Program Project Grant

Regulatory Mechanisms in Intestinal Motility

This Program Project seeks to understand basic cellular mechanisms responsible for gastrointestinal (GI) motility. Knowledge of the basic structures and mechanisms of the neuromuscular apparatus of the GI tract provides insights about how normal GI motility is accomplished and why dysmotilities develop in the abnormal GI tract. The long range benefit of this information will be to provide the basis for novel methods for treatment of abnormal GI transit and to improve the quality of life for human patients. The neuromuscular apparatus of the GI tract is extremely complex and function depends upon integrated activity of several types of cells. We have designed 4 projects that will explore various aspects of enteric neurotransmission, pacemaker activity, and smooth muscle function.

  • Project 1, using a novel murine genetic model in which interstitial cells of Cajal (ICC) express a fluorescent protein, will seek to understand the mechanism of pacemaker activity and how pacemaker function is affected in diabetes and ICC hyperplasia.
  • Project 3 will seek to understand regulation of smooth muscle excitability and how the activity of non-selective cation conductances contributes to normal and abnormal responses of muscle cells.
  • Project 4 will investigate the release, function and metabolism of a novel neurotransmitter substance that is important for regulating colonic motor function.
  • Project 5 will study the plasticity of ICC and how and why these cells are lost in type II diabetes. This project will also seek to develop techniques for restoring networks of ICC after damage.

These primary investigations will be supported by 3 Core facilities designed to provide administration and informatics support and cutting-edge techniques, including cell and organotypic cultures, construction of transgenic animals, cytometry and fluorescence activated cell sorting, analysis of molecular expression, and a variety of morphological techniques. For the purpose of translating our findings from animal models to the function of the human GI tract, many of our experiments will be conducted on tissues and cells of human patients that have been recovered from surgery for carcinomas. The investigative team is highly synergistic and collaborative, and the PPG has a 20 year track-record of productivity and novel discovery. The principle investigator of this project since its beginning is Dr. Kenton Sanders.

Projects within the Program Project Grant
ProjectTitleLeader
1 Mechanism of Electrical Rhythmicity in ICC Kenton M. Sanders, Ph.D.
3 Regulation of Non-selective Cation Conductances in GI Smooth Muscle Sang Don Koh, M.D., Ph.D.
4 Novel Mechanisms in Enteric Inhibitory Neurotransmission Violeta Mutafova, M.D., Ph.D.
5 Regulation of the Phenotype and Regeneration of ICC Sean M. Ward, Ph.D.
Core A Administration and Informatics Kenton M. Sanders, Ph.D.
Core B Cells, Tissues and Transgenics Kathleen Keef, Ph.D.
Core C Molecular Expression and Morphology Sean M. Ward, Ph.D.