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Center for Basic Research in Digestive Diseases, Division of Gastroenterology and Hepatology, Mayo Medical School, Clinic, and Foundation, Rochester, Minnesota 55905
We previously reported the development
of reproducible techniques for isolating and perfusing intact
intrahepatic bile duct units (IBDUs) from rats. Given the advantages of
transgenic and knockout mice for exploring ductal bile formation, we
report here the adaptation of those techniques to mice and their
initial application to the study of water transport across mouse
intrahepatic biliary epithelia. IBDUs were isolated from livers of
normal mice by microdissection combined with enzymatic digestion. After
culture, isolated IBDUs sealed to form intact, polarized compartments,
and a microperfusion system employing those isolated IBDUs developed. A
quantitative image analysis technique was used to observe a rapid
increase of luminal area when sealed IBDUs were exposed to a series of inward osmotic gradients reflecting net water secretion; the choleretic agonists secretin and forskolin also induced water secretion into IBDUs. The increase of IBDU luminal area induced by inward osmotic gradients and choleretic agonists was reversibly inhibited by HgCl2, a water channel inhibitor. With the use of a
quantitative epifluorescence technique in perfused mouse IBDUs, a high
osmotic water permeability (Pf = 2.5-5.6 × 10
2 cm/s) was found in response to
osmotic gradients, further supporting the presence of water channels.
These findings suggest that, as in the rat, water transport across
intrahepatic biliary epithelia in mice is water channel mediated.
epithelial cells; aquaporins; perfusion
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