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Review
. 2024 Jan 31:18:1210447.
doi: 10.3389/fnins.2024.1210447. eCollection 2024.

Can pluripotent/multipotent stem cells reverse Parkinson's disease progression?

Affiliations
Review

Can pluripotent/multipotent stem cells reverse Parkinson's disease progression?

Yongkang Wu et al. Front Neurosci. .

Abstract

Parkinson's disease (PD) is a progressive neurodegenerative disorder characterized by continuous and selective degeneration or death of dopamine neurons in the midbrain, leading to dysfunction of the nigrostriatal neural circuits. Current clinical treatments for PD include drug treatment and surgery, which provide short-term relief of symptoms but are associated with many side effects and cannot reverse the progression of PD. Pluripotent/multipotent stem cells possess a self-renewal capacity and the potential to differentiate into dopaminergic neurons. Transplantation of pluripotent/multipotent stem cells or dopaminergic neurons derived from these cells is a promising strategy for the complete repair of damaged neural circuits in PD. This article reviews and summarizes the current preclinical/clinical treatments for PD, their efficacies, and the advantages/disadvantages of various stem cells, including pluripotent and multipotent stem cells, to provide a detailed overview of how these cells can be applied in the treatment of PD, as well as the challenges and bottlenecks that need to be overcome in future translational studies.

Keywords: Parkinson’s disease; dopamine; multipotent stem cells; pluripotent stem cells; transplantation.

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Conflict of interest statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Figures

FIGURE 1
FIGURE 1
The complex pathogenesis of Parkinson’s disease.
FIGURE 2
FIGURE 2
A basic diagram showing how cell transplantation therapy can alleviate motor symptoms in PD patients.
FIGURE 3
FIGURE 3
Neuronal reprogramming strategy. (A) Injection of vectors into the brain using a microinjector. (B) Schematic of the protocol used to reprogram glial cells into neurons. (C) Commonly used delivery routes for in vivo reprogramming. (D) Targets for reprogramming.

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References

    1. Adler A., Björklund A., Parmar M. (2020). Transsynaptic tracing and its emerging use to assess graft-reconstructed neural circuits. Stem Cells 38 716–726. 10.1002/stem.3166 - DOI - PubMed
    1. Adler A., Cardoso T., Nolbrant S., Mattsson B., Hoban D., Jarl U., et al. (2019). hESC-derived dopaminergic transplants integrate into basal ganglia circuitry in a preclinical model of Parkinson’s disease. Cell Rep. 28 3462–3473.e5. 10.1016/j.celrep.2019.08.058 - DOI - PMC - PubMed
    1. Ahmed M., Selvakumar G., Kempuraj D., Raikwar S., Thangavel R., Bazley K., et al. (2020). Glia maturation factor (GMF) regulates microglial expression phenotypes and the associated neurological deficits in a mouse model of traumatic brain injury. Mol. Neurobiol. 57 4438–4450. 10.1007/s12035-020-02040-y - DOI - PubMed
    1. Ando M., Fiesel F., Hudec R., Caulfield T., Ogaki K., Górka-Skoczylas P., et al. (2017). The PINK1 p.I368N mutation affects protein stability and ubiquitin kinase activity. Mol. Neurodegener. 12:32. 10.1186/s13024-017-0174-z - DOI - PMC - PubMed
    1. Andrzejewska A., Dabrowska S., Lukomska B., Janowski M. (2021). Mesenchymal stem cells for neurological disorders. Adv. Sci. 8:2002944. - PMC - PubMed

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