Apoptosis Inhibition Can Be Threatening in Aβ-Induced Neuroinflammation, Through Promoting Cell Proliferation

被引:38
|
作者
Abdi, A. [1 ,2 ]
Sadraie, H. [3 ]
Dargahi, L. [1 ,2 ]
Khalaj, L. [1 ,2 ]
Ahmadiani, A. [1 ,2 ]
机构
[1] Shahid Beheshti Univ Med Sci, Neurosci Res Ctr, Tehran, Iran
[2] Shahid Beheshti Univ Med Sci, Dept Pharmacol, Tehran, Iran
[3] Baqiyatallah Univ Med Sci, Dept Anat, Sch Med, Tehran, Iran
关键词
Neuroinflammation; Apoptosis; NF-kappa B; Caspase-3; Cell proliferation; NF-KAPPA-B; NECROSIS-FACTOR-ALPHA; TNF-ALPHA; ALZHEIMERS-DISEASE; INFLAMMATION; DEATH; CANCER; EXPRESSION; LIFE; P53;
D O I
10.1007/s11064-010-0259-3
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Neuronal apoptosis in neurodegenerative diseases is correlated with inflammatory reactions. The beneficial or detrimental role of apoptosis in neuroinflammation is unclear. In this study, we injected beta-amyloid peptide into the rat cortex for induction of neuroinflammation in hippocampus. We observed an increase in TNF-alpha as an inflammatory cytokine and caspase3 and TUNEL-positive cells as apoptotic marker. As far as ability of TNF-alpha to induce apoptosis or activate NF-k beta, the question is what will happen if the balance between two pathways is disturbed by inhibition of apoptosis. Using caspase inhibitors, we inhibited apoptosis and assessed NF-k beta, Hsp 70 (a hallmark of cancer), cmyc (proto-oncogene) and p53 (tumor suppressor protein). There was an unexpected decrease in NF-k beta while Hsp70 and cmyc upregulated and p53 decreased. These results imply that inhibition of apoptosis due to increased susceptibility to abnormal mitosis may not provide a reliable strategy for treatment of neuroinflammatory diseases.
引用
收藏
页码:39 / 48
页数:10
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