Overexpression of Schizosaccharomyces pombe tRNA 3′-end processing enzyme Trz2 leads to an increased cellular iron level and apoptotic cell death

2019 ◽  
Vol 122 ◽  
pp. 11-20 ◽  
Author(s):  
Jinjie Shang ◽  
Lin Wu ◽  
Yanmei Yang ◽  
Yan Li ◽  
Zecheng Liu ◽  
...  
2019 ◽  
Vol 8 (2) ◽  
pp. 216-226 ◽  
Author(s):  
Hizlan Hincal Agus ◽  
Cansin Ogeday Sengoz ◽  
Sedanur Yilmaz

Camphor induces oxidative stress-mediated apoptotic cell death.


2020 ◽  
Vol 10 (1) ◽  
Author(s):  
Kinnosuke Yahiro ◽  
Kohei Ogura ◽  
Yoshiyuki Goto ◽  
Sunao Iyoda ◽  
Tatsuya Kobayashi ◽  
...  

Abstract Shiga-toxigenic Escherichia coli (STEC) infection causes severe bloody diarrhea, renal failure, and hemolytic uremic syndrome. Recent studies showed global increases in Locus for Enterocyte Effacement (LEE)-negative STEC infection. Some LEE-negative STEC produce Subtilase cytotoxin (SubAB), which cleaves endoplasmic reticulum (ER) chaperone protein BiP, inducing ER stress and apoptotic cell death. In this study, we report that SubAB induces expression of a novel form of Lipocalin-2 (LCN2), and describe its biological activity and effects on apoptotic cell death. SubAB induced expression of a novel LCN2, which was regulated by PRKR-like endoplasmic reticulum kinase via the C/EBP homologous protein pathway. SubAB-induced novel-sized LCN2 was not secreted into the culture supernatant. Increased intracellular iron level by addition of holo-transferrin or FeCl3 suppressed SubAB-induced PARP cleavage. Normal-sized FLAG-tagged LCN2 suppressed STEC growth, but this effect was not seen in the presence of SubAB- or tunicamycin-induced unglycosylated FLAG-tagged LCN2. Our study demonstrates that SubAB-induced novel-sized LCN2 does not have anti-STEC activity, suggesting that SubAB plays a crucial role in the survival of LEE-negative STEC as well as inducing apoptosis of the host cells.


2018 ◽  
Vol 7 (5) ◽  
pp. 848-858 ◽  
Author(s):  
Hizlan H. Agus ◽  
Cemaynur Sarp ◽  
Meryem Cemiloglu

Terpinolene induces apoptotic cell death via oxidative stress and mitochondrial impairment.


2020 ◽  
Vol 20 (4) ◽  
Author(s):  
Hizlan Hincal Agus ◽  
Gizem Kok ◽  
Ezgi Derinoz ◽  
Didem Oncel ◽  
Sedanur Yilmaz

ABSTRACT Alpha-thujone, widely used in beverages (1–5 mg/kg), is known to have cytotoxic effects, but the mode of action and the role of potential apoptotic proteins in yeast cell death should be unraveled. In this study, we used Schizosaccharomyces pombe, which is a promising unicellular model organism in mechanistic toxicology and cell biology, to investigate the involvement of pro-apoptotic factors in alpha-thujone-induced cell death. We showed alpha-thujone-induced ROS accumulation-dependent cytotoxicity and apoptosis. In addition, we used superoxide dismutase-deficient cells (sod1 and sod2 mutants) to understand the effect of oxidative stress. Alpha-thujone caused significant cytotoxicity and apoptotic cell death, particularly in sod mutants. Moreover, two potential apoptotic factors, pca1 and pnu1 (pombe caspase-1 and pombe nuc1) were investigated to understand which factor mediates alpha-thujone-induced cell death. Pca1-deficient cells showed increased survival rates and reduced apoptosis in comparison to parental cells after chemical treatment while pnu1 mutation did not cause any significant change and the response was found identical as of parental cells. Yeast responded to alpha-thujone in caspase-dependent manner which was very similar to that for acetic acid. In conclusion, alfa-thujone-induced apoptosis and accounting mechanisms, which were mediated by ROS and driven by Pca1, were clarified in the unicellular model, S. pombe.


Planta Medica ◽  
2007 ◽  
Vol 73 (09) ◽  
Author(s):  
YS Kim ◽  
EJ Sohn ◽  
HY Lee ◽  
CS Kim ◽  
YM Lee ◽  
...  

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