Australian Regenerative Medicine Institute, Monash University, Clayton, Victoria 3800, Australia.
J Anat. 2010 Oct;217(4):449-68. doi: 10.1111/j.1469-7580.2010.01275.x. Epub 2010 Aug 17.
The visual cortex comprises over 50 areas in the human, each with a specified role and distinct physiology, connectivity and cellular morphology. How these individual areas emerge during development still remains something of a mystery and, although much attention has been paid to the initial stages of the development of the visual cortex, especially its lamination, very little is known about the mechanisms responsible for the arealization and functional organization of this region of the brain. In recent years we have started to discover that it is the interplay of intrinsic (molecular) and extrinsic (afferent connections) cues that are responsible for the maturation of individual areas, and that there is a spatiotemporal sequence in the maturation of the primary visual cortex (striate cortex, V1) and the multiple extrastriate/association areas. Studies in both humans and non-human primates have started to highlight the specific neural underpinnings responsible for the maturation of the visual cortex, and how experience-dependent plasticity and perturbations to the visual system can impact upon its normal development. Furthermore, damage to specific nuclei of the visual cortex, such as the primary visual cortex (V1), is a common occurrence as a result of a stroke, neurotrauma, disease or hypoxia in both neonates and adults alike. However, the consequences of a focal injury differ between the immature and adult brain, with the immature brain demonstrating a higher level of functional resilience. With better techniques for examining specific molecular and connectional changes, we are now starting to uncover the mechanisms responsible for the increased neural plasticity that leads to significant recovery following injury during this early phase of life. Further advances in our understanding of postnatal development/maturation and plasticity observed during early life could offer new strategies to improve outcomes by recapitulating aspects of the developmental program in the adult brain.
人类的视觉皮层包含 50 多个区域,每个区域都有特定的作用和独特的生理学、连接和细胞形态。这些单个区域如何在发育过程中出现仍然是一个谜,尽管人们对视觉皮层的初始发育阶段,特别是其分层结构,给予了很多关注,但对于负责大脑这一区域的区域化和功能组织的机制却知之甚少。近年来,我们开始发现,正是内在(分子)和外在(传入连接)线索的相互作用,导致了各个区域的成熟,并且初级视觉皮层(纹状皮层,V1)和多个外纹状体/联合区域的成熟存在时空顺序。在人类和非人类灵长类动物中的研究已经开始强调负责视觉皮层成熟的特定神经基础,以及经验依赖性可塑性和对视觉系统的干扰如何影响其正常发育。此外,由于中风、神经创伤、疾病或缺氧,特定的视觉皮层核(如初级视觉皮层(V1))的损伤在新生儿和成年人中都很常见。然而,局灶性损伤的后果在未成熟和成年大脑之间存在差异,未成熟大脑表现出更高水平的功能弹性。随着检查特定分子和连接变化的技术的改进,我们现在开始揭示导致在生命早期受伤后显著恢复的增加的神经可塑性的机制。对出生后发育/成熟和可塑性的进一步了解,以及在生命早期观察到的可塑性,可以提供新的策略,通过在成年大脑中重现发育计划的某些方面来提高结果。