Jackson Travis C, Foster Thomas C
Department of Neuroscience, McKnight Brain Institute, University of Florida, P.O. Box 100244, Gainesville, FL 32610-0244, USA.
Biosci Hypotheses. 2009 Jun 8;2(4):245-251. doi: 10.1016/j.bihy.2009.02.013.
The hippocampus is especially vulnerable to damage caused by metabolic dysregulation. However distinct sub-regions within the hippocampus differ by their relative susceptibility to such damage. Region CA1 pyramidal neurons are most sensitive to metabolic perturbations while region CA3 pyramidal neurons show more resistance, and these unique profiles of susceptibility are but one example that differentiates CA1/CA3 neurons. We present here a hypothesis that inextricably links the unique biochemistries of learning and memory in region CA1, to that of cell survival signaling, and in so doing, suggest an explanation for region CA1 susceptibility to metabolic dysfunction. Further, we propose a signaling mechanism to explain how both pathways can be simultaneously regulated. Critical to this process is the protein phosphatase PHLPP1. Finally we discuss the implications of this hypothesis and the inherent challenges it poses for treatment of neurological disorders resulting in reduced hippocampal function by increased neuron death.
海马体特别容易受到代谢失调所造成的损伤。然而,海马体内不同的亚区域对这种损伤的相对易感性有所不同。CA1区的锥体神经元对代谢紊乱最为敏感,而CA3区的锥体神经元则表现出更强的抵抗力,这些独特的易感性特征只是区分CA1/CA3神经元的一个例子。我们在此提出一个假说,该假说将CA1区学习和记忆的独特生物化学与细胞存活信号紧密联系起来,并借此为CA1区对代谢功能障碍的易感性提供一种解释。此外,我们提出一种信号传导机制来解释这两条途径如何能够同时受到调节。这一过程的关键是蛋白磷酸酶PHLPP1。最后,我们讨论了这一假说的意义以及它对治疗因神经元死亡增加而导致海马体功能减退的神经系统疾病所带来的内在挑战。