Dermal connective tissue metabolism in photoageing

The term photoageing describes the clinical and histological cutaneous changes that are the consequence of repeated chronic sun exposures and are qualitatively different from those observed in chronological ageing. The connective tissue of the skin is composed mainly of collagen, glycosaminoglycans and elastin and, thus, alterations of these components in photoageing are briefly reviewed in the present article. Collagen changes in photoageing are partly explained by crosslinks as well as the unbalanced regulation of collagen production and breakdown. Some visible skin changes can be induced by the consequence of dermal glycosaminoglycans, because the total amount, as well as the composition of the main disaccharide units, is significantly altered in the exposed sites of both aged people and photoaged mice. As for the mechanism of solar elastosis, increased elastin mRNA levels resulting from transcriptional up‐regulation of the gene have been reported. Taken together, all components of the dermal connective tissue are affected by chronic actinic damage; however, further in vitro investigation is required to unmask the exact events in photoageing. With regard to this, our novel three‐dimensional culture system should be of great help because it mimics the in vivo condition by sell producing the extracellular matrices.

[1]  Y. Kuboki,et al.  Measurement of histidinohydroxylysinonorleucine and hydroxyproline in skin collagen by reversed-phase high-performance liquid chromatography after 9-fluorenylmethyl chloroformate labeling. , 1997, Analytical biochemistry.

[2]  Y. Miyachi,et al.  Morphological and biochemical analyses on fibroblasts and self‐produced collagens in a novel three‐dimensional culture , 1997, The British journal of dermatology.

[3]  J. Uitto,et al.  8‐Methoxypsoralen and Ultraviolet A Radiation Activate the Human Elastin Promoter in Transgenic Mice: In vivo and in vitro Evidence for Gene Induction , 1996, Photochemistry and photobiology.

[4]  Y. Igarashi,et al.  Disaccharide analysis of human skin glycosaminoglycans in sun-exposed and sun-protected skin of aged people. , 1996, Journal of dermatological science.

[5]  Y. Miyachi,et al.  Disaccharide analysis of the skin glycosaminoglycans in chronically ultraviolet light-irradiated hairless mice. , 1995, Journal of dermatological science.

[6]  F. Urbach,et al.  Ultraviolet radiation activates the human elastin promoter in transgenic mice: a novel in vivo and in vitro model of cutaneous photoaging. , 1995, The Journal of investigative dermatology.

[7]  J. Uitto,et al.  Differential expression of the versican and decorin genes in photoaged and sun-protected skin. Comparison by immunohistochemical and northern analyses. , 1995, Laboratory investigation; a journal of technical methods and pathology.

[8]  Y. Kato,et al.  FORMATION OF PROTEIN‐BOUND 3,4‐DIHYDROXYPHENYLALANINE IN COLLAGEN TYPES I AND IV EXPOSED TO ULTRAVIOLET LIGHT , 1995, Photochemistry and photobiology.

[9]  Y. Miyachi Photoaging from an oxidative standpoint. , 1995, Journal of dermatological science.

[10]  K. Scharffetter-Kochanek,et al.  Singlet oxygen may mediate the ultraviolet A-induced synthesis of interstitial collagenase. , 1995, The Journal of investigative dermatology.

[11]  Y. Miyachi,et al.  Disaccharide analysis of dermal fibroblast-derived glycosaminoglycans in the three-dimensional culture. , 1994, Journal of dermatological science.

[12]  J. Uitto,et al.  Enhanced elastin and fibrillin gene expression in chronically photodamaged skin. , 1994, The Journal of investigative dermatology.

[13]  Y. Miyachi,et al.  Changes in skin disaccharide components correlate with the severity of sclerotic skin in systemic sclerosis. , 1994, Acta dermato-venereologica.

[14]  T. Krieg,et al.  UVA‐INDUCED AUTOCRINE STIMULATION OF FIBROBLAST‐DERIVED COLLAGENASE/MMP‐1 BY INTERRELATED LOOPS OFINTERLEUKIN–1 andINTERLEUKIN–6 , 1994, Photochemistry and photobiology.

[15]  K. Scharffetter-Kochanek,et al.  UVA irradiation stimulates the synthesis of various matrix‐metalloproteinases (MMPs) in cultured human fibroblasts , 1993, Experimental dermatology.

[16]  S. Craig,et al.  Ultraviolet A irradiation stimulates collagenase production in cultured human fibroblasts. , 1992, The Journal of investigative dermatology.

[17]  M. Pathak,et al.  Skin photosensitizing agents and the role of reactive oxygen species in photoaging. , 1992, Journal of photochemistry and photobiology. B, Biology.

[18]  M. Yamauchi,et al.  Collagen cross-linking in sun-exposed and unexposed sites of aged human skin. , 1991, The Journal of investigative dermatology.

[19]  D. Bissett,et al.  CHRONIC ULTRAVIOLET B RADIATION‐INDUCED BIOCHEMICAL CHANGES IN THE SKIN OF HAIRLESS MICE * , 1990, Photochemistry and photobiology.

[20]  D. Bissett,et al.  WAVELENGTH DEPENDENCE OF HISTOLOGICAL, PHYSICAL, AND VISIBLE CHANGES IN CHRONICALLY UV‐IRRADIATED HAIRLESS MOUSE SKIN * , 1989, Photochemistry and photobiology.

[21]  I. Braverman,et al.  Scanning electron microscope study of elastic fibers of the loose connective tissue (superficial fascia) in the rat , 1988, The Anatomical record.

[22]  M. Yamauchi,et al.  Aging and cross-linking of skin collagen. , 1988, Biochemical and biophysical research communications.

[23]  M. Yamauchi,et al.  Structure and formation of a stable histidine-based trifunctional cross-link in skin collagen. , 1987, The Journal of biological chemistry.

[24]  I. Braverman Elastic fiber and microvascular abnormalities in aging skin. , 1986, Clinics in geriatric medicine.

[25]  N. Araki,et al.  Advanced glycation end products of the Maillard reaction and their relation to aging. , 1994, Gerontology.

[26]  早石 修,et al.  The Biological role of reactive oxygen species in skin , 1987 .