Basal forebrain subcortical projections.


Journal

Brain structure & function
ISSN: 1863-2661
Titre abrégé: Brain Struct Funct
Pays: Germany
ID NLM: 101282001

Informations de publication

Date de publication:
Apr 2019
Historique:
received: 13 06 2018
accepted: 16 12 2018
pubmed: 7 1 2019
medline: 31 8 2019
entrez: 7 1 2019
Statut: ppublish

Résumé

The basal forebrain (BF) contains at least three distinct populations of neurons (cholinergic, glutamatergic, and GABA-ergic) across its different regions (medial septum, diagonal band, magnocellular preoptic area, and substantia innominata). Much attention has focused on the BF's ascending projections to cortex, but less is known about descending projections to subcortical regions. Given the neurochemical and anatomical heterogeneity of the BF, we used conditional anterograde tracing to map the patterns of subcortical projections from multiple BF regions and neurochemical cell types using mice that express Cre recombinase only in cholinergic, glutamatergic, or GABAergic neurons. We confirmed that different BF regions innervate distinct subcortical targets, with more subcortical projections arising from neurons in the caudal and lateral BF (substantia innominata and magnocellular preoptic area). Additionally, glutamatergic and GABAergic BF neurons have distinct patterns of descending projections, while cholinergic descending projections are sparse. Considering the intensity of glutamatergic and GABAergic descending projections, the BF likely acts through subcortical targets to promote arousal, motivation, and other behaviors.

Identifiants

pubmed: 30612231
doi: 10.1007/s00429-018-01820-6
pii: 10.1007/s00429-018-01820-6
pmc: PMC6500474
mid: NIHMS1524933
doi:

Substances chimiques

Luminescent Proteins 0
Vesicular Glutamate Transport Protein 2 0
Vesicular Inhibitory Amino Acid Transport Proteins 0
Viaat protein, mouse 0
Glutamic Acid 3KX376GY7L
Dynorphins 74913-18-1
Choline O-Acetyltransferase EC 2.3.1.6

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1097-1117

Subventions

Organisme : NIH HHS
ID : NIH P01 HL095491-02S1
Pays : United States
Organisme : NHLBI NIH HHS
ID : T32 HL007901
Pays : United States
Organisme : NINDS NIH HHS
ID : K08 NS099425
Pays : United States
Organisme : NIH HHS
ID : NIH P01 HL095491
Pays : United States
Organisme : NHLBI NIH HHS
ID : P01 HL095491
Pays : United States

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Auteurs

Lindsay J Agostinelli (LJ)

Department of Neurology, Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, MA, 02215, USA.
Department of Neurology, Roy J. and Lucille A. Carver College of Medicine, University of Iowa, Iowa City, IA, 52242, USA.

Joel C Geerling (JC)

Department of Neurology, Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, MA, 02215, USA.
Department of Neurology, Roy J. and Lucille A. Carver College of Medicine, University of Iowa, Iowa City, IA, 52242, USA.

Thomas E Scammell (TE)

Department of Neurology, Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, MA, 02215, USA. tscammel@bidmc.harvard.edu.

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Classifications MeSH