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Gliotransmission: Beyond Black-and-White

机译:Gliotransmission:超越黑白

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Astrocytes are highly complex cells with many emerging putative roles in brain function. Of these, gliotransmission (active information transfer from glia to neurons) has probably the widest implications on our understanding of how the brain works: do astrocytes really contribute to information processing within the neural circuitry? “Positive evidence” for this stems from work of multiple laboratories reporting many examples of modulatory chemical signaling from astrocytes to neurons in the timeframe of hundreds of milliseconds to several minutes. This signaling involves, but is not limited to, Ca2+-dependent vesicular transmitter release, and results in a variety of regulatory effects at synapses in many circuits that are abolished by preventing Ca2+ elevations or blocking exocytosis selectively in astrocytes. In striking contradiction, methodologically advanced studies by a few laboratories produced “negative evidence,” triggering a heated debate on the actual existence and properties of gliotransmission. In this context, a skeptics' camp arose, eager to dismiss the whole positive evidence based on a number of assumptions behind the negative data, such as the following: (1) deleting a single Ca2+ release pathway (IP3R2) removes all the sources for Ca2+-dependent gliotransmission; (2) stimulating a transgenically expressed Gq-GPCR (MrgA1) mimics the physiological Ca2+ signaling underlying gliotransmitter release; (3) age-dependent downregulation of an endogenous GPCR (mGluR5) questions gliotransmitter release in adulthood; and (4) failure by transcriptome analysis to detect vGluts or canonical synaptic SNAREs in astrocytes proves inexistence/functional irrelevance of vesicular gliotransmitter release. We here discuss how the above assumptions are likely wrong and oversimplistic. In light of the most recent literature, we argue that gliotransmission is a more complex phenomenon than originally thought, possibly consisting of multiple forms and signaling processes, whose correct study and understanding require more sophisticated tools and finer scientific experiments than done until today. Under this perspective, the opposing camps can be reconciled and the field moved forward. Along the path, a more cautious mindset and an attitude to open discussion and mutual respect between opponent laboratories will be good companions.>Dual Perspectives Companion Paper:
机译:星形胶质细胞是高度复杂的细胞,在脑功能中具有许多新兴的假定作用。其中,神经胶质传输(从神经胶质到神经元的主动信息传递)可能对我们对大脑工作原理的理解具有最广泛的影响:星形胶质细胞确实对神经回路内的信息处理有作用吗?对此的“积极证据”来自多个实验室的工作,这些实验室报告了数百毫秒到几分钟时间范围内从星形胶质细胞到神经元的调节化学信号的许多例子。该信号传导涉及但不限于依赖Ca 2 + 的囊泡递质释放,并导致许多电路突触中的多种调节作用,这些作用通过预防Ca 2+而被取消。 升高或选择性阻断星形胶质细胞的胞吐作用。在相互矛盾的过程中,一些实验室在方法论上的先进研究产生了“负面证据”,引发了关于胶质传输的实际存在和性质的激烈辩论。在这种情况下,一个怀疑论者的阵营兴起,渴望基于负面数据背后的许多假设,驳斥全部积极证据,例如:(1)删除单个Ca 2 + 释放途径(IP3R2)消除了依赖Ca 2 + 的胶质细胞传输的所有来源; (2)刺激转基因表达的Gq-GPCR(MrgA1)模仿生理胶质递质释放的Ca 2 + 信号传导; (3)内源性GPCR(mGluR5)的年龄依赖性下调质疑成年胶质递质的释放; (4)转录组分析未能检测到星形胶质细胞中的vGluts或典型突触小网膜,证明水泡神经胶质递质释放不存在/与功能无关。我们在这里讨论上述假设可能是错误的和过于简单的。根据最新文献,我们认为神经胶质传输是一种比最初想像的更为复杂的现象,可能由多种形式和信号传导过程组成,其正确的研究和理解需要比今天更多的尖端工具和更精细的科学实验。在这种观点下,对立的阵营可以和解,田野可以向前推进。沿着这条道路,更加谨慎的心态以及在反对者实验室之间进行公开讨论和相互尊重的态度将是很好的伴侣。> Dual Perspectives Companion Paper:

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