scholarly journals Fas (CD95) May Mediate Delayed Cell Death in Hippocampal CA1 Sector after Global Cerebral Ischemia

2001 ◽  
Vol 21 (12) ◽  
pp. 1411-1421 ◽  
Author(s):  
Kunlin Jin ◽  
Steven H. Graham ◽  
Xiaoou Mao ◽  
Tetsuya Nagayama ◽  
Roger P. Simon ◽  
...  

Cell death–regulatory genes like caspases and bcl-2 family genes are involved in delayed cell death in the CA1 sector of hippocampus after global cerebral ischemia, but little is known about the mechanisms that trigger their expression. The authors found that expression of Fas and Fas-ligand messenger ribonucleic acid and protein was induced in vulnerable CA1 neurons at 24 and 72 hours after global ischemia. Fas-associating protein with a novel death domain (FADD) also was upregulated and immunoprecipitated and co-localized with Fas. Caspase-10 was activated and interacted with FADD protein to an increasing extent as the duration of ischemia increased. Moreover, caspase-10 co-localized with both FADD and caspase-3. These findings suggest that Fas-mediated death signaling may play an important role in signaling hippocampal neuronal death in CA1 after global cerebral ischemia.

Stroke ◽  
2009 ◽  
Vol 40 (2) ◽  
pp. 618-625 ◽  
Author(s):  
Kuniyasu Niizuma ◽  
Hidenori Endo ◽  
Chikako Nito ◽  
D. Jeannie Myer ◽  
Pak H. Chan

Resuscitation ◽  
2001 ◽  
Vol 50 (1) ◽  
pp. 117-125 ◽  
Author(s):  
Toshiyuki Yano ◽  
Ryosuke Nakayama ◽  
Takashi Imaizumi ◽  
Hidenori Terasaki ◽  
Kazuo Ushijima

2019 ◽  
Vol 16 (2) ◽  
pp. 156-165
Author(s):  
ChengPing Bai ◽  
ChenLiang Zhao

Introduction: The effect of hydrogen sulfide (H2S) on global cerebral ischemia remains partially understood. This study aimed to investigate the neuroprotective effect of sodium hydrosulfide (NaHS, a donor of H2S) post-conditioning and its underlying mechanism in a transient global cerebral ischemia (tGCI) model. Materials & Methods: The tGCI rat model was established by the four-vessel occlusion method. Wistar rats were randomly assigned into 6 groups: sham, tGCI, tGCI +NaHS, tGCI+vehicle, tGCI+U0126 and tGCI+U0126+NaHS groups. Neurons survival was assessed by Nissl staining and NeuN immunostaining. Levels of extracellular extracellular-regulated kinases (ERK)1/2 and p-ERK1/2 were determined by western blot and immunohistochemistry (IHC). Intraperitoneal injection of NaHS (24 μmol/kg) at 24 h post-tGCI attenuated tGCI-induced decrease of the survival and NeuN-positive neurons in the hippocampal CA1 subregion. Results: Compared to the sham group, tGCI significantly up-regulated p-ERK1/2 protein at 26 and 48 h post-tGCI. NaHS post-conditioning further enhanced the phosphorylation of ERK1/2 at 26, 48 and 168 h post-tGCI. Nevertheless, U0126 (an inhibitor of MEK1/2) pre-treatment reduced the p-ERK1/2 level in both the tGCI+ U0126 group and the tGCI+ U0126+ NaHS group. IHC staining revealed that p-ERK1/2-positive cell could be observed in several hippocampal subregions of the rats receiving NaHS post-conditioning. Immunofluorescence staining showed that some neurons were double-stained with p-ERK1/2 and NeuN. Furthermore, U0126 pre-treatment significantly attenuated the protective effect of NaHS post-conditioning on the neurons survival and NeuNpositive neurons in CA1 subregion. Conclusion: These results suggested that NaHS post-conditioning can protect hippocampal CA1 neurons from tGCI-induced injury, at least partially, through activation of ERK1/2 signaling.


2011 ◽  
Vol 43 (2) ◽  
pp. 187-193 ◽  
Author(s):  
Xing Su ◽  
Chang-Lai Zhu ◽  
Wei Shi ◽  
Lan-Chun Ni ◽  
Jian-Hong Shen ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document