Krasnov I B
Tsitologiia. 1982 Apr;24(4):497-503.
A direct method is described of measuring the thickness of cell fragments and histological structures isolated from freeze-dried tissue sections and a planimetric method of measuring their surface area is presented. A special device mounted on the object holder of the microscope has been used to smooth out and to turn the fragments. The thickness of fragment of the rabbit Deiter's nucleus neuron and that of the molecular layer of the rat cerebellar cortex was measured with errors of 3.1 and 1.5, respectively, and their surface areas were measured with errors of 2.2 and 0.8%, respectively. The methods can be used in quantitative cyto- and histochemistry for obtaining data needed for calculation of the volumes cell fragments or structures isolated from freeze-dried tissue sections. The mean thickness of the freeze-dried section may differ from the cryostat microtome feed setting by 20-50%; therefore the cryostat microtome feed setting cannot be used in calculations of the volume of a fragment isolated from the freeze dried section.
本文描述了一种直接测量从冻干组织切片分离出的细胞碎片和组织结构厚度的方法,并提出了一种测量其表面积的平面测量法。安装在显微镜载物台上的一种特殊装置用于平整和翻转这些碎片。测量了兔代特氏核神经元碎片和大鼠小脑皮质分子层的厚度,误差分别为3.1%和1.5%,并测量了它们的表面积,误差分别为2.2%和0.8%。这些方法可用于定量细胞化学和组织化学,以获取计算从冻干组织切片分离出的细胞碎片或结构体积所需的数据。冻干切片的平均厚度可能与低温恒温切片机的进样设置相差20 - 50%;因此,低温恒温切片机的进样设置不能用于计算从冻干切片分离出的碎片的体积。