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ERK-FosB signaling in dorsal MPOA neurons plays a major role in the initiation of parental behavior in mice

机译:背侧MPOA神经元中的ERK-FosB信号传导在小鼠父母行为的启动中起主要作用

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During mouse parental behavior, neurons in the dorsal medial preoptic area (MPOAd) are activated and express transcription factors such as c-Fos and FosB. FosB-knockout mice are reported to be defective in parental care. To clarify molecular signaling responsible for parental behavior, we investigated gene expression profiles in the MPOAd of parental versus nonparental mice. We identified upregulation of NGFI-B, SPRY1, and Rad in parental mice, together with c-Fos and FosB. A common inducer of these genes, the extracellular signal regulated kinase (ERK) was phosphorylated in MPOAd neurons upon pup exposure. Pharmacological blockade of ERK phosphorylation inhibited the FosB upregulation in MPOAd, and the initiation of pup retrieving in virgin female mice, but did not affect the established parenting in parous females. Furthermore, induction of SPRY1 and Rad was impaired in MPOAd of nonparental FosB-knockout mice. These results suggest the pivotal role of ERK-FosB signaling in the initiation of parental care. (c) 2007 Elsevier Inc. All rights reserved.
机译:在小鼠父母行为期间,后内侧视前区(MPOAd)中的神经元被激活并表达转录因子,例如c-Fos和FosB。据报道,FosB基因敲除小鼠在父母照护方面存在缺陷。为了阐明负责父母行为的分子信号传导,我们研究了父母与非父母小鼠MPOAd中的基因表达谱。我们在c-Fos和FosB亲本小鼠中鉴定了NGFI-B,SPRY1和Rad的上调。这些基因的常见诱导物,幼鼠暴露后MPOAd神经元中的细胞外信号调节激酶(ERK)被磷酸化。药理学上的ERK磷酸化抑制作用抑制了MPOAd中FosB的上调,并抑制了处女雌性小鼠的幼仔恢复,但并没有影响已成年雌性的成年育儿。此外,在非亲代FosB敲除小鼠的MPOAd中,对SPRY1和Rad的诱导被削弱。这些结果表明,ERK-FosB信号传导在父母监护中起着关键作用。 (c)2007 Elsevier Inc.保留所有权利。

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