Iwao H, Nakamura N, Ikemoto F, Yamamoto K
Jpn Circ J. 1983 Oct;47(10):1198-202. doi: 10.1253/jcj.47.1198.
Our recent findings on the subcellular localization of exogenously administered 125I-labeled mouse submaxillary renin in the mouse kidney are summarized herein. 125I-labeled renin was given intravenously to anesthetized male ICR mice (6 weeks) in a dose of 20 ng (2 muCi)/40 g body weight and the subcellular distribution was identified by the reaction with a specific antiserum of the mouse submaxillary renin. 125I-labeled renin was identified mainly by differential centrifugation in the heavy mitochondrial fraction. With discontinuous sucrose density gradient centrifugation, the radioactivity was most readily detected with 1.2 M and 1.5 M sucrose. Over 90% of the radioactivity was identified in the form of 125I-labeled renin with a molecular weight of 38,000 daltons in each fraction. Light and electron microscopic autoradiography revealed that the 125I-labeled renin had accumulated in the apical region of the proximal convoluted tubular cells and was mainly located in the lysosomal granules. All these data taken together indicate that the exogenous renin filtered through the glomerular capillaries is reabsorbed and localized in the lysosomes of the proximal convoluted tubular cells.
本文总结了我们最近关于外源性给予的125I标记的小鼠颌下肾素在小鼠肾脏中的亚细胞定位的研究结果。将125I标记的肾素以20 ng(2 μCi)/40 g体重的剂量静脉注射给麻醉的雄性ICR小鼠(6周龄),并通过与小鼠颌下肾素的特异性抗血清反应来确定亚细胞分布。125I标记的肾素主要通过差速离心法在重线粒体组分中被鉴定出来。通过不连续蔗糖密度梯度离心法,在1.2 M和1.5 M蔗糖中最容易检测到放射性。在每个组分中,超过90%的放射性以分子量为38,000道尔顿的125I标记的肾素形式被鉴定出来。光镜和电镜放射自显影显示,125I标记的肾素积聚在近端曲管细胞的顶端区域,主要位于溶酶体颗粒中。所有这些数据综合起来表明,通过肾小球毛细血管滤过的外源性肾素被重吸收并定位在近端曲管细胞的溶酶体中。