Activation of OR10A3 by Suberic Acid Promotes Collagen Synthesis in UVB-Irradiated Dermal Fibroblasts via the cAMP-Akt Pathway

Cells. 2022 Dec 7;11(24):3961. doi: 10.3390/cells11243961.

Abstract

In recent years, there has been a great deal of interest in the ectopic roles of olfactory receptors (ORs) throughout the human body. Especially, the ectopic function of OR in the skin is one of the most actively researched areas. Suberic acid, a scent compound, was hypothesized to increase collagen synthesis in the ultraviolet B (UVB)-irradiated human dermal fibroblasts (Hs68) through a specific olfactory receptor. Suberic acid ameliorated UVB-induced decreases in collagen production in Hs68 cells. Using in silico docking to predict the binding conformation and affinity of suberic acid to 15 ectopic ORs detectable in Hs68, several ORs were identified as promising candidates. The effect of suberic acid on collagen synthesis in UVB-exposed dermal fibroblasts was nullified only by a reduction in OR10A3 expression via specific siRNA. In addition, using the cells transiently expressing OR10A3, we demonstrated that suberic acid can activate OR10A3 by assessing the downstream effector cAMP response element (CRE) luciferase activity. We examined that the activation of OR10A3 by suberic acid subsequently stimulates collagen synthesis via the downstream cAMP-Akt pathway. The findings support OR10A3 as a promising target for anti-aging treatments of the skin.

Keywords: OR10A3; collagen; dermal fibroblast; olfactory receptor; suberic acid.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Collagen / metabolism
  • Fibroblasts / metabolism
  • Humans
  • Proto-Oncogene Proteins c-akt / metabolism
  • Receptors, Odorant* / genetics
  • Receptors, Odorant* / metabolism
  • Skin Aging* / drug effects
  • Skin Aging* / genetics
  • Skin Aging* / physiology

Substances

  • Collagen
  • Proto-Oncogene Proteins c-akt
  • suberic acid
  • Receptors, Odorant

Grants and funding

This research was funded by the National Research Foundation of Korea (NRF) grant funded by the Korean government (MSIT) (No. 2022R1A2C100667511).