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Resistin-like Molecule α Provides Vitamin-A-Dependent Antimicrobial Protection in the Skin.
Harris, Tamia A; Gattu, Sureka; Propheter, Daniel C; Kuang, Zheng; Bel, Shai; Ruhn, Kelly A; Chara, Andrew L; Edwards, Marshall; Zhang, Chenlu; Jo, Jay-Hyun; Raj, Prithvi; Zouboulis, Christos C; Kong, Heidi H; Segre, Julia A; Hooper, Lora V.
Afiliação
  • Harris TA; Department of Immunology, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA; Department of Dermatology, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA. Electronic address: tamia.harris-tryon@utsouthwestern.edu.
  • Gattu S; Department of Immunology, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.
  • Propheter DC; Department of Immunology, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.
  • Kuang Z; Department of Immunology, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.
  • Bel S; Department of Immunology, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.
  • Ruhn KA; Department of Immunology, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.
  • Chara AL; Department of Immunology, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.
  • Edwards M; Department of Dermatology, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.
  • Zhang C; Department of Dermatology, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.
  • Jo JH; Dermatology Branch, National Institute of Arthritis and Musculoskeletal and Skin Diseases, NIH, Bethesda, MD 20892, USA.
  • Raj P; Department of Immunology, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.
  • Zouboulis CC; Department of Dermatology, Venereology, Allergology and Immunology, Dessau Medical Center, Brandenburg Medical School Theodore Fontane, 06847 Dessau, Germany.
  • Kong HH; Dermatology Branch, National Institute of Arthritis and Musculoskeletal and Skin Diseases, NIH, Bethesda, MD 20892, USA.
  • Segre JA; Translational and Functional Genomics Branch, National Human Genome Research Institute, NIH, Bethesda, MD 20892, USA.
  • Hooper LV; Department of Immunology, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA; The Howard Hughes Medical Institute, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA. Electronic address: lora.hooper@utsouthwestern.edu.
Cell Host Microbe ; 25(6): 777-788.e8, 2019 Jun 12.
Article em En | MEDLINE | ID: mdl-31101494
ABSTRACT
Vitamin A deficiency increases susceptibility to skin infection. However, the mechanisms by which vitamin A regulates skin immunity remain unclear. Here, we show that resistin-like molecule α (RELMα), a small secreted cysteine-rich protein, is expressed by epidermal keratinocytes and sebocytes and serves as an antimicrobial protein that is required for vitamin-A-dependent resistance to skin infection. RELMα was induced by microbiota colonization of the murine skin, was bactericidal in vitro, and was protected against bacterial infection of the skin in vivo. RELMα expression required dietary vitamin A and was induced by the therapeutic vitamin A analog isotretinoin, which protected against skin infection in a RELMα-dependent manner. The RELM family member Resistin was expressed in human skin, was induced by vitamin A analogs, and killed skin bacteria, indicating a conserved function for RELM proteins in skin innate immunity. Our findings provide insight into how vitamin A promotes resistance to skin infection.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Pele / Vitamina A / Dermatopatias Bacterianas / Peptídeos Catiônicos Antimicrobianos / Peptídeos e Proteínas de Sinalização Intercelular / Fatores Imunológicos Tipo de estudo: Prognostic_studies Limite: Animals / Humans Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Pele / Vitamina A / Dermatopatias Bacterianas / Peptídeos Catiônicos Antimicrobianos / Peptídeos e Proteínas de Sinalização Intercelular / Fatores Imunológicos Tipo de estudo: Prognostic_studies Limite: Animals / Humans Idioma: En Ano de publicação: 2019 Tipo de documento: Article