The Anti-Inflammatory, Anti-Oxidative, and Anti-Apoptotic Benefits of Stem Cells in Acute Ischemic Kidney Injury.
Kuo-Hua LeeWei-Cheng TsengChih-Yu YangDer-Cherng TarngPublished in: International journal of molecular sciences (2019)
Ischemia-reperfusion injury (IRI) plays a significant role in the pathogenesis of acute kidney injury (AKI). The complicated interaction between injured tubular cells, activated endothelial cells, and the immune system leads to oxidative stress and systemic inflammation, thereby exacerbating the apoptosis of renal tubular cells and impeding the process of tissue repair. Stem cell therapy is an innovative approach to ameliorate IRI due to its antioxidative, immunomodulatory, and anti-apoptotic properties. Therefore, it is crucial to understand the biological effects and mechanisms of action of stem cell therapy in the context of acute ischemic AKI to improve its therapeutic benefits. The recent finding that treatment with conditioned medium (CM) derived from stem cells is likely an effective alternative to conventional stem cell transplantation increases the potential for future therapeutic uses of stem cell therapy. In this review, we discuss the recent findings regarding stem cell-mediated cytoprotection, with a focus on the anti-inflammatory effects via suppression of oxidative stress and uncompromised immune responses following AKI. Stem cell-derived CM represents a favorable approach to stem cell-based therapy and may serve as a potential therapeutic strategy against acute ischemic AKI.
Keyphrases
- cell therapy
- stem cells
- acute kidney injury
- ischemia reperfusion injury
- oxidative stress
- induced apoptosis
- cell cycle arrest
- anti inflammatory
- cell death
- stem cell transplantation
- liver failure
- cardiac surgery
- respiratory failure
- endoplasmic reticulum stress
- endothelial cells
- immune response
- drug induced
- dna damage
- aortic dissection
- high dose
- diabetic rats
- pi k akt
- signaling pathway
- high glucose
- mesenchymal stem cells
- intensive care unit
- current status
- dendritic cells
- blood brain barrier
- bone marrow
- risk assessment
- combination therapy
- heat shock protein