Zahlten R N, Hagler H K, Nejtek M E, Day C J
Department of Internal Medicine, University of Texas Health Science Center, Southwestern Medical School, Dallas 75235.
Gastroenterology. 1978 Jul;75(1):80-7.
Kupffer and endothelial cells of rat liver were purified by recirculating collagenase perfusion, metrizamide gradient, and counterflow elutriation. Every step of the isolation procedure was followed by light microscopy and histochemistry. The final fractions of purified sinusoidal cells were examined in their isolated state by transmission and scanning electron microscopy. The scope of this manuscript is the detailed documentation and discussion of all technical aspects and problems of a rather new isolation technique, as well as the detailed description of the purified sinusoidal cells of the liver by scanning electron microscopy. Broader acceptance of this isolation procedure should lead to the specific characterization of biochemical and immunological functions of these cells and elucidate their pathophysiological significance.
通过循环胶原酶灌注、甲泛葡胺梯度离心和逆流淘析法纯化大鼠肝脏的库普弗细胞和内皮细胞。分离过程的每一步之后都进行光学显微镜检查和组织化学检查。通过透射电子显微镜和扫描电子显微镜对纯化的肝窦细胞的最终组分进行分离状态下的检查。本手稿的范围是详细记录和讨论一种相当新的分离技术的所有技术方面和问题,以及通过扫描电子显微镜对纯化的肝脏窦状细胞进行详细描述。这种分离方法的更广泛接受应该能够对这些细胞的生化和免疫功能进行特异性表征,并阐明它们的病理生理意义。