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John Geibel

DSc, MD, AGAF, MS, FRS
Professor of Surgery (Gastrointestinal) and of Cellular And Molecular Physiology; Vice Chair, Surgery; Director, Surgical Research; American Gastroenterological Association Fellow; Fellow of the Royal Society of Medicine

Contact Information

John Geibel, DSc, MD, AGAF, MS, FRS

Lab Location

Mailing Addresses

  • Gastrointestinal Surgery

    PO Box 208062

    New Haven, CT, 06520-8062

    United States

  • Yale University

    BML 232, 310 Cedar Street

    New Haven, CT, 06510

    United States

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Research Summary

Our primary focus is on real time monitoring of ion transport mechanisms in epithelia, using high-resolution microscopy. One of the crucial problems facing all epithelial cells is the control of the intracellular milieu. In an effort to maintain ionic homeostasis, epithelial cells have devised a variety of ion channels, transport proteins, and carriers to regulate and maintain the intracellular ionic concentrations. To further understand how ions are transported in epithelial cells, we have developed a variety of optical techniques to continuously monitor intracellular ionic concentrations in real time. Using high-resolution video or confocal microscopy we are presently able to monitor intracellular Ca2+, Na+, K+, Cl-, pH, and membrane potential. We are currently investigating various aspects of renal tubule and gastric tissue ion transport in intact renal tubules and gastric glands. We also are characterizing the secretory and reabsorptive properties of the colonic crypt, with a special focus on diarrheal disease.

Specialized Terms: Gastric Acid Secretion; Colonic Fluid Transport; Renal Physiology; Intracellular Ion Activity Measurements; Calcium Sensing Receptor; Diarrheal disease; electrophysiology; CFTR; AMPKinase volume regulation

Extensive Research Description

We are focused on 3 main areas; gastric ion transport in health and disease, intestinal ion transport in health and disease, and 3DBioprinting. For gastric ion transport we are focusing on means to modulate acid secretion and reverse erosion. We use a combination of natural products and biochemical modifications to treat acid disease at the cellular level. For studies of intestinal ion transport, we are focusing on how the calcium sensing receptor(CaSR) can modulate fluid transport during toxin induced diarrhea. We are also looking at nanoparticle therapies for Ulcerative Colitis. In addition we are investigating means to prevent ischemic injury by activating ionic pathways using the AMPKinase. Finally we are trying to prevent IBD/IBS associated epithelial injury in the gut by CaSR activation using nutraceuticals . For the 3DBioprinting area we are developing replacement conduits that can be used for the aorta, the inferior vena cava, and also as small and large intestine repair tool. Along with this research we are now examining the potential for intestinal elongation using a 3D printed replacement.

Coauthors

Research Interests

Diarrhea; Electrophysiology; Gastric Acid; Gastroenterology; Gastrointestinal Agents; Physiology; Bioprinting; Chemicals and Drugs

Research Image

Isolated Human Gastric Gland

Isolated gastric gland loaded with the pH sensitive dye BCECF and a lysosomal tracker on a Zeiss Spinning Disk confocal. Image shows 3-D reconstruction of the gland in real time.

Selected Publications

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