Rabinowitz S, Horstmann H, Gordon S, Griffiths G
Sir William Dunn School of Pathology, Oxford, England.
J Cell Biol. 1992 Jan;116(1):95-112. doi: 10.1083/jcb.116.1.95.
We have used endocytic and phagocytic tracers in an EM immunocytochemical study to define the compartments of the phagocytic and endocytic pathways in mouse peritoneal macrophages. Endocytosed BSA-gold appeared successively in early endosomes, spherical endosomal vesicles, a late endosomal tubuloreticular compartment (TC), and terminal lysosomes. The TC appeared as an elaborate structure enriched for the lysosomal membrane glycoproteins Lamp 1 and Lamp 2, and expressing significant levels of rab7, a late endosome-specific GTP-binding protein. The cation-independent mannose-6-phosphate receptor was restricted to specialized regions of the TC that were predominantly adjacent to the Golgi complex. Both the early endosome and the TC had coated bud structures whose composition and function are presently unknown. Phagolysosomes containing latex beads expressed the same membrane antigens and received endocytic tracers simultaneously with the TC. Since the membrane surrounding both organelles was also in direct continuity, we assume that both structures form one functional compartment. Macrosialin, an antigen confined to macrophages and dendritic cells, was heavily expressed in TC and phagolysosomal membranes with low levels being detected in other endosomal compartments and on the cell surface. Treatment of cells with wheat germ agglutinin drastically altered the morphology of the TC, giving rise to sheets of tightly adherent membrane and greatly expanded vesicles, in which cell-associated wheat germ agglutinin was concentrated. The spherical endosomal carrier vesicles loaded with internalized gold tracers clustered nearby, often making contact without fusing. Since the delivery of endocytic tracer to the TC was significantly delayed these experiments suggest that the lectin is somehow preventing the endosome vesicles from fusing with the TC. Collectively, our data argue first that the PLC is equivalent to the "tubular lysosomes" commonly described in macrophages, and second that the meeting of the phagocytic and endocytic pathway occurs in this compartment.
在一项电子显微镜免疫细胞化学研究中,我们使用了内吞和吞噬示踪剂来确定小鼠腹膜巨噬细胞中吞噬和内吞途径的区室。内吞的牛血清白蛋白-金先后出现在早期内体、球形内体小泡、晚期内体管状网状区室(TC)和终末溶酶体中。TC呈现为一种复杂的结构,富含溶酶体膜糖蛋白Lamp 1和Lamp 2,并表达高水平的rab7,一种晚期内体特异性GTP结合蛋白。不依赖阳离子的甘露糖-6-磷酸受体局限于TC的特定区域,这些区域主要与高尔基体复合体相邻。早期内体和TC都有包被芽结构,其组成和功能目前尚不清楚。含有乳胶珠的吞噬溶酶体表达相同的膜抗原,并与TC同时接收内吞示踪剂。由于围绕这两种细胞器的膜也直接连续,我们假设这两种结构形成一个功能区室。巨唾液酸蛋白是一种局限于巨噬细胞和树突状细胞的抗原,在TC和吞噬溶酶体膜中大量表达,在其他内体区室和细胞表面检测到的水平较低。用小麦胚凝集素处理细胞会极大地改变TC的形态,产生紧密粘附的膜片和大大扩张的小泡,其中细胞相关的小麦胚凝集素集中在其中。装载内化金示踪剂的球形内体载体小泡聚集在附近,常常接触但不融合。由于向内吞示踪剂向TC的递送明显延迟,这些实验表明凝集素以某种方式阻止内体小泡与TC融合。总的来说,我们的数据首先表明PLC等同于巨噬细胞中通常描述的“管状溶酶体”,其次表明吞噬和内吞途径的交汇发生在这个区室中。