Cartography of hevin-expressing cells in the adult brain reveals prominent expression in astrocytes and parvalbumin neurons.


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: 08 02 2018
accepted: 08 01 2019
pubmed: 19 1 2019
medline: 31 8 2019
entrez: 19 1 2019
Statut: ppublish

Résumé

Hevin, also known as SPARC-like 1, is a member of the secreted protein acidic and rich in cysteine family of matricellular proteins, which has been implicated in neuronal migration and synaptogenesis during development. Unlike previously characterized matricellular proteins, hevin remains strongly expressed in the adult brain in both astrocytes and neurons, but its precise pattern of expression is unknown. The present study provides the first systematic description of hevin mRNA distribution in the adult mouse brain. Using isotopic in situ hybridization, we showed that hevin is strongly expressed in the cortex, hippocampus, basal ganglia complex, diverse thalamic nuclei and brainstem motor nuclei. To identify the cellular phenotype of hevin-expressing cells, we used double fluorescent in situ hybridization in mouse and human adult brains. In the mouse, hevin mRNA was found in the majority of astrocytes but also in specific neuronal populations. Hevin was expressed in almost all parvalbumin-positive projection neurons and local interneurons. In addition, hevin mRNA was found in: (1) subsets of other inhibitory GABAergic neuronal subtypes, including calbindin, cholecystokinin, neuropeptide Y, and somatostatin-positive neurons; (2) subsets of glutamatergic neurons, identified by the expression of the vesicular glutamate transporters VGLUT1 and VGLUT2; and (3) the majority of cholinergic neurons from motor nuclei. Hevin mRNA was absent from all monoaminergic neurons and cholinergic neurons of the ascending pathway. A similar cellular profile of expression was observed in human, with expression of hevin in parvalbumin interneurons and astrocytes in the cortex and caudate nucleus as well as in cortical glutamatergic neurons. Furthermore, hevin transcript was enriched in ribosomes of astrocytes and parvalbumin neurons providing a direct evidence of hevin mRNAs translation in these cell types. This study reveals the unique and complex expression profile of the matricellular protein hevin in the adult brain. This distribution is compatible with a role of hevin in astrocytic-mediated adult synaptic plasticity and in the regulation of network activity mediated by parvalbumin-expressing neurons.

Identifiants

pubmed: 30656447
doi: 10.1007/s00429-019-01831-x
pii: 10.1007/s00429-019-01831-x
doi:

Substances chimiques

Calcium-Binding Proteins 0
Excitatory Amino Acid Transporter 1 0
Extracellular Matrix Proteins 0
Nerve Tissue Proteins 0
Parvalbumins 0
RNA, Messenger 0
SPARCL1 protein, human 0
Vesicular Glutamate Transport Proteins 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1219-1244

Subventions

Organisme : National Alliance for Research on Schizophrenia and Depression
ID : 17566
Organisme : FP7 People: Marie-Curie Actions
ID : 618807
Organisme : Agence Nationale de la Recherche
ID : JCJC 2015
Organisme : Eusko Jaurlaritza
ID : IT616/13
Organisme : Fondation pour la Recherche M?dicale
ID : DEQ20160334919
Organisme : Fundaci?n Vital
ID : 2018
Organisme : ERAB: The European Foundation for Alcohol Research
ID : EA 18 19
Organisme : Marie Curie Intra-European Fellowship
ID : IEF327648

Auteurs

Raphaële Mongrédien (R)

Sorbonne Université, INSERM, CNRS, Neuroscience Paris Seine, Institut de Biologie Paris Seine, Paris, France.

Amaia M Erdozain (AM)

Department of Pharmacology, University of the Basque Country, UPV/EHU, Bizkaia, Spain.
Centro de Investigación Biomédica en Red de Salud Mental (CIBERSAM), Madrid, Spain.

Sylvie Dumas (S)

Oramacell, Paris, France.

Laura Cutando (L)

IGF, CNRS, INSERM, University of Montpellier, Montpellier, France.

Amaia Nuñez Del Moral (AN)

Department of Pharmacology, University of the Basque Country, UPV/EHU, Bizkaia, Spain.

Emma Puighermanal (E)

IGF, CNRS, INSERM, University of Montpellier, Montpellier, France.

Sara Rezai Amin (S)

Sorbonne Université, INSERM, CNRS, Neuroscience Paris Seine, Institut de Biologie Paris Seine, Paris, France.

Bruno Giros (B)

Sorbonne Université, INSERM, CNRS, Neuroscience Paris Seine, Institut de Biologie Paris Seine, Paris, France.

Emmanuel Valjent (E)

IGF, CNRS, INSERM, University of Montpellier, Montpellier, France.

J Javier Meana (JJ)

Department of Pharmacology, University of the Basque Country, UPV/EHU, Bizkaia, Spain.
Centro de Investigación Biomédica en Red de Salud Mental (CIBERSAM), Madrid, Spain.

Sophie Gautron (S)

Sorbonne Université, INSERM, CNRS, Neuroscience Paris Seine, Institut de Biologie Paris Seine, Paris, France.

Luis F Callado (LF)

Department of Pharmacology, University of the Basque Country, UPV/EHU, Bizkaia, Spain.
Centro de Investigación Biomédica en Red de Salud Mental (CIBERSAM), Madrid, Spain.

Véronique Fabre (V)

Sorbonne Université, INSERM, CNRS, Neuroscience Paris Seine, Institut de Biologie Paris Seine, Paris, France.

Vincent Vialou (V)

Sorbonne Université, INSERM, CNRS, Neuroscience Paris Seine, Institut de Biologie Paris Seine, Paris, France. vincent.vialou@inserm.fr.

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Classifications MeSH