» Articles » PMID: 27829839

Therapeutic Potential of Stem Cells Strategy for Cardiovascular Diseases

Overview
Journal Stem Cells Int
Publisher Wiley
Specialty Cell Biology
Date 2016 Nov 11
PMID 27829839
Citations 14
Authors
Affiliations
Soon will be listed here.
Abstract

Despite development of medicine, cardiovascular diseases (CVDs) are still the leading cause of mortality and morbidity worldwide. Over the past 10 years, various stem cells have been utilized in therapeutic strategies for the treatment of CVDs. CVDs are characterized by a broad range of pathological reactions including inflammation, necrosis, hyperplasia, and hypertrophy. However, the causes of CVDs are still unclear. While there is a limit to the currently available target-dependent treatments, the therapeutic potential of stem cells is very attractive for the treatment of CVDs because of their paracrine effects, anti-inflammatory activity, and immunomodulatory capacity. Various studies have recently reported increased therapeutic potential of transplantation of microRNA- (miRNA-) overexpressing stem cells or small-molecule-treated cells. In addition to treatment with drugs or overexpressed miRNA in stem cells, stem cell-derived extracellular vesicles also have therapeutic potential because they can deliver the stem cell-specific RNA and protein into the host cell, thereby improving cell viability. Here, we reported the state of stem cell-based therapy for the treatment of CVDs and the potential for cell-free based therapy.

Citing Articles

Epicardial transplantation of antioxidant polyurethane scaffold based human amniotic epithelial stem cell patch for myocardial infarction treatment.

Li J, Yao Y, Zhou J, Yang Z, Qiu C, Lu Y Nat Commun. 2024; 15(1):9105.

PMID: 39438477 PMC: 11496666. DOI: 10.1038/s41467-024-53531-8.


Progress in Biomaterials for Cardiac Tissue Engineering and Regeneration.

Udriste A, Niculescu A, Iliuta L, Bajeu T, Georgescu A, Grumezescu A Polymers (Basel). 2023; 15(5).

PMID: 36904419 PMC: 10007484. DOI: 10.3390/polym15051177.


Extracellular Vesicles from NMN Preconditioned Mesenchymal Stem Cells Ameliorated Myocardial Infarction via miR-210-3p Promoted Angiogenesis.

Pu Y, Li C, Qi X, Xu R, Dong L, Jiang Y Stem Cell Rev Rep. 2023; 19(4):1051-1066.

PMID: 36696015 PMC: 10185590. DOI: 10.1007/s12015-022-10499-6.


Cardiac stem cells: Current knowledge and future prospects.

Mehanna R, Essawy M, Barkat M, Awaad A, Thabet E, Hamed H World J Stem Cells. 2022; 14(1):1-40.

PMID: 35126826 PMC: 8788183. DOI: 10.4252/wjsc.v14.i1.1.


Hyaluronate supports hESC-cardiomyocyte cell therapy for cardiac regeneration after acute myocardial infarction.

Tan Y, Wang L, Chen G, Liu W, Li Z, Wang Y Cell Prolif. 2020; 53(12):e12942.

PMID: 33107673 PMC: 7705924. DOI: 10.1111/cpr.12942.


References
1.
Perea-Gil I, Monguio-Tortajada M, Galvez-Monton C, Bayes-Genis A, Borras F, Roura S . Preclinical evaluation of the immunomodulatory properties of cardiac adipose tissue progenitor cells using umbilical cord blood mesenchymal stem cells: a direct comparative study. Biomed Res Int. 2015; 2015:439808. PMC: 4377370. DOI: 10.1155/2015/439808. View

2.
Zhao T, Zhang Z, Rong Z, Xu Y . Immunogenicity of induced pluripotent stem cells. Nature. 2011; 474(7350):212-5. DOI: 10.1038/nature10135. View

3.
Yde P, Mengel B, Jensen M, Krishna S, Trusina A . Modeling the NF-κB mediated inflammatory response predicts cytokine waves in tissue. BMC Syst Biol. 2011; 5:115. PMC: 3152534. DOI: 10.1186/1752-0509-5-115. View

4.
Chang W, Lee C, Park J, Park M, Maeng L, Yoon C . Survival of hypoxic human mesenchymal stem cells is enhanced by a positive feedback loop involving miR-210 and hypoxia-inducible factor 1. J Vet Sci. 2013; 14(1):69-76. PMC: 3615234. DOI: 10.4142/jvs.2013.14.1.69. View

5.
Lai R, Arslan F, Lee M, Sze N, Choo A, Chen T . Exosome secreted by MSC reduces myocardial ischemia/reperfusion injury. Stem Cell Res. 2010; 4(3):214-22. DOI: 10.1016/j.scr.2009.12.003. View