Calcium-dependent up-regulation of mitochondrial electron transfer chain gene expressions in human luteinized granulosa cells

Fertil Steril. 2005 Oct:84 Suppl 2:1104-8. doi: 10.1016/j.fertnstert.2005.03.072.

Abstract

Objective: To evaluate the transcription and translation ability of mitochondria in terminally differentiated granulosa cells, these cells were incubated with ionic calcium.

Design: Prospective laboratory research.

Setting: In vitro fertilization laboratory in a university hospital.

Patient(s): Granulosa cells were harvested from 50 female patients undergoing IVF.

Intervention(s): Analysis of mitochondrial gene expression by semiquantitative reverse transcription-polymerase chain reaction (RT-PCR) and of mitochondrial-encoded proteins by Western blot.

Main outcome measure(s): Comparison of the RNA expression levels of genes including cytochrome c oxidase subunit I (COX I), adenosine triphosphate synthase 6 (ATPase 6), flavoprotein, and succinate-ubiquinone oxidoreductase, and protein levels of COX I and flavoprotein in different calcium ion treatment groups.

Result(s): There were dose-dependent increases in RNA expressions of the four genes analyzed from granulosa cells cultured in a serial concentration of calcium ions. This effect was abolished when cells were preincubated with the extracellular calcium-chelating agent, Ethylene glycol-bis (2-aminoethylether)-N,N,N',N'-tetraacetic acid (EGTA). The effect of ionic calcium on both the nuclear- and mitochondrial-encoded subunits also was determined. Expression levels of mitochondrial transcription factor A in RNA significantly increased in granulosa cells that were exposed for 24 and 48 hours to 0.5 and 1 microM A23187.

Conclusion(s): The present study is the first report to present calcium-dependent increases in the transcription and translation levels of both nuclear-encoded and mitochondrial-encoded mitochondrial respiratory enzyme subunits and also indicates that mitochondrial transcription factor A is involved in mitochondrial biogenesis.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Calcium / physiology*
  • Cells, Cultured
  • Dose-Response Relationship, Drug
  • Electron Transport / drug effects
  • Electron Transport / physiology
  • Electron Transport Chain Complex Proteins / biosynthesis*
  • Electron Transport Chain Complex Proteins / genetics*
  • Female
  • Gene Expression Profiling*
  • Granulosa Cells / enzymology
  • Granulosa Cells / metabolism*
  • Humans
  • Luteinization / genetics
  • Luteinization / metabolism*
  • Mitochondria / enzymology
  • Mitochondria / genetics
  • Mitochondria / metabolism*
  • Prospective Studies
  • Up-Regulation / physiology*

Substances

  • Electron Transport Chain Complex Proteins
  • Calcium