Cited by 177Mesenchymal stem cell researchNeurogenesis and neuroplasticity mechanismsMultiple Sclerosis Research Studies

Functional role of mesenchymal stem cells in the treatment of chronic neurodegenerative diseases

Lo Furno, Debora, Mannino, Giuliana, Giuffrida, Rosario·2018·Journal of Cellular Physiology

Abstract

Mesenchymal stem cells (MSCs) can differentiate into not only cells of mesodermal lineages, but also into endodermal and ectodermal derived elements, including neurons and glial cells. For this reason, MSCs have been extensively investigated to develop cell‐based therapeutic strategies, especially in pathologies whose pharmacological treatments give poor results, if any. As in the case of irreversible neurological disorders characterized by progressive neuronal death, in which behavioral and cognitive functions of patients inexorably decline as the disease progresses. In this review, we focus on the possible functional role exerted by MSCs in the treatment of some disabling neurodegenerative disorders such as Alzheimer's Disease, Amyotrophic Lateral Sclerosis, Huntington's Disease, and Parkinson's Disease. Investigations have been mainly performed in vitro and in animal models by using MSCs generally originated from umbilical cord, bone marrow, or adipose tissue. Positive results obtained have prompted several clinical trials, the number of which is progressively increasing worldwide. To date, many of them have been primarily addressed to verify the safety of the procedures but some improvements have already been reported, fortunately. Although the exact mechanisms of MSC‐induced beneficial activities are not entirely defined, they include neurogenesis and angiogenesis stimulation, antiapoptotic, immunomodulatory, and anti‐inflammatory actions. Most effects would be exerted through their paracrine expression of neurotrophic factors and cytokines, mainly delivered at damaged regions, given the innate propensity of MSCs to home to injured sites. Hopefully, in the near future more efficacious cell‐replacement therapies will be developed to substantially restore disease‐disrupted brain circuitry.

Integrity signals

Registry

Crossref · 10.1002/jcp.26192

Cites

2 of 2 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Claims the paper makes

We couldn’t retrieve this paper’s full text, so its claims and self-check weren’t run. The registry and citation checks still apply.

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

  • NSCs may have to be obtained by harvesting cells from nervous tissue, and their insufficient amount in the human body would not make this method feasible for patients.

    “First, NSCs may have to be obtained by harvesting cells from nervous tissue. Their insufficient amount in the human body would not make this method feasible for patients [109].”

Cites

Flagged first, then by citations

Cited by

Sorted by citations

Authors
Lo Furno, D., Mannino, G., & Giuffrida, R.
Affiliations
  • Department of Biomedical and Biotechnological Sciences, Section of Physiology University of Catania Catania Italy
  • University of Catania (IT)
Corresponding author
Giuffrida, Rosario
Venue
Journal of Cellular Physiology
Publisher
Wiley
Published
2017-10-20
Volume
233
Issue
5
Pages
3982-3999
ISSN
  • 0021-9541 (ISSN-L)
  • 1097-4652
OpenAlex
W2754685511
Cited by
177
References
2
Citations by year
2026: 8 · 2025: 13 · 2024: 17 · 2023: 28 · 2022: 23 · 2021: 27 · 2020: 29 · 2019: 19 · 2018: 13
FWCI
2.35
Type
journal article
Language
en
Open access
closed
Locations
  • Journal of Cellular Physiology (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Health Sciences › Medicine › Genetics › Mesenchymal stem cell research
  • Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
  • Health Sciences › Medicine › Pathology and Forensic Medicine › Multiple Sclerosis Research Studies
Keywords
mesenchymal stem cells, neurodegenerative diseases, cell therapy, Alzheimer's disease, amyotrophic lateral sclerosis, Huntington's disease, Parkinson's disease, neurogenesis, angiogenesis, immunomodulation, anti-inflammatory activity, neurotrophic factors, paracrine signaling, stem cell homing, cell replacement therapy, stem cell clinical trials
MeSH terms
Alzheimer Disease, Amyotrophic Lateral Sclerosis, Humans, Huntington Disease, Neurons, Parkinson Disease, Umbilical Cord, Neurodegenerative Diseases, Mesenchymal Stem Cell Transplantation, Neurogenesis, Mesenchymal Stem Cells, Cell- and Tissue-Based Therapy

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review