共 23 条
Calbindin-D28K, parvalbumin and calretinin in primate lower motor neurons
被引:25
作者:

Fahandejsaadi, A
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机构: Harvard Univ, Sch Med, Dept Med, Lab Neurodegenerat & Aging Res, Boston, MA 02215 USA

Leung, E
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机构: Harvard Univ, Sch Med, Dept Med, Lab Neurodegenerat & Aging Res, Boston, MA 02215 USA

Rahaii, R
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h-index: 0
机构: Harvard Univ, Sch Med, Dept Med, Lab Neurodegenerat & Aging Res, Boston, MA 02215 USA

Bu, J
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h-index: 0
机构: Harvard Univ, Sch Med, Dept Med, Lab Neurodegenerat & Aging Res, Boston, MA 02215 USA

Geula, C
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机构: Harvard Univ, Sch Med, Dept Med, Lab Neurodegenerat & Aging Res, Boston, MA 02215 USA
机构:
[1] Harvard Univ, Sch Med, Dept Med, Lab Neurodegenerat & Aging Res, Boston, MA 02215 USA
[2] Beth Israel Deaconess Med Ctr, Sect Gerontol, Boston, MA 02215 USA
来源:
关键词:
amyotrophic lateral sclerosis;
Calbindin-D-28K;
calretinin;
common marmoset;
non-phosphorylated neurofilaments;
parvalbumin;
rhesus monkey;
D O I:
10.1097/00001756-200403010-00012
中图分类号:
Q189 [神经科学];
学科分类号:
071006 ;
摘要:
It has been suggested that lower motor neurons containing calcium-binding proteins (CBP) may be resistant to degeneration in motor neuron disease. The testing of this hypothesis is hampered by lack of comprehensive information regarding the presence of CBPs in motor neurons. To address this shortcoming, we investigated the distribution of the CBPs calbindin-D-28K (CB), parvalbumin (PV) and calretinin (CRT) in lower motor neurons in the normal human and two non-human primates (rhesus monkey and common marmoset) using immunohistochemistry. A variable proportion of motor neurons in cranial nerve motor nuclei contained immunoreactivity for one or more CBPs. A subpopulation of spinal cord alpha-motor neurons was also CBP-positive. Comparison of staining for choline acetyltransferase (ChAT) and CBPs in the human spinal cord demonstrated that approximately 63% of ventral horn motor neurons contained PV, 53% contained CRT and 56% contained CB. CBP immunoreactivity within motor neurons was of variable staining intensity. It remains to be established whether the presence of these CBPs confers protection against the pathogenic mechanisms of motor neuron disease.
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页码:443 / 448
页数:6
相关论文
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