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Molecular mechanisms of renal aging
Open accessAbstract
Epidemiologic, clinical, and molecular evidence suggest that aging is a major contributor to the increasing incidence of acute kidney injury and chronic kidney disease. The aging kidney undergoes complex changes that predispose to renal pathology. The underlying molecular mechanisms could be the target of therapeutic strategies in the future. Here, we summarize recent insight into cellular and molecular processes that have been shown to contribute to the renal aging phenotype.The main clinical finding of renal aging is the decrease in glomerular filtration rate, and its structural correlate is the loss of functioning nephrons. Mechanistically, this has been linked to different processes, such as podocyte hypertrophy, glomerulosclerosis, tubular atrophy, and gradual microvascular rarefaction. Renal functional recovery after an episode of acute kidney injury is significantly worse in elderly patients. This decreased regenerative potential, which is a hallmark of the aging process, may be caused by cellular senescence. Accumulation of senescent cells could explain insufficient repair and functional loss, a view that has been strengthened by recent studies showing that removal of senescent cells results in attenuation of renal aging. Other potential mechanisms are alterations in autophagy as an important component of a disturbed renal stress response and functional differences in the inflammatory system. Promising therapeutic measures to counteract these age-related problems include mimetics of caloric restriction, pharmacologic renin-angiotensin-aldosterone system inhibition, and novel strategies of senotherapy with the goal of reducing the number of senescent cells to decrease aging-related disease in the kidney.
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“As individuals age, the kidneys undergo various structural impairments, such as fibrosis, and experience functional issues, including mitochondrial dysfunction (Fig. 3).144–146”
From Inflammation and aging: signaling pathways and intervention therapies (2023) · cites this paper as [146]
Citations
Cites
A biomarker that identifies senescent human cells in culture and in aging skin in vivo.
Dimri, G. P., Lee, X., Basile, G., Acosta, M., Scott, G., Roskelley, C., Medrano, E. E., Linskens, M., Rubelj, I., & Pereira-Smith, O. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.20.9363 · Cited by 7,477
The limited in vitro lifetime of human diploid cell strains
Hayflick, L. (1965) · Experimental Cell Research · doi:10.1016/0014-4827(65)90211-9 · Cited by 5,876
Telomeres shorten during ageing of human fibroblasts
Harley, C. B., Futcher, A. B., & Greider, C. W. (1990) · Nature · doi:10.1038/345458a0 · Cited by 5,750
The retinoblastoma protein and cell cycle control
Weinberg, R. A. (1995) · Cell · doi:10.1016/0092-8674(95)90385-2 · Cited by 4,862
Clearance of p16Ink4a-positive senescent cells delays ageing-associated disorders
Baker, D. J., Wijshake, T., Tchkonia, T., LeBrasseur, N. K., Childs, B. G., van de Sluis, B., Kirkland, J. L., & van Deursen, J. M. (2011) · Nature · doi:10.1038/nature10600 · Cited by 3,670
Empagliflozin and Progression of Kidney Disease in Type 2 Diabetes
Wanner, C., Inzucchi, S. E., Lachin, J. M., Fitchett, D., von Eynatten, M., Mattheus, M., Johansen, O. E., Woerle, H. J., Broedl, U. C., & Zinman, B. (2016) · New England Journal of Medicine · doi:10.1056/nejmoa1515920 · Cited by 3,655
Aging, Cellular Senescence, and Cancer
Campisi, J. (2013) · Annual Review of Physiology · doi:10.1146/annurev-physiol-030212-183653 · Cited by 2,954 · cited 1×
“Active p53 is able to initiate either apoptosis or senescence via transcriptional upregulation of proapoptotic genes or the cyclin-dependent kinase inhibitor p21CIP1/WAF1, the latter of which inhibits cyclindependent kinases that inactivate the retinoblastoma protein.(52) Hypophosphorylation of the retinoblastoma”
BackgroundNaturally occurring p16Ink4a-positive cells shorten healthy lifespan
Baker, D. J., Childs, B. G., Durik, M., Wijers, M. E., Sieben, C. J., Zhong, J., A. Saltness, R., Jeganathan, K. B., Verzosa, G. C., Pezeshki, A., et al. (2016) · Nature · doi:10.1038/nature16932 · Cited by 2,876
The role of senescent cells in ageing
van Deursen, J. M. (2014) · Nature · doi:10.1038/nature13193 · Cited by 2,623
Cellular senescence in aging and age-related disease: from mechanisms to therapy
Childs, B. G., Durik, M., Baker, D. J., & van Deursen, J. M. (2015) · Nature Medicine · doi:10.1038/nm.4000 · Cited by 2,363
Switching and Signaling at the Telomere
