Transcription regulators differentiate mesenchymal stem cells into chondroprogenitors, and their

Gene expression Human umbilical cord Intervertebral disc degeneration Mesenchymal stem cells Regeneration Transcription factors

Journal

World journal of stem cells
ISSN: 1948-0210
Titre abrégé: World J Stem Cells
Pays: United States
ID NLM: 101535826

Informations de publication

Date de publication:
26 Feb 2022
Historique:
received: 28 02 2021
revised: 02 05 2021
accepted: 06 01 2022
entrez: 18 4 2022
pubmed: 19 4 2022
medline: 19 4 2022
Statut: ppublish

Résumé

Intervertebral disc degeneration (IVDD) is the leading cause of lower back pain. Disc degeneration is characterized by reduced cellularity and decreased production of extracellular matrix (ECM). Mesenchymal stem cells (MSCs) have been envisioned as a promising treatment for degenerative illnesses. Cell-based therapy using ECM-producing chondrogenic derivatives of MSCs has the potential to restore the functionality of the intervertebral disc (IVD). To investigate the potential of chondrogenic transcription factors to promote differentiation of human umbilical cord MSCs into chondrocytes, and to assess their therapeutic potential in IVD regeneration. MSCs were isolated and characterized morphologically and immunologically by the expression of specific markers. MSCs were then transfected with Isolated cells showed fibroblast-like morphology and expressed CD105, CD90, CD73, CD29, and Vimentin but not CD45 antigens. Overexpression of Genetically modified MSCs accelerate cartilage regeneration, providing a unique opportunity and impetus for stem cell-based therapeutic approach for degenerative disc diseases.

Sections du résumé

BACKGROUND BACKGROUND
Intervertebral disc degeneration (IVDD) is the leading cause of lower back pain. Disc degeneration is characterized by reduced cellularity and decreased production of extracellular matrix (ECM). Mesenchymal stem cells (MSCs) have been envisioned as a promising treatment for degenerative illnesses. Cell-based therapy using ECM-producing chondrogenic derivatives of MSCs has the potential to restore the functionality of the intervertebral disc (IVD).
AIM OBJECTIVE
To investigate the potential of chondrogenic transcription factors to promote differentiation of human umbilical cord MSCs into chondrocytes, and to assess their therapeutic potential in IVD regeneration.
METHODS METHODS
MSCs were isolated and characterized morphologically and immunologically by the expression of specific markers. MSCs were then transfected with
RESULTS RESULTS
Isolated cells showed fibroblast-like morphology and expressed CD105, CD90, CD73, CD29, and Vimentin but not CD45 antigens. Overexpression of
CONCLUSION CONCLUSIONS
Genetically modified MSCs accelerate cartilage regeneration, providing a unique opportunity and impetus for stem cell-based therapeutic approach for degenerative disc diseases.

Identifiants

pubmed: 35432734
doi: 10.4252/wjsc.v14.i2.163
pmc: PMC8963382
doi:

Types de publication

Journal Article

Langues

eng

Pagination

163-182

Informations de copyright

©The Author(s) 2022. Published by Baishideng Publishing Group Inc. All rights reserved.

Déclaration de conflit d'intérêts

Conflict-of-interest statement: No conflict of interest.

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Auteurs

Shumaila Khalid (S)

Dr. Panjwani Center for Molecular Medicine and Drug Research, International Center for Chemical and Biological Sciences, University of Karachi, Karachi 75270, Sindh, Pakistan.

Sobia Ekram (S)

Dr. Panjwani Center for Molecular Medicine and Drug Research, International Center for Chemical and Biological Sciences, University of Karachi, Karachi 75270, Sindh, Pakistan.

Asmat Salim (A)

Dr. Panjwani Center for Molecular Medicine and Drug Research, International Center for Chemical and Biological Sciences, University of Karachi, Karachi 75270, Sindh, Pakistan.

G Rasul Chaudhry (GR)

Department of Biological Sciences, Oakland University, Rochester, MI 48309, United States.

Irfan Khan (I)

Dr. Panjwani Center for Molecular Medicine and Drug Research, International Center for Chemical and Biological Sciences, University of Karachi, Karachi 75270, Sindh, Pakistan. khan@iccs.edu.

Classifications MeSH