Department of Cell Modulation, Institute of Molecular Embryology and Genetics, Kumamoto University, Kumamoto 860-0811, Japan.
Department of Mental Disorder Research, National Institute of Neuroscience, National Center of Neurology and Psychiatry (NCNP), Tokyo 187-8551, Japan.
Int J Mol Sci. 2018 Nov 19;19(11):3650. doi: 10.3390/ijms19113650.
It is well known that brain-derived neurotrophic factor, BDNF, has an important role in a variety of neuronal aspects, such as differentiation, maturation, and synaptic function in the central nervous system (CNS). BDNF stimulates mitogen-activated protein kinase/extracellular signal-regulated kinase (MAPK/ERK), phosphoinositide-3kinase (PI3K), and phospholipase C (PLC)-gamma pathways via activation of tropomyosin receptor kinase B (TrkB), a high affinity receptor for BDNF. Evidence has shown significant contributions of these signaling pathways in neurogenesis and synaptic plasticity in in vivo and in vitro experiments. Importantly, it has been demonstrated that dysfunction of the BDNF/TrkB system is involved in the onset of brain diseases, including neurodegenerative and psychiatric disorders. In this review, we discuss actions of BDNF and related signaling molecules on CNS neurons, and their contributions to the pathophysiology of brain diseases.
众所周知,脑源性神经营养因子(BDNF)在中枢神经系统(CNS)中的多种神经元方面具有重要作用,例如分化、成熟和突触功能。BDNF 通过激活其高亲和力受体 tropomyosin receptor kinase B(TrkB),刺激丝裂原活化蛋白激酶/细胞外信号调节激酶(MAPK/ERK)、磷酸肌醇-3-激酶(PI3K)和磷脂酶 C(PLC)-γ途径。有证据表明,这些信号通路在体内和体外实验中的神经发生和突触可塑性中具有重要贡献。重要的是,已经证明 BDNF/TrkB 系统的功能障碍与包括神经退行性和精神疾病在内的脑部疾病的发生有关。在这篇综述中,我们讨论了 BDNF 及其相关信号分子对 CNS 神经元的作用,以及它们对脑部疾病病理生理学的贡献。