Blackburn, E. H. (2001) · Cell · doi:10.1016/s0092-8674(01)00492-5 · Cited by 2,139
Rubinsztein, D. C., Mariño, G., & Kroemer, G. (2011) · Cell · doi:10.1016/j.cell.2011.07.030 · Cited by 2,107
Autophagy: from phenomenology to molecular understanding in less than a decade
Klionsky, D. J. (2007) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2245 · Cited by 1,977
Clearance of senescent cells by ABT263 rejuvenates aged hematopoietic stem cells in mice
Chang, J., Wang, Y., Shao, L., Laberge, R.-M., Demaria, M., Campisi, J., Janakiraman, K., Sharpless, N. E., Ding, S., Feng, W., et al. (2016) · Nature Medicine · doi:10.1038/nm.4010 · Cited by 1,819
Cellular senescence and the senescent secretory phenotype: therapeutic opportunities
Tchkonia, T., Zhu, Y., van Deursen, J., Campisi, J., & Kirkland, J. L. (2013) · Journal of Clinical Investigation · doi:10.1172/jci64098 · Cited by 1,774
Role of the INK4a Locus in Tumor Suppression and Cell Mortality
Serrano, M., Lee, H.-W., Chin, L., Cordon-Cardo, C., Beach, D., & DePinho, R. A. (1996) · Cell · doi:10.1016/s0092-8674(00)81079-x · Cited by 1,585
Epithelial cell cycle arrest in G2/M mediates kidney fibrosis after injury
Yang, L., Besschetnova, T. Y., Brooks, C. R., Shah, J. V., & Bonventre, J. V. (2010) · Nature Medicine · doi:10.1038/nm.2144 · Cited by 1,333
Cardioprotection and lifespan extension by the natural polyamine spermidine
Eisenberg, T., Abdellatif, M., Schroeder, S., Primessnig, U., Stekovic, S., Pendl, T., Harger, A., Schipke, J., Zimmermann, A., Schmidt, A., et al. (2016) · Nature Medicine · doi:10.1038/nm.4222 · Cited by 1,168
Vascular and Neurogenic Rejuvenation of the Aging Mouse Brain by Young Systemic Factors
Katsimpardi, L., Litterman, N. K., Schein, P. A., Miller, C. M., Loffredo, F. S., Wojtkiewicz, G. R., Chen, J. W., Lee, R. T., Wagers, A. J., & Rubin, L. L. (2014) · Science · doi:10.1126/science.1251141 · Cited by 1,037
Directed elimination of senescent cells by inhibition of BCL-W and BCL-XL
Yosef, R., Pilpel, N., Tokarsky-Amiel, R., Biran, A., Ovadya, Y., Cohen, S., Vadai, E., Dassa, L., Shahar, E., Condiotti, R., et al. (2016) · Nature Communications · doi:10.1038/ncomms11190 · Cited by 1,032
p16INK4a induces an age-dependent decline in islet regenerative potential
Krishnamurthy, J., Ramsey, M. R., Ligon, K. L., Torrice, C., Koh, A., Bonner-Weir, S., & Sharpless, N. E. (2006) · Nature · doi:10.1038/nature05092 · Cited by 1,003 · cited 1×
“senescence depends on cell type and stress and occurs at different rates in different organs.(62) Shorter telomeres occur in the kidney with older age and are present mainly in the cortical region.”
BackgroundLoffredo, F. S., Steinhauser, M. L., Jay, S. M., Gannon, J., Pancoast, J. R., Yalamanchi, P., Sinha, M., Dall’Osso, C., Khong, D., Shadrach, J. L., et al. (2013) · Cell · doi:10.1016/j.cell.2013.04.015 · Cited by 948
Xu, M., Tchkonia, T., Ding, H., Ogrodnik, M., Lubbers, E. R., Pirtskhalava, T., White, T. A., Johnson, K. O., Stout, M. B., Mezera, V., et al. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1515386112 · Cited by 915
Kurz, D. J., Decary, S., Hong, Y., & Erusalimsky, J. D. (2000) · Journal of Cell Science · doi:10.1242/jcs.113.20.3613 · Cited by 899
Mechanisms of maladaptive repair after AKI leading to accelerated kidney ageing and CKD
Ferenbach, D. A., & Bonventre, J. V. (2015) · Nature Reviews Nephrology · doi:10.1038/nrneph.2015.3 · Cited by 892
Restoring systemic GDF11 levels reverses age-related dysfunction in mouse skeletal muscle
Sinha, M., Jang, Y. C., Oh, J., Khong, D., Wu, E. Y., Manohar, R., Miller, C., Regalado, S. G., Loffredo, F. S., Pancoast, J. R., et al. (2014) · Science · doi:10.1126/science.1251152 · Cited by 824
Angiotensin II revisited: new roles in inflammation, immunology and aging
Benigni, A., Cassis, P., & Remuzzi, G. (2010) · EMBO Molecular Medicine · doi:10.1002/emmm.201000080 · Cited by 757
Hartleben, B., Gödel, M., Meyer-Schwesinger, C., Liu, S., Ulrich, T., Köbler, S., Wiech, T., Grahammer, F., Arnold, S. J., Lindenmeyer, M. T., et al. (2010) · Journal of Clinical Investigation · doi:10.1172/jci39492 · Cited by 721
The Aging Kidney: Physiological Changes
Weinstein, J., & Anderson, S. (2010) · Advances in Chronic Kidney Disease · doi:10.1053/j.ackd.2010.05.002 · Cited by 661
Kume, S., Uzu, T., Horiike, K., Chin-Kanasaki, M., Isshiki, K., Araki, S.-I., Sugimoto, T., Haneda, M., Kashiwagi, A., & Koya, D. (2010) · Journal of Clinical Investigation · doi:10.1172/jci41376 · Cited by 640
Autophagy and aging: keeping that old broom working
Cuervo, A. M. (2008) · Trends in Genetics · doi:10.1016/j.tig.2008.10.002 · Cited by 527
