Abstract

We have demonstrated that the number of pseudopodia is directly correlated with cell differentiation and carcinogenesis in the squamous epithelium. Microprocesses over T-lymphocytes may also reflect cell differentiation or a functional state of the cells as seen in the epithelial cell model, although their functions are not well understood. Visual quantification of spatially distributed bodies such as microprocesses observed with a scanning electron microscope (SEM) is inherently poor. That is, exact quantitation of the number of microprocesses per cell may be necessary to demonstrate a smaller difference in frequency of such structure. One drawback of previous attempts to use such a method was that the quantitation of a structure over a surface which was at a steep angle to the film plane could not be accurate. We developed a modified method of enumeration with SEM and another method with a transmission electron microscope (TEM), using cultured murine T-lymphoma cells (EL-4) as a model, and the results were compared.

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