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Opposing Actions of Ethanol and Nicotine on Micro RNAs are Mediated by Nicotinic Acetylcholine Receptors in Fetal Cerebral Cortical-Derived Neural Progenitor Cells.
- Source :
- Alcoholism: Clinical & Experimental Research; Oct2012, Vol. 36 Issue 10, p1669-1677, 9p
- Publication Year :
- 2012
-
Abstract
- Background Ethanol ( EtOH) and nicotine are often co-abused. However, their combined effects on fetal neural development, particularly on fetal neural stem cells ( NSCs), which generate most neurons of the adult brain during the second trimester of pregnancy, are poorly understood. We previously showed that EtOH influenced NSC maturation in part, by suppressing the expression of specific micro RNAs (mi RNAs). Here, we tested in fetal NSCs the extent to which EtOH and nicotine coregulated known EtOH-sensitive (mi R-9, mi R-21, mi R-153, and mi R-335), a nicotine-sensitive mi RNA (mi R-140-3p), and mRNAs for nicotinic acetylcholine receptor ( nAChR) subunits. Additionally, we tested the extent to which these effects were nAChR dependent. Methods Gestational day 12.5 mouse fetal murine cerebral cortical-derived neurosphere cultures were exposed to EtOH, nicotine, and mecamylamine, a noncompetitive nAChR antagonist, individually or in combination, for short (24 hour) and long (5 day) periods, to mimic exposure during the in vivo period of neurogenesis. Levels of mi RNAs, mi RNA-regulated transcripts, and nAChR subunit mRNAs were assessed by quantitative reverse transcription polymerase chain reaction. Results EtOH suppressed the expression of known EtOH-sensitive mi RNAs and miR-140-3p, while nicotine at concentrations attained by cigarette smokers induced a dose-related increase in these mi RNAs. Nicotine's effect was blocked by EtOH and by mecamylamine. Finally, EtOH decreased the expression of nAChR subunit mRNAs and, like mecamylamine, prevented the nicotine-associated increase in α4 and β2 nAChR transcripts. Conclusions EtOH and nicotine exert mutually antagonistic, nAChR-mediated effects on teratogen-sensitive mi RNAs in fetal NSCs. These data suggest that concurrent exposure to EtOH and nicotine disrupts mi RNA regulatory networks that are important for NSC maturation. [ABSTRACT FROM AUTHOR]
- Subjects :
- RNA analysis
CHOLINERGIC receptors
ANALYSIS of variance
ANIMAL experimentation
CEREBRAL cortex
ETHANOL
FISHER exact test
HYDROCARBONS
MICE
NEURONS
NICOTINE
PARASYMPATHOMIMETIC agents
POLYMERASE chain reaction
RESEARCH funding
STATISTICS
DATA analysis
REVERSE transcriptase polymerase chain reaction
DATA analysis software
DESCRIPTIVE statistics
Subjects
Details
- Language :
- English
- ISSN :
- 01456008
- Volume :
- 36
- Issue :
- 10
- Database :
- Complementary Index
- Journal :
- Alcoholism: Clinical & Experimental Research
- Publication Type :
- Academic Journal
- Accession number :
- 82070273
- Full Text :
- https://doi.org/10.1111/j.1530-0277.2012.01793.x