Conditioned Media of Choroid Plexus Epithelial Cells Induces Nrf2-Activated Phase II Antioxidant Response Proteins and Suppresses Oxidative Stress-Induced Apoptosis in PC12 Cells

被引:16
作者
Aliaghaei, Abbas [1 ,2 ]
Khodagholi, Fariba [1 ,2 ]
Ahmadiani, Abolhassan [1 ,2 ,3 ]
机构
[1] Shahid Beheshti Univ Med Sci, NeuroBiol Res Ctr, Tehran, Iran
[2] Shahid Beheshti Univ Med Sci, Neurosci Res Ctr, Tehran, Iran
[3] Univ Malaya, Fac Med, Dept Pharmacol, Kuala Lumpur 50603, Malaysia
关键词
Choroid plexus epithelial cells; Nrf2; Condition media; Oxidative stress; Apoptosis; ENDOTHELIAL GROWTH-FACTOR; BLOOD-BRAIN-BARRIER; NEURITE OUTGROWTH; HYDROGEN-PEROXIDE; RODENT MODEL; EXPRESSION; NRF2; NEUROPROTECTION; TRANSTHYRETIN; NEURONS;
D O I
10.1007/s12031-014-0228-4
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
Based on the critical role of the choroid plexus (CP) in detoxification processes in the central nervous system (CNS), herein we investigated the effect of choroid plexus epithelial cells conditioned media (CPECs-CM) under oxidative conditions. CPECs were isolated from rat brains, cultured, and the conditioned media were collected. Then pheochromocytoma neuron-like cells (PC12) were treated simultaneously with CPECs-CM and H2O2 as the oxidative stressor. Next, the effect of CPECs-CM on neurite outgrowth and cell differentiation in the presence of H2O2 was determined. Our results showed that CPECs-CM improved the expansion of neurites and differentiation in PC12 cells under oxidative stress conditions. Changes in apoptotic factors, nuclear factor erythroid 2-related factor 2 (Nrf2) and gamma-glutamylcysteine synthetase as the highlighted pathway in the antioxidant defense system were determined by western blot. Also, the activity of antioxidant enzymes and lipid peroxidation level were determined. CPECs-CM-treated PC12 cells could survive after exposure to H2O2 by reduction of caspase-3 cleavage and Bax level and elevation of anti-apoptotic factor Bcl2. Our data also revealed that Nrf2 activation, and consequently its downstream protein levels, increased in the presence of CPECs-CM. Based on our data, we can conclude that CPECs-CM protects PC12 cells against oxidative stress and apoptosis. It seems that CPECs secrete antioxidative agents and neurotrophic factors that have a role in the health of the CNS.
引用
收藏
页码:617 / 625
页数:9
相关论文
共 47 条
[1]   Neuroprotection by encapsulated choroid plexus in a rodent model of Huntington's disease [J].
Borlongan, CV ;
Skinner, SJM ;
Geaney, M ;
Vasconcellos, AV ;
Elliott, RB ;
Emerich, DF .
NEUROREPORT, 2004, 15 (16) :2521-2525
[2]   Intracerebral transplantation of porcine choroid plexus provides structural and functional neuroprotection in a rodent model of stroke [J].
Borlongan, CV ;
Skinner, SJM ;
Geaney, M ;
Vasconcellos, AV ;
Elliott, RB ;
Emerich, DF .
STROKE, 2004, 35 (09) :2206-2210
[3]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[4]   Choroid plexus ependymal cells enhance neurite outgrowth from dorsal root ganglion neurons in vitro [J].
Chakrabortty, S ;
Kitada, M ;
Matsumoto, N ;
Taketomi, M ;
Kimura, K ;
Ide, C .
JOURNAL OF NEUROCYTOLOGY, 2000, 29 (10) :707-717
[5]   Expression of the Nrf2-system at the blood-CSF barrier is modulated by neonatal inflammation and hypoxia-ischemia [J].
D'Angelo, Barbara ;
Ek, C. Joakim ;
Sandberg, Mats ;
Mallard, Carina .
JOURNAL OF INHERITED METABOLIC DISEASE, 2013, 36 (03) :479-490
[6]   CHOROID PLEXUS - A HISTORICAL REVIEW [J].
DOHRMANN, GJ .
BRAIN RESEARCH, 1970, 18 (02) :197-+
[7]  
DRAPER HH, 1990, METHOD ENZYMOL, V186, P421
[8]   TISSUE SULFHYDRYL GROUPS [J].
ELLMAN, GL .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1959, 82 (01) :70-77
[9]   The choroid plexus: function, pathology and therapeutic potential of its transplantation [J].
Emerich, DF ;
Vasconcellos, AV ;
Elliott, RB ;
Skinner, SJM ;
Borlongan, CV .
EXPERT OPINION ON BIOLOGICAL THERAPY, 2004, 4 (08) :1191-1201
[10]   Promoting neurite outgrowth from spiral ganglion neuron explants using polypyrrole/BDNF-coated electrodes [J].
Evans, Alison J. ;
Thompson, Brianna C. ;
Wallace, Gordon G. ;
Millard, Rodney ;
O'Leary, Stephen J. ;
Clark, Graeme M. ;
Shepherd, Robert K. ;
Richardson, Rachael T. .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART A, 2009, 91A (01) :241-250