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Ischemia-Like Stress Conditions Stimulate Trophic Activities of Adipose-Derived Stromal/Stem Cells

Overview
Journal Cells
Publisher MDPI
Date 2020 Aug 23
PMID 32825678
Citations 7
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Abstract

Adipose-derived stromal/stem cells (ASCs) have been shown to exert regenerative functions, which are mainly attributed to the secretion of trophic factors. Upon transplantation, ASCs are facing an ischemic environment characterized by oxygen and nutrient deprivation. However, current knowledge on the secretion capacity of ASCs under such conditions is limited. Thus, the present study focused on the secretory function of ASCs under glucose and oxygen deprivation as major components of ischemia. After exposure to glucose/oxygen deprivation, ASCs maintained distinct viability, but the metabolic activity was greatly reduced by glucose limitation. ASCs were able to secrete a broad panel of factors under glucose/oxygen deprivation as revealed by a cytokine antibody array. Quantification of selected factors by ELISA demonstrated that glucose deprivation in combination with hypoxia led to markedly higher secretion levels of the angiogenic and anti-apoptotic factors IL-6, VEGF, and stanniocalcin-1 as compared to the hypoxic condition alone. A conditioned medium of glucose/oxygen-deprived ASCs promoted the viability and tube formation of endothelial cells, and the proliferation and migration of fibroblasts. These findings indicate that ASCs are stimulated by ischemia-like stress conditions to secrete trophic factors and would be able to exert their beneficial function in an ischemic environment.

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References
1.
Frazier T, Gimble J, Kheterpal I, Rowan B . Impact of low oxygen on the secretome of human adipose-derived stromal/stem cell primary cultures. Biochimie. 2013; 95(12):2286-96. DOI: 10.1016/j.biochi.2013.07.011. View

2.
Choi S, Shin I, Je K, Min E, Kim E, Kim H . Hypoxia antagonizes glucose deprivation on interleukin 6 expression in an Akt dependent, but HIF-1/2α independent manner. PLoS One. 2013; 8(3):e58662. PMC: 3592797. DOI: 10.1371/journal.pone.0058662. View

3.
DiPietro L, Reintjes M, Low Q, Levi B, Gamelli R . Modulation of macrophage recruitment into wounds by monocyte chemoattractant protein-1. Wound Repair Regen. 2001; 9(1):28-33. DOI: 10.1046/j.1524-475x.2001.00028.x. View

4.
Li C, Ye L, Yang L, Yu X, He Y, Chen Z . Rapamycin Promotes the Survival and Adipogenesis of Ischemia-Challenged Adipose Derived Stem Cells by Improving Autophagy. Cell Physiol Biochem. 2017; 44(5):1762-1774. DOI: 10.1159/000485783. View

5.
Vyas K, Vasconez H, Morrison S, Mogni B, Linton S, Hockensmith L . Fat Graft Enrichment Strategies: A Systematic Review. Plast Reconstr Surg. 2020; 145(3):827-841. DOI: 10.1097/PRS.0000000000006557. View