A molecular gradient along the longitudinal axis of the human hippocampus informs large-scale behavioral systems.


Journal

Nature communications
ISSN: 2041-1723
Titre abrégé: Nat Commun
Pays: England
ID NLM: 101528555

Informations de publication

Date de publication:
19 02 2020
Historique:
received: 05 04 2019
accepted: 09 12 2019
entrez: 21 2 2020
pubmed: 23 2 2020
medline: 30 4 2020
Statut: epublish

Résumé

The functional organization of the hippocampus is distributed as a gradient along its longitudinal axis that explains its differential interaction with diverse brain systems. We show that the location of human tissue samples extracted along the longitudinal axis of the adult human hippocampus can be predicted within 2mm using the expression pattern of less than 100 genes. Futhermore, this model generalizes to an external set of tissue samples from prenatal human hippocampi. We examine variation in this specific gene expression pattern across the whole brain, finding a distinct anterioventral-posteriodorsal gradient. We find frontal and anterior temporal regions involved in social and motivational behaviors, and more functionally connected to the anterior hippocampus, to be clearly differentiated from posterior parieto-occipital regions involved in visuospatial cognition and more functionally connected to the posterior hippocampus. These findings place the human hippocampus at the interface of two major brain systems defined by a single molecular gradient.

Identifiants

pubmed: 32075960
doi: 10.1038/s41467-020-14518-3
pii: 10.1038/s41467-020-14518-3
pmc: PMC7031290
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

960

Subventions

Organisme : NIA NIH HHS
ID : P30 AG066444
Pays : United States
Organisme : NIA NIH HHS
ID : P01 AG026276
Pays : United States
Organisme : NIA NIH HHS
ID : P30 AG062422
Pays : United States
Organisme : NIA NIH HHS
ID : P01 AG019724
Pays : United States
Organisme : NIA NIH HHS
ID : P01 AG003991
Pays : United States
Organisme : NIA NIH HHS
ID : P50 AG005681
Pays : United States

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Auteurs

Jacob W Vogel (JW)

Montreal Neurological Institute, McGill University, Montréal, QC, Canada. jacob.vogel@mail.mcgill.ca.

Renaud La Joie (R)

Memory and Aging Center, University of California, San Francisco, CA, USA.

Michel J Grothe (MJ)

German Center for Neurodegenerative Diseases (DZNE), Rostock, Germany.

Alexandr Diaz-Papkovich (A)

McGill University and Genome Quebec Innovation Centre, Montréal, QC, Canada.
Quantitative Life Sciences, McGill University, Montreal, QC, H3A 0G1, Canada.

Andrew Doyle (A)

Montreal Neurological Institute, McGill University, Montréal, QC, Canada.

Etienne Vachon-Presseau (E)

Faculty of Dentistry, Department of Anesthesia, McGill University, Montréal, QC, Canada.
Alan Edwards Centre for Research on Pain (AECRP), McGill University, Montréal, QC, Canada.

Claude Lepage (C)

Montreal Neurological Institute, McGill University, Montréal, QC, Canada.

Reinder Vos de Wael (R)

Montreal Neurological Institute, McGill University, Montréal, QC, Canada.

Rhalena A Thomas (RA)

Montreal Neurological Institute, McGill University, Montréal, QC, Canada.

Yasser Iturria-Medina (Y)

Montreal Neurological Institute, McGill University, Montréal, QC, Canada.

Boris Bernhardt (B)

Montreal Neurological Institute, McGill University, Montréal, QC, Canada.

Gil D Rabinovici (GD)

Memory and Aging Center, University of California, San Francisco, CA, USA.

Alan C Evans (AC)

Montreal Neurological Institute, McGill University, Montréal, QC, Canada. alan.evans@mcgill.ca.

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