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Mitochondrial Activity of Human Umbilical Cord Mesenchymal Stem Cells

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Journal Brain Circ
Date 2021 Jun 4
PMID 34084975
Citations 11
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Abstract

Human umbilical cord mesenchymal stem cells (hUC-MSCs) serve as a potential cell-based therapy for degenerative disease. They provide immunomodulatory and anti-inflammatory properties, multipotent differentiation potential and are harvested with no ethical concern. It is unknown whether MSCs collected from different areas of the human umbilical cord elicit more favorable effects than others. Three MSC populations were harvested from various regions of the human umbilical cord: cord lining (CL-MSCs), perivascular region (PV-MSCs), and Wharton's jelly (WJ-MSCs). Mesenchymal markers (CD90 and CD73) were expressed by all three cell populations. Stemness marker (OCT4), endothelial cell adhesion molecular marker (CD146), and monocyte-macrophage marker (CD14) were expressed by WJ-MSCs, PV-MSCs, and CL-MSCs, respectively. Stroke presents with oxygen and glucose deprivation and leads to dysfunctional mitochondria and consequently cell death. Targeting the restoration of mitochondrial function in the stroke brain through mitochondrial transfer may be effective in treating stroke. exposure to ambient and OGD conditions resulted in CL-MSCs number decreasing the least post-OGD/R exposure, and PV-MSCs exhibiting the greatest mitochondrial activity. All three hUC-MSC populations presented similar metabolic activity and survival in normal and pathologic environments. These characteristics indicate hUC-MSCs potential as a potent therapeutic in regenerative medicine.

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References
1.
Tajiri N, Duncan K, Antoine A, Pabon M, Acosta S, De la Pena I . Stem cell-paved biobridge facilitates neural repair in traumatic brain injury. Front Syst Neurosci. 2014; 8:116. PMC: 4068001. DOI: 10.3389/fnsys.2014.00116. View

2.
Russo E, Nguyen H, Lippert T, Tuazon J, Borlongan C, Napoli E . Mitochondrial targeting as a novel therapy for stroke. Brain Circ. 2018; 4(3):84-94. PMC: 6187947. DOI: 10.4103/bc.bc_14_18. View

3.
Lavrentieva A, Majore I, Kasper C, Hass R . Effects of hypoxic culture conditions on umbilical cord-derived human mesenchymal stem cells. Cell Commun Signal. 2010; 8:18. PMC: 2918620. DOI: 10.1186/1478-811X-8-18. View

4.
Xia C, Yin H, Borlongan C, Chao J, Chao L . Adrenomedullin gene delivery protects against cerebral ischemic injury by promoting astrocyte migration and survival. Hum Gene Ther. 2005; 15(12):1243-54. DOI: 10.1089/hum.2004.15.1243. View

5.
Yang J, Mukda S, Chen S . Diverse roles of mitochondria in ischemic stroke. Redox Biol. 2018; 16:263-275. PMC: 5854930. DOI: 10.1016/j.redox.2018.03.002. View