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Department of Medicine, Division of Gastroenterology/Hepatology, Indiana University School of Medicine and The Richard L. Roudebush Veterans Affairs Medical Center, Indianapolis, Indiana 46202 - 5121
Cell volume
regulation plays a vital role in many cell functions. Recent study
indicates that both K+ and Cl
channels are
important for the regulatory volume decrease (RVD) of
cholangiocarcinoma cells, but its physiological significance is unclear
due to the tumorous nature of the cells used. This present study
reports the RVD of normal mouse cholangiocytes by using freshly
isolated bile duct cell clusters (BDCC). A relatively simple and
practical method of measuring the cross-sectional area of BDCCs by
quantitative videomicroscopy was used to indirectly measure their
volumes. Mouse cholangiocytes exhibited RVD, which was inhibited by
5-nitro-2'-(3-phenylpropylamino)-benzoate, DIDS, and glibenclamide,
suggesting its dependence on certain chloride channels, such as
volume-activated chloride channels. It is also inhibited by barium
chloride but not by tetraethylammonium chloride, indicating its
dependence on certain potassium channels. However, cAMP agonists had no
significant effect on the RVD of BDCCs. This indirect method described
can be used to study the RVD of cholangiocytes from normal as well as
genetically altered mouse livers.
ion channel; quantitative videomicroscopy
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