Disruption of the Ang II type 1 receptor promotes longevity in mice
Benigni, A., Corna, D., Zoja, C., Sonzogni, A., Latini, R., Salio, M., Conti, S., Rottoli, D., Longaretti, L., Cassis, P., et al. (2009) · Journal of Clinical Investigation · doi:10.1172/jci36703 · Cited by 486
Differentiated kidney epithelial cells repair injured proximal tubule
Kusaba, T., Lalli, M., Kramann, R., Kobayashi, A., & Humphreys, B. D. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1310653110 · Cited by 476
Protein Homeostasis and Aging: the importance of exquisite quality control
Koga, H., Kaushik, S., & Cuervo, A. M. (2011) · Ageing research reviews · doi:10.1016/j.arr.2010.02.001 · Cited by 476
Pathways to nephron loss starting from glomerular diseases—Insights from animal models
Kriz, W., & LeHir, M. (2005) · Kidney International · doi:10.1111/j.1523-1755.2005.67097.x · Cited by 462
The Substantial Loss of Nephrons in Healthy Human Kidneys with Aging
Đenić, A., Lieske, J. C., Chakkera, H. A., Poggio, E. D., Alexander, M. P., Singh, P. Y., Kremers, W. K., Lerman, L. O., & Rule, A. D. (2016) · Journal of the American Society of Nephrology · doi:10.1681/asn.2016020154 · Cited by 453
Rethinking Chronic Allograft Nephropathy
Halloran, P. F., Melk, A., & BARTH, C. (1999) · Journal of the American Society of Nephrology · doi:10.1681/asn.v101167 · Cited by 448
Self-citationWiggins, J. E., Goyal, M., Sanden, S. K., Wharram, B. L., Shedden, K. A., Misek, D. E., Kuick, R. D., & Wiggins, R. C. (2005) · Journal of the American Society of Nephrology · doi:10.1681/asn.2005050488 · Cited by 422
BRD4 Connects Enhancer Remodeling to Senescence Immune Surveillance
Tasdemir, N., Banito, A., Roe, J.-S., Alonso-Curbelo, D., Camiolo, M., Tschaharganeh, D. F., Huang, C.-H., Aksoy, O., Bolden, J. E., Chen, C.-C., et al. (2016) · Cancer Discovery · doi:10.1158/2159-8290.cd-16-0217 · Cited by 415 · cited 1×
“However, the recent finding that bromodomain-containing protein 4 inhibition interferes with immune cell–mediated targeting and elimination of senescent cells points to the possibility to combat SASP more specifically.(148)”
BackgroundWright, W. E., & Shay, J. W. (2000) · Nature Medicine · doi:10.1038/78592 · Cited by 398
Hoy, W. E., Douglas-Denton, R. N., Hughson, M. D., Cass, A., Johnson, K., & Bertram, J. F. (2003) · Kidney International · doi:10.1046/j.1523-1755.63.s83.8.x · Cited by 390
Repair of injured proximal tubule does not involve specialized progenitors
Humphreys, B. D., Czerniak, S., DiRocco, D. P., Hasnain, W., Cheema, R., & Bonventre, J. V. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1100629108 · Cited by 369
Melk, A., Schmidt, B. M. W., Takeuchi, O., Sawitzki, B., Rayner, D. C., & Halloran, P. F. (2004) · Kidney International · doi:10.1111/j.1523-1755.2004.00438.x · Cited by 362
Self-citationThe Search for Antiaging Interventions: From Elixirs to Fasting Regimens
de Cabo, R., Carmona-Gutierrez, D., Bernier, M., Hall, M. N., & Madeo, F. (2014) · Cell · doi:10.1016/j.cell.2014.05.031 · Cited by 345
Ketoanalogue-Supplemented Vegetarian Very Low–Protein Diet and CKD Progression
Gârneaţă, L., Stancu, A., Dragomir, D. R., Ştefan, G., & Mircescu, G. (2016) · Journal of the American Society of Nephrology · doi:10.1681/asn.2015040369 · Cited by 339
Schmitt, R., Coca, S. G., Kanbay, M., Tinetti, M. E., Cantley, L. G., & Parikh, C. R. (2008) · American Journal of Kidney Diseases · doi:10.1053/j.ajkd.2008.03.005 · Cited by 323
Self-citationAntioxidant Supplementation in the Treatment of Aging-Associated Diseases
Conti, V., Izzo, V., Corbi, G., Russomanno, G., Manzo, V., Lise, F. D., Donato, A. D., & Filippelli, A. (2016) · Frontiers in Pharmacology · doi:10.3389/fphar.2016.00024 · Cited by 302
Calorie restriction as an intervention in ageing
López‐Lluch, G., & Navas, P. (2015) · The Journal of Physiology · doi:10.1113/jp270543 · Cited by 301
Glassock, R. J., & Rule, A. D. (2012) · Kidney International · doi:10.1038/ki.2012.65 · Cited by 292
Senescent Cells: A Novel Therapeutic Target for Aging and Age-Related Diseases
Naylor, R. M., Baker, D. J., & van Deursen, J. M. (2012) · Clinical Pharmacology & Therapeutics · doi:10.1038/clpt.2012.193 · Cited by 287
Kosar, M., Bartkova, J., Hubackova, S., Hodny, Z., Lukas, J., & Bartek, J. (2011) · Cell Cycle · doi:10.4161/cc.10.3.14707 · Cited by 283
Kang, D., Anderson, S., Kim, Y.-G., Mazzalli, M., Suga, S., Jefferson, J. A., GORDON, K. L., Oyama, T., Hughes, J., Hugo, C., et al. (2001) · American Journal of Kidney Diseases · doi:10.1053/ajkd.2001.22087 · Cited by 283
Cellular senescence and the senescent secretory phenotype in age-related chronic diseases
