Hamberg H, Edman P
Acta Pathol Microbiol Immunol Scand A. 1983 Jan;91(1):1-8. doi: 10.1111/j.1699-0463.1983.tb02719.x.
Cultured mouse peritoneal macrophages were exposed for 48 h to a large and toxic dose of polyacrylamide microspheres (previously designed for use as a lysosomotropic carrier for the intracellular delivery of enzymes and other macromolecules). This treatment induced autophagocytosis in the macrophages, which contained abundant autophagic vacuoles at 24 h post exposure. Transmission electron microscopical studies including enzyme cytochemistry showed that the segregating membranes in autophagosome formation consisted of flattened, smooth-surfaced vacuoles with a granular matrix in which reaction product indicating acid phosphatase activity could be demonstrated. The autophagic vacuole formation was apparently effected by wrapping of a portion of the cytoplasm in a sheet formed by flattening and fusion of multiple small vacuoles with acid phosphatase activity in their matrices. The conclusion is drawn that the segregating membranes are derived from lysosomes or GERL structures in this particular system of induced autophagocytosis.
将培养的小鼠腹腔巨噬细胞暴露于大剂量且有毒的聚丙烯酰胺微球(先前设计用作酶和其他大分子细胞内递送的溶酶体亲和载体)48小时。这种处理在巨噬细胞中诱导了自噬作用,在暴露后24小时巨噬细胞中含有丰富的自噬泡。包括酶细胞化学在内的透射电子显微镜研究表明,自噬体形成过程中的隔离膜由扁平、表面光滑的空泡组成,其具有颗粒状基质,在其中可以证明有指示酸性磷酸酶活性的反应产物。自噬泡的形成显然是通过将一部分细胞质包裹在由多个小空泡扁平化和融合形成的薄片中实现的,这些小空泡的基质中具有酸性磷酸酶活性。得出的结论是,在这个特定的诱导自噬系统中,隔离膜源自溶酶体或GERL结构。