Improvements in the primary culture of neonate rat myocardial cells by study of the mechanism of endoplasmic reticulum stress

Cell Stress Chaperones. 2013 May;18(3):367-75. doi: 10.1007/s12192-012-0390-y. Epub 2013 Jan 18.

Abstract

We previously found that endoplasmic reticulum stress (ERS) might be exhibited in the conventional protocol of the primary culture of neonate rat myocardial cells (NRMCs) and that the high glucose concentration (25 mmol/L) in the culture medium might be the cause. Here, we investigated if the high concentration of glucose might influence ERS in myocardial cells during culture. GRP78 expression (ERS marker) was similar in groups with tunicamycin (TM) and without TM in high glucose cultured cells (p > 0.01). Different glucose concentrations elicited different GRP78 expressions according to analyses of protein and RNA levels, which showed ERS in H/H groups. Finally, we found that GRP78 expression was higher in TM groups compared with M/M groups (p < 0.01). The conventional high-glucose culture media during primary culture of NRMCs induced ERS. We propose that medium-glucose culture media should be used and describe an improved protocol for the primary culture of NRMCs.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Animals, Newborn
  • Blotting, Western
  • Cell Culture Techniques / methods*
  • Cell Shape / drug effects
  • Cells, Cultured
  • Culture Media / pharmacology
  • Endoplasmic Reticulum Chaperone BiP
  • Endoplasmic Reticulum Stress* / drug effects
  • Gene Expression Regulation / drug effects
  • Glucose / pharmacology
  • Heart Rate / drug effects
  • Heat-Shock Proteins / genetics
  • Heat-Shock Proteins / metabolism
  • Myocardium / cytology*
  • Rats
  • Rats, Sprague-Dawley
  • Reverse Transcriptase Polymerase Chain Reaction
  • Time Factors
  • Tunicamycin / pharmacology

Substances

  • Culture Media
  • Endoplasmic Reticulum Chaperone BiP
  • Heat-Shock Proteins
  • Tunicamycin
  • Glucose