Bile secretion is a major hepatic function, frequently impaired in diseases of the liver resulting in the syndrome of cholestasis and occasionally resulting in progressive liver injury and death. Since 1974, this grant has focused on the development of new techniques to understand the basic mechanisms of this secretory process. I. Utilizing isolated hepatocyte couplets (a novel primary secretory unit that transports solutes and secretes bile in short term cultures), and subconfluent hepatocyte monolayers, we will examine the functional role of previously identified ion transports systems (Na+/H+exchange, HC03/Cl-exchange Na+/HC03 symport) and ion channels (K+, CL-), in the regulation of cell pH and cell volume and the relationship of these transport events to bile secretion (bile acid independent secretion). Agents that stimulate (DBcAMP) and inhibit (phorbol esters) this secretory process will be examined for an effect on these events. These studies will be facilitated by fluorescent techniques for measurement of intracellular pH and Ca++, and intracanalicular pH, and confocal imaging equipment for intracellular and canalicular resolution. DIC optical systems with image enhancement equipment will permit measurements of canalicular volume to be made to assess secretory rates in the isolated cells. II. The transcytotic vesicle pathway, and its mechanism of regulation by agents such as DBcAMP and phorbol esters will be assessed in isolated perfused rat livers using fluid phase markers (HRP, dextran). Techniques will also be explored for developing an in-vitro fusion assay between intracellular vesicles and canalicular membranes as a model for examining both stimulation and inhibition of this pathway. III. Finally, techniques will be developed for the isolation of bile duct epithelial cells and establishment of monolayers in order to characterize the membrane transport systems used for maintaining pHi, cell volume and secretory and absorptive functions, using techniques developed for the study of isolated hepatocytes.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
2R01DK025636-14
Application #
3566175
Study Section
General Medicine A Subcommittee 2 (GMA)
Project Start
1978-09-01
Project End
1995-06-30
Budget Start
1990-09-01
Budget End
1991-06-30
Support Year
14
Fiscal Year
1990
Total Cost
Indirect Cost
Name
Yale University
Department
Type
DUNS #
082359691
City
New Haven
State
CT
Country
United States
Zip Code
06520
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Pan, Qiong; Zhang, Xiaoxun; Zhang, Liangjun et al. (2018) Solute Carrier Organic Anion Transporter Family Member 3A1 Is a Bile Acid Efflux Transporter in Cholestasis. Gastroenterology 155:1578-1592.e16
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Cai, Shi-Ying; Boyer, James L (2017) Studies on the mechanisms of bile acid initiated hepatic inflammation in cholestatic liver injury. Inflamm Cell Signal 4:
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Li, Man; Mennone, Albert; Soroka, Carol J et al. (2015) Na(+) /H(+) exchanger regulatory factor 1 knockout mice have an attenuated hepatic inflammatory response and are protected from cholestatic liver injury. Hepatology 62:1227-36
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Wheeler, Sadie G; Hammond, Christine L; Jornayvaz, François R et al. (2014) Ost?-/- mice exhibit altered expression of intestinal lipid absorption genes, resistance to age-related weight gain, and modestly improved insulin sensitivity. Am J Physiol Gastrointest Liver Physiol 306:G425-38
Soroka, Carol J; Boyer, James L (2014) Biosynthesis and trafficking of the bile salt export pump, BSEP: therapeutic implications of BSEP mutations. Mol Aspects Med 37:3-14

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