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Role of Mesenchymal Stem/Stromal Cells (MSCs) and MSC-Derived Extracellular Vesicles (EVs) in Prevention of Telomere Length Shortening, Cellular Senescence, and Accelerated Biological Aging.
Arellano, Myrna Y Gonzalez; VanHeest, Matthew; Emmadi, Sravya; Abdul-Hafez, Amal; Ibrahim, Sherif Abdelfattah; Thiruvenkataramani, Ranga P; Teleb, Rasha S; Omar, Hady; Kesaraju, Tulasi; Mohamed, Tarek; Madhukar, Burra V; Omar, Said A.
Affiliation
  • Arellano MYG; Division of Neonatology, Department of Pediatrics and Human Development, College of Human Medicine, Michigan State University, East Lansing, MI 48824, USA.
  • VanHeest M; College of Human Medicine, Michigan State University, East Lansing, MI 48824, USA.
  • Emmadi S; Regional Neonatal Intensive Care Unit, Sparrow Hospital, Lansing, MI 48912, USA.
  • Abdul-Hafez A; College of Human Medicine, Michigan State University, East Lansing, MI 48824, USA.
  • Ibrahim SA; College of Human Medicine, Michigan State University, East Lansing, MI 48824, USA.
  • Thiruvenkataramani RP; Division of Neonatology, Department of Pediatrics and Human Development, College of Human Medicine, Michigan State University, East Lansing, MI 48824, USA.
  • Teleb RS; College of Human Medicine, Michigan State University, East Lansing, MI 48824, USA.
  • Omar H; Division of Neonatology, Department of Pediatrics and Human Development, College of Human Medicine, Michigan State University, East Lansing, MI 48824, USA.
  • Kesaraju T; College of Human Medicine, Michigan State University, East Lansing, MI 48824, USA.
  • Mohamed T; Histology and Cell Biology Department, Faculty of Medicine, Mansoura University, Mansoura 35516, Egypt.
  • Madhukar BV; Division of Neonatology, Department of Pediatrics and Human Development, College of Human Medicine, Michigan State University, East Lansing, MI 48824, USA.
  • Omar SA; College of Human Medicine, Michigan State University, East Lansing, MI 48824, USA.
Bioengineering (Basel) ; 11(6)2024 May 21.
Article in En | MEDLINE | ID: mdl-38927760
ABSTRACT
Biological aging is defined as a progressive decline in tissue function that eventually results in cell death. Accelerated biologic aging results when the telomere length is shortened prematurely secondary to damage from biological or environmental stressors, leading to a defective reparative mechanism. Stem cells therapy may have a potential role in influencing (counteract/ameliorate) biological aging and maintaining the function of the organism. Mesenchymal stem cells, also called mesenchymal stromal cells (MSCs) are multipotent stem cells of mesodermal origin that can differentiate into other types of cells, such as adipocytes, chondrocytes, and osteocytes. MSCs influence resident cells through the secretion of paracrine bioactive components such as cytokines and extracellular vesicles (EVs). This review examines the changes in telomere length, cellular senescence, and normal biological age, as well as the factors contributing to telomere shortening and accelerated biological aging. The role of MSCs-especially those derived from gestational tissues-in prevention of telomere shortening (TS) and accelerated biological aging is explored. In addition, the strategies to prevent MSC senescence and improve the antiaging therapeutic application of MSCs and MSC-derived EVs in influencing telomere length and cellular senescence are reviewed.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Bioengineering (Basel) Year: 2024 Document type: Article Affiliation country: Estados Unidos

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Bioengineering (Basel) Year: 2024 Document type: Article Affiliation country: Estados Unidos
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