scholarly journals MECHANISMS OF METABOLIC ADAPTATION AND OXIDATIVE STRESS IN HERPESVIRUS INFECTIONS

2019 ◽  
Vol 9 (1) ◽  
pp. 149-150
Author(s):  
Yekaterina Kasymova ◽  
Olga Bashkina ◽  
Aleksei Zhidovinov
2021 ◽  
Author(s):  
Sarah Tessier ◽  
Omar Ferhi ◽  
Marie-Claude Geoffroy ◽  
Roman Gonzalez-Prieto ◽  
Antoine Canat ◽  
...  

Membrane-less organelles are condensates formed by phase separation whose functions often remain enigmatic. Upon oxidative stress, PML scaffolds Nuclear Bodies (NBs) to regulate senescence or metabolic adaptation, but their role in pluripotency remains elusive. Here we establish that PML is required for basal SUMO2/3 conjugation in mESCs and oxidative stress-driven sumoylation in mESCs or in vivo. PML NBs create an oxidation-protective environment for UBC9-driven SUMO2/3 conjugation of PML partners, often followed by their poly-ubiquitination and degradation. Differential in vivo proteomics identified several members of the KAP1 complex as PML NB-dependent SUMO2-targets. The latter drives functional activation of this key epigenetic repressor. Accordingly, Pml-/- mESCs re-express transposable elements and display features of totipotent-like cells, a process further enforced by PML-controlled SUMO2-conjugation of DPPA2. Finally, PML is required for adaptive stress responses in mESCs. Collectively, PML orchestrates mESC fate through SUMO2-conjugation of key transcriptional or epigenetic regulators, raising new mechanistic hypotheses about PML roles in normal or cancer stem cells.


JAMA ◽  
2006 ◽  
Vol 295 (13) ◽  
pp. 1539 ◽  
Author(s):  
Leonie K. Heilbronn ◽  
Lilian de Jonge ◽  
Madlyn I. Frisard ◽  
James P. DeLany ◽  
D. Enette Larson-Meyer ◽  
...  

2013 ◽  
Vol 141 (3-4) ◽  
pp. 109-115 ◽  
Author(s):  
R. Turk ◽  
O. Podpečan ◽  
J. Mrkun ◽  
M. Kosec ◽  
Z. Flegar-Meštrić ◽  
...  

Author(s):  
Hasan Haci Yeter ◽  
Berfu Korucu ◽  
Elif Burcu Bali ◽  
Ulver Derici

Abstract. Background: The pathophysiological basis of chronic kidney disease and its complications, including cardiovascular disease, are associated with chronic inflammation and oxidative stress. We investigated the effects of active vitamin D (calcitriol) and synthetic vitamin D analog (paricalcitol) on oxidative stress in hemodialysis patients. Methods: This cross-sectional study was composed of 83 patients with a minimum hemodialysis vintage of one year. Patients with a history of any infection, malignancy, and chronic inflammatory disease were excluded. Oxidative markers (total oxidant and antioxidant status) and inflammation markers (C-reactive protein and interleukin-6) were analyzed. Results: A total of 47% (39/83) patients were using active or analog vitamin D. Total antioxidant status was significantly higher in patients with using active or analog vitamin D than those who did not use (p = 0.006). Whereas, total oxidant status and oxidative stress index were significantly higher in patients with not using vitamin D when compared with the patients who were using vitamin D preparation (p = 0.005 and p = 0.004, respectively). On the other hand, total antioxidant status, total oxidant status, and oxidative stress index were similar between patients who used active vitamin D or vitamin D analog (p = 0.6; p = 0.4 and p = 0.7, respectively). Conclusion: The use of active or selective vitamin D analog in these patients decreases total oxidant status and increases total antioxidant status. Also, paricalcitol is as effective as calcitriol in decreasing total oxidant status and increasing total antioxidant status in patients with chronic kidney disease.


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