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Am J Physiol Gastrointest Liver Physiol (April 23, 2003). doi:10.1152/ajpgi.00421.2002
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Submitted on September 26, 2002
Accepted on April 15, 2003

PROTEIN KINASE C{epsilon} TRANSLOCATION IN ENTERIC NEURONS AND INTERSTITIAL CELLS OF CAJAL IN RESPONSE TO MUSCARINIC STIMULATION

Xuan-Yu Wang1, Sean M. Ward1, William T. Gerthoffer2, and Kenton M. Sanders1*

1 Department of Physiology and Cell Biology, University of Nevada School of Medicine, Reno, NV, USA
2 Department of Pharmacology, University of Nevada School of Medicine, Reno, NV, USA

* To whom correspondence should be addressed. E-mail: kent{at}physio.unr.edu.

Interstitial cells of Cajal in the deep muscular plexus (ICC-DMP) of the small intestine express excitatory neurotransmitter receptors. We tested whether ICC-DMP are functionally innervated by cholinergic neurons in the murine intestine. Muscles were stimulated by intrinsic nerves and acetylcholine and processed for immunohistochemistry to determine these effects on protein kinase C{epsilon} (PKC{epsilon}) activation. Under control conditions, PKC{epsilon}-LI was only observed in myenteric neurons within the tunica muscularis. Electrical field stimulation or ACh caused translocation of neural PKC{epsilon}-LI from the cytosol to a peripheral compartment. After stimulation, PKC{epsilon}-LI was found in spindle-shaped cells in the deep muscular plexus. These cells were identified as ICC-DMP by Kit-LI and vimentin-LI. PKC{epsilon}-LI in ICC-DMP and translocation of PKC{epsilon}-LI in neurons was blocked by tetrodotoxin or atropine suggesting these responses was due to activation of muscarinic receptors. Western blots also confirmed translocation of PKC{epsilon}-LI. In conclusion, PKC{epsilon} translocation is linked to muscarinic receptor activation in ICC-DMP and a sub-population of myenteric neurons. These studies demonstrate that ICC-DMP are functionally innervated by excitatory motor neurons.




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