Identification of differentially expressed genes after heat shock in isolated rat aorta

Clin Exp Pharmacol Physiol. 2007 Jul;34(7):636-40. doi: 10.1111/j.1440-1681.2007.04620.x.

Abstract

1. In a previous study, we demonstrated that heat shock augments vascular contractility through the stress response. 2. The current study was designed to identify differentially expressed genes after heat shock by using a novel annealing control primer (ACP) system, which was developed recently to identify authentic genes. 3. Rat aortic rings were mounted in organ baths, exposed to 42 degrees C for 45 min and harvested 4 h after the end of heat shock. Total RNA were used for amplification by the reverse transcriptase-polymerase chain reaction (RT-PCR) with ACP system. Differentially amplified PCR products were sequenced, searched against the GenBank and confirmed by RT-PCR. 4. Genes for connective tissue growth factor, stress-inducible protein 1 and heat shock protein 25 were upregulated, whereas a gene for interferon regulatory factor 1 was downregulated. Immunohistochemistry revealed upregulation of the phosphorylated form of Hsp25 in aortic rings after heat shock. 5. These results suggest that phosphorylated Hsp25 plays a pivotal role in the augmentation of vascular contraction after heat shock.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Aorta, Thoracic / metabolism*
  • Aorta, Thoracic / physiopathology
  • Connective Tissue Growth Factor
  • Databases, Genetic
  • Gene Expression Profiling / methods
  • Gene Expression*
  • HSP27 Heat-Shock Proteins
  • Heat Stress Disorders / genetics*
  • Heat Stress Disorders / metabolism
  • Heat Stress Disorders / physiopathology
  • Heat-Shock Proteins / genetics
  • Heat-Shock Proteins / metabolism
  • Hot Temperature*
  • Immediate-Early Proteins / genetics
  • Immediate-Early Proteins / metabolism
  • Immunohistochemistry
  • In Vitro Techniques
  • Intercellular Signaling Peptides and Proteins / genetics
  • Intercellular Signaling Peptides and Proteins / metabolism
  • Interferon Regulatory Factor-1 / genetics
  • Interferon Regulatory Factor-1 / metabolism
  • Male
  • Neoplasm Proteins / genetics
  • Neoplasm Proteins / metabolism
  • Phosphorylation
  • RNA, Messenger / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Reproducibility of Results
  • Reverse Transcriptase Polymerase Chain Reaction
  • Vasoconstriction / genetics*

Substances

  • CCN2 protein, rat
  • HSP27 Heat-Shock Proteins
  • Heat-Shock Proteins
  • Hspb1 protein, rat
  • Immediate-Early Proteins
  • Intercellular Signaling Peptides and Proteins
  • Interferon Regulatory Factor-1
  • Irf1 protein, rat
  • Neoplasm Proteins
  • RNA, Messenger
  • Stip1 protein, rat
  • Connective Tissue Growth Factor