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The Developing Aging Neocortex: How Genetics and Epigenetics Influence Early Developmental Patterning and Age-Related Change

机译:发育中老化的新皮层:遗传学和表观遗传学如何影响早期发育模式和与年龄有关的变化

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摘要

A hallmark of mammalian development is the generation of functional subdivisions within the nervous system. In humans, this regionalization creates a complex system that regulates behavior, cognition, memory, and emotion. During development, specification of neocortical tissue that leads to functional sensory and motor regions results from an interplay between cortically intrinsic, molecular processes, such as gene expression, and extrinsic processes regulated by sensory input. Cortical specification in mice occurs pre- and perinatally, when gene expression is robust and various anatomical distinctions are observed alongside an emergence of physiological function. After patterning, gene expression continues to shift and axonal connections mature into an adult form. The function of adult cortical gene expression may be to maintain neocortical subdivisions that were established during early patterning. As some changes in neocortical gene expression have been observed past early development into late adulthood, gene expression may also play a role in the altered neocortical function observed in age-related cognitive decline and brain dysfunction. This review provides a discussion of how neocortical gene expression and specific patterns of neocortical sensori-motor axonal connections develop and change throughout the lifespan of the animal. We posit that a role of neocortical gene expression in neocortex is to regulate plasticity mechanisms that impact critical periods for sensory and motor plasticity in aging. We describe results from several studies in aging brain that detail changes in gene expression that may relate to microstructural changes observed in brain anatomy. We discuss the role of altered glucocorticoid signaling in age-related cognitive and functional decline, as well as how aging in the brain may result from immune system activation. We describe how caloric restriction or reduction of oxidative stress may ameliorate effects of aging on the brain.
机译:哺乳动物发育的标志是神经系统内功能细分的产生。在人类中,这种区域划分创建了一个复杂的系统,该系统调节行为,认知,记忆和情感。在发育过程中,导致功能性感觉和运动区域的新皮质组织的规范是由皮质内在的,分子的过程(如基因表达)和由感觉输入调节的外在过程之间的相互作用产生的。当基因表达稳定并且在生理功能出现的同时观察到各种解剖学区别时,小鼠的皮质规格会发生在产前和围产期。图案化后,基因表达继续移动,轴突连接成熟为成年形式。成人皮层基因表达的功能可能是维持在早期模式化过程中建立的新皮层细分。由于已经观察到新皮质基因表达的一些变化已经超过早期发展到成年后期,因此基因表达也可能在与年龄有关的认知下降和脑功能障碍中观察到的新皮质功能改变中起作用。这篇综述提供了关于在整个动物寿命中新皮质基因表达和新皮质感觉运动轴突连接的特定模式是如何发展和变化的讨论。我们认为,新皮质基因表达在新皮质中的作用是调节可塑性机制,该机制影响衰老过程中感觉和运动可塑性的关键时期。我们描述了一些关于大脑老化的研究的结果,这些研究详述了基因表达的变化,该变化可能与在大脑解剖结构中观察到的微结构变化有关。我们讨论了糖皮质激素信号转导在与年龄有关的认知和功能下降中的作用,以及免疫系统激活如何导致脑部衰老。我们描述了热量限制或氧化应激的减少如何改善衰老对大脑的影响。

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