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Unconjugated bile salts shuttle through hepatocyte peroxisomes for taurine conjugation
Author(s) -
Rembacz Krzysztof P.,
Woudenberg Jannes,
Hoekstra Mark,
Jonkers Elles Z.,
van den Heuvel Fiona A.J.,
BuistHoman Ma,
WoudenbergVrenken Titia E.,
Rohacova Jana,
Marin M. Luisa,
Miranda Miguel A.,
Moshage Han,
Stellaard Frans,
Faber Klaas Nico
Publication year - 2010
Publication title -
hepatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.488
H-Index - 361
eISSN - 1527-3350
pISSN - 0270-9139
DOI - 10.1002/hep.23954
Subject(s) - taurine , digitonin , peroxisome , biochemistry , hepatocyte , enterohepatic circulation , bile acid , cholic acid , chemistry , cytosol , glycine , biology , chromatography , enzyme , amino acid , in vitro , gene
Abstract Bile acid‐CoA:amino acid N‐acyltransferase (BAAT) conjugates bile salts to glycine or taurine, which is the final step in bile salt biosynthesis. In addition, BAAT is required for reconjugation of bile salts in the enterohepatic circulation. Recently, we showed that BAAT is a peroxisomal protein, implying shuttling of bile salts through peroxisomes for reconjugation. However, the subcellular location of BAAT remains a topic of debate. The aim of this study was to obtain direct proof for reconjugation of bile salts in peroxisomes. Primary rat hepatocytes were incubated with deuterium‐labeled cholic acid (D 4 CA). Over time, media and cells were collected and the levels of D 4 CA, D 4 ‐tauro‐CA (D 4 TCA), and D 4 ‐glyco‐CA (D 4 GCA) were quantified by liquid chromatography‐tandem mass spectrometry (LC/MS/MS). Subcellular accumulation of D 4 ‐labeled bile salts was analyzed by digitonin permeabilization assays and subcellular fractionation experiments. Within 24 hours, cultured rat hepatocytes efficiently (>90%) converted and secreted 100 μM D 4 CA to D 4 TCA and D 4 GCA. The relative amounts of D 4 TCA and D 4 GCA produced were dependent on the presence of glycine or taurine in the medium. Treatment of D 4 CA‐exposed hepatocytes with 30‐150 μg/mL digitonin led to the complete release of D 4 CA, D 4 GCA, and glyceraldehyde 3‐phosphate dehydrogenase (GAPDH) (cytosolic marker). Full release of D 4 TCA, catalase, and BAAT was only observed at 500 μg/mL digitonin, indicating the presence of D 4 TCA in membrane‐enclosed organelles. D 4 TCA was detected in fractions of purified peroxisomes, which did not contain D 4 CA and D 4 GCA. Conclusion: We established a novel assay to study conjugation and intra‐ and transcellular transport of bile salts. Using this assay, we show that cholic acid shuttles through peroxisomes for taurine‐conjugation. (H EPATOLOGY 2010)