Center for Developmental Genetics and Department of Anesthesiology, Stony Brook University, Stony Brook, NY, United States; Moscow Institute of Physics and Technology, Moscow, Russia; P.K. Anokhin Institute for Normal Physiology, Moscow, Russia.
Center for Developmental Genetics and Department of Anesthesiology, Stony Brook University, Stony Brook, NY, United States; Koltzov Institute of Developmental Biology, Moscow, Russia.
Behav Brain Res. 2019 Nov 18;374:112118. doi: 10.1016/j.bbr.2019.112118. Epub 2019 Jul 29.
Hippocampal neurogenesis presents an unorthodox form of neuronal plasticity and may be relevant for the normal or abnormal functioning of the human and animal brain. As production of new neurons decreases after birth, purposefully activating stem cells to create additional new neurons may augment brain function or slow a disease's progression. Here, we describe current models of hippocampal stem cell maintenance and differentiation, and emphasize key features of neural stem cells' turnover that may define hippocampal neurogenesis enhancement attempts' long-term consequences. We argue that even the basic blueprint of how stem cells are maintained, divide, differentiate, and are eliminated is still contentious, with different models potentially leading to vastly different outcomes in regard to neuronal production and stem cell pool preservation. We propose that to manipulate neurogenesis for a long-term benefit, we must first understand the outline of the neural stem cells' lifecycle.
海马体神经发生呈现出一种非传统的神经元可塑性形式,可能与人和动物大脑的正常或异常功能有关。由于出生后新神经元的产生减少,有目的地激活干细胞以产生额外的新神经元可能会增强大脑功能或减缓疾病的进展。在这里,我们描述了海马体干细胞维持和分化的当前模型,并强调了神经干细胞更替的关键特征,这些特征可能定义了海马体神经发生增强尝试的长期后果。我们认为,即使是干细胞如何维持、分裂、分化和消除的基本蓝图仍然存在争议,不同的模型可能会导致神经元产生和干细胞池保存方面的结果大相径庭。我们提出,为了获得长期的益处而进行神经发生的操作,我们必须首先了解神经干细胞生命周期的大致轮廓。