Feirabend H K, Choufoer H, Voogd J
Department of Physiology, Leiden University, The Netherlands.
J Comp Neurol. 1996 May 27;369(2):236-51. doi: 10.1002/(SICI)1096-9861(19960527)369:2<236::AID-CNE5>3.0.CO;2-4.
Low magnification light microscopic examination of the white matter in appropriately stained avian and mammalian cerebellum reveals a mediolateral succession in which areas of large, heavily myelinated fibers alternate with areas containing nearly exclusively small fibers. A large fiber accumulation (LFA) and its medially adjoining small fiber area (SFA) form a fiber compartment, which, with related parts of cortex and central nuclei, constitutes a so-called cerebellar module. The composition and the apparent mediolateral heterogeneity of cerebellar fiber compartments was quantified in the chicken by morphometrical analysis of myelinated fiber profiles in light (LM) and electron (EM) microscopic micrographs. In LM versus EM, approximately 37% of the myelinated fiber population is neglected. This deficit concerns profiles that are smaller than 1.2 micron2 (diameter < 1.2 microns). EM analysis is therefore considered a prerequisite and forms the main part of this study. The myelinated fiber population has a left-skewed log normal size distribution. Ninety-nine percent of the myelinated fibers fall within the range of 0.1 to 20 microns2 (diameter = 0.4-5.0 microns) and 90% are even smaller than 7 micron2 (diameter < 3.0 microns). Small fibers are abundant in both parts of the compartment. Statistical comparisons provide quantitative confirmation of the LM distinction of LFAs and SFAs. It appears, moreover, that, apart from typical LFAs and SFAs, transitional zones rather than sharp borders can be distinguished between the two. The medial border of the LFA appears to be more sharply defined than its lateral border. Distinct mediolateral fluctuations were found with respect to fiber density (166-243 fibers/1,000 microns2), mean profile area (2.4-4.0 microns2), and interspace (31-47%). These differences reflect the contrast between LFA (lower density, larger mean profile area) and SFA (higher density, smaller mean profile area). The interspace discriminates less well between LFA and SFA but is often smaller in the LFA and larger in the SFA. The presented quantitative characteristics of mediolateral heterogeneity in the cerebellar fiber layer can be used as reference for morphometric studies on the different fiber systems of the cerebellar white matter and the functional organization of the compartments.
对经过适当染色的鸟类和哺乳动物小脑白质进行低倍光学显微镜检查,可发现其在内外侧呈现出一种连续性,其中大的、髓鞘厚的纤维区域与几乎仅含小纤维的区域交替出现。一个大纤维聚集区(LFA)及其内侧相邻的小纤维区域(SFA)形成一个纤维间隔,该间隔与皮质和中央核的相关部分共同构成一个所谓的小脑模块。通过对光镜(LM)和电镜(EM)显微照片中髓鞘纤维轮廓进行形态计量分析,对鸡小脑纤维间隔的组成和明显的内外侧异质性进行了量化。在光镜与电镜对比中,约37%的髓鞘纤维群体被忽略。这种遗漏涉及面积小于1.2平方微米(直径<1.2微米)的轮廓。因此,电镜分析被视为一项先决条件,且构成本研究的主要部分。髓鞘纤维群体具有左偏态对数正态大小分布。99%的髓鞘纤维面积在0.1至20平方微米范围内(直径=0.4 - 5.0微米),90%甚至小于7平方微米(直径<3.0微米)。小纤维在间隔的两个部分都很丰富。统计比较为光镜下对LFA和SFA的区分提供了定量证实。此外,似乎除了典型的LFA和SFA之外,两者之间可区分出过渡区而非清晰的边界。LFA的内侧边界似乎比其外侧边界更清晰。在纤维密度(166 - 243根纤维/1000平方微米)、平均轮廓面积(2.4 - 4.0平方微米)和间隙(31 - 47%)方面发现了明显的内外侧波动。这些差异反映了LFA(较低密度、较大平均轮廓面积)和SFA(较高密度、较小平均轮廓面积)之间的对比。间隙在区分LFA和SFA方面效果较差,但通常在LFA中较小,在SFA中较大。所呈现的小脑纤维层内外侧异质性的定量特征可作为小脑白质不同纤维系统形态计量学研究及间隔功能组织研究的参考。