Mitochondrial DNA Oxidative Damage Triggering Mitochondrial Dysfunction and Apoptosis in High Glucose-Induced HRECs

2008 ◽  
Vol 49 (9) ◽  
pp. 4203 ◽  
Author(s):  
Lin Xie ◽  
Xiaobo Zhu ◽  
Yiqun Hu ◽  
Tao Li ◽  
Yi Gao ◽  
...  



2005 ◽  
Vol 39 (1) ◽  
pp. 34-42 ◽  
Author(s):  
Liu-Ji Chen ◽  
Yan-Qin Gao ◽  
Xue-Jun Li ◽  
Di-Han Shen ◽  
Feng-Yan Sun


2012 ◽  
Vol 44 (11) ◽  
pp. 1942-1951 ◽  
Author(s):  
Zhenfen Chi ◽  
Linghu Nie ◽  
Zhao Peng ◽  
Qiong Yang ◽  
Kuan Yang ◽  
...  


2014 ◽  
Vol 10 (6) ◽  
pp. 2861-2867 ◽  
Author(s):  
ZHENGDE DU ◽  
QIONG YANG ◽  
TAO ZHOU ◽  
LIN LIU ◽  
SHUO LI ◽  
...  


2020 ◽  
Vol 2020 ◽  
pp. 1-21
Author(s):  
Yingchao Li ◽  
Haitao Yu ◽  
Chongyang Chen ◽  
Shupeng Li ◽  
Zaijun Zhang ◽  
...  

The deleterious effects of aging on the brain remain to be fully elucidated. In the present study, proteomic changes of young (4-month) and aged (16-month) B6129SF2/J male mouse hippocampus and cerebral cortex were investigated by using nano liquid chromatography tandem mass spectrometry (NanoLC-ESI-MS/MS) combined with tandem mass tag (TMT) labeling technology. Compared with the young animals, 390 hippocampal proteins (121 increased and 269 decreased) and 258 cortical proteins (149 increased and 109 decreased) changed significantly in the aged mouse. Bioinformatic analysis indicated that these proteins are mainly involved in mitochondrial functions (FIS1, DRP1), oxidative stress (PRDX6, GSTP1, and GSTM1), synapses (SYT12, GLUR2), ribosome (RPL4, RPS3), cytoskeletal integrity, transcriptional regulation, and GTPase function. The mitochondrial fission-related proteins FIS1 and DRP1 were significantly increased in the hippocampus and cerebral cortex of the aged mice. Further results in the hippocampus showed that ATP content was significantly reduced in aged mice. A neurotrophin brain-derived neurotrophic factor (BNDF), a protein closely related with synaptic plasticity and memory, was also significantly decreased in the hippocampus of the aged mice, with the tendency of synaptic protein markers including complexin-2, synaptophysin, GLUR2, PSD95, NMDAR2A, and NMDAR1. More interestingly, 8-hydroxydeoxyguanosine (8-OHdG), a marker of DNA oxidative damage, increased as shown by immunofluorescence staining. In summary, we demonstrated that aging is associated with systemic changes involving mitochondrial dysfunction, energy reduction, oxidative stress, loss of neurotrophic factor, synaptic proteins, and ribosomal proteins, as well as molecular deficits involved in various physiological/pathological processes.



2021 ◽  
pp. 2008065
Author(s):  
Han Jiang ◽  
Yuedong Guo ◽  
Chenyang Wei ◽  
Ping Hu ◽  
Jianlin Shi


2015 ◽  
Vol 230 (9) ◽  
pp. 2128-2141 ◽  
Author(s):  
Rongchuan Yue ◽  
Xuewei Xia ◽  
Jiahui Jiang ◽  
Dezhong Yang ◽  
Yu Han ◽  
...  


2001 ◽  
Vol 226 (5) ◽  
pp. 450-457 ◽  
Author(s):  
Muyao Li ◽  
P. Marlene Absher ◽  
Ping Liang ◽  
James C. Russell ◽  
Burton E. Sobel ◽  
...  


2013 ◽  
Vol 18 (18) ◽  
pp. 2444-2457 ◽  
Author(s):  
Renato X. Santos ◽  
Sónia C. Correia ◽  
Xiongwei Zhu ◽  
Mark A. Smith ◽  
Paula I. Moreira ◽  
...  


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