| Literature DB >> 29444427 |
Yonglu Tian1, Chaojuan Yang2, Yaxuan Cui2, Feng Su3, Yongjie Wang4, Yangzhen Wang5, Peijiang Yuan6, Shujiang Shang2, Hao Li7, Jizong Zhao7, Desheng Zhu2, Shiming Tang2, Peng Cao8, Yunbo Liu9, Xunli Wang10, Liecheng Wang11, Wenbo Zeng12, Haifei Jiang12, Fei Zhao12, Minhua Luo12, Wei Xiong13, Zilong Qiu14, Xiang-Yao Li15, Chen Zhang16.
Abstract
Short-term memory (STM) is crucial for animals to hold information for a small period of time. Persistent or recurrent neural activity, together with neural oscillations, is known to encode the STM at the cellular level. However, the coding mechanisms at the microcircuitry level remain a mystery. Here, we performed two-photon imaging on behaving mice to monitor the activity of neuronal microcircuitry. We discovered a neuronal subpopulation in the medial prefrontal cortex (mPFC) that exhibited emergent properties in a context-dependent manner underlying a STM-like behavior paradigm. These neuronal subpopulations exclusively comprise excitatory neurons and mainly represent a group of neurons with stronger functional connections. Microcircuitry plasticity was maintained for minutes and was absent in an animal model of Alzheimer's disease (AD). Thus, these results point to a functional coding mechanism that relies on the emergent behavior of a functionally defined neuronal assembly to encode STM.Entities:
Keywords: Alzheimer’s disease; microcircuitry; prefrontal cortex; short-term memory
Mesh:
Year: 2018 PMID: 29444427 DOI: 10.1016/j.celrep.2018.01.050
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423