A histological study of human wrinkle structures: comparison between sun‐exposed areas of the face, with or without wrinkles, and sun‐protected areas

Wrinkles are a major topic in dermocosmetology; the purpose of this work has been to go deeper into the knowledge of cutaneous damage underlying these modifications of skin surface. Up to now, the number of published works about the histological structure of wrinkles is not very large. Therefore to complete the findings, we studied 46 subjects of both sexes, between 57 and 98‐year‐old, enabling us to obtain 157 skin biopsies of wrinkles (face) and sun‐protected areas (abdomen). We used different histological techniques involving histochemistry, immunohistochemistry, electron microscopy and quantification by image analysis in addition to classic standard techniques. This study has allowed us to confirm published structural modifications of wrinkles, but also to display many other original alterations. The increased thinning of the epidermis atrophied with age is confirmed by the study of desmoplakins outlining the cellular contours of keratinocytes. Such a thinning is accompanied by a decrease in several markers of epidermal differentiation at the bottom of the wrinkles: filaggrin, keratohyalin granules and transglutaminase I, disturbing desquamation and the capacity of the horny layer to retain water. The dermoepidermal junction is modified by a decrease of collagen IV and VII, which, combined with fewer and fewer oxytalan fibres under wrinkles, weakens this interface. The deposition of abnormal elastotic tissue in the dermis, with an interruption of these deposits under wrinkles and an atrophy of dermal collagen more pronounced under wrinkles, boosts the magnitude and depth of wrinkles. The composition of the other dermal constituents is also altered with, more particularly, a marked decrease of chondroitin sulphates in the papillary dermis under wrinkles, combined with an asymmetrical variation of glycosaminoglycans on both edges of wrinkles. The atrophy of the hypodermis, also more marked under wrinkles, with a thickening of fibrous lines, also makes the depth of wrinkles more pronounced. Wrinkle formation appears at the same time as numerous modifications in different cutaneous structures, which may be mutually amplified. Such a study by pointing out altered elements in skin physiology, makes the development of specific treatments possible in order to mitigate this unwelcome cutaneous deterioration.

[1]  G. Piérard,et al.  The microanatomical basis of facial frown lines. , 1989, Archives of dermatology.

[2]  G. M. Ridder,et al.  Age, sunlight, and facial skin: a histologic and quantitative study. , 1991, Journal of the American Academy of Dermatology.

[3]  R. Dobson,et al.  British Association of Dermatologists , 2014 .

[4]  N. Morris,et al.  Type VII collagen is a major structural component of anchoring fibrils , 1986, The Journal of cell biology.

[5]  W. Shellow,et al.  The Histopathology of Wrinkles , 1973 .

[6]  R. Lavker,et al.  The anatomy and pathogenesis of wrinkles , 1985, The British journal of dermatology.

[7]  T. Tsuji,et al.  Light and scanning electron microscopic studies on wrinkles in aged persons' skin , 1986, The British journal of dermatology.

[8]  I. Braverman,et al.  Studies in cutaneous aging: I. The elastic fiber network. , 1982, The Journal of investigative dermatology.

[9]  H. L. Li,et al.  Ultraviolet A irradiation upregulates type VII collagen expression in human dermal fibroblasts. , 1997, The Journal of investigative dermatology.

[10]  J. Leyden What is photoaged skin? , 2001, European journal of dermatology : EJD.

[11]  D. Schmitt,et al.  HB8: a monoclonal antibody recognizing elastic fibre microfibrils , 1986, The British journal of dermatology.

[12]  T. Tezuka,et al.  Terminal differentiation of facial epidermis of the aged: immunohistochemical studies. , 1994, Dermatology.

[13]  C. Griffiths,et al.  Clinical features of photodamaged human skin are associated with a reduction in collagen VII , 1997, The British journal of dermatology.

[14]  E. Davidson,et al.  Alterations in human dermal connective tissue with age and chronic sun damage. , 1962, The Journal of investigative dermatology.

[15]  R. Timpl Macromolecular organization of basement membranes. , 1996, Current opinion in cell biology.

[16]  R. Bashey,et al.  Human dermal glycosaminoglycans and aging. , 1972, Biochimica et biophysica acta.

[17]  A M Kligman,et al.  Early destructive effect of sunlight on human skin. , 1969, JAMA.

[18]  G. Cotta-Pereira,et al.  Oxytalan, elaunin, and elastic fibers in the human skin. , 1976, The Journal of investigative dermatology.

[19]  E. Aubiniere Rides et élastose , 1985 .

[20]  M. Siciliano,et al.  Type I keratinocyte transglutaminase: expression in human skin and psoriasis. , 1992, The Journal of investigative dermatology.

[21]  K. Yoneda,et al.  Expression of transglutaminase 1 in human epidermis. , 1995, The Journal of investigative dermatology.

[22]  A. Caplan,et al.  Patterns of glycosaminoglycan/proteoglycan immunostaining in human skin during aging. , 1990, The Journal of investigative dermatology.