Laminar and Dorsoventral Molecular Organization of the Medial Entorhinal Cortex Revealed by Large-scale Anatomical Analysis of Gene Expression

被引:42
作者
Ramsden, Helen L. [1 ,2 ]
Suermeli, Guelsen [1 ]
McDonagh, Steven G. [3 ]
Nolan, Matthew F. [1 ,4 ]
机构
[1] Univ Edinburgh, Ctr Integrat Physiol, Edinburgh, Midlothian, Scotland
[2] Univ Edinburgh, Sch Informat, Neuroinformat Doctoral Training Ctr, Edinburgh, Midlothian, Scotland
[3] Univ Edinburgh, Inst Percept Act & Behav, Sch Informat, Edinburgh, Midlothian, Scotland
[4] inStem, Ctr Brain Dev & Repair, Bangalore, Karnataka, India
基金
英国生物技术与生命科学研究理事会; 英国惠康基金; 英国工程与自然科学研究理事会;
关键词
PREFERENTIAL NEURONAL LOSS; GENOME-WIDE ASSOCIATION; LAYER V NEURONS; GRID CELLS; ELECTROPHYSIOLOGICAL CHARACTERISTICS; PARAHIPPOCAMPAL REGION; IDENTIFIES VARIANTS; PYRAMIDAL NEURONS; MOUSE-BRAIN; ADULT;
D O I
10.1371/journal.pcbi.1004032
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Neural circuits in the medial entorhinal cortex (MEC) encode an animal's position and orientation in space. Within the MEC spatial representations, including grid and directional firing fields, have a laminar and dorsoventral organization that corresponds to a similar topography of neuronal connectivity and cellular properties. Yet, in part due to the challenges of integrating anatomical data at the resolution of cortical layers and borders, we know little about the molecular components underlying this organization. To address this we develop a new computational pipeline for high-throughput analysis and comparison of in situ hybridization (ISH) images at laminar resolution. We apply this pipeline to ISH data for over 16,000 genes in the Allen Brain Atlas and validate our analysis with RNA sequencing of MEC tissue from adult mice. We find that differential gene expression delineates the borders of the MEC with neighboring brain structures and reveals its laminar and dorsoventral organization. We propose a new molecular basis for distinguishing the deep layers of the MEC and show that their similarity to corresponding layers of neocortex is greater than that of superficial layers. Our analysis identifies ion channel-, cell adhesion-and synapse-related genes as candidates for functional differentiation of MEC layers and for encoding of spatial information at different scales along the dorsoventral axis of the MEC. We also reveal laminar organization of genes related to disease pathology and suggest that a high metabolic demand predisposes layer II to neurodegenerative pathology. In principle, our computational pipeline can be applied to high-throughput analysis of many forms of neuro-anatomical data. Our results support the hypothesis that differences in gene expression contribute to functional specialization of superficial layers of the MEC and dorsoventral organization of the scale of spatial representations.
引用
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页数:38
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