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齿状回颗粒细胞的树突通过控制稀疏性来促进模式分离。

Dendrites of dentate gyrus granule cells contribute to pattern separation by controlling sparsity.

作者信息

Chavlis Spyridon, Petrantonakis Panagiotis C, Poirazi Panayiota

机构信息

Institute of Molecular Biology and Biotechnology (IMBB), Foundation for Research and Technology, Hellas (FORTH), Heraklion, Crete, Greece.

Department of Biology, School of Sciences and Engineering, University of Crete, Heraklion, Crete, Greece.

出版信息

Hippocampus. 2017 Jan;27(1):89-110. doi: 10.1002/hipo.22675. Epub 2016 Nov 10.

DOI:10.1002/hipo.22675
PMID:27784124
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5217096/
Abstract

The hippocampus plays a key role in pattern separation, the process of transforming similar incoming information to highly dissimilar, nonverlapping representations. Sparse firing granule cells (GCs) in the dentate gyrus (DG) have been proposed to undertake this computation, but little is known about which of their properties influence pattern separation. Dendritic atrophy has been reported in diseases associated with pattern separation deficits, suggesting a possible role for dendrites in this phenomenon. To investigate whether and how the dendrites of GCs contribute to pattern separation, we build a simplified, biologically relevant, computational model of the DG. Our model suggests that the presence of GC dendrites is associated with high pattern separation efficiency while their atrophy leads to increased excitability and performance impairments. These impairments can be rescued by restoring GC sparsity to control levels through various manipulations. We predict that dendrites contribute to pattern separation as a mechanism for controlling sparsity. © 2016 The Authors Hippocampus Published by Wiley Periodicals, Inc.

摘要

海马体在模式分离中起着关键作用,模式分离是将相似的传入信息转化为高度不同、不重叠表征的过程。齿状回(DG)中稀疏放电的颗粒细胞(GCs)被认为承担了这种计算,但对于它们的哪些特性影响模式分离却知之甚少。在与模式分离缺陷相关的疾病中已报道有树突萎缩,这表明树突在这一现象中可能发挥作用。为了研究GCs的树突是否以及如何对模式分离做出贡献,我们构建了一个简化的、具有生物学相关性的DG计算模型。我们的模型表明,GCs树突的存在与高模式分离效率相关,而其萎缩会导致兴奋性增加和性能受损。通过各种操作将GCs的稀疏性恢复到控制水平,可以挽救这些损伤。我们预测,树突作为控制稀疏性的一种机制,对模式分离有贡献。© 2016作者 海马体 由威利期刊公司出版

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0129/5217096/27bafea25231/HIPO-27-89-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0129/5217096/a6913fcde047/HIPO-27-89-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0129/5217096/b94b3ed3cee5/HIPO-27-89-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0129/5217096/5b3b835d83f3/HIPO-27-89-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0129/5217096/6f13f844ea61/HIPO-27-89-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0129/5217096/38a84295fa3f/HIPO-27-89-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0129/5217096/10540c1956e2/HIPO-27-89-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0129/5217096/6084d01c4a45/HIPO-27-89-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0129/5217096/aedaaa286f78/HIPO-27-89-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0129/5217096/27bafea25231/HIPO-27-89-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0129/5217096/a6913fcde047/HIPO-27-89-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0129/5217096/b94b3ed3cee5/HIPO-27-89-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0129/5217096/5b3b835d83f3/HIPO-27-89-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0129/5217096/6f13f844ea61/HIPO-27-89-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0129/5217096/38a84295fa3f/HIPO-27-89-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0129/5217096/10540c1956e2/HIPO-27-89-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0129/5217096/6084d01c4a45/HIPO-27-89-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0129/5217096/aedaaa286f78/HIPO-27-89-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0129/5217096/27bafea25231/HIPO-27-89-g009.jpg

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