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
相关论文
共 47 条
[1]   Nuclear factor-κ-B:: The enemy within [J].
Aggarwal, BB .
CANCER CELL, 2004, 6 (03) :203-208
[2]   Inflammation and Alzheimer's disease [J].
Akiyama, H ;
Barger, S ;
Barnum, S ;
Bradt, B ;
Bauer, J ;
Cole, GM ;
Cooper, NR ;
Eikelenboom, P ;
Emmerling, M ;
Fiebich, BL ;
Finch, CE ;
Frautschy, S ;
Griffin, WST ;
Hampel, H ;
Hull, M ;
Landreth, G ;
Lue, LF ;
Mrak, R ;
Mackenzie, IR ;
McGeer, PL ;
O'Banion, MK ;
Pachter, J ;
Pasinetti, G ;
Plata-Salaman, C ;
Rogers, J ;
Rydel, R ;
Shen, Y ;
Streit, W ;
Strohmeyer, R ;
Tooyoma, I ;
Van Muiswinkel, FL ;
Veerhuis, R ;
Walker, D ;
Webster, S ;
Wegrzyniak, B ;
Wenk, G ;
Wyss-Coray, T .
NEUROBIOLOGY OF AGING, 2000, 21 (03) :383-421
[3]   Neuronal survival activity of S100ββ is enhanced by calcineurin inhibitors and requires activation of NF-κB [J].
Alexanian, AR ;
Bamburg, JR .
FASEB JOURNAL, 1999, 13 (12) :1611-1620
[4]   Inflammation in central nervous system injury [J].
Allan, SM ;
Rothwell, NJ .
PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES, 2003, 358 (1438) :1669-1677
[5]   Hyperthermia inhibits cell proliferation and induces apoptosis: Relative signaling status of p53, S100A4, and notch in heat sensitive and resistant cell lines [J].
Basile, Antonio ;
Biziato, Daniela ;
Sherbet, Gajanan V. ;
Comi, Paola ;
Cajone, Francesco .
JOURNAL OF CELLULAR BIOCHEMISTRY, 2008, 103 (01) :212-220
[6]   Apoptosis and Alzheimer's disease [J].
Behl, C .
JOURNAL OF NEURAL TRANSMISSION, 2000, 107 (11) :1325-1344
[7]   Nuclear imaging of neuroinflammation: a comprehensive review of [11C]PK11195 challengers [J].
Chauveau, Fabien ;
Boutin, Herve ;
Van Camp, Nadja ;
Dolle, Frederic ;
Tavitian, Bertrand .
EUROPEAN JOURNAL OF NUCLEAR MEDICINE AND MOLECULAR IMAGING, 2008, 35 (12) :2304-2319
[8]   Heat shock proteins in cancer: diagnostic, prognostic, predictive, and treatment implications [J].
Ciocca, DR ;
Calderwood, SK .
CELL STRESS & CHAPERONES, 2005, 10 (02) :86-103
[9]  
Combs CK, 2001, J NEUROSCI, V21, P1179
[10]   z-VAD-fmk augmentation of TNFα-stimulated neutrophil apoptosis is compound specific and does not involve the generation of reactive oxygen species [J].
Cowburn, AS ;
White, JF ;
Deighton, J ;
Walmsley, SR ;
Chilvers, ER .
BLOOD, 2005, 105 (07) :2970-2972