Retinoids Enhance the Expression of Cathelicidin Antimicrobial Peptide during Reactive Dermal Adipogenesis

J Immunol. 2019 Sep 15;203(6):1589-1597. doi: 10.4049/jimmunol.1900520. Epub 2019 Aug 16.

Abstract

A subset of dermal fibroblasts undergo rapid differentiation into adipocytes in response to infection and acutely produce the cathelicidin antimicrobial peptide gene Camp Vitamin A and other retinoids inhibit adipogenesis yet can show benefit to skin disorders, such as cystic acne, that are exacerbated by bacteria. We observed that retinoids potently increase and sustain the expression of Camp in preadipocytes undergoing adipogenesis despite inhibition of markers of adipogenesis, such as Adipoq, Fabp4, and Rstn Retinoids increase cathelicidin in both mouse and human preadipocytes, but this enhancement of antimicrobial peptide expression did not occur in keratinocytes or a sebocyte cell line. Preadipocytes undergoing adipogenesis more effectively inhibited growth of Staphylococcus aureus when exposed to retinoic acid. Whole transcriptome analysis identified hypoxia-inducible factor 1-α (HIF-1α) as a mechanism through which retinoids mediate this response. These observations uncouple the lipid accumulation element of adipogenesis from the innate immune response and uncover a mechanism, to our knowledge previously unsuspected, that may explain therapeutic benefits of retinoids in some skin disorders.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • 3T3-L1 Cells
  • Adipocytes / drug effects*
  • Adipocytes / metabolism
  • Adipogenesis / drug effects*
  • Animals
  • Antimicrobial Cationic Peptides / metabolism*
  • Cathelicidins
  • Cell Differentiation / drug effects
  • Cell Line
  • Dermis / drug effects*
  • Dermis / metabolism
  • Fibroblasts / drug effects
  • Fibroblasts / metabolism
  • Keratinocytes / drug effects
  • Keratinocytes / metabolism
  • Mice
  • Retinoids / pharmacology*
  • Skin / drug effects
  • Skin / metabolism
  • Staphylococcal Infections / drug therapy
  • Staphylococcal Infections / metabolism
  • Staphylococcus aureus / drug effects
  • Tretinoin / pharmacology

Substances

  • Antimicrobial Cationic Peptides
  • Retinoids
  • Tretinoin
  • Cathelicidins