Subtractive hybridization unravels a role for the ion cotransporter NKCC1 in the murine intestinal pacemaker.

Wouters M, De Laet A, Donck LV, Delpire E, van Bogaert PP, Timmermans JP, de Kerchove d'Exaerde A, Smans K, Vanderwinden JM
Am J Physiol Gastrointest Liver Physiol. 2006 290 (6): G1219-27

PMID: 16123204 · DOI:10.1152/ajpgi.00032.2005

In the small intestine, interstitial cells of Cajal (ICC) surrounding the myenteric plexus generate the pacemaking slow waves that are essential for an efficient intestinal transit. The underlying molecular mechanisms of the slow wave are poorly known. Our aim was to identify ICC-specific genes and their function in the mouse jejunum. Suppression subtractive hybridization using two independent ICC-deficient mouse models identified 56 genes putatively downregulated in the muscularis propria compared with wild-type littermates. Differential expression was confirmed by real-time quantitative PCR for the tyrosine kinase receptor KIT, the established marker for ICC, and for the Na(+)-K(+)-2Cl(-) cotransporter (NKCC1). Immunoreactivity for NKCC1 was detected in myenteric ICC but not in the ICC population located at the deep muscular plexus. NKCC1 was also expressed in enteric neurons and mucosal crypts. Bumetanide, an NKCC1 inhibitor, reversibly affected the shape, amplitude, and frequency of the slow waves. Similar alterations were observed in NKCC1 knockout mice. These data support the hypothesis that NKCC1 expressed in myenteric ICC is involved in the mechanism of slow waves in the murine jejunum.

MeSH Terms (11)

Action Potentials Animals Biological Clocks Cells, Cultured In Situ Hybridization Intestine, Small Mice Mice, Transgenic Myocytes, Smooth Muscle Sodium-Potassium-Chloride Symporters Solute Carrier Family 12, Member 2

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