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不同的靶点特异性机制通过稳态调节使突触前和突触后区室的传递稳定。

Distinct Target-Specific Mechanisms Homeostatically Stabilize Transmission at Pre- and Post-synaptic Compartments.

作者信息

Goel Pragya, Nishimura Samantha, Chetlapalli Karthik, Li Xiling, Chen Catherine, Dickman Dion

机构信息

Department of Neurobiology, University of Southern California, Los Angeles, CA, United States.

出版信息

Front Cell Neurosci. 2020 Jun 26;14:196. doi: 10.3389/fncel.2020.00196. eCollection 2020.

Abstract

Neurons must establish and stabilize connections made with diverse targets, each with distinct demands and functional characteristics. At neuromuscular junctions (NMJs), synaptic strength remains stable in a manipulation that simultaneously induces hypo-innervation on one target and hyper-innervation on the other. However, the expression mechanisms that achieve this exquisite target-specific homeostatic control remain enigmatic. Here, we identify the distinct target-specific homeostatic expression mechanisms. On the hypo-innervated target, an increase in postsynaptic glutamate receptor (GluR) abundance is sufficient to compensate for reduced innervation, without any apparent presynaptic adaptations. In contrast, a target-specific reduction in presynaptic neurotransmitter release probability is reflected by a decrease in active zone components restricted to terminals of hyper-innervated targets. Finally, loss of postsynaptic GluRs on one target induces a compartmentalized, homeostatic enhancement of presynaptic neurotransmitter release called presynaptic homeostatic potentiation (PHP) that can be precisely balanced with the adaptations required for both hypo- and hyper-innervation to maintain stable synaptic strength. Thus, distinct anterograde and retrograde signaling systems operate at pre- and post-synaptic compartments to enable target-specific, homeostatic control of neurotransmission.

摘要

神经元必须建立并稳定与各种不同靶标的连接,每个靶标都有独特的需求和功能特征。在神经肌肉接头(NMJ)处,当同时对一个靶标诱导低神经支配而对另一个靶标诱导高神经支配时,突触强度仍保持稳定。然而,实现这种精确的靶标特异性稳态控制的表达机制仍然是个谜。在这里,我们确定了不同的靶标特异性稳态表达机制。在低神经支配的靶标上,突触后谷氨酸受体(GluR)丰度的增加足以补偿神经支配的减少,而没有任何明显的突触前适应性变化。相反,突触前神经递质释放概率的靶标特异性降低表现为活性区成分的减少,且仅限于高神经支配靶标的终末。最后,一个靶标上突触后GluR的缺失会诱导一种局部化的、突触前神经递质释放的稳态增强,称为突触前稳态增强(PHP),它可以与低神经支配和高神经支配所需的适应性变化精确平衡,以维持稳定的突触强度。因此,不同的顺行和逆行信号系统在突触前和突触后区室发挥作用,以实现对神经传递的靶标特异性稳态控制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1f28/7333441/c9b43bd93aaf/fncel-14-00196-g0001.jpg

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