Pokaż uproszczony rekord

dc.contributor.authorPieniążek, Anna
dc.contributor.authorBernasińska-Słomczewska, Joanna
dc.contributor.authorHikisz, Paweł
dc.date.accessioned2023-08-31T12:56:00Z
dc.date.available2023-08-31T12:56:00Z
dc.date.issued2023
dc.identifier.citationPieniazek, A., Bernasinska-Slomczewska, J. & Hikisz, P. Indoxyl sulfate induces apoptosis in mononuclear blood cells via mitochondrial pathway. Sci Rep 13, 14044 (2023). https://doi.org/10.1038/s41598-023-40824-zpl_PL
dc.identifier.urihttp://hdl.handle.net/11089/47832
dc.description.abstractThe consequence of chronic kidney disease is the accumulation of metabolic products called uremic toxins in the body. Indoxyl sulfate (IS) is a toxin with a high affinity for proteins. This study focuses on the deleterious effect of IS, especially apoptosis induction, in mononuclear blood cells (MNCs). Thus, in MNCs treated with IS at three different concentrations for 24 h, the survival, mitochondrial potential, caspases activity and expression, Bcl-2 and Bax protein expression, DNA damage, and PARP degradation were estimated. The study showed a decrease in survival and mitochondrial potential of MNCs treated with IS compared to the control. IS increased the activity of caspase 2-, 3-, 9-, and the expression of caspase 3-, and 9- in MNCs but does not affect the activity of caspase 6- and 8. The treatment of MNCs with IS also increased DNA damage and degradation of PARP. Indoxyl sulfate significantly influences the expression of Bcl-2 and Bax proteins. Indoxyl sulfate induces the programmed death of MNCs through the intrinsic mitochondrial apoptotic pathway. The observed cellular changes are mostly dose-dependent.pl_PL
dc.language.isoenpl_PL
dc.publisherSpringer Naturepl_PL
dc.relation.ispartofseriesScientific Reports;14044
dc.rightsUznanie autorstwa 4.0 Międzynarodowe*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subjectDiseasespl_PL
dc.subjectCell biologypl_PL
dc.titleIndoxyl sulfate induces apoptosis in mononuclear blood cells via mitochondrial pathwaypl_PL
dc.typeArticlepl_PL
dc.page.number11pl_PL
dc.contributor.authorAffiliationDepartment of Oncobiology and Epigenetics, Faculty of Biology and Environmental Protection, University of Lodz, Ul. Pomorska 141/143, 90-236, Lodz, Polandpl_PL
dc.contributor.authorAffiliationDepartment of Oncobiology and Epigenetics, Faculty of Biology and Environmental Protection, University of Lodz, Ul. Pomorska 141/143, 90-236, Lodz, Polandpl_PL
dc.contributor.authorAffiliationDepartment of Oncobiology and Epigenetics, Faculty of Biology and Environmental Protection, University of Lodz, Ul. Pomorska 141/143, 90-236, Lodz, Polandpl_PL
dc.identifier.eissn2045-2322
dc.referencesVanholder, R. et al. Review on uremic toxins: Classification, concentration, and interindividual variability. Kidney Int. 63, 1934–1943 (2003).pl_PL
dc.referencesItoh, Y., Ezawa, A., Kikuchi, K., Tsuruta, Y. & Niwa, T. Protein-bound uremic toxins in hemodialysis patients measured by liquid chromatography/tandem mass spectrometry and their effects on endothelial ROS production. Anal. Bioanal. Chem. 403, 1841–1850 (2012).pl_PL
dc.referencesVanholder, R., van Laecke, S. & Glorieux, G. What is new in uremic toxicity?. Pediatr. Nephrol. (Berlin, Germany) 23, 1211–1221 (2008).pl_PL
dc.referencesPieniazek, A., Bernasinska-Slomczewska, J. & Gwozdzinski, L. Uremic toxins and their relation with oxidative stress induced in patients with CKD. Int. J. Mol. Sci. 22, 6196 (2021).pl_PL
dc.referencesAddi, T., Dou, L. & Burtey, S. Tryptophan-derived uremic toxins and thrombosis in chronic kidney disease. Toxins 10, 412 (2018).pl_PL
dc.referencesHung, S.-C. et al. Indoxyl sulfate suppresses endothelial progenitor cell-mediated neovascularization. Kidney Int. 89, 574–585 (2016).pl_PL
dc.referencesAkchurin, O. M. & Kaskel, F. Update on inflammation in chronic kidney disease. Blood Purif. 39, 84–92 (2015).pl_PL
dc.referencesHung, S.-C., Kuo, K.-L., Wu, C.-C. & Tarng, D.-C. Indoxyl sulfate: A novel cardiovascular risk factor in chronic kidney disease. J. Am. Heart Assoc. 6, e005022 (2017).pl_PL
