HORMESIS, CELL DEATH, AND REGENERATIVE MEDICINE FOR NEURODEGENERATIVE DISEASES

被引:7
作者
Wang, Guanghu [1 ]
机构
[1] Georgia Hlth Sci Univ, Med Coll Georgia, Inst Mol Med & Genet, Augusta, GA 30912 USA
关键词
hormesis; preconditioning; regenerative medicine; stem cells; cell death; apoptosis; necrosis; autophagy; molecular chaperone; Hsp90; inhibitors; MESENCHYMAL STEM-CELLS; PRECONDITIONING-MEDIATED NEUROPROTECTION; NEURAL PROGENITOR CELLS; HEAT-SHOCK; ISCHEMIA/REPERFUSION INJURY; ENHANCED NEUROGENESIS; MOLECULAR-MECHANISMS; ADULT NEUROGENESIS; OXIDATIVE STRESS; HSP90; INHIBITOR;
D O I
10.2203/dose-response.12-019.Wang
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Although the adult human brain has a small number of neural stem cells, they are insufficient to repair the damaged brain to achieve significant functional recovery for neurodegenerative diseases and stroke. Stem cell therapy, by either enhancing endogenous neurogenesis, or transplanting stem cells, has been regarded as a promising solution. However, the harsh environment of the diseased brain posts a severe threat to the survival and correct differentiation of those new stem cells. Hormesis (or preconditioning, stress adaptation) is an adaptation mechanism by which cells or organisms are potentiated to survive an otherwise lethal condition, such as the harsh oxidative stress in the stroke brain. Stem cells treated by low levels of chemical, physical, or pharmacological stimuli have been shown to survive better in the neurodegenerative brain. Thus combining hormesis and stem cell therapy might improve the outcome for treatment of these diseases. In addition, since the cell death patterns and their underlying molecular mechanism may vary in different neurodegenerative diseases, even in different progression stages of the same disease, it is essential to design a suitable and optimum hormetic strategy that is tailored to the individual patient.
引用
收藏
页码:238 / 254
页数:17
相关论文
共 140 条
[1]   Cell death pathology: Perspective for human diseases [J].
Agostini, Massimiliano ;
Tucci, Paola ;
Melino, Gerry .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2011, 414 (03) :451-455
[2]   Potential role for adult neurogenesis in the encoding of time in new memories [J].
Aimone, James B. ;
Wiles, Janet ;
Gage, Fred H. .
NATURE NEUROSCIENCE, 2006, 9 (06) :723-727
[3]   Ataxia telangiectasia mutated is essential during adult neurogenesis [J].
Allen, DR ;
van Praag, H ;
Ray, J ;
Weaver, Z ;
Winrow, CJ ;
Carter, TA ;
Braquet, R ;
Harrington, E ;
Ried, T ;
Brown, KD ;
Gage, FH ;
Barlow, C .
GENES & DEVELOPMENT, 2001, 15 (05) :554-566
[4]   Loss of protein kinase C delta alters mammary gland development and apoptosis [J].
Allen-Petersen, B. L. ;
Miller, M. R. ;
Neville, M. C. ;
Anderson, S. M. ;
Nakayama, K. I. ;
Reyland, M. E. .
CELL DEATH & DISEASE, 2010, 1 :e17-e17
[5]   Preconditioning-mediated neuroprotection - Role of nitric oxide, cGMP, and new protein expression [J].
Andoh, T ;
Chock, PB ;
Chiueh, CC .
NITRIC OXIDE: NOVEL ACTIONS, DELETERIOUS EFFECTS AND CLINICAL POTENTIAL, 2002, 962 :1-7
[6]   The protective effect of hypoxic preconditioning on cortical neuronal cultures is associated with increases in the activity of several antioxidant enzymes [J].
Arthur, PG ;
Lim, SCC ;
Meloni, BP ;
Munns, SE ;
Chan, A ;
Knuckey, NW .
BRAIN RESEARCH, 2004, 1017 (1-2) :146-154
[7]   Hormesis/preconditioning mechanisms, the nervous system and aging [J].
Arumugam, Thiruma V. ;
Gleichmann, Marc ;
Tang, Sung-Chun ;
Mattson, Mark P. .
AGEING RESEARCH REVIEWS, 2006, 5 (02) :165-178
[8]   Apaf-1/cytochrome capoptosome: an essential initiator of caspase activation or just a sideshow? [J].
Baliga, B ;
Kumar, S .
CELL DEATH AND DIFFERENTIATION, 2003, 10 (01) :16-18
[9]   Androgens modulate autophagy and cell death via regulation of the endoplasmic reticulum chaperone glucose-regulated protein 78/BiP in prostate cancer cells [J].
Bennett, H. L. ;
Fleming, J. T. ;
O'Prey, J. ;
Ryan, K. M. ;
Leung, H. Y. .
CELL DEATH & DISEASE, 2010, 1 :e72-e72
[10]   Linking calorie restriction to longevity through sirtuins and autophagy: any role for TOR [J].
Blagosklonny, M. V. .
CELL DEATH & DISEASE, 2010, 1 :e12-e12