β-Glucuronidase latency in isolated murine hepatocytes

Miklós Csala, Gábor Bánhegyi, László Braun, Rita Szirmai, Ann Burchell, Brian Burchell, Angelo Benedetti, József Mandl

Research output: Contribution to journalArticle

18 Citations (Scopus)

Abstract

The physiological function of microsomal β-glucuronidase is unclear. Substrates may be either glucuronides produced in the lumen of endoplasmic reticulum (ER) or those taken up by hepatocytes. In the latter case, efficient inward transport of glucuronides at the plasma membrane and the ER membrane would be required. Therefore, the potential role of β-glucuronidase in ER was investigated. Isolated mouse hepatocytes and mouse and rat liver microsomal vesicles were used in the experiments. Selective permeabilization of the plasma membrane of isolated hepatocytes with saponin or digitonin resulted in an almost 4-fold elevation in the rate of p-nitrophenol glucuronide hydrolysis, while the permeabilization of plasma membrane plus ER membrane by Triton X-100 caused a further 2-fold elevation. In microsomal vesicles, the p-nitrophenol glucuronide or phenolphthalein glucuronide β-glucuronidase activity showed about 50% latency as revealed by alamethicin or Triton X-100 treatment. A light-scattering study indicated that the microsomes are relatively impermeable to both glucuronides and to glucuronate. On the basis of our results, the role of liver microsomal β-glucuronidase in the deconjugation of glucuronides taken up by the liver seems unlikely. Hydrolysis of the glucuronides produced in the ER lumen may play a role in substrate supply for ascorbate synthesis or in 'proofreading' of glucuronidation. Copyright (C) 2000 Elsevier Science Inc.

Original languageEnglish
Pages (from-to)801-805
Number of pages5
JournalBiochemical Pharmacology
Volume59
Issue number7
DOIs
Publication statusPublished - Apr 1 2000

Keywords

  • Endoplasmic reticulum
  • Glucuronide
  • Latency
  • Liver
  • Transport

ASJC Scopus subject areas

  • Biochemistry
  • Pharmacology

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