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TRAIL contributes to the apoptotic effect of 13‐ cis retinoic acid in human sebaceous gland cells
Author(s) -
Nelson A.M.,
Cong Z.,
Gilliland K.L.,
Thiboutot D.M.
Publication year - 2011
Publication title -
british journal of dermatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.304
H-Index - 179
eISSN - 1365-2133
pISSN - 0007-0963
DOI - 10.1111/j.1365-2133.2011.10392.x
Subject(s) - retinoic acid , apoptosis , sebaceous gland , tretinoin , cancer research , endocrinology , chemistry , medicine , biology , biochemistry , gene
Summary Background The full mechanism of action of isotretinoin [13‐ cis retinoic acid (13‐ cis RA)] in treating acne is unknown. 13‐ cis RA induces key genes in sebocytes that are involved in apoptosis, including T umor necrosis factor R elated A poptosis I nducing L igand (TRAIL). Objectives In this study, we investigated the role of 13‐ cis RA‐induced TRAIL within SEB‐1 sebocytes. Methods Using 13‐ cis RA and recombinant human TRAIL (rhTRAIL) protein, we assessed induction of TRAIL and apoptosis in SEB‐1 sebocytes, normal keratinocytes and patient skin biopsies. Results Treatment with rhTRAIL protein increased TUNEL‐positive staining in SEB‐1 sebocytes. TRAIL siRNA significantly decreased the percentage of TUNEL‐positive SEB‐1 sebocytes in response to 13‐ cis RA treatment. Furthermore, TRAIL expression increased in the skin of patients with acne after 1 week of isotretinoin therapy compared with baseline. TRAIL expression localized within sebaceous glands. Unlike sebocytes, TRAIL protein expression was not increased in normal human epidermal keratinocytes in response to 13‐ cis RA, nor did rhTRAIL induce apoptosis in keratinocytes, suggesting that TRAIL is key in the sebocyte‐specific apoptotic effects of 13‐ cis RA. Conclusions Taken together, our data suggest that TRAIL, like the neutrophil gelatinase‐associated lipocalin, is involved in mediating 13‐ cis RA apoptosis of sebocytes.