Brown D H, Byrd B L, Carlton J E, Swartzendruber D C, Hayes R L
Cancer Res. 1976 Mar;36(3):956-63.
This paper describes a quantitative procedure for the isolation of 67 Ga-binding granules (GBG) from normal rat liver and Morris 5123C hepatoma homogenates by a combination of rate and isopyknic density gradient zonal centrifugation. Another class of GBG has been found that is much smaller than the lysosomal GBG we have previously described. These smaller particles, or microvesicles, bind the largest portion of the 67Ga found in the hepatoma whereas, in the liver, the GBG lysosomes are the major binding component. Previously, we had shown that considerably more 67Ga is taken up in hepatoma than in liver (as percentage of administered dose per g of tissue). The preferential association of 67Ga with these microvesicles in the 5123C hepatoma may be indicative of a basic difference between normal and malignant tissue.
本文描述了一种通过速率和等密度密度梯度区带离心相结合的方法,从正常大鼠肝脏和莫里斯5123C肝癌匀浆中定量分离67Ga结合颗粒(GBG)的程序。已发现另一类GBG比我们之前描述的溶酶体GBG小得多。这些较小的颗粒或微泡结合了肝癌中发现的大部分67Ga,而在肝脏中,GBG溶酶体是主要的结合成分。此前,我们已经表明,肝癌摄取的67Ga比肝脏多得多(以每克组织中给药剂量的百分比计算)。67Ga在5123C肝癌中与这些微泡的优先结合可能表明正常组织和恶性组织之间存在根本差异。