TRAIL contributes to the apoptotic effect of 13-cis retinoic acid in human sebaceous gland cells

Br J Dermatol. 2011 Sep;165(3):526-33. doi: 10.1111/j.1365-2133.2011.10392.x. Epub 2011 Aug 17.

Abstract

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 Tumor necrosis factor Related Apoptosis Inducing Ligand (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.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acne Vulgaris / drug therapy
  • Acne Vulgaris / metabolism
  • Acne Vulgaris / pathology
  • Acute-Phase Proteins / metabolism
  • Apoptosis / drug effects*
  • Cells, Cultured
  • Dermatologic Agents / pharmacology*
  • Humans
  • In Situ Nick-End Labeling
  • Isotretinoin / pharmacology*
  • Lipocalin-2
  • Lipocalins / metabolism
  • Proto-Oncogene Proteins / metabolism
  • RNA, Small Interfering / pharmacology
  • Recombinant Proteins / pharmacology
  • Sebaceous Glands / cytology*
  • Sebaceous Glands / metabolism
  • TNF-Related Apoptosis-Inducing Ligand / metabolism
  • TNF-Related Apoptosis-Inducing Ligand / pharmacology*
  • Transfection

Substances

  • Acute-Phase Proteins
  • Dermatologic Agents
  • LCN2 protein, human
  • Lipocalin-2
  • Lipocalins
  • Proto-Oncogene Proteins
  • RNA, Small Interfering
  • Recombinant Proteins
  • TNF-Related Apoptosis-Inducing Ligand
  • Isotretinoin