Zhu, Y., Armstrong, J. L., Tchkonia, T., & Kirkland, J. L. (2014) · Current Opinion in Clinical Nutrition and Metabolic Care · doi:10.1097/mco.0000000000000065 · Cited by 273
Autophagy plays a critical role in kidney tubule maintenance, aging and ischemia-reperfusion injury
Liu, S., Hartleben, B., Kretz, O., Wiech, T., Igarashi, P., Mizushima, N., Walz, G., & Huber, T. B. (2012) · Autophagy · doi:10.4161/auto.19419 · Cited by 271
Emerging role of autophagy in kidney function, diseases and aging
Huber, T. B., Edelstein, C. L., Hartleben, B., Inoki, K., Jiang, M., Koya, D., Kume, S., Lieberthal, W., Pallet, N., Quiroga, A., et al. (2012) · Autophagy · doi:10.4161/auto.19821 · Cited by 261
Zhao, Y., Banerjee, S., Dey, N., LeJeune, W. S., Sarkar, P. S., Brobey, R. K. B., Rosenblatt, K. P., Tilton, R. G., & Choudhary, S. (2011) · Diabetes · doi:10.2337/db10-1262 · Cited by 232
Flatt, T. (2012) · Frontiers in Genetics · doi:10.3389/fgene.2012.00148 · Cited by 229
How autophagy both activates and inhibits cellular senescence
Kang, C., & Elledge, S. J. (2016) · Autophagy · doi:10.1080/15548627.2015.1121361 · Cited by 228 · cited 3×
“The level of autophagic flux, on the other hand, might directly regulate crucial senescence features, such as the SASP.(90) In addition, the consequences of autophagy for senescence induction are highly variable: ablation of Atg5 limited to the S3 segment of the proximal tubule resulted in protection from postischemic…”
BackgroundInfluentialTubulointerstitial disease in aging
Thomas, S. E., Anderson, S., GORDON, K. L., Oyama, T., Shankland, S. J., & Johnson, R. J. (1998) · Journal of the American Society of Nephrology · doi:10.1681/asn.v92231 · Cited by 219
Aging and the Kidneys: Anatomy, Physiology and Consequences for Defining Chronic Kidney Disease
Glassock, R. J., & Rule, A. D. (2016) · The Nephron journals/Nephron journals · doi:10.1159/000445450 · Cited by 216
Glomerular Aging and Focal Global Glomerulosclerosis
Hodgin, J. B., Bitzer, M., Wickman, L. T., Afshinnia, F., Wang, S. Q., O'Connor, C. L., Yang, Y., Meadowbrooke, C. C., Chowdhury, M., Kikuchi, M., et al. (2015) · Journal of the American Society of Nephrology · doi:10.1681/asn.2014080752 · Cited by 215
Human POT1 Facilitates Telomere Elongation by Telomerase
Colgin, L. M., Baran, K., Baumann, P., Cech, T. R., & Reddel, R. R. (2003) · Current Biology · doi:10.1016/s0960-9822(03)00339-7 · Cited by 212
New Autophagy Reporter Mice Reveal Dynamics of Proximal Tubular Autophagy
Li, L., Wang, Z. V., Hill, J. A., & Lin, F. (2014) · Journal of the American Society of Nephrology · doi:10.1681/asn.2013040374 · Cited by 206
Melk, A., Kittikowit, W., Sandhu, I., Halloran, K. M., Grimm, P., Schmidt, B. M. W., & Halloran, P. F. (2003) · Kidney International · doi:10.1046/j.1523-1755.2003.00032.x · Cited by 205
Self-citationBábíčková, J., Klinkhammer, B. M., Buhl, E. M., Djudjaj, S., Hoß, M., Heymann, F., Tacke, F., Floege, J., Becker, J. U., & Boor, P. (2016) · Kidney International · doi:10.1016/j.kint.2016.07.038 · Cited by 195
Telomere Shortening in Kidneys with Age
MELK, A., RAMASSAR, V., HELMS, L. M. H., MOORE, R., RAYNER, D., SOLEZ, K., & HALLORAN, P. F. (2000) · Journal of the American Society of Nephrology · doi:10.1681/asn.v113444 · Cited by 189
Self-citationUnraveling the Role of Podocyte Turnover in Glomerular Aging and Injury
Wanner, N., Hartleben, B., Herbach, N., Goedel, M., Stickel, N., Zeiser, R., Walz, G., Moeller, M. J., Grahammer, F., & Huber, T. B. (2014) · Journal of the American Society of Nephrology · doi:10.1681/asn.2013050452 · Cited by 189
Cellular Senescence Limits Regenerative Capacity and Allograft Survival
Braun, H., Schmidt, B. M. W., Raiss, M., Baisantry, A., Mircea-Constantin, D., Wang, S., Groß, M.-L., Serrano, M., Schmitt, R., & Melk, A. (2012) · Journal of the American Society of Nephrology · doi:10.1681/asn.2011100967 · Cited by 180
Self-citationGrowth-Dependent Podocyte Failure Causes Glomerulosclerosis
Fukuda, A., Chowdhury, M. A., Venkatareddy, M. P., Wang, S. Q., Nishizono, R., Suzuki, T., Wickman, L. T., Wiggins, J. E., Muchayi, T., Fingar, D. C., et al. (2012) · Journal of the American Society of Nephrology · doi:10.1681/asn.2012030271 · Cited by 170
The impact of aging on kidney repair
Schmitt, R., & Cantley, L. G. (2008) · American Journal of Physiology-Renal Physiology · doi:10.1152/ajprenal.00543.2007 · Cited by 169
Self-citationDNA Damage Response and Autophagy: A Meaningful Partnership
Eliopoulos, A. G., Havaki, S., & Gorgoulis, V. G. (2016) · Frontiers in Genetics · doi:10.3389/fgene.2016.00204 · Cited by 169
