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In vivo dynamics of senescence in rhabdomyolysis-induced acute kidney injury.
- Source :
-
Biochemical and biophysical research communications [Biochem Biophys Res Commun] 2023 Sep 17; Vol. 673, pp. 121-130. Date of Electronic Publication: 2023 Jun 15. - Publication Year :
- 2023
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Abstract
- Cellular senescence is involved in the pathogenesis of various diseases, including acute kidney injury (AKI). AKI is defined as a sudden loss of kidney function. In severe AKI, irreversible loss of kidney cells can occur. Cellular senescence might contribute to this maladaptive tubular repair, though, its pathophysiological role in vivo is incompletely understood. In this study, we used p16-CreERT2-tdTomato mice in which cells with high p16 expression, a prototypical senescent marker, are labeled with tdTomato fluorescence. Then, we induced AKI by rhabdomyolysis and traced the cells with high p16 expression following AKI. We proved that the induction of senescence was observed predominantly in proximal tubular epithelial cells (PTECs) and occurred in a relatively acute phase within 1-3 days after AKI. These acute senescent PTECs were spontaneously eliminated by day 15. On the contrary, the generation of senescence in PTECs persisted during the chronic recovery phase. We also confirmed that the kidney function did not fully recover on day 15. These results suggest that the chronic generation of senescent PTECs might contribute to maladaptive recovery from AKI and lead to chronic kidney disease progression.<br />Competing Interests: Declaration of competing interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests:Makoto Nakanishi reports financial support was provided by reverSASP Therapeutics Co., Airweave Co. Makoto Nakanishi reports a relationship with Airweave Co., reverSASP Therapeutics Co. that includes: consulting or advisory.<br /> (Copyright © 2023 Elsevier Inc. All rights reserved.)
Details
- Language :
- English
- ISSN :
- 1090-2104
- Volume :
- 673
- Database :
- MEDLINE
- Journal :
- Biochemical and biophysical research communications
- Publication Type :
- Academic Journal
- Accession number :
- 37385006
- Full Text :
- https://doi.org/10.1016/j.bbrc.2023.06.046