Vanacore Giada, Christensen Jens Bager, Bayin N Sumru
Gurdon Institute, University of Cambridge, Cambridge, U.K.
Department of Physiology, Development and Neuroscience, University of Cambridge, Cambridge, U.K.
Biochem Soc Trans. 2024 Dec 19;52(6):2243-2252. doi: 10.1042/BST20230547.
Repairing the adult mammalian brain represents one of the greatest clinical challenges in medicine. Injury to the adult brain often results in substantial loss of neural tissue and permanent functional impairment. In contrast with the adult, during development, the mammalian brain exhibits a remarkable capacity to replace lost cells. A plethora of cell-intrinsic and extrinsic factors regulate the age-dependent loss of regenerative potential in the brain. As the developmental window closes, neural stem cells undergo epigenetic changes, limiting their proliferation and differentiation capacities, whereas, changes in the brain microenvironment pose additional challenges opposing regeneration, including inflammation and gliosis. Therefore, studying the regenerative mechanisms during development and identifying what impairs them with age may provide key insights into how to stimulate regeneration in the brain. Here, we will discuss how the mammalian brain engages regenerative mechanisms upon injury or neuron loss. Moreover, we will describe the age-dependent changes that affect these processes. We will conclude by discussing potential therapeutic approaches to overcome the age-dependent regenerative decline and stimulate regeneration.
修复成年哺乳动物的大脑是医学领域最重大的临床挑战之一。成年大脑损伤往往会导致大量神经组织丧失和永久性功能障碍。与成年期不同,在发育过程中,哺乳动物的大脑具有显著的替代丢失细胞的能力。大量细胞内在和外在因素调节大脑中与年龄相关的再生潜能丧失。随着发育窗口关闭,神经干细胞会发生表观遗传变化,限制其增殖和分化能力,而大脑微环境的变化对再生构成了额外挑战,包括炎症和胶质增生。因此,研究发育过程中的再生机制并确定衰老过程中哪些因素会损害这些机制,可能为如何刺激大脑再生提供关键见解。在此,我们将讨论哺乳动物大脑在损伤或神经元丢失时如何启动再生机制。此外,我们将描述影响这些过程的与年龄相关的变化。我们将通过讨论克服与年龄相关的再生衰退并刺激再生的潜在治疗方法来结束本文。