dc.referencesPark, J. S., Choi, H. I., Bae, E. H., Ma, S. K. & Kim, S. W. Paricalcitol attenuates indoxyl sulfate-induced apoptosis through the inhibition of MAPK, Akt, and NF-kB activation in HK-2 cells. Korean J. Intern. Med. 34, 146–155 (2019).pl_PL
dc.referencesDias, G. F. et al. Indoxyl sulfate, a uremic toxin, stimulates reactive oxygen species production and erythrocyte cell death supposedly by an organic anion transporter 2 (OAT2) and NADPH oxidase activity-dependent pathways. Toxins 10, 280 (2018).pl_PL
dc.referencesPieniazek, A., Gwozdzinski, L., Hikisz, P. & Gwozdzinski, K. Indoxyl sulfate generates free radicals, decreases antioxidant defense, and leads to damage to mononuclear blood cells. Chem. Res. Toxicol. 31, 869–875 (2018).pl_PL
dc.referencesAdesso, S. et al. Effect of indoxyl sulfate on the repair and intactness of intestinal epithelial cells: Role of reactive oxygen species’ release. Int. J. Mol. Sci. 20, 2280 (2019).pl_PL
dc.referencesDeng, M. et al. Short-chain fatty acids alleviate hepatocyte apoptosis induced by gut-derived protein-bound uremic toxins. Front. Nutr. 8, 756730 (2021).pl_PL
dc.referencesEnoki, Y. et al. Potential therapeutic interventions for chronic kidney disease-associated sarcopenia via indoxyl sulfate-induced mitochondrial dysfunction. J. Cachexia Sarcopenia Muscle 8, 735–747 (2017).pl_PL
dc.referencesEllis, R. J. et al. Indoxyl sulfate induces apoptosis and hypertrophy in human kidney proximal tubular cells. Toxicol. Pathol. 46, 449–459 (2018).pl_PL
dc.referencesWang, W.-J., Cheng, M.-H., Sun, M.-F., Hsu, S.-F. & Weng, C.-S. Indoxyl sulfate induces renin release and apoptosis of kidney mesangial cells. J. Toxicol. Sci. 39, 637–643 (2014).pl_PL
dc.referencesRodrigues, G. G. C. et al. Indoxyl sulfate contributes to uremic sarcopenia by inducing apoptosis in myoblasts. Arch. Med. Res. 51, 21–29 (2020).pl_PL
dc.referencesFotakis, G. & Timbrell, J. A. In vitro cytotoxicity assays: comparison of LDH, neutral red, MTT and protein assay in hepatoma cell lines following exposure to cadmium chloride. Toxicol. Lett. 160, 171–177 (2006).pl_PL
dc.referencesMeijers, B. & Lowenstein, J. The evolving view of uremic toxicity. Toxins 14, 274 (2022).pl_PL
dc.referencesShimizu, H. et al. Indoxyl sulfate downregulates renal expression of Klotho through production of ROS and activation of nuclear factor-ĸB. Am. J. Nephrol. 33, 319–324 (2011).pl_PL
dc.referencesShimizu, H., Yisireyili, M., Higashiyama, Y., Nishijima, F. & Niwa, T. Indoxyl sulfate upregulates renal expression of ICAM-1 via production of ROS and activation of NF-κB and p53 in proximal tubular cells. Life Sci. 92, 143–148 (2013).pl_PL
dc.referencesMilanesi, S. et al. Indoxyl sulfate induces renal fibroblast activation through a targetable heat shock protein 90-dependent pathway. Oxid. Med. Cell. Longev. 2019, 2050183 (2019).pl_PL
dc.referencesKim, Y.-H., Kwak, K.-A., Gil, H.-W., Song, H.-Y. & Hong, S.-Y. Indoxyl sulfate promotes apoptosis in cultured osteoblast cells. BMC Pharmacol. Toxicol. 14, 60 (2013).pl_PL
dc.referencesGreen, D. R. Caspase activation and inhibition. Cold Spring Harbor Perspect. Biol. 14, 1020 (2022).pl_PL
dc.referencesTheofilas, P. et al. Caspase-6-cleaved tau is relevant in Alzheimer’s disease and marginal in four-repeat tauopathies: Diagnostic and therapeutic implications. Neuropathol. Appl. Neurobiol. 48, e12819 (2022).pl_PL
dc.referencesGreen, D. R. The mitochondrial pathway of apoptosis part II: The BCL-2 protein family. Cold Spring Harbor Perspect. Biol. 14, 1046 (2022).pl_PL
dc.referencesLalier, L., Vallette, F. & Manon, S. Bcl-2 family members and the mitochondrial import machineries: The roads to death. Biomolecules 12, 162 (2022).pl_PL
dc.referencesDuangchan, T. et al. Indoxyl sulfate impairs in vitro erythropoiesis by triggering apoptosis and senescence. Exp. Biol. Med. (Maywood, N.J.) 247, 1350–1363 (2022).pl_PL
dc.referencesAltintas, M. M., DiBartolo, S., Tadros, L., Samelko, B. & Wasse, H. Metabolic changes in peripheral blood mononuclear cells isolated from patients with end stage renal disease. Front. Endocrinol. 12, 629239 (2021).pl_PL
