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Integration of gene expression and brain-wide connectivity reveals the multiscale organization of mouse hippocampal networks

Understanding the organization of the hippocampus is fundamental to understanding brain function related to learning, memory, emotions, and diseases like Alzheimer’s disease. Physiological studies in humans and rodents suggest both structural and functional heterogeneity along the longitudinal axis...

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Autores principales: Bienkowski, Michael S., Bowman, Ian, Song, Monica Y., Gou, Lin, Ard, Tyler, Cotter, K., Zhu, Muye, Benavidez, Nora L., Yamashita, Seita, Abu-Jaber, Jaspar, Azam, Sana, Lo, Darrick, Foster, Nicholas N., Hintiryan, Houri, Dong, Hong-Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6398347/
https://www.ncbi.nlm.nih.gov/pubmed/30297807
http://dx.doi.org/10.1038/s41593-018-0241-y
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author Bienkowski, Michael S.
Bowman, Ian
Song, Monica Y.
Gou, Lin
Ard, Tyler
Cotter, K.
Zhu, Muye
Benavidez, Nora L.
Yamashita, Seita
Abu-Jaber, Jaspar
Azam, Sana
Lo, Darrick
Foster, Nicholas N.
Hintiryan, Houri
Dong, Hong-Wei
author_facet Bienkowski, Michael S.
Bowman, Ian
Song, Monica Y.
Gou, Lin
Ard, Tyler
Cotter, K.
Zhu, Muye
Benavidez, Nora L.
Yamashita, Seita
Abu-Jaber, Jaspar
Azam, Sana
Lo, Darrick
Foster, Nicholas N.
Hintiryan, Houri
Dong, Hong-Wei
author_sort Bienkowski, Michael S.
collection PubMed
description Understanding the organization of the hippocampus is fundamental to understanding brain function related to learning, memory, emotions, and diseases like Alzheimer’s disease. Physiological studies in humans and rodents suggest both structural and functional heterogeneity along the longitudinal axis of the hippocampus. Yet the recent discovery of discrete gene expression domains within the mouse hippocampus has provided the opportunity to re-evaluate hippocampal connectivity. To integrate mouse hippocampal gene expression and connectivity, we mapped the distribution of distinct gene expression patterns within mouse hippocampus and subiculum to create the Hippocampus Gene Expression Atlas (HGEA). Notably, novel subiculum gene expression patterns revealed a hidden laminar organization. Guided by the HGEA, we constructed the most detailed hippocampal connectome available using Mouse Connectome Project (www.MouseConnectome.org) tract tracing data. Our results define the hippocampus’ multiscale network organization and demonstrate each subnetwork’s unique brain-wide connectivity patterns.
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spelling pubmed-63983472019-04-08 Integration of gene expression and brain-wide connectivity reveals the multiscale organization of mouse hippocampal networks Bienkowski, Michael S. Bowman, Ian Song, Monica Y. Gou, Lin Ard, Tyler Cotter, K. Zhu, Muye Benavidez, Nora L. Yamashita, Seita Abu-Jaber, Jaspar Azam, Sana Lo, Darrick Foster, Nicholas N. Hintiryan, Houri Dong, Hong-Wei Nat Neurosci Article Understanding the organization of the hippocampus is fundamental to understanding brain function related to learning, memory, emotions, and diseases like Alzheimer’s disease. Physiological studies in humans and rodents suggest both structural and functional heterogeneity along the longitudinal axis of the hippocampus. Yet the recent discovery of discrete gene expression domains within the mouse hippocampus has provided the opportunity to re-evaluate hippocampal connectivity. To integrate mouse hippocampal gene expression and connectivity, we mapped the distribution of distinct gene expression patterns within mouse hippocampus and subiculum to create the Hippocampus Gene Expression Atlas (HGEA). Notably, novel subiculum gene expression patterns revealed a hidden laminar organization. Guided by the HGEA, we constructed the most detailed hippocampal connectome available using Mouse Connectome Project (www.MouseConnectome.org) tract tracing data. Our results define the hippocampus’ multiscale network organization and demonstrate each subnetwork’s unique brain-wide connectivity patterns. 2018-10-08 2018-11 /pmc/articles/PMC6398347/ /pubmed/30297807 http://dx.doi.org/10.1038/s41593-018-0241-y Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Bienkowski, Michael S.
Bowman, Ian
Song, Monica Y.
Gou, Lin
Ard, Tyler
Cotter, K.
Zhu, Muye
Benavidez, Nora L.
Yamashita, Seita
Abu-Jaber, Jaspar
Azam, Sana
Lo, Darrick
Foster, Nicholas N.
Hintiryan, Houri
Dong, Hong-Wei
Integration of gene expression and brain-wide connectivity reveals the multiscale organization of mouse hippocampal networks
title Integration of gene expression and brain-wide connectivity reveals the multiscale organization of mouse hippocampal networks
title_full Integration of gene expression and brain-wide connectivity reveals the multiscale organization of mouse hippocampal networks
title_fullStr Integration of gene expression and brain-wide connectivity reveals the multiscale organization of mouse hippocampal networks
title_full_unstemmed Integration of gene expression and brain-wide connectivity reveals the multiscale organization of mouse hippocampal networks
title_short Integration of gene expression and brain-wide connectivity reveals the multiscale organization of mouse hippocampal networks
title_sort integration of gene expression and brain-wide connectivity reveals the multiscale organization of mouse hippocampal networks
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6398347/
https://www.ncbi.nlm.nih.gov/pubmed/30297807
http://dx.doi.org/10.1038/s41593-018-0241-y
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