| Literature DB >> 30609022 |
Saeed Farzamfar1, Akram Hasanpour2, Niloufar Nazeri2, Hengameh Razavi1, Majid Salehi3,4, Shilan Shafei5, Vajiheh T Nooshabadi6, Ahmad Vaez1, Arian Ehterami7, Hamed Sahrapeyma8, Jafar Ai1.
Abstract
Acute renal failure (ARF) is a clinical challenge that is highly resistant to treatment, and its high rate of mortality is alarming. Ischemia-reperfusion injury (IRI) is the most common cause of ARF. Especially IRI is implicated in kidney transplantation and can determine graft survival. Although the exact pathophysiology of renal IRI is unknown, the role of inflammatory responses has been elucidated. Because mesenchymal stromal cells (MSCs) have strong immunomodulatory properties, they are under extensive investigation as a therapeutic modality for renal IRI. Extracellular vesicles (EVs) play an integral role in cell-to-cell communication. Because the regenerative potential of the MSCs can be recapitulated by their EVs, the therapeutic appeal of MSC-derived EVs has dramatically increased in the past decade. Higher safety profile and ease of preservation without losing function are other advantages of EVs compared with their producing cells. In the current review, the preliminary results and potential of MSC-derived EVs to alleviate kidney IRI are summarized. We might be heading toward a cell-free approach to treat renal IRI.Entities:
Keywords: exosomes; extracellular vesicles (EVs); ischemia-reperfusion injury (IRI); microvesicles (MVs); renal failure
Mesh:
Year: 2019 PMID: 30609022 DOI: 10.1002/jcp.27998
Source DB: PubMed Journal: J Cell Physiol ISSN: 0021-9541 Impact factor: 6.384