Two- and three-dimensional computer graphic evaluation of the subacute spinal cord injury

被引:30
作者
Moriarty, LJ
Duerstock, BS
Bajaj, CL
Lin, KN
Borgens, RB
机构
[1] Purdue Univ, Sch Vet Med, Ctr Paralysis Res, Dept Basic Med Sci, W Lafayette, IN 47907 USA
[2] Purdue Univ, Dept Comp Sci, W Lafayette, IN 47907 USA
关键词
macrophage; spinal cord injury; cavitation; 3-D morphometry; neurotrauma; computer graphics;
D O I
10.1016/S0022-510X(97)00203-7
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
We have evaluated three-week-old compression lesions of the rat spinal cord using two-dimensional and three-dimensional morphometry, reconstruction, and visualization techniques. We offer a new computer assisted method to determine the number and density of macrophages within the spinal lesion using the macrophage specific monoclonal label ED1. We also provide quantitative information on pathological cyst formation and cavitation. This technique does not require: (1) subjective identification of the cell type, (2) human interaction with the data during the phase of quantification, and (3) can be applied to any sampling paradigm based on immunocytochemical labeling. Using novel algorithms based on solutions to 'correspondence' and 'branching' problems inherent in cross-sectional histological data, we provide three-dimensional reconstructions and visualizations of the macrophagic lesions and cysts imbedded within it. Our three-dimensional surface reconstructions can be interrogated to determine volumes and surface areas of structures within the data set. Using these methods we have learned that macrophage numbers approach the maximum density possible for such isodiametric cells (similar to 12 mu m diameter) in the central lesion ranging from 4000-7000 cells per mm(2) of lesion. At the time point studied, macrophage numbers would have peaked following the initial insult, and would not be expected to decline for several months. While the density of macrophages is highest in the region of most tissue damage, we show that the central regions of cavitated and cystic spinal parenchyma is not. We discuss how this density of cells may effect the secondary pathological responses of the spinal cord to injury. (C) 1998 Elsevier Science B.V.
引用
收藏
页码:121 / 137
页数:17
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