[Expressiona of c-Jun and collagens I and III in cultured human skin fibroblasts are affected by infrared ray radiation]

Nan Fang Yi Ke Da Xue Xue Bao. 2016 Feb;36(2):163-9.
[Article in Chinese]

Abstract

Objective: To observe the effect of solar infrared ray (IR) radiation on the expressions of c-Jun and collagens I and III in cultured human skin fibroblasts (HSFs) and explore the molecular mechanism by which IR radiation causes aging of the skin.

Methods: Primarily cultured HSFs exposed to IR radiation were examined for changes of the cell viability with MTT assay. The mRNA and protein expressions of c-Jun and collagens I and III was detected with real-time quantitative PCR and immunocytochemistry.

Results: MTT assay showed that IR irradiation caused inhibition of cell proliferation compared with the control cells. The mRNA and protein expression of collagen I was decreased significantly by IR irradiation with the increase of the irradiation dose (P<0.01). HSFs irradiated by IR for 12 h showed a dose-dependent reduction of the expression of collagen type III mRNA and protein (P<0.05, P<0.01), but the expression increased dose-dependently in response to IR exposure for 24 h (P<0.05 or 0.01). IR irradiation enhanced the mRNA and protein expression of c-Jun in a dose-dependence manner (P<0.05 or 0.01).

Conclusions: IR irradiation can increase the expression of c-Jun, inhibit the expression of collagen I, and cause disturbance in collagen III expression in human skin fibroblasts, which may be one of the mechanism of IR radiation to initiate and promote skin photoaging.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Proliferation
  • Cell Survival
  • Cells, Cultured
  • Collagen Type I / metabolism*
  • Collagen Type III / metabolism*
  • Fibroblasts / metabolism
  • Fibroblasts / radiation effects*
  • Humans
  • Infrared Rays*
  • Proto-Oncogene Proteins c-jun / metabolism*
  • RNA, Messenger / metabolism
  • Skin / cytology
  • Skin Aging
  • Ultraviolet Rays*

Substances

  • Collagen Type I
  • Collagen Type III
  • Proto-Oncogene Proteins c-jun
  • RNA, Messenger