Clinical strategies and animal models for developing senolytic agents
Kirkland, J. L., & Tchkonia, T. (2015) · Experimental Gerontology · doi:10.1016/j.exger.2014.10.012 · Cited by 168 · cited 1×
“This approach was first tested by using senolytic transgene strategies, as described previously in the context of p16INK4a,(45,141) and has recently been extended to pharmacologic strategies.(142) The induction of apoptosis in senescent cells through BH3-mimetics ABT-737 and ABT-263 that inhibit prosurvival genes Bcl-…”
MethodHard, G. C., & Khan, K. N. (2004) · Toxicologic Pathology · doi:10.1080/01926230490422574 · Cited by 167
Alimbetov, D., Davis, T., Brook, A. J. C., Cox, L. S., Faragher, R. G. A., Nurgozhin, T., Zhumadilov, Z., & Kipling, D. (2016) · Biogerontology · doi:10.1007/s10522-015-9610-z · Cited by 162
Autophagy in kidney disease and aging: lessons from rodent models
Lenoir, O., Tharaux, P., & Huber, T. B. (2016) · Kidney International · doi:10.1016/j.kint.2016.04.014 · Cited by 156
Melk, A., Schmidt, B. M. W., Vongwiwatana, A., Rayner, D. C., & Halloran, P. F. (2005) · American Journal of Transplantation · doi:10.1111/j.1600-6143.2005.00846.x · Cited by 154
Self-citationEhling, J., Bábíčková, J., Gremse, F., Klinkhammer, B. M., Baetke, S. C., Knuechel, R., Kiessling, F. M., Floege, J., Lammers, T., & Boor, P. (2015) · Journal of the American Society of Nephrology · doi:10.1681/asn.2015020204 · Cited by 154
Westhoff, J. H., Hilgers, K. F., Steinbach, M. P., Hartner, A., Klanke, B., Amann, K., & Melk, A. (2008) · Hypertension · doi:10.1161/hypertensionaha.107.099432 · Cited by 152
Self-citationKitada, K., Nakano, D., Ohsaki, H., Hitomi, H., Minamino, T., Yatabe, J., Felder, R. A., Mori, H., Masaki, T., Kobori, H., et al. (2014) · Journal of Diabetes and its Complications · doi:10.1016/j.jdiacomp.2014.05.010 · Cited by 151
Regression of sclerosis in aging by an angiotensin inhibition-induced decrease in PAI-1
Ma, L., Nakamura, S., Whitsitt, J. S., Marcantoni, C., Davidson, J. M., & Fogo, A. B. (2000) · Kidney International · doi:10.1046/j.1523-1755.2000.00426.x · Cited by 144
Telomere Shortening Reduces Regenerative Capacity after Acute Kidney Injury
Westhoff, J. H., Schildhorn, C., Jacobi, C., Hömme, M., Hartner, A., Braun, H., Kryzer, C., Wang, C., von Zglinicki, T., Kränzlin, B., et al. (2010) · Journal of the American Society of Nephrology · doi:10.1681/asn.2009010072 · Cited by 139
Self-citationYamamoto, T., Takabatake, Y., Kimura, T., Takahashi, A., Namba, T., Matsuda, J., Minami, S., Kaimori, J.-Y., Matsui, I., Kitamura, H., et al. (2016) · Autophagy · doi:10.1080/15548627.2016.1159376 · Cited by 135
The aging kidney: increased susceptibility to nephrotoxicity
Wang, X., Bonventre, J., & Parrish, A. (2014) · International Journal of Molecular Sciences · doi:10.3390/ijms150915358 · Cited by 132
Prattichizzo, F., De Nigris, V., La Sala, L., Procopio, A. D., Olivieri, F., & Ceriello, A. (2016) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2016/1810327 · Cited by 129
CDK4/6 inhibition induces epithelial cell cycle arrest and ameliorates acute kidney injury
DiRocco, D. P., Bisi, J., Roberts, P. J., Strum, J. C., Wong, K., Sharpless, N. E., & Humphreys, B. D. (2013) · American Journal of Physiology-Renal Physiology · doi:10.1152/ajprenal.00475.2013 · Cited by 127
From Mitochondria to Disease: Role of the Renin-Angiotensin System
de Cavanagh, E. M. V., Inserra, F., Ferder, M., & Ferder, L. (2007) · American Journal of Nephrology · doi:10.1159/000107757 · Cited by 124
Markers of cellular senescence in zero hour biopsies predict outcome in renal transplantation
Koppelstaetter, C., Schratzberger, G., Perco, P., Hofer, J., Mark, W., Öllinger, R., Oberbauer, R., Schwarz, C., Mitterbauer, C., Kainz, A., et al. (2008) · Aging Cell · doi:10.1111/j.1474-9726.2008.00398.x · Cited by 124
Clements, M. E., Chaber, C. J., Ledbetter, S. R., & Zuk, A. (2013) · PLoS ONE · doi:10.1371/journal.pone.0070464 · Cited by 123
Mitochondrial Biogenesis in Kidney Disease
Weinberg, J. M. (2011) · Journal of the American Society of Nephrology · doi:10.1681/asn.2010060643 · Cited by 119
Peritubular capillary rarefaction: a new therapeutic target in chronic kidney disease
Kida, Y., Tchao, B. N., & Yamaguchi, I. (2013) · Pediatric Nephrology · doi:10.1007/s00467-013-2430-y · Cited by 117
Zhou, X., Chen, K., Lei, H., & Sun, Z. (2014) · Journal of the American Society of Nephrology · doi:10.1681/asn.2013101033 · Cited by 115
Pabla, N., Gibson, A. A., Buege, M., Ong, S. S., Li, L., Hu, S., Du, G., Sprowl, J. A., Vasilyeva, A., Janke, L. J., et al. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1424313112 · Cited by 110
