Abstract
Summary
Cells from mouse fetal liver were dispersed by various methods and tested for their ability to protect lethally irradiated mice. Intravenous injection of 105, 106 or 107 cells dispersed by means of trypsin plus methocel protected well. Cells dispersed by forcing tissue through a 27-gauge needle or by exposure to pancreatin plus methocel protected well only when 107 cells were injected. Cells obtained by forcing fetal liver through monel mesh did not protect as well as cells dispersed by trypsin plus methocel when either 106 or 107 cells were injected. From the results of these experiments it is concluded that dispersion of mouse fetal liver cells by means of trypsin and methocel permits more multipotential cells to remain viable and that these cells are very susceptible to manipulation.
Get full access to this article
View all access options for this article.
