Distinct melanogenic response of human melanocytes in mono-culture, in co-culture with keratinocytes and in reconstructed epidermis, to UV exposure

被引:82
作者
Duval, C [1 ]
Régnier, M [1 ]
Schmidt, R [1 ]
机构
[1] LOreal, Ctr Charles Zviak, Life Sci Res, F-92583 Clichy, France
来源
PIGMENT CELL RESEARCH | 2001年 / 14卷 / 05期
关键词
epidermal-melanin unit; keratinocyte-melanocyte interaction; UVB; UVA; tanning;
D O I
10.1034/j.1600-0749.2001.140506.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 [细胞生物学]; 090102 [作物遗传育种];
摘要
Striking differences are observed in the melanogenic response of normal human melanocytes to UVA and UVB irradiation depending on culture conditions and the presence of keratinocytes. Exposure of melanocytes co-cultured with keratinocytes to UVB irradiation triggered, already at low doses (5 mJ/cm(2)), an increase in melanin synthesis whereas in melanocyte mono-cultures, UVB doses up to 50 mJ/cm(2) had no melanogenic effect. Unlike UVB, UVA exposure caused the same melanogenic response in both mono- and co-cultures. Removing certain keratinocyte growth factors from the co-culture medium abolished the melanogenic response to UVB, but not to UVA,exposure. When integrated into the basal layer of a reconstructed human epidermis, human melanocytes similarly reacted to UVA and UVB irradiation as in vivo by increasing their production and transfer of melanin to the neighboring keratinocytes which resulted in a noticeable tanning of the reconstructed epidermis. The presence of a dense stratum corneum, known to scatter and absorb UV light, is responsible for higher minimal UVB and UVA doses required to trigger a melanogenic response in the reconstructed epidermis compared to keratinocyte-melanocyte co-cultures. Furthermore, an immediate tanning response was observed in the pigmented epidermis following UVA irradiation. From these results we conclude that: (i) keratinocytes play an important role in mediating UVB-induced pigmentation, (ii) UVA-Induced pigmentation is the result of a rather direct effect on melanocytes and (iii) reconstructed pigmented epidermis is the most appropriate model to study UV-induced pigmentation in vitro.
引用
收藏
页码:348 / 355
页数:8
相关论文
共 55 条
[1]
ANALYSIS OF THE UV-INDUCED MELANOGENESIS AND GROWTH ARREST OF HUMAN MELANOCYTES [J].
ABDELMALEK, Z ;
SWOPE, V ;
SMALARA, D ;
BABCOCK, G ;
DAWES, S .
PIGMENT CELL RESEARCH, 1994, 7 (05) :326-332
[2]
ABERDAM E, 1993, J CELL SCI, V106, P1015
[3]
THE OPTICS OF HUMAN-SKIN [J].
ANDERSON, RR ;
PARRISH, JA .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1981, 77 (01) :13-19
[4]
KERATINOCYTES AND FIBROBLASTS IN A HUMAN SKIN EQUIVALENT MODEL ENHANCE MELANOCYTE SURVIVAL AND MELANIN SYNTHESIS AFTER ULTRAVIOLET-IRRADIATION [J].
ARCHAMBAULT, M ;
YAAR, M ;
GILCHREST, BA .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1995, 104 (05) :859-867
[5]
EFFECT OF CUTANEOUS HYPOXIA UPON ERYTHEMA AND PIGMENT RESPONSES TO UVA, UVB, AND PUVA (8-MOP+UVA) IN HUMAN-SKIN [J].
AULETTA, M ;
GANGE, RW ;
TAN, OT ;
MATZINGER, E .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1986, 86 (06) :649-652
[6]
Ex vivo reconstruction of the epidermis with melanocytes and the influence of UVB [J].
Bessou, S ;
SurleveBazeille, JE ;
Sorbier, E ;
Taieb, A .
PIGMENT CELL RESEARCH, 1995, 8 (05) :241-249
[7]
TRANSMISSION OF HUMAN-EPIDERMIS AND STRATUM-CORNEUM AS A FUNCTION OF THICKNESS IN THE ULTRAVIOLET AND VISIBLE WAVELENGTHS [J].
BRULS, WAG ;
SLAPER, H ;
VANDERLEUN, JC ;
BERRENS, L .
PHOTOCHEMISTRY AND PHOTOBIOLOGY, 1984, 40 (04) :485-494
[8]
CASBERG CJ, 1994, J CELL SCI, V107, P2591
[9]
Pigmentary changes in aged and photoaged skin [J].
Castanet, J ;
Ortonne, JP .
ARCHIVES OF DERMATOLOGY, 1997, 133 (10) :1296-1299
[10]
Production and release of proopiomelanocortin (POMC) derived peptides by human melanocytes and keratinocytes in culture: Regulation by ultraviolet B [J].
Chakraborty, AK ;
Funasaka, Y ;
Slominski, A ;
Ermak, G ;
Hwang, J ;
Pawelek, JM ;
Ichihashi, M .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH, 1996, 1313 (02) :130-138