Effects of Donor Age and Cell Senescence on Kidney Allograft Survival
Melk, A., Schmidt, B. M. W., Braunc, H., Vongwiwatana, A., Urmson, J. R., Zhu, L. F., Rayner, D. C., & Halloran, P. F. (2008) · American Journal of Transplantation · doi:10.1111/j.1600-6143.2008.02500.x · Cited by 109
Self-citationCellular senescence in pretransplant renal biopsies predicts postoperative organ function
McGlynn, L. M., Stevenson, K. S., Lamb, K. J., Zino, S., Brown, M., Prina, A., Kingsmore, D. B., & Shiels, P. G. (2008) · Aging Cell · doi:10.1111/j.1474-9726.2008.00447.x · Cited by 108
Hard, G. C., Johnson, K. J., & Cohen, S. M. (2009) · Critical Reviews in Toxicology · doi:10.1080/10408440802368642 · Cited by 106
Zag Expression during Aging Suppresses Proliferation after Kidney Injury
Schmitt, R., Marlier, A., & Cantley, L. G. (2008) · Journal of the American Society of Nephrology · doi:10.1681/asn.2008010035 · Cited by 106
Self-citationElsherbiny, H. E., Alexander, M. P., Kremers, W. K., Park, W. D., Poggio, E. D., Prieto, M., Lieske, J. C., & Rule, A. D. (2014) · Clinical Journal of the American Society of Nephrology · doi:10.2215/cjn.02560314 · Cited by 105
Bonventre, J. V. (2014) · Kidney International Supplements · doi:10.1038/kisup.2014.8 · Cited by 103
Cell Senescence and Its Implications for Nephrology
Melk, A., & Halloran, P. F. (2001) · Journal of the American Society of Nephrology · doi:10.1681/asn.v122385 · Cited by 101
Self-citationAutophagy Induces Prosenescent Changes in Proximal Tubular S3 Segments
Baisantry, A., Bhayana, S., Rong, S., Ermeling, E., Wrede, C., Hegermann, J., Pennekamp, P., Sörensen-Zender, I., Haller, H., Melk, A., et al. (2016) · Journal of the American Society of Nephrology · doi:10.1681/asn.2014111059 · Cited by 97
Self-citationBaylis, C. (2005) · Experimental Gerontology · doi:10.1016/j.exger.2005.01.008 · Cited by 95
Senescence of renal cells: molecular basis and clinical implications
Melk, A. (2003) · Nephrology Dialysis Transplantation · doi:10.1093/ndt/gfg322 · Cited by 92
Self-citationAutophagy and the kidney: health and disease
Takabatake, Y., Kimura, T., Takahashi, A., & Isaka, Y. (2014) · Nephrology Dialysis Transplantation · doi:10.1093/ndt/gft535 · Cited by 92
Ning, Y., Cai, G., Zhuo, L., Gao, J., Dong, D. F., Cui, S., Feng, Z., Shi, S., Bai, X., Sun, X., et al. (2013) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2013.11.006 · Cited by 91
Cheng, H., Fan, X., Lawson, W. E., Paueksakon, P., & Harris, R. C. (2015) · Kidney International · doi:10.1038/ki.2015.69 · Cited by 89
van der Heijden, R. A., Bijzet, J., Meijers, W. C., Yakala, G. K., Kleemann, R., Nguyen, T. Q., de Boer, R. A., Schalkwijk, C. G., Hazenberg, B. P. C., Tietge, U. J. F., et al. (2015) · Scientific Reports · doi:10.1038/srep16474 · Cited by 83
Ablation of the p16INK4a tumour suppressor reverses ageing phenotypes of klotho mice
Sato, S., Kawamata, Y., Takahashi, A., Imai, Y., Hanyu, A., Okuma, A., Takasugi, M., Yamakoshi, K., Sorimachi, H., Kanda, H., et al. (2015) · Nature Communications · doi:10.1038/ncomms8035 · Cited by 77
Reliability of Transcutaneous Measurement of Renal Function in Various Strains of Conscious Mice
Schock‐Kusch, D., Geraci, S., Ermeling, E., Shulhevich, Y., Sticht, C., Hesser, J. W., Stsepankou, D., Neudecker, S., Pill, J., Schmitt, R., et al. (2013) · PLoS ONE · doi:10.1371/journal.pone.0071519 · Cited by 72
Self-citationZeng, Y., Wang, P.-H., Zhang, M., & Du, J. (2015) · Aging Clinical and Experimental Research · doi:10.1007/s40520-015-0371-y · Cited by 68
Donor age intensifies the early immune response after transplantation
Reutzel‐Selke, A., Jurisch, A., Denecke, C., Pascher, A., Martins, P. N. A., Kessler, H., Tamura, A., Utku, N., Pratschke, J., Neuhaus, P., et al. (2007) · Kidney International · doi:10.1038/sj.ki.5002098 · Cited by 68
Wiggins, J. E. (2012) · The Journals of Gerontology Series A · doi:10.1093/gerona/gls157 · Cited by 65
Aging and endothelin: Determinants of disease
Barton, M. (2014) · Life Sciences · doi:10.1016/j.lfs.2014.09.009 · Cited by 63
McKiernan, S. H., Tuen, V. C., Baldwin, K. R., Wanagat, J., Djamali, A., & Aiken, J. M. (2007) · American Journal of Physiology-Renal Physiology · doi:10.1152/ajprenal.00307.2006 · Cited by 63
Berkenkamp, B., Susnik, N., Baisantry, A., Kuznetsova, I., Jacobi, C., Sörensen-Zender, I., Broecker, V., Haller, H. G., Melk, A., & Schmitt, R. (2014) · PLoS ONE · doi:10.1371/journal.pone.0088071 · Cited by 60
Self-citationGlomerular Function, Structure, and Number in Renal Allografts from Older Deceased Donors
