloproteinases that degrade human skin in vivo. , 1998, The journal of investigative dermatology. Symposium proceedings.

[38]  J. Voorhees,et al.  Ultraviolet Irradiation Blocks Cellular Responses to Transforming Growth Factor-β by Down-regulating Its Type-II Receptor and Inducing Smad7* , 2001, The Journal of Biological Chemistry.

[39]  J. Chung,et al.  Ultraviolet modulation of human macrophage metalloelastase in human skin in vivo. , 2002, The Journal of investigative dermatology.

[40]  K. Scharffetter-Kochanek,et al.  Ultraviolet‐B Irradiation and Matrix Metalloproteinases , 2002 .