Generation of a fluorescent hESC reporter line (Kle033-A-1) for the isolation of distinct midbrain progenitor cell types

Midbrain dopaminergic (mDA) neurons derived from human pluripotent stem cells (hPSCs) offer a promising cell source for cell replacement therapy in Parkinson's disease (PD). Single-cell RNA sequencing (scRNA-seq) of the developing human ventral midbrain has identified four cell types expressing markers used to define correctly patterned mDA progenitors. Here, we use CRISPR/Cas9 to generate a fluorescent human embryonic stem cell line for the isolation of two potential mDA progenitors, Rgl1 and ProgM. We expect that by isolating specific mDA progenitor cell type/s and defining their function, it may be possible to develop more precise cell replacement strategies for PD.

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Publication Details

Journal
Stem Cell Research
Published
2024-08-12
DOI
https://doi.org/10.1016/j.scr.2024.103523
Citations
1
Primary Topic
Pluripotent Stem Cells Research
Type
article
Field-Weighted Citation Impact
0.23

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article

Generation of a fluorescent hESC reporter line (Kle033-A-1) for the isolation of distinct midbrain progenitor cell types

Ernest Arenas, Emilía Sif Ásgrímsdóttir
1 citations
Stem Cell Research
Pluripotent Stem Cells Research
0.23
article

Generation of a fluorescent hESC reporter line (Kle033-A-1) for the isolation of distinct midbrain progenitor cell types

Ernest Arenas, Emilía Sif Ásgrímsdóttir
article en
1 citations

Abstract

Midbrain dopaminergic (mDA) neurons derived from human pluripotent stem cells (hPSCs) offer a promising cell source for cell replacement therapy in Parkinson's disease (PD). Single-cell RNA sequencing (scRNA-seq) of the developing human ventral midbrain has identified four cell types expressing markers used to define correctly patterned mDA progenitors. Here, we use CRISPR/Cas9 to generate a fluorescent human embryonic stem cell line for the isolation of two potential mDA progenitors, Rgl1 and ProgM. We expect that by isolating specific mDA progenitor cell type/s and defining their function, it may be possible to develop more precise cell replacement strategies for PD.

Stem Cell ResearchVol. 81
Karolinska Institutet (SE)
Knut och Alice Wallenbergs Stiftelse, Vetenskapsrådet, HORIZON EUROPE Framework Programme, H2020 European Research Council
Zero hunger
Openalex Percentile: Top 43%
Pluripotent Stem Cells Research
0.23
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