De Vincenti Ana Paula, Ríos Antonella S, Paratcha Gustavo, Ledda Fernanda
División de Neurociencia Molecular y Celular, Instituto de Biología Celular y Neurociencias, Universidad de Buenos Aires, CONICET, Buenos Aires, Argentina.
Fundación Instituto Leloir, Instituto de Investigaciones Bioquímicas de Buenos Aires, CONICET, Buenos Aires, Argentina.
Front Cell Neurosci. 2019 Apr 9;13:135. doi: 10.3389/fncel.2019.00135. eCollection 2019.
Brain-derived neurotrophic factor (BDNF) is a neurotrophin that has pleiotropic effects on neuronal morphology and synaptic plasticity that underlie hippocampal circuit development and cognition. Recent advances established that BDNF function is controlled and diversified by molecular and cellular mechanisms including trafficking and subcellular compartmentalization of different mRNA species, pre- vs. postsynaptic release of BDNF, control of BDNF signaling by tropomyosin receptor kinase B (TrkB) receptor interactors and conversion of pro-BDNF to mature BDNF and BDNF-propeptide. Defects in these regulatory mechanisms affect dendritic spine formation and morphology of pyramidal neurons as well as synaptic integration of newborn granule cells (GCs) into preexisting circuits of mature hippocampus, compromising the cognitive function. Here, we review recent findings describing novel dynamic mechanisms that diversify and locally control the function of BDNF in hippocampal neurons.
脑源性神经营养因子(BDNF)是一种神经营养因子,对神经元形态和突触可塑性具有多效性作用,这些作用构成了海马回路发育和认知的基础。最近的进展表明,BDNF的功能受到分子和细胞机制的控制和多样化,这些机制包括不同mRNA种类的运输和亚细胞区室化、BDNF的突触前与突触后释放、原肌球蛋白受体激酶B(TrkB)受体相互作用物对BDNF信号传导的控制以及前体BDNF向成熟BDNF和BDNF前肽的转化。这些调节机制的缺陷会影响锥体神经元的树突棘形成和形态,以及新生颗粒细胞(GCs)与成熟海马体现有回路的突触整合,从而损害认知功能。在这里,我们回顾了最近的研究发现,这些发现描述了使BDNF在海马神经元中的功能多样化并进行局部控制的新型动态机制。