p-Cresol mediates autophagic cell death in renal proximal tubular cells

被引:14
|
作者
Lin, Hsin-Hung [1 ,2 ,3 ]
Huang, Chiu-Ching [1 ,2 ,3 ]
Lin, Tze-Yi [4 ]
Lin, Ching-Yuang [3 ,5 ,6 ]
机构
[1] China Med Univ Hosp, Dept Med, Div Nephrol, Taipei, Taiwan
[2] China Med Univ Hosp, Kidney Inst, Dept Med, Taipei, Taiwan
[3] China Med Univ, Coll Med, Grad Inst Clin Med Sci, Taichung 40403, Taiwan
[4] China Med Univ Hosp, Dept Pathol, Taipei, Taiwan
[5] China Med Univ, Childrens Hosp, Clin Immunol Ctr, Taichung 40403, Taiwan
[6] China Med Univ, Childrens Hosp, Div Pediat Nephrol, Taichung 40403, Taiwan
关键词
p-Cresol; Renal proximal tubular cell; Chronic kidney disease; Apoptosis; Autophagy; p62/SQSTM1; UREMIC TOXIN; MECHANISMS; APOPTOSIS; CASPASE-8; DISEASE; SERUM; VIEW; LIFE; P62;
D O I
10.1016/j.toxlet.2015.02.003
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Higher serum level of p-cresol (PC) in chronic kidney disease (CKD) patients has been linked with CKD progression. The toxic effect of PC on diverse cells has been reported by prior studies, except for renal tubular cells. Both autophagy and apoptosis contribute to renal tubular cell death, yet evidence of its response to PC is limited and their crosstalk is still unclear. Autophagy is an important cellular process involved in toxin-induced cell death. Renal tubular cell death in tubular injury is thought to be one of the key events causing the progression of CKD. Thus, we treated rat (NRK-52E) and human (HRPTEC) renal proximal tubular cells (RPTC) with PC and found the cell proliferation was significantly decreased. Cell apoptosis was significantly increased and accompanied with the activation of autophagy as evidenced by increases in LC3-II, beclin 1 and Atg 4. We also found an increase of p62 by c-Jun activation. p62 accumulation could mediate the activation of caspase 8-dependent cell apoptosis. Conversely, knockdown of p62 by siRNA of p62 had the opposite effect by arresting LC3-II accumulation and promoting increasing cell viability. We conclude that PC triggered autophagic RPTC death via JNK-mediated p62 accumulation and then activated caspase 8-dependent cell death pathway. PC can be considered as one of the key events causing progression of CKD, which might affect drug disposition in CKD cases. (C) 2015 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:20 / 29
页数:10
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