Giorgi Corinna, Marinelli Silvia
CNR, Institute of Molecular Biology and Pathology, Rome, Italy.
European Brain Research Institute (EBRI), Fondazione Rita Levi-Montalcini, Rome, Italy.
Front Mol Neurosci. 2021 Jun 15;14:689952. doi: 10.3389/fnmol.2021.689952. eCollection 2021.
Increasing evidence supports a model whereby memories are encoded by sparse ensembles of neurons called engrams, activated during memory encoding and reactivated upon recall. An engram consists of a network of cells that undergo long-lasting modifications of their transcriptional programs and connectivity. Ground-breaking advancements in this field have been made possible by the creative exploitation of the characteristic transcriptional responses of neurons to activity, allowing both engram labeling and manipulation. Nevertheless, numerous aspects of engram cell-type composition and function remain to be addressed. As recent transcriptomic studies have revealed, memory encoding induces persistent transcriptional and functional changes in a plethora of neuronal subtypes and non-neuronal cells, including glutamatergic excitatory neurons, GABAergic inhibitory neurons, and glia cells. Dissecting the contribution of these different cellular classes to memory engram formation and activity is quite a challenging yet essential endeavor. In this review, we focus on the role played by the GABAergic inhibitory component of the engram through two complementary lenses. On one hand, we report on available physiological evidence addressing the involvement of inhibitory neurons to different stages of memory formation, consolidation, storage and recall. On the other, we capitalize on a growing number of transcriptomic studies that profile the transcriptional response of inhibitory neurons to activity, revealing important clues on their potential involvement in learning and memory processes. The picture that emerges suggests that inhibitory neurons are an essential component of the engram, likely involved in engram allocation, in tuning engram excitation and in storing the memory trace.
越来越多的证据支持这样一种模型,即记忆由称为记忆印迹的稀疏神经元集合编码,在记忆编码过程中被激活,并在回忆时重新激活。记忆印迹由一组细胞网络组成,这些细胞的转录程序和连接性会发生持久的改变。通过创造性地利用神经元对活动的特征性转录反应,该领域取得了突破性进展,这使得记忆印迹的标记和操纵成为可能。然而,记忆印迹细胞类型的组成和功能的许多方面仍有待解决。正如最近的转录组学研究所揭示的,记忆编码会在大量神经元亚型和非神经元细胞中诱导持续的转录和功能变化,包括谷氨酸能兴奋性神经元、γ-氨基丁酸能抑制性神经元和神经胶质细胞。剖析这些不同细胞类别对记忆印迹形成和活动的贡献是一项极具挑战性但又至关重要的工作。在这篇综述中,我们通过两个互补的视角聚焦于记忆印迹中γ-氨基丁酸能抑制成分所起的作用。一方面,我们报告了现有的生理学证据,这些证据涉及抑制性神经元在记忆形成、巩固、存储和回忆的不同阶段的参与情况。另一方面,我们利用越来越多的转录组学研究,这些研究描绘了抑制性神经元对活动的转录反应,揭示了它们在学习和记忆过程中潜在参与的重要线索。出现的情况表明,抑制性神经元是记忆印迹的重要组成部分,可能参与记忆印迹的分配、调节记忆印迹的兴奋性以及存储记忆痕迹。