Tissue-specific and time-dependent regulation of the endothelin axis by the circadian clock protein Per1

Life Sci. 2014 Nov 24;118(2):255-62. doi: 10.1016/j.lfs.2014.03.028. Epub 2014 Apr 8.

Abstract

Aims: The present study is designed to consider a role for the circadian clock protein Per1 in the regulation of the endothelin axis in mouse kidney, lung, liver and heart. Renal endothelin-1 (ET-1) is a regulator of the epithelial sodium channel (ENaC) and blood pressure (BP), via activation of both endothelin receptors, ETA and ETB. However, ET-1 mediates many complex events in other tissues.

Main methods: Tissues were collected in the middle of murine rest and active phases, at noon and midnight, respectively. ET-1, ETA and ETB mRNA expressions were measured in the lung, heart, liver, renal inner medulla and renal cortex of wild type and Per1 heterozygous mice using real-time quantitative RT-PCR.

Key findings: The effect of reduced Per1 expression on levels of mRNAs and the time-dependent regulation of expression of the endothelin axis genes appeared to be tissue-specific. In the renal inner medulla and the liver, ETA and ETB exhibited peaks of expression in opposite circadian phases. In contrast, expressions of ET-1, ETA and ETB in the lung did not appear to vary with time, but ET-1 expression was dramatically decreased in this tissue in Per1 heterozygous mice. Interestingly, ET-1 and ETA, but not ETB, were expressed in a time-dependent manner in the heart.

Significance: Per1 appears to regulate expression of the endothelin axis genes in a tissue-specific and time-dependent manner. These observations have important implications for our understanding of the best time of day to deliver endothelin receptor antagonists.

Keywords: ETA; ETB; Endothelin-A receptor; Endothelin-B receptor; Gene regulation.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Circadian Clocks* / genetics
  • Endothelin-1 / metabolism
  • Endothelins / metabolism*
  • Gene Expression Profiling
  • Gene Expression Regulation
  • Kidney / metabolism
  • Mice
  • Organ Specificity* / genetics
  • Period Circadian Proteins / metabolism*
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Receptor, Endothelin A / metabolism
  • Receptor, Endothelin B / metabolism
  • Time Factors

Substances

  • Endothelin-1
  • Endothelins
  • Per1 protein, mouse
  • Period Circadian Proteins
  • RNA, Messenger
  • Receptor, Endothelin A
  • Receptor, Endothelin B