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人黑素细胞在单培养、与角质形成细胞共培养以及在重建表皮中对紫外线照射的不同黑素生成反应。

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

作者信息

Duval C, Régnier M, Schmidt R

机构信息

Life Sciences Research, L'Oreal, Centre Charles Zviak, Clichy, France.

出版信息

Pigment Cell Res. 2001 Oct;14(5):348-55. doi: 10.1034/j.1600-0749.2001.140506.x.

Abstract

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/cm2), an increase in melanin synthesis whereas in melanocyte mono-cultures, UVB doses up to 50 mJ/cm2 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.

摘要

根据培养条件和角质形成细胞的存在情况,正常人黑素细胞对UVA和UVB照射的黑素生成反应存在显著差异。与角质形成细胞共培养的黑素细胞暴露于UVB照射下,即使在低剂量(5 mJ/cm2)时,也会引发黑色素合成增加,而在黑素细胞单培养中,高达50 mJ/cm2的UVB剂量没有黑素生成作用。与UVB不同,UVA暴露在单培养和共培养中引起相同的黑素生成反应。从共培养基中去除某些角质形成细胞生长因子可消除对UVB的黑素生成反应,但对UVA暴露无影响。当整合到重建的人表皮基底层时,人黑素细胞对UVA和UVB照射的反应与体内相似,通过增加黑色素的产生并将其转移到相邻的角质形成细胞,导致重建表皮出现明显的晒黑。已知致密角质层会散射和吸收紫外线,这导致与角质形成细胞 - 黑素细胞共培养相比,重建表皮引发黑素生成反应所需的最小UVB和UVA剂量更高。此外,UVA照射后在色素沉着的表皮中观察到即时晒黑反应。从这些结果我们得出结论:(i)角质形成细胞在介导UVB诱导的色素沉着中起重要作用,(ii)UVA诱导的色素沉着是对黑素细胞相当直接作用的结果,(iii)重建的色素沉着表皮是体外研究紫外线诱导色素沉着的最合适模型。

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