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稳态信号传导:负反馈的积极一面。

Homeostatic signaling: the positive side of negative feedback.

作者信息

Turrigiano Gina

机构信息

Brandeis University Department of Biology, MS08 and Center for Behavioral Genomics, 415 South Street, Waltham, MA 02454, USA.

出版信息

Curr Opin Neurobiol. 2007 Jun;17(3):318-24. doi: 10.1016/j.conb.2007.04.004. Epub 2007 Apr 23.

Abstract

Synaptic homeostasis provides a means for neurons and circuits to maintain stable function in the face of perturbations such as developmental or activity-dependent changes in synapse number or strength. These forms of plasticity are thought to utilize negative feedback signaling to sense some aspect of activity, compare this with an internal set point, and then adjust synaptic properties to keep activity close to this set point. However, the molecular identity of these signaling components has not been firmly established. Recent work suggests that there are likely to be multiple forms of synaptic homeostasis, mediated by distinct signaling pathways and with distinct expression mechanisms. These include presynaptic forms that depend on retrograde signaling to presynaptic Ca(2+) channels, and postsynaptic forms influenced by BDNF, TNFalpha and Arc signaling. Current challenges include matching signaling elements to their functions (i.e. as detectors of activity, as part of the set-point mechanism and/or as effectors of synaptic change), and fitting these molecular candidates into a unified view of the signaling pathways that underlie synaptic homeostasis.

摘要

突触稳态为神经元和神经回路提供了一种手段,使其在面对诸如发育或活动依赖的突触数量或强度变化等扰动时,仍能维持稳定的功能。这些可塑性形式被认为利用负反馈信号来感知活动的某些方面,将其与内部设定点进行比较,然后调整突触特性以使活动接近该设定点。然而,这些信号成分的分子身份尚未得到确凿证实。最近的研究表明,可能存在多种形式的突触稳态,由不同的信号通路介导并具有不同的表达机制。这些包括依赖逆行信号至突触前Ca(2+)通道的突触前形式,以及受脑源性神经营养因子(BDNF)、肿瘤坏死因子α(TNFalpha)和Arc信号影响的突触后形式。当前的挑战包括将信号元件与其功能相匹配(即作为活动的检测器、作为设定点机制的一部分和/或作为突触变化的效应器),以及将这些分子候选物纳入构成突触稳态基础的信号通路的统一观点中。

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