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自噬机制的研究:自噬泡的形成。

Studies on the mechanisms of autophagy: formation of the autophagic vacuole.

作者信息

Dunn W A

机构信息

Department of Anatomy and Cell Biology, University of Florida College of Medicine, Gainesville 32610.

出版信息

J Cell Biol. 1990 Jun;110(6):1923-33. doi: 10.1083/jcb.110.6.1923.

Abstract

Autophagic vacuoles form within 15 min of perfusing a liver with amino acid-depleted medium. These vacuoles are bound by a "smooth" double membrane and do not contain acid phosphatase activity. In an attempt to identify the membrane source of these vacuoles, I have used morphological techniques combined with immunological probes to localize specific membrane antigens to the limiting membranes of newly formed or nascent autophagic vacuoles. Antibodies to three integral membrane proteins of the plasma membrane (CE9, HA4, and epidermal growth factor receptor) and one of the Golgi apparatus (sialyltransferase) did not label these vacuoles. Internalized epidermal growth factor and its membrane receptor were not found in nascent autophagic vacuoles but were present in lysosome-like degradative autophagic vacuoles. All these results suggested that autophagic vacuoles were not formed from plasma membrane, Golgi apparatus, or endosome constituents. Antisera prepared against integral membrane proteins (14, 25, and 40 kD) of the RER was found to label the inner and outer limiting membranes of almost all nascent autophagic vacuoles. In addition, ribophorin II was identified at the limiting membranes of many nascent autophagic vacuoles. Finally, secretory proteins, rat serum albumin and alpha 2u-globulin, were localized to the lumen of the RER and to the intramembrane space between the inner and outer membranes of some of these vacuoles. The results were consistent with the formation of autophagic vacuoles from ribosome-free regions of the RER.

摘要

在用缺乏氨基酸的培养基灌注肝脏后的15分钟内,自噬泡开始形成。这些泡由“光滑”的双层膜包裹,且不含有酸性磷酸酶活性。为了确定这些泡的膜来源,我运用形态学技术结合免疫探针,将特定的膜抗原定位到新形成的或新生的自噬泡的界膜上。针对质膜的三种整合膜蛋白(CE9、HA4和表皮生长因子受体)以及高尔基体的一种蛋白(唾液酸转移酶)的抗体并未标记这些泡。在新生自噬泡中未发现内化的表皮生长因子及其膜受体,但在溶酶体样的降解性自噬泡中存在。所有这些结果表明,自噬泡并非由质膜、高尔基体或内体成分形成。针对粗面内质网的整合膜蛋白(14、25和40 kD)制备的抗血清被发现可标记几乎所有新生自噬泡的内界膜和外界膜。此外,在许多新生自噬泡的界膜上鉴定出了核糖体结合蛋白II。最后,分泌蛋白、大鼠血清白蛋白和α2u球蛋白被定位到粗面内质网的管腔以及其中一些泡内外膜之间的膜内空间。这些结果与自噬泡由粗面内质网的无核糖体区域形成一致。

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