Project 1 is investigating the mechanismof electrical rhythmicityin GImuscles. Phasiccontractions are timed by electrical slow waves that are generated by a specializedpopulationof cells known as interstitial cells of Cajal (ICC). We developed a cell culture model of ICCduringthe previous funding period. These cells are spontaneously active, producingspontaneous transient inward currents (STICs), but the cells do not fully recapitulate electrical rhythmicityin intact musclestrips. For example,we could not activate large amplitude currents responsible for slow waves in these cells. Molecular studies showed that cultured ICC rapidly dedifferentiate and lose the ICC phenotype withina few days in culture. Afresh preparation of ICCwas difficult to develop because ICC are difficult to identify in mixedpopulationsof cells. In the next funding period we will utilize a new genetic tool we have created by engineeringexpression of a bright green fluoresccent protein (copGFP) in ICC. Expression of the reporter makes it easy to find ICCin cell dispersions and to sort ICCby fluorescence activated cell sorting for molecularstudies. Cells from these mice displayspontaneous rhythmicity in the form oflarge amplitude spontaneous depolarizations that we believe are equivalent to slow waves in intact ICC networks. We will characterize the spontaneous activityof single ICCand describe the properties of the large amplitude 'autonomous'currents that underlyspontaneous depolarization. Autonomouscurrents can be pace by depolarization of single cells. We will explore the voltage-dependence of autonomous currents and determine the underlyingvoltage-sensor and mechanismthat initiates these currents. We will also investigate how spontaneous activity in single ICCis regulated with the goal of understanding how slow wavefrequency (and ultimately phasic contractile activity) is regulated. Several clinical studies have demosntrate loss of ICCin pathophysiological conditions, and this has resulted in hypotheses about the cause of GI motilitydisorders. We hypothesize that changes in ICCmay precede the loss of cells, and we will characterize changes in ICCfunction during the development of type II diabetes. We will also study changes in ICCduring the development of hyperplasia in pre-GIST ICCnetworks. New ideas about pacemaker activity in the gut will result from this work.

Public Health Relevance

Interstitial cells of Cajal generate pacemaker activity in the GI tract that is responsible for peristaltic and segmental contractions in motility. Defects in pacemaker activity lead to disordered motility and unregulated transit of food and nutrients. Understanding how pacemaker cells work will provide new ideas about how to control GI motility and offer new suggestions about how to treat GI motility disoders.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Program Projects (P01)
Project #
5P01DK041315-25
Application #
8469485
Study Section
Special Emphasis Panel (ZDK1-GRB-9)
Project Start
Project End
Budget Start
2013-05-01
Budget End
2014-04-30
Support Year
25
Fiscal Year
2013
Total Cost
$169,156
Indirect Cost
$48,760
Name
University of Nevada Reno
Department
Type
DUNS #
146515460
City
Reno
State
NV
Country
United States
Zip Code
89557
Sanders, Kenton M; Salter, Anna K; Hennig, Grant W et al. (2014) Responses to enteric motor neurons in the gastric fundus of mice with reduced intramuscular interstitial cells of cajal. J Neurogastroenterol Motil 20:171-84
Zheng, Haifeng; Park, Kyung Sik; Koh, Sang Don et al. (2014) Expression and function of a T-type Ca2+ conductance in interstitial cells of Cajal of the murine small intestine. Am J Physiol Cell Physiol 306:C705-13
McCann, Conor J; Hwang, Sung-Jin; Hennig, Grant W et al. (2014) Bone Marrow Derived Kit-positive Cells Colonize the Gut but Fail to Restore Pacemaker Function in Intestines Lacking Interstitial Cells of Cajal. J Neurogastroenterol Motil 20:326-37
Durnin, Leonie; Hwang, Sung Jin; Kurahashi, Masaaki et al. (2014) Uridine adenosine tetraphosphate is a novel neurogenic P2Y1 receptor activator in the gut. Proc Natl Acad Sci U S A 111:15821-6
Okamoto, T; Barton, M J; Hennig, G W et al. (2014) Extensive projections of myenteric serotonergic neurons suggest they comprise the central processing unit in the colon. Neurogastroenterol Motil 26:556-70
Drumm, Bernard T; Koh, Sang Don; Andersson, Karl-Erik et al. (2014) Calcium signalling in Cajal-like interstitial cells of the lower urinary tract. Nat Rev Urol 11:555-64
Mutafova-Yambolieva, Violeta N; Durnin, Leonie (2014) The purinergic neurotransmitter revisited: a single substance or multiple players? Pharmacol Ther 144:162-91
Sanders, Kenton M; Ward, Sean M; Koh, Sang Don (2014) Interstitial cells: regulators of smooth muscle function. Physiol Rev 94:859-907
Kurahashi, Masaaki; Nakano, Yasuko; Peri, Lauren E et al. (2013) A novel population of subepithelial platelet-derived growth factor receptor *-positive cells in the mouse and human colon. Am J Physiol Gastrointest Liver Physiol 304:G823-34
Keef, K D; Saxton, S N; McDowall, R A et al. (2013) Functional role of vasoactive intestinal polypeptide in inhibitory motor innervation in the mouse internal anal sphincter. J Physiol 591:1489-506

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