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Defective Intracellular Processing of Lactase‐Phlorizin Hydrolase Protein in Rats Prenatally Exposed to Ethanol
Author(s) -
Estrada Gemma,
Krasinski Stephen D.,
Grand Richard J.,
LópezTejero M. Dolores
Publication year - 1998
Publication title -
alcoholism: clinical and experimental research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.267
H-Index - 153
eISSN - 1530-0277
pISSN - 0145-6008
DOI - 10.1111/j.1530-0277.1998.tb03719.x
Subject(s) - lactase , enterocyte , medicine , endocrinology , intracellular , maltase , ethanol , chemistry , alcohol dehydrogenase , messenger rna , brush border , biochemistry , biology , microbiology and biotechnology , enzyme , small intestine , vesicle , membrane , gene
We have previously shown that fetal exposure to ethanol in rats produces both structural and biochemical abnormalities in absorptive enterocytes. Among the indicators of injury are derangements in the expression of lactase‐phlorizin hydrolase (LPH), which is an essential enzyme for the assimilation of milk. In an animal model of fetal alcohol syndrome, unsuckled newborn rats prenatally exposed to maternal ethanol revealed a 10‐ to 15‐fold increase in the number of LPH mRNA molecules per absorptive enterocyte, compared with controls (Estrada et al., Alcohol. Clin. Exp. Res. 20:1662–1668,1996). However, lactase activity per cell was similar in both groups. The aim of this study was to characterize the effect of prenatal exposure to ethanol on the processing of LPH mRNA and protein. RNase protection assays using 3′‐ and 5′‐directed antisense RNA probes revealed that the LPH mRNA from ethanol‐exposed pups is full length. However, metabolic labeling, followed by immunoprecipitation using an anti‐LPH monoclonal antibody, demonstrated a significant alteration in LPH protein processing. Intestinal explants from 21‐day ethanol‐exposed fetuses that were chased 30 min after a [ 35 S]methionine pulse showed greater amounts of newly synthesized LPH precursors (205 and 220 kDa) and low molecular weight degradation products than controls. However, despite the increases in LPH precursor, the amount of 130 kDa mature LPH was similar in ethanol‐exposed and control explants. These data suggest an increase in intracellular degradation of LPH precursor in rats prenatally exposed to ethanol, which occurs before its insertion into the microvillus membrane. Biosynthesis of LPH appears to be upregulated at the transcriptional level, which overcomes the degradation of LPH precursor during processing.