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J. Biol. Chem., Vol. 265, Issue 11, 5942-5945, 04, 1990
P von Dippe and D Levy
The expression of the hepatocyte Na(+)-dependent bile acid transport
protein during liver development and in hepatoma cells has been
characterized using a monoclonal antibody (mAb 25D-1) which specifically
recognizes this 49-kDa carrier system. mAb binding studies demonstrated a
greatly reduced concentration of this transport protein on the surface of
hepatoma tissue culture (HTC) cells, a result consistent with the greater
than 95% reduction in bile acid transport capacity when compared with
normal adult hepatocytes. Immunoprecipitation procedures with 25D-1 were
utilized to quantitate the presence of this transport protein in HTC cells
as well as in adult hepatocytes that had been labeled with [35S]methionine
or Na125I. These studies indicate that the 49-kDa transport protein is not
expressed either on the surface or in any intracellular compartment in HTC
cells. mAb binding to fetal cells (day 17) also indicated a greatly
decreased number of transport molecules in the plasma membrane. Total cell
content of this carrier protein during the next 7 weeks of liver
development, as measured by immunoprecipitation, increased in a linear
fashion reaching 92% of the adult level at 4 weeks after birth, which
parallels the increase in transport function. These results demonstrate
that bile acid transport capacity is directly related to the level of
expression of this 49-kDa membrane protein.
Expression of the bile acid transport protein during liver development and in hepatoma cells
Department of Biochemistry, University of Southern California School of Medicine, Los Angeles 90033.
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