Acute Kidney Injury as a Condition of Renal Senescence

• Published in: Cell transplantation Vol. 27; no. 5; pp. 739 - 753
• Main Authors: Andrade, Lucia, Rodrigues, Camila E., Gomes, Samirah A., Noronha, Irene L.
• Format: Journal Article
• Language: English
• Published: Los Angeles, CA SAGE Publications 01.05.2018; Sage Publications Ltd; SAGE Publishing
• Subjects: Acute Kidney Injury - pathology; Acute Kidney Injury - therapy; Aging - pathology; Angiogenesis; Animals; Apoptosis; Atrophy; Cell cycle; Cell Cycle Checkpoints; Cell death; Cell injury; Cell membranes; Cytoskeleton; Disease Progression; DNA damage; Epithelial cells; Fibrosis; Glucuronidase - genetics; Humans; Immunomodulation; Ischemia; Kidney - pathology; Kidney diseases; Kidneys; Klotho protein; Mesenchymal stem cells; Mesenchyme; miRNA; Oxidative stress; Phagocytosis; Phenotypes; Recovery of function; Reviews; Senescence; Stem cells; Umbilical cord; acute kidney injury; cell cycle arrest; Klotho; oxidative stress; telomeres; mesenchymal stromal cells
• ISSN: 0963-6897; 1555-3892; 1555-3892
• DOI: 10.1177/0963689717743512

Acute kidney injury (AKI), characterized by a sharp drop in glomerular filtration, continues to be a significant health burden because it is associated with high initial mortality, morbidity, and substantial health-care costs. There is a strong connection between AKI and mechanisms of senescence activation. After ischemic or nephrotoxic insults, a wide range of pathophysiological events occur. Renal tubular cell injury is characterized by cell membrane damage, cytoskeleton disruption, and DNA degradation, leading to tubular cell death by necrosis and apoptosis. The senescence mechanism involves interstitial fibrosis, tubular atrophy, and capillary rarefaction, all of which impede the morphological and functional recovery of the kidneys, suggesting a strong link between AKI and the progression of chronic kidney disease. During abnormal kidney repair, tubular epithelial cells can assume a senescence-like phenotype. Cellular senescence can occur as a result of cell cycle arrest due to increased expression of cyclin kinase inhibitors (mainly p21), downregulation of Klotho expression, and telomere shortening. In AKI, cellular senescence is aggravated by other factors including oxidative stress and autophagy. Given this scenario, the main question is whether AKI can be repaired and how to avoid the senescence process. Stem cells might constitute a new therapeutic approach. Mesenchymal stem cells (MSCs) can ameliorate kidney injury through angiogenesis, immunomodulation, and fibrosis pathway blockade, as well as through antiapoptotic and promitotic processes. Young umbilical cord–derived MSCs are better at increasing Klotho levels, and thus protecting tissues from senescence, than are adipose-derived MSCs. Umbilical cord–derived MSCs improve glomerular filtration and tubular function to a greater degree than do those obtained from adult tissue. Although senescence-related proteins and microRNA are upregulated in AKI, they can be downregulated by treatment with umbilical cord–derived MSCs. In summary, stem cells derived from young tissues, such as umbilical cord–derived MSCs, could slow the post-AKI senescence process.