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内质网膜的生物发生。II. 发育中大鼠肝细胞组成型微粒体酶的合成。

Biogenesis of endoplasmic reticulum membranes. II. Synthesis of constitutive microsomal enzymes in developing rat hepatocyte.

作者信息

Dallner G, Siekevitz P, Palade G E

出版信息

J Cell Biol. 1966 Jul;30(1):97-117. doi: 10.1083/jcb.30.1.97.

Abstract

The constitutive enzymes of microsomal membranes were investigated during a period of rapid ER development (from 3 days before to 8 days after birth) in rat hepatocytes. The activities studied (electron transport enzymes and phosphatases) appear at different times and increase at different rates. The increase in the enzyme activities tested was inhibited by Actinomycin D and puromycin. G-6-Pase and NADPH-cytochrome c reductase activities appeared first in the rough microsomes, and subsequently in smooth microsomes, eventually reaching a uniform concentration as in adult liver. The evidence suggests that the enzymes are synthesized in the rough part, then transferred to the smooth part, of the ER. Changes in the fat supplement of the maternal diet brought about changes in the fatty acid composition of microsomal phospholipids but did not influence the enzymic pattern of the suckling. Microsomes from 8-day-old and adult rats lose 95% of PLP and 80% of NADH-cytochrome c reductase activity after acetone-H(2)O (10:1) extraction. However, one-half the original activity could be regained by adding back phospholipid micelles prepared from purified phospholipid, or from lipid extracts of heart mitochondria, or of liver microsomes of 8-day or adult rats, thus demonstrating an activation of the enzyme by nonspecific phospholipid. The results suggest that during development the enzymic pattern is not influenced by the fatty acid or phospholipid composition of ER membranes.

摘要

在大鼠肝细胞内质网快速发育阶段(从出生前3天到出生后8天),对微粒体膜的组成酶进行了研究。所研究的酶活性(电子传递酶和磷酸酶)在不同时间出现,且以不同速率增加。放线菌素D和嘌呤霉素可抑制所测试酶活性的增加。葡萄糖-6-磷酸酶和NADPH-细胞色素c还原酶活性首先出现在粗面微粒体中,随后出现在滑面微粒体中,最终达到与成年肝脏相同的均匀浓度。证据表明这些酶是在内质网的粗面部分合成,然后转移到滑面部分。母体饮食中脂肪补充的变化导致微粒体磷脂脂肪酸组成发生变化,但不影响哺乳幼崽的酶谱。8日龄和成年大鼠的微粒体在丙酮-H₂O(10:1)提取后,会丧失95%的磷脂酰吡哆醛和80%的NADH-细胞色素c还原酶活性。然而,通过添加由纯化磷脂、心脏线粒体脂质提取物或8日龄或成年大鼠肝脏微粒体制备的磷脂微团,可恢复一半的原始活性,从而证明非特异性磷脂对该酶具有激活作用。结果表明,在发育过程中,酶谱不受内质网膜脂肪酸或磷脂组成的影响。

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