Podocyte Senescence and Aging
Kidney360, ISSN: 2641-7650, Vol: 4, Issue: 12, Page: 1784-1793
2023
- 5Citations
- 10Captures
- 1Mentions
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Citations5
- Citation Indexes5
- CrossRef1
- Captures10
- Readers10
- 10
- Mentions1
- News Mentions1
- 1
Most Recent News
Studies from University of Washington in the Area of Podocytes Described (Podocyte Senescence and Aging)
2023 NOV 28 (NewsRx) -- By a News Reporter-Staff News Editor at Genomics & Genetics Daily -- Current study results on podocytes have been published.
Article Description
As the population in many industrial countries is aging, the risk, incidence, and prevalence of CKD increases. In the kidney, advancing age results in a progressive decrease in nephron number and an increase in glomerulosclerosis. In this review, we focus on the effect of aging on glomerular podocytes, the post-mitotic epithelial cells critical for the normal integrity and function of the glomerular filtration barrier. The podocytes undergo senescence and transition to a senescence-associated secretory phenotype typified by the production and secretion of inflammatory cytokines that can influence neighboring glomerular cells by paracrine signaling. In addition to senescence, the aging podocyte phenotype is characterized by ultrastructural and functional changes; hypertrophy; cellular, oxidative, and endoplasmic reticulum stress; reduced autophagy; and increased expression of aging genes. This results in a reduced podocyte health span and a shortened life span. Importantly, these changes in the pathways/processes characteristic of healthy podocyte aging are also often similar to pathways in the disease-induced injured podocyte. Finally, the better understanding of podocyte aging and senescence opens therapeutic options to slow the rate of podocyte aging and promote kidney health.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85181159622&origin=inward; http://dx.doi.org/10.34067/kid.0000000000000284; http://www.ncbi.nlm.nih.gov/pubmed/37950369; https://journals.lww.com/10.34067/KID.0000000000000284; https://dx.doi.org/10.34067/kid.0000000000000284; https://journals.lww.com/kidney360/abstract/9900/podocyte_senescence_and_aging.260.aspx
Ovid Technologies (Wolters Kluwer Health)
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