Tan, J. C., Workeneh, B., Busque, S., Blouch, K. L., Derby, G. C., & Myers, B. D. (2008) · Journal of the American Society of Nephrology · doi:10.1681/asn.2008030306 · Cited by 60
Endostatin and transglutaminase 2 are involved in fibrosis of the aging kidney
Lin, C. H. S., Chen, J., Zhang, Z., Johnson, G. V. W., Cooper, A. J. L., Feola, J., Bank, A., Shein, J., Ruotsalainen, H. J., Pihlajaniemi, T. A., et al. (2016) · Kidney International · doi:10.1016/j.kint.2016.01.030 · Cited by 59
Renal tubular Notch signaling triggers a prosenescent state after acute kidney injury
Sörensen-Zender, I., Rong, S., Susnik, N., Zender, S., Pennekamp, P., Melk, A., Haller, H. G., & Schmitt, R. (2014) · American Journal of Physiology-Renal Physiology · doi:10.1152/ajprenal.00030.2014 · Cited by 58
Self-citationGDF11 improves tubular regeneration after acute kidney injury in elderly mice
Zhang, Y., Li, Q., Liu, D., Huang, Q., Cai, G., Cui, S., Sun, X., & Chen, X. (2016) · Scientific Reports · doi:10.1038/srep34624 · Cited by 58
Ge, S., Nie, S., Liu, Z., Chen, C., Zha, Y., Qian, J., Liu, B., Teng, S., Xu, A., Wei, B., et al. (2016) · BMC Nephrology · doi:10.1186/s12882-016-0351-2 · Cited by 54
Zinc-α2-Glycoprotein Exerts Antifibrotic Effects in Kidney and Heart
Sörensen-Zender, I., Bhayana, S., Susnik, N., Rolli, V., Bátkai, S., Baisantry, A., Bahram, S., Sen, P., Teng, B., Lindner, R. M., et al. (2015) · Journal of the American Society of Nephrology · doi:10.1681/asn.2014050485 · Cited by 50
Self-citationReplicative senescence in kidney aging, renal disease, and renal transplantation.
Naesens, M. (2011) · PubMed · Cited by 45
Aging-associated renal disease in mice is fructokinase dependent
Roncal-Jiménez, C. A., Ishimoto, T., Lanaspa, M. A., Milagres, T., Andrés-Hernando, A., Jensen, T., Miyazaki, M., Doke, T., Hayasaki, T., Nakagawa, T., et al. (2016) · American Journal of Physiology-Renal Physiology · doi:10.1152/ajprenal.00306.2016 · Cited by 45
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Stefańska, A., Eng, D. G., Kaverina, N. V., Duffield, J. S., Pippin, J. W., Rabinovitch, P. S., & Shankland, S. J. (2015) · Aging · doi:10.18632/aging.100756 · Cited by 44
Baylis, C. (2012) · The Journals of Gerontology Series A · doi:10.1093/gerona/gls171 · Cited by 44
Hochegger, K., Koppelstaetter, C., Tagwerker, A., Huber, J., Heininger, D., Mayer, G. J., & Rosenkranz, A. R. (2006) · American Journal of Physiology-Renal Physiology · doi:10.1152/ajprenal.00084.2006 · Cited by 41
Age-dependent renal cortical microvascular loss in female mice
Urbieta-Caceres, V. H., Syed, F. A., Lin, J., Zhu, X.-Y., Jordan, K. L., Bell, C. C., Bentley, M. D., Lerman, A., Khosla, S., & Lerman, L. O. (2012) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00411.2011 · Cited by 41
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Schmitt, R., & Melk, A. (2012) · American Journal of Transplantation · doi:10.1111/j.1600-6143.2012.04214.x · Cited by 39
Self-citationImmunosenescence in renal transplantation
Seyda, M., Quante, M., Uehara, H., Slegtenhorst, B. R., Elkhal, A., & Tullius, S. G. (2015) · Current Opinion in Organ Transplantation · doi:10.1097/mot.0000000000000210 · Cited by 35
Xu, X.-M., Ning, Y., Wang, W., Liu, J., Bai, X., Sun, X., Cai, G., & Chen, X. (2015) · Cellular Physiology and Biochemistry · doi:10.1159/000430248 · Cited by 34
Quantitative podocyte parameters predict human native kidney and allograft half-lives
Naik, A. S., Afshinnia, F., Cibrik, D. M., Hodgin, J. B., Wu, F., Zhang, M., Kikuchi, M., Wickman, L. T., Samaniego, M., Bitzer, M., et al. (2016) · JCI Insight · doi:10.1172/jci.insight.86943 · Cited by 32
Bellière, J., de Lizarrondo, S. M., Choudhury, R. P., Quenault, A., Béhot, A. L., Delage, C., Chauveau, D., Schanstra, J. P., Bascands, J., Vivien, D., et al. (2015) · Theranostics · doi:10.7150/thno.11835 · Cited by 31
Identification of Novel Genes Associated with Renal Tertiary Lymphoid Organ Formation in Aging Mice
Huang, Y., Caputo, C. R., Noordmans, G. A., Yazdani, S., Monteiro, L. H., van den Born, J., van Goor, H., Heeringa, P., Korstanje, R., & Hillebrands, J. (2014) · PLoS ONE · doi:10.1371/journal.pone.0091850 · Cited by 30
Vusser, K. D., Pieters, N., Janssen, B. G., Lerut, E., Kuypers, D. R. J., Jochmans, I., Monbaliu, D. R. L., Pirenne, J., Nawrot, T. S., & Naesens, M. (2015) · Aging · doi:10.18632/aging.100814 · Cited by 28
Aging aggravates long-term renal ischemia-reperfusion injury in a rat model
Xu, X., Fan, M., He, X., Liu, J., Qin, J., & Ye, J. (2013) · Journal of Surgical Research · doi:10.1016/j.jss.2013.10.008 · Cited by 27
Zha, Y., Taguchi, T., Nazneen, A., Shimokawa, I., Higami, Y., & Razzaque, M. S. (2008) · American Journal of Nephrology · doi:10.1159/000128607 · Cited by 27
