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通过注射亮抑酶肽诱导细胞质酶在自噬泡-溶酶体系统中隔离。

Sequestration of cytoplasmic enzymes in an autophagic vacuole-lysosomal system induced by injection of leupeptin.

作者信息

Kominami E, Hashida S, Khairallah E A, Katunuma N

出版信息

J Biol Chem. 1983 May 25;258(10):6093-100.

PMID:6133857
Abstract

Administration of leupeptin to rats induces the accumulation of numerous autophagic vacuoles in the liver. Furuno et al. (Furuno, K., Ishikawa, T., and Kato, K. (1982) J. Biochem. (Tokyo) 91, 1485-1494) have recently devised a method for Percoll density gradient equilibrium fractionation of crude lysosomal fractions to isolate a highly enriched preparation of autophagic vacuoles. This system was used to determine whether cytoplasmic enzymes are normally sequestered into autophagic vacuoles in fed animals. Within 30 min following the administration of leupeptin to fed rats, several cytoplasmic enzymes could be demonstrated in vacuolar fractions heavier than mitochondria and normal lyosomes. The activities of tyrosine aminotransferase and lactic dehydrogenase as well as antigens of fructose-bisphosphate aldolase were detectable in fractions with densities of 1.115 to 1.15 g/ml containing cathepsins and acid phosphatase. The cytoplasmic enzymes in these fractions exhibited latency and were sequestered within membranous organelles. Six hours after the administration of leupeptin, the autophagic vacuoles gradually disappeared from these fractions concurrently with the loss of both cytoplasmic and lysosomal marker enzymes. For 6 h after injection of leupeptin the activities of cathepsin D and acid phosphatase increased in autophagic vacuoles and decreased in the postvacuolar lysosomal fraction. Administration of dexamethasone, which induces the synthesis of tyrosine aminotransferase and cytosolic aspartate aminotransferase, selectively increased the sequestration of these enzymes to proportional degrees. Cycloheximide administered simultaneously with leupeptin rapidly inhibited formation of autophagic vacuoles and the sequestrations of both cytoplasmic and lysosomal enzymes. However, when cycloheximide was administered 1 h after leupeptin, the formation of autophagosomes and the sequestration of cytoplasmic enzymes were inhibited but the vacuolar uptake of acid phosphatase and cathepsin D continued to increase for several hours. When cycloheximide was injected 1 h after leupeptin, losses of lactic dehydrogenase and aldolase proteins were observed in autophagic vacuoles isolated 1 and 2 h later.

摘要

给大鼠注射亮抑酶肽会诱导肝脏中大量自噬泡的积累。古野等人(古野健、石川彻、加藤和男(1982年)《生物化学杂志》(东京)91卷,1485 - 1494页)最近设计了一种用于粗溶酶体组分的Percoll密度梯度平衡分级分离法,以分离高度富集的自噬泡制剂。该系统用于确定在喂食动物中细胞质酶是否正常地被隔离到自噬泡中。给喂食的大鼠注射亮抑酶肽后30分钟内,在比线粒体和正常溶酶体密度大的液泡组分中可检测到几种细胞质酶。在密度为1.115至1.15克/毫升、含有组织蛋白酶和酸性磷酸酶的组分中可检测到酪氨酸转氨酶和乳酸脱氢酶的活性以及果糖 - 双磷酸醛缩酶的抗原。这些组分中的细胞质酶表现出潜伏性,并被隔离在膜性细胞器内。注射亮抑酶肽6小时后,自噬泡从这些组分中逐渐消失,同时细胞质和溶酶体标记酶也消失。注射亮抑酶肽后6小时内,组织蛋白酶D和酸性磷酸酶的活性在自噬泡中增加,而在液泡后溶酶体组分中降低。地塞米松可诱导酪氨酸转氨酶和胞质天冬氨酸转氨酶的合成,其给药选择性地增加了这些酶的隔离程度。与亮抑酶肽同时给药的环己酰亚胺迅速抑制自噬泡的形成以及细胞质和溶酶体酶的隔离。然而,当在亮抑酶肽给药1小时后给予环己酰亚胺时,自噬体的形成和细胞质酶的隔离受到抑制,但酸性磷酸酶和组织蛋白酶D的液泡摄取在数小时内持续增加。当在亮抑酶肽给药1小时后注射环己酰亚胺时,在1小时和2小时后分离的自噬泡中观察到乳酸脱氢酶和醛缩酶蛋白的损失。

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