Jadot M, Misquith S, Dubois F, Wattiaux-De Coninck S, Wattiaux R
Eur J Biochem. 1986 Dec 15;161(3):695-700. doi: 10.1111/j.1432-1033.1986.tb10495.x.
Yeast invertase, when injected into rats, is endocytosed by the liver, mainly by sinusoidal cells. The work reported here aims at investigating the organelles involved in the intracellular journey of this protein. Experiments were performed on rats injected with 125I-invertase (25 micrograms/100 g body wt) and killed at various times after injection. Homogenates were fractioned by differential centrifugation, according to de Duve, Pressman, Gianetto, Wattiaux and Appelmans [(1955) Biochem. J. 63, 604-617]. Early after injection the radioactivity was recovered mainly in the microsomal fraction P; later it was found in the mitochondrial fractions (ML). At all times a peak of relative specific activity was observed in the light mitochondrial fraction L. After isopycnic centrifugation in a sucrose gradient, structures bearing 125I-invertase, present in P, exhibited a relatively flattened distribution with a density of around 1.17 g/ml, relatively similar to that of alkaline phosphodiesterase a plasma membrane marker. The organelles located in ML were endowed with a more homogeneous distribution, their median equilibrium density increasing up to 30 min after injection (1.20 g/ml----1.23 g/ml); with time the radioactivity distribution became more closely related to the distribution of arylsulfatase, a lysosomal enzyme. ML fractions, isolated 10 min and 180 min after 125I-invertase injection, were subjected to isopycnic centrifugation in Percoll gradient with, as solvent, 0.25 M, 0.5 M and 0.75 M sucrose. The change of density of the particles bearing 125I-invertase, as a function of the sucrose concentration, paralleled the change of density of the lysosomes as ascertained by the behaviour of arylsulfatase. The distribution of radioactivity and arylsulfatase in a sucrose gradient was established after isopycnic centrifugation of the ML fraction of rats injected with 125I-invertase, the animals having received or not an injection of 900 micrograms/100 g body weight of unlabelled invertase 15 h before killing. In agreement with our previous results, a shift towards higher densities of about 25% or arylsulfatase takes place in rats pretreated with unlabelled invertase. At 10 min, invertase preinjection did not change the radioactivity distribution curve. Later, it caused a progressive shift of the distribution towards higher-density regions of the gradient where the arylsulfatase, which had been shifted, was located.(ABSTRACT TRUNCATED AT 400 WORDS)
将酵母转化酶注射到大鼠体内后,肝脏会对其进行内吞作用,主要是由肝血窦细胞完成。本文报道的研究旨在探究参与该蛋白细胞内运输过程的细胞器。对注射了125I标记的转化酶(25微克/100克体重)的大鼠进行实验,并在注射后的不同时间点将其处死。根据德·迪夫、普雷斯曼、贾内托、瓦蒂奥克斯和阿佩尔曼斯[(1955)《生物化学杂志》63, 604 - 617]的方法,通过差速离心对匀浆进行分级分离。注射后早期,放射性主要在微粒体组分P中检测到;之后在线粒体组分(ML)中发现。在整个时间段内,在轻线粒体组分L中均观察到相对比活性的峰值。在蔗糖梯度中进行等密度离心后,存在于P中的携带125I标记转化酶的结构呈现出相对扁平的分布,密度约为1.17克/毫升,与质膜标记物碱性磷酸二酯酶的密度相对相似。位于ML中的细胞器具有更均匀的分布,其平均平衡密度在注射后30分钟内增加(从1.20克/毫升增加到1.23克/毫升);随着时间推移,放射性分布与溶酶体酶芳基硫酸酯酶的分布关系更为密切。在注射125I标记的转化酶后10分钟和180分钟分离得到的ML组分,在含有0.25 M、0.5 M和0.75 M蔗糖作为溶剂的Percoll梯度中进行等密度离心。携带125I标记转化酶的颗粒密度随蔗糖浓度的变化,与通过芳基硫酸酯酶行为确定的溶酶体密度变化平行。在处死前15小时,对注射了125I标记转化酶的大鼠,分别注射或未注射900微克/100克体重的未标记转化酶,然后对其ML组分进行等密度离心,确定在蔗糖梯度中放射性和芳基硫酸酯酶的分布。与我们之前的结果一致,预先注射未标记转化酶的大鼠中,芳基硫酸酯酶的密度向更高值偏移约25%。在10分钟时,预先注射转化酶并未改变放射性分布曲线。之后,它导致分布逐渐向梯度中更高密度区域偏移,而已经发生偏移的芳基硫酸酯酶就位于该区域。(摘要截选至400字)