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Differential gene expression in functional classes of interstitial cells of Cajal in murine small intestine

Publication ,  Journal Article
Chen, H; Ördög, T; Chen, J; Young, DL; Bardsley, MR; Redelman, D; Ward, SM; Sanders, KM
Published in: Physiological Genomics
November 2007

Interstitial cells of Cajal (ICC) have important functions in regulation of motor activity in the gastrointestinal tract. In murine small intestine, ICC are gathered in the regions of the myenteric plexus (ICC-MY) and the deep muscular plexus (ICC-DMP). These two classes of ICC have different physiological functions. ICC-MY are pacemaker cells and generate the slow-wave electrical rhythmicity of gastrointestinal organs. ICC-DMP form synaptic connections with the varicose nerve terminals of enteric motor neurons and are involved in reception and transduction of motor neurotransmission. Gene expression underlying specific functions of ICC classes is incompletely understood. In the present study, we used recently developed highly selective techniques to isolate the two functional ICC classes from enzymatically dispersed intestinal muscles by fluorescence-activated cell sorting. The transcriptomes of ICC-MY and ICC-DMP were investigated using oligonucleotide microarray analysis. Differential expression of functional groups of genes defined by standard gene ontology terms was also studied. There were substantial numbers of genes expressed more abundantly in ICC than in the tunica muscularis, and we also detected marked phenotypic differences between ICC-MY and ICC-DMP. Notably, genes related to cell junction, process guidance, and vesicle trafficking were upregulated in ICC. Consistent with their specific functions, metabolic and Catransport genes were relatively upregulated in ICC-MY, whereas genes for signaling proteins involved in transduction of neurotransmitter functions were relatively upregulated in ICC-DMP. Our results may lead to the identification of novel biomarkers for ICC and provide directions for further studies designed to understand ICC function in health and disease.

Duke Scholars

Published In

Physiological Genomics

DOI

EISSN

1531-2267

ISSN

1094-8341

Publication Date

November 2007

Volume

31

Issue

3

Start / End Page

492 / 509

Publisher

American Physiological Society

Related Subject Headings

  • Biochemistry & Molecular Biology
  • 1116 Medical Physiology
 

Citation

APA
Chicago
ICMJE
MLA
NLM
Chen, H., Ördög, T., Chen, J., Young, D. L., Bardsley, M. R., Redelman, D., … Sanders, K. M. (2007). Differential gene expression in functional classes of interstitial cells of Cajal in murine small intestine. Physiological Genomics, 31(3), 492–509. https://doi.org/10.1152/physiolgenomics.00113.2007
Chen, Hui, Tamás Ördög, Junwei Chen, David L. Young, Michael R. Bardsley, Doug Redelman, Sean M. Ward, and Kenton M. Sanders. “Differential gene expression in functional classes of interstitial cells of Cajal in murine small intestine.” Physiological Genomics 31, no. 3 (November 2007): 492–509. https://doi.org/10.1152/physiolgenomics.00113.2007.
Chen H, Ördög T, Chen J, Young DL, Bardsley MR, Redelman D, et al. Differential gene expression in functional classes of interstitial cells of Cajal in murine small intestine. Physiological Genomics. 2007 Nov;31(3):492–509.
Chen, Hui, et al. “Differential gene expression in functional classes of interstitial cells of Cajal in murine small intestine.” Physiological Genomics, vol. 31, no. 3, American Physiological Society, Nov. 2007, pp. 492–509. Crossref, doi:10.1152/physiolgenomics.00113.2007.
Chen H, Ördög T, Chen J, Young DL, Bardsley MR, Redelman D, Ward SM, Sanders KM. Differential gene expression in functional classes of interstitial cells of Cajal in murine small intestine. Physiological Genomics. American Physiological Society; 2007 Nov;31(3):492–509.

Published In

Physiological Genomics

DOI

EISSN

1531-2267

ISSN

1094-8341

Publication Date

November 2007

Volume

31

Issue

3

Start / End Page

492 / 509

Publisher

American Physiological Society

Related Subject Headings

  • Biochemistry & Molecular Biology
  • 1116 Medical Physiology