Individual variability in the structural properties of neurons in the human inferior olive

被引:5
|
作者
Baizer, Joan S. [1 ]
Wong, Keit Men [1 ]
Sherwood, Chet C. [2 ,3 ]
Hof, Patrick R. [4 ,5 ]
Witelson, Sandra F. [6 ]
机构
[1] Univ Buffalo, Sch Med & Biomed Sci, Dept Physiol & Biophys, 123 Sherman Hall, Buffalo, NY 14214 USA
[2] George Washington Univ, Dept Anthropol, Washington, DC 20052 USA
[3] George Washington Univ, Ctr Adv Study Human Paleobiol, Washington, DC 20052 USA
[4] Icahn Sch Med Mt Sinai, Fishberg Dept Neurosci, New York, NY 10029 USA
[5] Icahn Sch Med Mt Sinai, Friedman Brain Inst, New York, NY 10029 USA
[6] McMaster Univ, Michael G DeGroote Sch Med, Dept Psychiat & Behav Neurosci, Hamilton, ON L8S 4K1, Canada
来源
BRAIN STRUCTURE & FUNCTION | 2018年 / 223卷 / 04期
关键词
Cerebellar cortex; Purkinje cells; Aging; Climbing fibers; Lysosomes; Lipofuscin; Hyperphosphorylated tau protein; Tauopathies; HUMAN NERVOUS-SYSTEM; ALZHEIMERS-DISEASE; LIPOFUSCIN CONTENT; NEUROCHEMICAL ORGANIZATION; NEUROFIBRILLARY TANGLES; ENTORHINAL CORTEX; CEREBELLAR CORTEX; HYPOXIA-ISCHEMIA; HUMAN BRAIN; MOTOR;
D O I
10.1007/s00429-017-1580-2
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
The inferior olive (IO) is the sole source of the climbing fibers innervating the cerebellar cortex. We have previously shown both individual differences in the size and folding pattern of the principal nucleus (IOpr) in humans as well as in the expression of different proteins in IOpr neurons. This high degree of variability was not present in chimpanzee samples. The neurochemical differences might reflect static differences among individuals, but might also reflect age-related processes resulting in alterations of protein synthesis. Several observations support the latter idea. First, accumulation of lipofuscin, the "age pigment" is well documented in IOpr neurons. Second, there are silver- and abnormal tau-immunostained intraneuronal granules in IOpr neurons (Ikeda et al. Neurosci Lett 258:113-116, 1998). Finally, Olszewski and Baxter (Cytoarchitecture of the human brain stem, Second edn. Karger, Basel, 1954) observed an apparent loss of IOpr neurons in older individuals. We have further investigated the possibility of age-related changes in IOpr neurons using silver- and immunostained sections. We found silver-labeled intraneuronal granules in neurons of the IOpr in all human cases studied (n = 17, ages 25-71). We did not, however, confirm immunostaining with antibodies to abnormal tau. There was individual variability in the density of neurons as well as in the expression of the calcium-binding protein calretinin. In the chimpanzee, there were neither silver-stained intraneuronal granules nor irregularities in immunostaining. Overall, the data support the hypothesis that in some, but not all, humans there are functional changes in IOpr neurons and ultimately cell death. Neurochemical changes of IOpr neurons may contribute to age-related changes in motor and cognitive skills mediated by the cerebellum.
引用
收藏
页码:1667 / 1681
页数:15
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