Microarray comparison of normal and W/Wv mice in the gastric fundus indicates a supersensitive phenotype

Physiol Genomics. 2002 Oct 2;11(1):1-9. doi: 10.1152/physiolgenomics.00052.2002.

Abstract

Interstitial cells of Cajal (ICC) have been identified in specific areas throughout the smooth musculature of the gastrointestinal (GI) tract. Located within the circular and longitudinal muscle layers of the gastric fundus lies a specific type of ICC, termed "intramuscular" ICC or IC-IM. The principal function of this cell type is to act as "mediators of excitatory and inhibitory enteric neurotransmission." The functional role of these cells has been investigated using W/W(v) mutant mice that specifically lack IC-IM, resulting in disrupted enteric neurotransmission. The aim of the present study was to investigate differential gene expression in W/W(v) mutant mice, from the tunica muscularis of the gastric fundus using a mouse cDNA microarray containing 1,081 known genes. Verification of the microarray data was attained using real-time "quantitative" PCR (qPCR). Of the 1,081 arrayed genes, 36 demonstrated differential expression by >2-fold in the W/W(v) mice. An agreement rate of 50% (7 of 14 tested) was obtained using qPCR. Of the seven confirmed changes in expression, several were indicative of a supersensitive phenotype, observed in denervation models. Expression of several putative neurotransmitter receptors including P2Y, the receptor for the inhibitory neurotransmitter ATP, was upregulated. The functional role of the P2Y receptor was also investigated using electrophysiological recordings. These results offer a new insight into the molecular changes that occur in W/W(v) fundic smooth muscle and may also provide novel information with regard to the importance of IC-IM in enteric neurotransmission.

Publication types

  • Comparative Study
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Evoked Potentials
  • Gastric Fundus / cytology*
  • Gastric Fundus / metabolism*
  • Gastric Fundus / physiology
  • Gene Expression Profiling
  • Mice
  • Mice, Mutant Strains
  • Muscle, Smooth / cytology
  • Muscle, Smooth / metabolism
  • Oligonucleotide Array Sequence Analysis
  • Phenotype
  • Proto-Oncogene Proteins c-kit / genetics*
  • Receptors, Purinergic P2 / physiology
  • Reverse Transcriptase Polymerase Chain Reaction

Substances

  • Receptors, Purinergic P2
  • Proto-Oncogene Proteins c-kit