Bowers W E
J Cell Biol. 1973 Oct;59(1):177-84. doi: 10.1083/jcb.59.1.177.
A method of zonal centrifugation was developed which separates rat thoracic duct lymphocytes (TDL) mainly according to size. The validity of the fractionation method was supported by light microscope observations, Coulter Counter sizing, and in vivo and in vitro labeling of lymphocytes. The distributions of lysosomal acid hydrolases in TDL fractionated by zonal centrifugation are similar to the distribution obtained for the cells. This result indicates that the large lymphocyte is not the sole bearer of either lysosomes or the large amount of soluble cathepsin D found in homogenates of TDL. Both reside mainly in small lymphocytes. This point was clearly established by fractionating homogenates of purified small lymphocytes by means of differential centrifugation and isopycnic density gradient centrifugation.
开发了一种区带离心方法,该方法主要根据大小分离大鼠胸导管淋巴细胞(TDL)。通过光学显微镜观察、库尔特计数器测量大小以及淋巴细胞的体内和体外标记,支持了分级分离方法的有效性。通过区带离心分级分离的TDL中溶酶体酸性水解酶的分布与细胞的分布相似。该结果表明,大淋巴细胞不是TDL匀浆中发现的溶酶体或大量可溶性组织蛋白酶D的唯一载体。两者主要存在于小淋巴细胞中。通过差速离心和等密度密度梯度离心对纯化的小淋巴细胞匀浆进行分级分离,明确证实了这一点。