Protective role of female gender in programmed accelerated renal aging in the rat
Pijacka, W., Clifford, B. L., Tilburgs, C., Joles, J. A., Langley‐Evans, S. C., & McMullen, S. (2015) · Physiological Reports · doi:10.14814/phy2.12342 · Cited by 27
McNicholas, B., Eng, D. G., Lichtnekert, J., Rabinowitz, P. S., Pippin, J. W., & Shankland, S. J. (2016) · American Journal of Physiology-Renal Physiology · doi:10.1152/ajprenal.00196.2016 · Cited by 27
Calvo-Rubio, M., Burón, M. I., López-Lluch, G., Navas, P., de Cabo, R., Ramsey, J. J., Villalba, J. M., & González-Reyes, J. A. (2016) · Aging Cell · doi:10.1111/acel.12451 · Cited by 26
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Schmitt, R., Jacobi, C., Susnik, N., Broecker, V., Haller, H. G., & Melk, A. (2009) · Nephrology Dialysis Transplantation · doi:10.1093/ndt/gfp232 · Cited by 25
Self-citationThe impact of autophagy on the development of senescence in primary tubular epithelial cells
Baisantry, A., Bhayana, S., Wrede, C., Hegermann, J., Haller, H. G., Melk, A., & Schmitt, R. (2016) · Cell Cycle · doi:10.1080/15384101.2016.1234547 · Cited by 22
Self-citationReutzel‐Selke, A., Filatenkov, A., Jurisch, A., Denecke, C., Martins, P. N. A., Pascher, A., Jonas, S., Pratschke, J., Neuhaus, P., & Tullius, S. G. (2005) · Transplantation Proceedings · doi:10.1016/j.transproceed.2005.01.005 · Cited by 19
Aging and Age-Related Disorders
Jellinger, K. A. (2010) · European Journal of Neurology · doi:10.1111/j.1468-1331.2010.03327.x · Cited by 17
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Schildhorn, C., Jacobi, C., Weißbrodt, A., Hermstedt, C., Westhoff, J. H., Hömme, M., Bhayadia, R., Gretz, N., Falk, C. S., Schmitt, R., et al. (2015) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2015.08.004 · Cited by 16
Self-citationSusnik, N., Melk, A., & Schmitt, R. (2015) · Cell Cycle · doi:10.1080/15384101.2015.1032636 · Cited by 16
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Çakatay, U. (2010) · Humana Press eBooks · doi:10.1007/978-1-60761-602-3_1 · Cited by 15
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Harris, R. C., & Cheng, H. (2016) · The Nephron journals/Nephron journals · doi:10.1159/000446665 · Cited by 15
Uesugi, N., Shimazu, Y., Kikuchi, K., & Nagata, M. (2016) · International Journal of Molecular Sciences · doi:10.3390/ijms17111831 · Cited by 13
Amor, S., Garcı́a-Villalón, Á. L., Rubio, C., Carrascosa, J. M., Monge, L., Fernández, N., Martín-Carro, B., & Granado, M. (2016) · Experimental Gerontology · doi:10.1016/j.exger.2016.12.020 · Cited by 7
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Bhayana, S., Baisantry, A., Kraemer, T. D., Wrede, C., Hegermann, J., Bräsen, J. H., Bockmeyer, C. L., Becker, J. U., Ochs, M., Gwinner, W., et al. (2016) · Journal of Nephropathology · doi:10.15171/jnp.2017.15 · Cited by 6
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“Functional and structural impairment in aged kidneys as well as chronic inflammatory traits contribute to increased risk for AKI to CKD progression and developing AKI in the elderly (37, 121, 142).”
Background
Metadata
- Authors
- Schmitt, R., & Melk, A.
- Affiliations
- Medizinische Hochschule Hannover (DE)
- Venue
- Kidney International
- Publisher
- Elsevier BV
- Published
- 2017-09
- Volume
- 92
- Issue
- 3
- Pages
- 569-579
- ISSN
- 0085-2538 (ISSN-L)
- OpenAlex
- W2737090018
- Cited by
- 235
- References
- 149
- Citations by year
- 2026: 18 · 2025: 27 · 2024: 31 · 2023: 32 · 2022: 30 · 2021: 32 · 2020: 29 · 2019: 19 · 2018: 15 · 2017: 2
- FWCI
- 2.37
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Kidney International (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Nephrology › Chronic Kidney Disease and Diabetes
- Health Sciences › Medicine › Nephrology › Acute Kidney Injury Research
- Health Sciences › Medicine › Nephrology › Renal Diseases and Glomerulopathies
- Keywords
- kidney aging, acute kidney injury, chronic kidney disease, glomerular filtration rate decline, nephron loss, podocyte hypertrophy, glomerulosclerosis, tubular atrophy, microvascular rarefaction, cellular senescence, senolytics, autophagy, renal inflammation, caloric restriction mimetics, renin-angiotensin-aldosterone system inhibition, kidney regeneration
- MeSH terms
- Aging, Angiotensin-Converting Enzyme Inhibitors, Animals, Autophagy, Disease Models, Animal, Disease Susceptibility, Glomerular Filtration Rate, Humans, Kidney, Renin-Angiotensin System, Cellular Senescence, Caloric Restriction, Acute Kidney Injury
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