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Reproducible Large-Scale Isolation of Exosomes from Adipose Tissue-Derived Mesenchymal Stem/Stromal Cells and Their Application in Acute Kidney Injury. | LitMetric

AI Article Synopsis

  • AKI is a serious condition that can quickly lead to death due to sudden kidney failure.
  • Previous research shows that exosomes from mesenchymal stem/stromal cells can help improve kidney injuries in animal models, but mass-producing these exosomes for clinical use has been difficult.
  • This study highlights the successful large-scale production of ASC-exosomes using tangential flow filtration (TFF) and their potential lifesaving effects in a specific rat model of AKI, suggesting they could be a valuable treatment for severe kidney issues.

Article Abstract

Acute kidney injury (AKI) is a fatal medical episode caused by sudden kidney damage or failure, leading to the death of patients within a few hours or days. Previous studies demonstrated that exosomes derived from various mesenchymal stem/stromal cells (MSC-exosomes) have positive effects on renal injuries in multiple experimental animal models of kidney diseases including AKI. However, the mass production of exosomes is a challenge not only in preclinical studies with large animals but also for successful clinical applications. In this respect, tangential flow filtration (TFF) is suitable for good manufacturing practice (GMP)-compliant large-scale production of high-quality exosomes. Until now, no studies have been reported on the use of TFF, but rather ultracentrifugation has been almost exclusively used, to isolate exosomes for AKI therapeutic application in preclinical studies. Here, we demonstrated the reproducible large-scale production of exosomes derived from adipose tissue-derived MSC (ASC-exosomes) using TFF and the lifesaving effect of the ASC-exosomes in a lethal model of cisplatin-induced rat AKI. Our results suggest the possibility of large-scale stable production of ASC-exosomes without loss of function and their successful application in life-threatening diseases.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7370182PMC
http://dx.doi.org/10.3390/ijms21134774DOI Listing

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