Expression of p53 and ALZ-50 immunoreactivity in rat cortex: Effect of prenatal exposure to ethanol

被引:23
|
作者
Kuhn, PE [1 ]
Miller, MW
机构
[1] Rutgers State Univ, Program Cell & Dev Biol, Piscataway, NJ 08854 USA
[2] Vet Affairs Med Ctr, Res Serv, Iowa City, IA 52246 USA
[3] Univ Iowa, Coll Med, Dept Psychiat, Iowa City, IA 52242 USA
[4] Univ Iowa, Coll Med, Dept Pharmacol, Iowa City, IA 52242 USA
关键词
alcohol; fetal alcohol syndrome; apoptosis; cell death; cerebral cortex;
D O I
10.1006/exnr.1998.6907
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Neuronal death is an active process that results in the upregulation of antigens recognized by ALZ-50 and p53. Since prenatal exposure to ethanol can induce the postnatal death of cortical neurons, we examined the effects of ethanol on the in vivo expression of both the ALZ-50-positive antigen and p53. Pregnant rats were fed one of three diets, a liquid diet containing ethanol (Et), an isocaloric and isonutritive diet (Ct), or chow and water (Ch). Segments of frontoparietal cortex from fetuses and pups were examined for ethanol-induced changes (a) in the expression of ALZ-50 and p53 immunoreactivity using a quantitative immunoblotting assay and (b) in the distribution of ALZ-50- and p53-positive cells using immunohistochemistry. In control rats, ALZ-50 identified a 56-kDa peptide that was transiently expressed postnatally and peak expression occurred on postnatal day (P) 6 to P12. In Et-treated rats, peak expression was attained earlier (on P3) and was about three times of that achieved in the controls. The anti-p53 antibody identified three proteins (28, 56, and 58 kDa). Peak expression in control rats occurred during the second postnatal week and only the 58-kDa protein was expressed in appreciable amounts in adult cortex. Each p53-positive protein was affected by ethanol exposure. The 28- and 56-kDa p53-positive proteins were affected by ethanol much in the same way as was the ALZ-50-positive antigen, That is, the timing and amount of peak expression were earlier and lower, respectively, in the Et-treated rats, The postnatal expression of the 58-kDa protein was halved following prenatal exposure to ethanol. Both ALZ-50 and anti-p53 immunoprecipitated proteins are p53- and ALZ-50-positive, respectively. Thus, ethanol alters the expression of the ALZ-50- and p53-positive proteins and presumably the timing of neuronal death in the developing cortex. The parallel effects of prenatal ethanol exposure on the 56-kDa ALZ-50-positive antigen and the 28- and 56-kDa p53-positive proteins and the coprecipitation of the proteins are consistent with the notion that ALZ-50 recognizes a form of p53. (C) 1998 Academic Press.
引用
收藏
页码:418 / 429
页数:12
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