ACCUMULATING AUTOFLUORESCENT MATERIAL AS A MARKER FOR EARLY CHANGES IN THE SPINAL-CORD OF THE MND MOUSE

被引:27
作者
MESSER, A
PLUMMER, J
机构
[1] NEW YORK STATE DEPT HLTH, WADSWORTH CTR LABS & RES, ALBANY, NY 12201 USA
[2] SUNY, DEPT BIOMED SCI, ALBANY, NY 12222 USA
关键词
MOTOR NEURON DEGENERATION; AMYOTROPHIC LATERAL SCLEROSIS; AUTOFLUORESCENCE;
D O I
10.1016/0960-8966(93)90004-4
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The mouse mutant Motor neuron degeneration (Mnd) displays an adult-onset progressive degeneration of upper and lower motor neurons, with mild symptoms recognizable at 6 months, leading to spastic paralysis and premature death at 10-12 months on the C57B1/6 background. Despite this late onset, abnormally-accumulating autofluorescent material can be seen in both the spinal cord and other regions as early as the first month. This pigmented material is present in both increasing numbers of cells, and in increasing amounts within individual cells, as the animals age. Motor neurons then go on to degenerate, while most other cell types stabilize. The level of pathological involvement, well before the onset of clear clinical symptoms, suggests that the full degenerative process is an extremely gradual and protracted one with some selectivity for motor neurons.
引用
收藏
页码:129 / 134
页数:6
相关论文
共 20 条
[1]   ABNORMAL LYSOSOMAL CATHEPSIN ACTIVITIES IN LEUKOCYTES AND CULTURED SKIN FIBROBLASTS IN LATE INFANTILE, BUT NOT IN JUVENILE NEURONAL CEROID-LIPOFUSCINOSIS (BATTEN DISEASE) [J].
BENNETT, MJ ;
CHERN, L ;
CARPENTER, KH ;
SLADKY, JT .
CLINICA CHIMICA ACTA, 1992, 208 (1-2) :111-117
[2]   NEUROFILAMENT DISTRIBUTION IS ALTERED IN THE MND (MOTOR-NEURON DEGENERATION) MOUSE [J].
CALLAHAN, LM ;
WYLEN, EL ;
MESSER, A ;
MAZURKIEWICZ, JE .
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 1991, 50 (04) :491-504
[3]   LYSOSOMAL HYDROLASES OF DIFFERENT CLASSES ARE ABNORMALLY DISTRIBUTED IN BRAINS OF PATIENTS WITH ALZHEIMER-DISEASE [J].
CATALDO, AM ;
PASKEVICH, PA ;
KOMINAMI, E ;
NIXON, RA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (24) :10998-11002
[4]   THE ADULT AND A NEW LATE ADULT FORMS OF NEURONAL CEROID LIPOFUSCINOSIS [J].
CONSTANTINIDIS, J ;
WISNIEWSKI, KE ;
WISNIEWSKI, TM .
ACTA NEUROPATHOLOGICA, 1992, 83 (05) :461-468
[5]  
CORK LC, 1989, LAB INVEST, V61, P333
[6]  
CORK LC, 1982, LAB INVEST, V46, P89
[7]   LINKAGE ANALYSIS IN JUVENILE NEURONAL CEROID LIPOFUSCINOSIS [J].
HAINES, JL ;
YAN, WL ;
BOUSTANY, RM ;
JEWELL, A ;
JULIER, C ;
BREAKEFIELD, XO ;
GUSELLA, JF .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1992, 42 (04) :542-545
[8]   NEUROVISCERAL CEROID-LIPOFUSCINOSIS IN BLIND DEVON CATTLE [J].
HARPER, PAW ;
WALKER, KH ;
HEALY, PJ ;
HARTLEY, WJ ;
GIBSON, AJ ;
SMITH, JS .
ACTA NEUROPATHOLOGICA, 1988, 75 (06) :632-636
[9]  
Iwata M, 1979, PROGR NEUROPATHOLOGY, P277
[10]  
JOLLY RD, 1990, CAN J VET RES, V54, P15