dc.referencesHsu, Y.-J. et al. Indoxyl sulfate upregulates the cannabinoid type 1 receptor gene via an ATF3/c-Jun complex-mediated signaling pathway in the model of uremic cardiomyopathy. Int. J. Cardiol. 252, 128–135 (2018).pl_PL
dc.referencesZhang, R., Guo, F., Xue, X., Yang, R. & Wang, L. Uremia toxin helps to induce inflammation in intestines by activating the ATM/NEMO/NF-kB signalling pathway in human intestinal epithelial cells. IJBB https://doi.org/10.56042/ijbb.v57i5.31780 (2020).pl_PL
dc.referencesDaenen, K. et al. Oxidative stress in chronic kidney disease. Pediatr. Nephrol. (Berlin, Germany) 34, 975–991 (2019).pl_PL
dc.referencesMagliocca, G., Mone, P., Di Iorio, B. R., Heidland, A. & Marzocco, S. Short-chain fatty acids in chronic kidney disease: Focus on inflammation and oxidative stress regulation. Int. J. Mol. Sci. 23, 5354 (2022).pl_PL
dc.referencesChen, C.-H. et al. Indoxyl sulfate, homocysteine, and antioxidant capacities in patients at different stages of chronic kidney disease. Nurs. Res. Pract. 16, 464–475 (2022).pl_PL
dc.referencesColombo, G. et al. Effects of the uremic toxin indoxyl sulphate on human microvascular endothelial cells. J. Appl. Toxicol. JAT 42, 1948–1961 (2022).pl_PL
dc.referencesLai, Y.-R. et al. The effects of indoxyl sulfate and oxidative stress on the severity of peripheral nerve dysfunction in patients with chronic kidney diseases. Antioxidants (Basel, Switzerland) 11, 2350 (2022).pl_PL
dc.referencesPieniazek, A., Kopera, M., Gwozdzinski, L. & Gwozdzinski, K. Indoxyl sulfate induces oxidative changes in plasma and hemolysate. Molecules (Basel, Switzerland) 27, 3848 (2022).pl_PL
dc.referencesArmand, L., Fofana, M., Couturier-Becavin, K., Andriamihaja, M. & Blachier, F. Dual effects of the tryptophan-derived bacterial metabolite indole on colonic epithelial cell metabolism and physiology: Comparison with its co-metabolite indoxyl sulfate. Amino Acids 54, 1371–1382 (2022).pl_PL
dc.referencesChen, Q. et al. Truncated PARP1 mediates ADP-ribosylation of RNA polymerase III for apoptosis. Cell Discov. 8, 3 (2022).pl_PL
dc.referencesRichard, I. A., Burgess, J. T., O’Byrne, K. J. & Bolderson, E. Beyond PARP1: The potential of other members of the poly (ADP-ribose) polymerase family in DNA repair and cancer therapeutics. Front. Cell Dev. Biol. 9, 801200 (2021).pl_PL
dc.referencesRepetto, G., del Peso, A. & Zurita, J. L. Neutral red uptake assay for the estimation of cell viability/cytotoxicity. Nat. Protoc. 3, 1125–1131 (2008).pl_PL
dc.referencesPieniazek, A. & Gwozdzinski, K. Carbamylation and oxidation of proteins lead to apoptotic death of lymphocytes. Chem. Biol. Interact. 270, 24–32 (2017).pl_PL
dc.referencesNuydens, R. et al. A rapid method for the evaluation of compounds with mitochondria-protective properties. J. Neurosci. Methods 92, 153–159 (1999).pl_PL
dc.referencesSingh, N. P., McCoy, M. T., Tice, R. R. & Schneider, E. L. A simple technique for quantitation of low levels of DNA damage in individual cells. Exp. Cell Res. 175, 184–191 (1988).pl_PL
dc.referencesTowbin, H., Staehelin, T. & Gordon, J. Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: Procedure and some applications. Proc. Natl. Acad. Sci. U.S.A. 76, 4350–4354 (1979).pl_PL
dc.referencesLowry, O. H., Rosebrough, N. J., Farr, A. L. & Randall, R. J. Protein measurement with the Folin phenol reagent. J. Biol. Chem. 193, 265–275 (1951).pl_PL
dc.referencesLeary, J. J., Brigati, D. J. & Ward, D. C. Rapid and sensitive colorimetric method for visualizing biotin-labeled DNA probes hybridized to DNA or RNA immobilized on nitrocellulose: Bio-blots. Proc. Natl. Acad. Sci. U.S.A. 80, 4045–4049 (1983).pl_PL
dc.referencesHikisz, P., Namiecińska, E., Paneth, P. & Budzisz, E. Mechanistic studies of arene-ruthenium(II) complexes with carbothioamidopyrazoles as alternative cancer drugs. Molecules (Basel, Switzerland) 28, 3969 (2023).pl_PL
dc.identifier.doi10.1038/s41598-023-40824-z
dc.relation.volume13pl_PL


Pliki tej pozycji

Thumbnail
Thumbnail

Pozycja umieszczona jest w następujących kolekcjach

Pokaż uproszczony rekord

Uznanie autorstwa 4.0 Międzynarodowe
Poza zaznaczonymi wyjątkami, licencja tej pozycji opisana jest jako Uznanie autorstwa 4.0 Międzynarodowe