Temperature compensation and temperature resetting of circadian rhythms in mammalian cultured fibroblasts

Genes Cells. 2003 Aug;8(8):713-20. doi: 10.1046/j.1365-2443.2003.00669.x.

Abstract

Background: Circadian rhythms control many physiological processes. One of characteristic properties of circadian rhythms is insensitivity to temperature, called temperature compensation. Although this temperature-insensitive property has repeatedly been observed mainly in circadian output rhythms, temperature effect on autoregulatory feedback loops of clock gene expression, the rhythm-generating mechanisms, has not been fully investigated.

Results: We show first that the circadian oscillation of clock gene expression in NIH3T3 fibroblasts, which is induced by TPA (12-O-tetradecanoylphorbol-13-acetate) treatment, is strongly temperature-compensated over the temperature range of 33-42 degrees C. We then show that heat treatment at 42 degrees C is able to trigger circadian oscillation of clock gene expression in NIH3T3 cells. This 42 degrees C heat treatment, unlike serum shock or TPA treatment, did not induce immediate expression of mPer1 mRNA, suggesting the existence of several different resetting mechanisms.

Conclusions: This is the first demonstration of temperature compensation of the rhythm-generating core feedback loops of clock gene expression in mammalian cultured cells. It is possible that cells in the periphery could sense the change of ambient temperature as a resetting cue and that the whole organism thus could be entrained rapidly at dawn, in cooperation with the resetting mechanism by light.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • CLOCK Proteins
  • Carcinogens / pharmacology
  • Cell Cycle Proteins
  • Circadian Rhythm / drug effects
  • Circadian Rhythm / physiology*
  • Fibroblasts / drug effects
  • Fibroblasts / metabolism*
  • Gene Expression Regulation*
  • Mice
  • NIH 3T3 Cells
  • Nuclear Proteins / metabolism
  • Period Circadian Proteins
  • RNA, Messenger / metabolism
  • Reverse Transcriptase Polymerase Chain Reaction
  • Temperature*
  • Tetradecanoylphorbol Acetate / pharmacology
  • Time Factors
  • Trans-Activators / genetics
  • Trans-Activators / metabolism*
  • Transcription Factors
  • Transcription, Genetic

Substances

  • Carcinogens
  • Cell Cycle Proteins
  • Nuclear Proteins
  • Per1 protein, mouse
  • Per2 protein, mouse
  • Per3 protein, mouse
  • Period Circadian Proteins
  • RNA, Messenger
  • Trans-Activators
  • Transcription Factors
  • CLOCK Proteins
  • Clock protein, mouse
  • Tetradecanoylphorbol Acetate