Single-cell transcriptomics reveals multiple neuronal cell types in human midbrain-specific organoids.

Electrophysiological activity Midbrain organoids Neural stem cells Neuronal subtypes Single-cell RNA sequencing

Journal

Cell and tissue research
ISSN: 1432-0878
Titre abrégé: Cell Tissue Res
Pays: Germany
ID NLM: 0417625

Informations de publication

Date de publication:
Dec 2020
Historique:
received: 23 01 2020
accepted: 22 06 2020
pubmed: 2 8 2020
medline: 11 8 2021
entrez: 2 8 2020
Statut: ppublish

Résumé

Human stem cell-derived organoids have great potential for modelling physiological and pathological processes. They recapitulate in vitro the organization and function of a respective organ or part of an organ. Human midbrain organoids (hMOs) have been described to contain midbrain-specific dopaminergic neurons that release the neurotransmitter dopamine. However, the human midbrain contains also additional neuronal cell types, which are functionally interacting with each other. Here, we analysed hMOs at high-resolution by means of single-cell RNA sequencing (scRNA-seq), imaging and electrophysiology to unravel cell heterogeneity. Our findings demonstrate that hMOs show essential neuronal functional properties as spontaneous electrophysiological activity of different neuronal subtypes, including dopaminergic, GABAergic, glutamatergic and serotonergic neurons. Recapitulating these in vivo features makes hMOs an excellent tool for in vitro disease phenotyping and drug discovery.

Identifiants

pubmed: 32737576
doi: 10.1007/s00441-020-03249-y
pii: 10.1007/s00441-020-03249-y
pmc: PMC7683480
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

463-476

Subventions

Organisme : Fonds National de la Recherche Luxembourg
ID : C14/BM/7975668/CaSCAD
Organisme : Fonds National de la Recherche Luxembourg
ID : PRIDE/10907093/CRITICS
Organisme : Fonds National de la Recherche Luxembourg
ID : C13/BM/5791363; PoC15/11180855; PoC16/11559169; INTER/JPND/14/02; INTER/JPND/15/11092422
Organisme : Fonds National de la Recherche Luxembourg
ID : AFR
Organisme : Wellcome Trust
Pays : United Kingdom
Organisme : H2020 Excellent Science
ID : 668738
Organisme : NIH HHS
ID : GM103426
Pays : United States

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Auteurs

Lisa M Smits (LM)

Luxembourg Centre for Systems Biomedicine (LCSB), Developmental and Cellular Biology, University of Luxembourg, Belvaux, Luxembourg.

Stefano Magni (S)

Luxembourg Centre for Systems Biomedicine (LCSB), Developmental and Cellular Biology, University of Luxembourg, Belvaux, Luxembourg.

Kaoru Kinugawa (K)

Department of Future Basic Medicine, Nara Medical University, Kashihara, Nara, Japan.

Kamil Grzyb (K)

Luxembourg Centre for Systems Biomedicine (LCSB), Developmental and Cellular Biology, University of Luxembourg, Belvaux, Luxembourg.

Joachim Luginbühl (J)

Division of Genomic Technologies, RIKEN Center for Life Science Technologies, Yokohama, Kanagawa, Japan.

Sonia Sabate-Soler (S)

Luxembourg Centre for Systems Biomedicine (LCSB), Developmental and Cellular Biology, University of Luxembourg, Belvaux, Luxembourg.

Silvia Bolognin (S)

Luxembourg Centre for Systems Biomedicine (LCSB), Developmental and Cellular Biology, University of Luxembourg, Belvaux, Luxembourg.

Jay W Shin (JW)

Division of Genomic Technologies, RIKEN Center for Life Science Technologies, Yokohama, Kanagawa, Japan.

Eiichiro Mori (E)

Department of Future Basic Medicine, Nara Medical University, Kashihara, Nara, Japan.

Alexander Skupin (A)

Luxembourg Centre for Systems Biomedicine (LCSB), Developmental and Cellular Biology, University of Luxembourg, Belvaux, Luxembourg.
University California San Diego, La Jolla, CA, USA.

Jens C Schwamborn (JC)

Luxembourg Centre for Systems Biomedicine (LCSB), Developmental and Cellular Biology, University of Luxembourg, Belvaux, Luxembourg. jens.schwamborn@uni.lu.

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