Varela-Nieto Isabel, de la Rosa Enrique J, Valenciano Ana I, León Yolanda
Instituto de Investigaciones Biomédicas "Alberto Sols," Consejo Superior de Investigaciones Científicas-Universidad Autónoma de Madrid (CSIC-UAM), Arturo Duperier 4, E-28029 Madrid, Spain.
Mol Neurobiol. 2003 Aug;28(1):23-50. doi: 10.1385/MN:28:1:23.
Programmed cell death is an essential process for proper neural development. Cell death, with its similar regulatory and executory mechanisms, also contributes to the origin or progression of many or even all neurodegenerative diseases. An understanding of the mechanisms that regulate cell death during neural development may provide new targets and tools to prevent neurodegeneration. Many studies that have focused mainly on insulin-like growth factor-I (IGF-I), have shown that insulin-related growth factors are widely expressed in the developing and adult nervous system, and positively modulate a number of processes during neural development, as well as in adult neuronal and glial physiology. These factors also show neuroprotective effects following neural damage. Although some specific actions have been demonstrated to be anti-apoptotic, we propose that a broad neuroprotective role is the foundation for many of the observed functions of the insulin-related growth factors, whose therapeutical potential for nervous system disorders may be greater than currently accepted.
程序性细胞死亡是神经正常发育的一个重要过程。细胞死亡具有相似的调节和执行机制,也与许多甚至所有神经退行性疾病的起源或进展有关。了解神经发育过程中调节细胞死亡的机制可能会为预防神经退行性变提供新的靶点和工具。许多主要聚焦于胰岛素样生长因子-I(IGF-I)的研究表明,胰岛素相关生长因子在发育中的和成年神经系统中广泛表达,并在神经发育过程以及成年神经元和神经胶质细胞生理学中对许多过程产生正向调节作用。这些因子在神经损伤后也表现出神经保护作用。尽管已证明一些特定作用具有抗凋亡作用,但我们认为广泛的神经保护作用是胰岛素相关生长因子许多已观察到的功能的基础,其对神经系统疾病的治疗潜力可能比目前所公认的更大。