Singh-Taylor Akanksha, Korosi Aniko, Molet Jenny, Gunn Benjamin G, Baram Tallie Z
Departments of Pediatrics, University of California-Irvine, Irvine, CA 92697-4475, USA.
Swammerdam Institute for Life Sciences, University of Amsterdam, Science Park 904, 1098 XH Amsterdam. The Netherlands.
Neurobiol Stress. 2015 Jan 1;1:109-115. doi: 10.1016/j.ynstr.2014.10.007.
Genes and environment interact to influence cognitive and emotional functions throughout life. Early-life experiences in particular contribute to vulnerability or resilience to a number of emotional and cognitive illnesses in humans. In rodents, early-life experiences directly lead to resilience or vulnerability to stress later in life, and influence the development of cognitive and emotional deficits. The mechanisms for the enduring effects of early-life experiences on cognitive and emotional outcomes are not completely understood. Here, we present emerging information supporting experience-dependent modulation of the number and efficacy of synaptic inputs onto stress-sensitive neurons. This synaptic 'rewiring', in turn, may influence the expression of crucial neuronal genes. The persistent changes in gene expression in resilient versus vulnerable rodent models are likely maintained via epigenetic mechanisms. Thus, early-life experience may generate resilience by altering synaptic input to neurons, which informs them to modulate their epigenetic machinery.
基因与环境相互作用,在整个生命过程中影响认知和情感功能。尤其是早年经历会导致人类对多种情感和认知疾病的易感性或恢复力。在啮齿动物中,早年经历直接导致其成年后对应激的恢复力或易感性,并影响认知和情感缺陷的发展。早年经历对认知和情感结果产生持久影响的机制尚未完全明了。在此,我们展示了新出现的信息,这些信息支持依赖于经验对压力敏感神经元突触输入的数量和效能进行调节。这种突触“重新布线”进而可能影响关键神经元基因的表达。在有恢复力和易受影响的啮齿动物模型中,基因表达的持续变化可能通过表观遗传机制得以维持。因此,早年经历可能通过改变神经元的突触输入来产生恢复力,而这会促使神经元调节其表观遗传机制。