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小脑单极刷状神经元中异常的神经丝组成。

Unusual neurofilament composition in cerebellar unipolar brush neurons.

作者信息

Harris J, Moreno S, Shaw G, Mugnaini E

机构信息

Department of Neuroscience, University of Florida, Gainesville 32610-0244.

出版信息

J Neurocytol. 1993 Dec;22(12):1039-59. doi: 10.1007/BF01235748.

DOI:10.1007/BF01235748
PMID:8106879
Abstract

During antibody screening on sections of rat cerebellum, we noticed a group of small neurons which exhibited unusual staining properties. They were robustly immunopositive for the high molecular weight neurofilament protein, moderately immunostained with antibodies to the low molecular weight neurofilament protein and alpha-internexin, but only faintly immunoreactive (in PAP sections) or essentially immunonegative (in immunofluorescent sections) with all members of a panel of antibodies directed against the middle molecular weight neurofilament protein. Since neurons generally react equally well with phosphate-independent, (antibodies to) low, middle and high molecular weight neurofilament protein, we conclude that middle molecular weight neurofilament protein is present in these cells in an unusually low relative amount. These cells are found in the granular layer and appear concentrated in the flocculus, ventral paraflocculus, and vermis, particularly in the ventral uvula and nodulus (lobules IXd and X). Previous studies performed by Hockfield defined a population of neurons of similar appearance and distribution using the monoclonal antibody Rat-302, which recognized an uncharacterized 160 kDa protein. We show here that the cells described by Hockfield are identical to those we have found and furthermore that the Rat-302 antibody specifically recognizes the dephosphorylated form of the lysine-serine-proline repeated sequences of high molecular weight neurofilament protein. These cells were studied by pre-embedding immunoelectron microscopy. The nucleus is deeply indented and shows little condensed chromatin. The cytoplasm contains scattered microtubules and a larger number of neurofilaments than expected in a small cell. There are numerous large dense core vesicles, an unusual organelle consisting of ringlet subunits, and relatively little granular endoplasmic reticulum. A thin axon and a single stout dendritic trunk emanate from the perikaryon. Although the cell body and the dendritic shaft may form either complex contacts with mossy fibres (resembling those previously termed en marron synapses) or simple symmetric synapses with small boutons containing pleomorphic vesicles, most of the synaptic relations are established on the shafts of brush-like branchlets that form at the tip of the dendrite and enter one or two glomeruli. Each branchlet forms an extraordinarily extensive asymmetric synapse with the mossy fibre rosette and the subsynaptic region shows a microfibrillar web connected to the postsynaptic density. In addition to other organelles, the branchlets contain numerous mitochondria and large dense core vesicles. Short, non-synaptic appendages with few cytoplasmic organelles emanated from the cell body, dendritic shaft and branchlets.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

在对大鼠小脑切片进行抗体筛选时,我们注意到一组小神经元呈现出异常的染色特性。它们对高分子量神经丝蛋白呈强免疫阳性,对低分子量神经丝蛋白和α-中间丝蛋白的抗体呈中度免疫染色,但在用针对中分子量神经丝蛋白的一组抗体进行检测时,仅呈微弱免疫反应(在过氧化物酶-抗过氧化物酶(PAP)切片中)或基本呈免疫阴性(在免疫荧光切片中)。由于神经元通常对与磷酸盐无关的低、中、高分子量神经丝蛋白抗体反应良好,我们得出结论,这些细胞中的中分子量神经丝蛋白相对含量异常低。这些细胞位于颗粒层,集中在绒球、腹侧旁绒球和蚓部,特别是在腹侧小舌和小结(小叶IXd和X)。霍克菲尔德先前的研究使用单克隆抗体Rat - 302定义了一群外观和分布相似的神经元,该抗体识别一种未鉴定的160 kDa蛋白。我们在此表明,霍克菲尔德描述的细胞与我们发现的细胞相同,此外,Rat - 302抗体特异性识别高分子量神经丝蛋白赖氨酸 - 丝氨酸 - 脯氨酸重复序列的去磷酸化形式。通过包埋前免疫电子显微镜对这些细胞进行了研究。细胞核深陷,几乎没有浓缩染色质。细胞质中含有散在的微管和比小细胞预期数量更多的神经丝。有许多大的致密核心囊泡,一种由小环亚基组成的不寻常细胞器,以及相对较少的颗粒内质网。一个细轴突和一个粗壮的树突干从胞体发出。尽管细胞体和树突轴可能与苔藓纤维形成复杂接触(类似于先前称为棕褐色突触的那些)或与含有多形性囊泡的小突触终扣形成简单对称突触,但大多数突触关系是在树突末端形成并进入一个或两个小球体的刷状小分支的轴上建立的。每个小分支与苔藓纤维花结形成极其广泛的不对称突触,突触下区域显示出与突触后致密区相连的微纤维网。除了其他细胞器外,小分支还含有许多线粒体和大的致密核心囊泡。短的、无突触的附属物从细胞体、树突轴和小分支发出,附属物中细胞质细胞器很少。(摘要截取自400字)

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