A screen for apoptotic synergism between clinical relevant nephrotoxicant and the cytokine TNF-α

被引:6
|
作者
Benedetti, Giulia [1 ]
Ramaiahgaris, Sreenivasa [1 ]
Herpers, Bram [1 ]
van de Water, Bob [1 ]
Price, Leo S. [1 ]
de Graauw, Marjo [1 ]
机构
[1] Leiden Univ, Leiden Acad Ctr Drug Res, Div Toxicol, NL-2333 CC Leiden, Netherlands
关键词
Nephrotoxicity; Mouse immortalized proximal tubular; epithelial cells; TNF-alpha; In vitro cytotoxicity assay; Synergistic apoptosis; NF-KAPPA-B; RENAL-TRANSPLANT RECIPIENTS; ANNEXIN A1 PROTEIN; CYCLOSPORINE-A; IN-VITRO; GENE-EXPRESSION; ANGIOTENSIN-II; CELLS; NECROSIS; TOXICITY;
D O I
10.1016/j.tiv.2013.09.004
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Nephrotoxicity remains one of the main reasons for post-market drug withdrawal. Tumour necrosis factor alpha (TNF-alpha) secretion has been shown to underlie the nephrotoxicity induced by some of these drugs. Yet, there is currently no reliable and sensitive in vitro assay available to screen for nephrotoxicants of which toxicity largely depends on TNF-alpha secretion. Therefore, we developed and applied a sensitive fluorescence-based in vitro assay for TNF-alpha-mediated nephrotoxicity screening using mouse immortalized proximal tubular epithelial cells (IM-PTECs). Our assay allows rapid evaluation of TNF-alpha-mediated toxicant-induced apoptosis and necrosis using fixed endpoint and live cell measurements. To evaluate our assay, sixteen nephrotoxicants and two control non-nephrotoxicants were used. Out of the sixteen nephrotoxicants, eight induced cell death, of which five induced apoptosis as well as necrosis. Moreover, TNF-alpha significantly enhanced apoptotic cell death induced by cisplatin, cyclosporine A, tacrolimus and azidothymidine. These nephrotoxicants are known to induce inflammation in vivo which has been linked to an enhancement of nephrotoxicity for cisplatin, cyclosporine A and tacrolimus, confirming the functionality of our assay. Overall, our assay allows rapid and sensitive measurement of apoptosis and necrosis induced by a combination of nephrotoxicants and inflammatory components such as TNF-alpha and can be used as an alternative assay for nephrotoxicity prediction in vitro. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2264 / 2272
页数:9
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