S100B protein and 4-hydroxynonenal in the spinal cord of wobbler mice

被引:15
作者
Corvino, V
Businaro, R
Geloso, MC
Bigini, P
Cavallo, V
Pompili, E
Mennini, T
Fumagalli, L
Michetti, F
机构
[1] Catholic Univ, Inst Anat, I-00168 Rome, Italy
[2] Univ Roma La Sapienza, Dept Cardiovasc Sci, Rome, Italy
关键词
S100B protein; 4-hydroxinonenal; wobbler mice; neurodegeneration; oxidative stress;
D O I
10.1023/A:1022345720852
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
S100B is a calcium-binding protein that, in the nervous system, is mainly concentrated in glial cells. Although its biological role is still unclear, the protein is hypothesized, at high concentrations, to act in the pathogenesis of neurodegenerative processes, possibly through oxidative stress mechanisms. To investigate this hypothesis we studied the spinal cord of wobbler mice, an animal model of motor neuron degeneration. Using immunocytochemistry, we detected an overexpression of S100B in astrocytes of the cervical spinal cord of these animals. We also confirmed this finding by reverse transcriptase polymerase chain reaction. In the same spinal cord regions, scattered neurons appeared to be immunostained for 4-hydroxynonenal-modified proteins, an indicator of lipid peroxidation. This finding constitutes a sign of oxidative stress-induced neurodegeneration.
引用
收藏
页码:341 / 345
页数:5
相关论文
共 26 条
[1]   THE LOSS OF MOTORNEURONS CORRESPONDING TO SPECIFIC MUSCLES IN THE WOBBLER MUTANT MOUSE [J].
BAULAC, M ;
RIEGER, F ;
MEININGER, V .
NEUROSCIENCE LETTERS, 1983, 37 (01) :99-104
[2]   Glutamate transporters in the spinal cord of the wobbler mouse [J].
Bigini, P ;
Bastone, A ;
Mennini, T .
NEUROREPORT, 2001, 12 (09) :1815-1820
[3]  
Cookson MR, 1999, BRAIN PATHOL, V9, P165
[4]   Cellular basis of steroid neuroprotection in the Wobbler mouse, a genetic model of motoneuron disease [J].
Deniselle, MCG ;
González, SL ;
De Nicola, AF .
CELLULAR AND MOLECULAR NEUROBIOLOGY, 2001, 21 (03) :237-254
[5]   S100: a multigenic family of calcium-modulated proteins of the EF-hand type with intracellular and extracellular functional roles [J].
Donato, R .
INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 2001, 33 (07) :637-668
[6]  
DUCHEN LW, 1966, J PHYSIOL-LONDON, V183, pP53
[7]   AN HEREDITARY MOTOR NEURONE DISEASE WITH PROGRESSIVE DENERVATION OF MUSCLE IN MOUSE - MUTANTWOBBLER [J].
DUCHEN, LW ;
STRICH, SJ .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 1968, 31 (06) :535-&
[8]  
Falconer D., 1956, MOUSE NEWS LETT, V15, P23
[9]   Specific features of chronic astrocyte gliosis after experimental central nervous system (CNS) xenografting and in Wobbler neurological mutant CNS [J].
Hantaz-Ambroise, D ;
Jacque, C ;
Ikhlef, AA ;
Parmentier, C ;
Leclerc, P ;
Cambier, D ;
Zadigue, G ;
Rieger, F .
DIFFERENTIATION, 2001, 69 (2-3) :100-107
[10]   ABNORMAL ASTROCYTE DIFFERENTIATION AND DEFECTIVE CELLULAR INTERACTIONS IN WOBBLER MOUSE SPINAL-CORD [J].
HANTAZAMBROISE, D ;
BLONDET, B ;
MURAWSKY, M ;
RIEGER, F .
JOURNAL OF NEUROCYTOLOGY, 1994, 23 (03) :179-192