Gibson K F, Phadke S
Division of Pulmonary, Allergy, and Critical Care Medicine, University of Pittsburgh, School of Medicine, Pennsylvania 15261.
Exp Lung Res. 1994 Nov-Dec;20(6):595-611. doi: 10.3109/01902149409031739.
This study investigated the intracellular distribution of lysozyme, a protein that is synthesized and secreted by rat alveolar type II epithelial (ATII) cells and alveolar macrophages, using a polyclonal antibody generated against purified rat lysozyme. Lysozyme was immunoprecipitated with this antibody from Triton X-100 lysates of ATII cells cultured on a basement membrane derived from Englebreth-Holme-Swarm mouse sarcoma (EHS) and radiolabeled with 35S-methionine. ATII cells cultured on EHS basement membrane for several days were fixed and labeled with antibodies to surfactant apoprotein A (SP-A) and lgp-120 (a lysosomal glycoprotein), or lysozyme and lgp-120, and studied by confocal microscopy. Organelles were identified that stained positively for either anti-lysozyme or anti-lgp-120; a second population of organelles contained both markers. Similarly, two populations of SP-A-containing organelles were identified; one contained the lysosomal glycoprotein lgp-120. In addition, confocal images demonstrated that both SP-A and lysozyme were secreted by ATII cells, as evidenced by the accumulation of secretory products within the lumen of the cyst-like aggregates. When the subcellular localization of SP-A and lysozyme was studied by analytical cell fractionation, two populations of organelles were identified that contained SP-A or lysozyme. The lighter population accounted for approximately 32% of SP-A and 33% of total intracellular lysozyme and was recovered in the same region of the gradient as secretory lamellar bodies. The more dense population co-localized with lysosomes and accounted for approximately 67% of both SP-A and lysozyme recovered. Western blots of cell fractions revealed intact lysozyme in all the cell fractions. The results of these experiments suggest that lysozyme has a similar intracellular distribution as surfactant apoprotein A in ATII cells. Lysozyme is found in fractions containing lamellar bodies where it is packaged for secretion, and in lysosomal fractions where it may undergo degradation.
本研究利用针对纯化大鼠溶菌酶产生的多克隆抗体,调查了溶菌酶在细胞内的分布情况。溶菌酶是一种由大鼠II型肺泡上皮(ATII)细胞和肺泡巨噬细胞合成并分泌的蛋白质。用该抗体从培养在源自Englebreth-Holme-Swarm小鼠肉瘤(EHS)的基底膜上的ATII细胞的Triton X-100裂解物中免疫沉淀溶菌酶,并用35S-甲硫氨酸进行放射性标记。在EHS基底膜上培养数天的ATII细胞经固定后,用针对表面活性蛋白A(SP-A)和lgp-120(一种溶酶体糖蛋白)的抗体,或溶菌酶和lgp-120的抗体进行标记,然后通过共聚焦显微镜进行研究。鉴定出了对抗溶菌酶或抗lgp-120呈阳性染色的细胞器;另一群细胞器同时含有这两种标记物。同样,鉴定出了两群含有SP-A的细胞器;其中一群含有溶酶体糖蛋白lgp-120。此外,共聚焦图像显示SP-A和溶菌酶均由ATII细胞分泌,囊状聚集体腔内分泌产物的积累证明了这一点。当通过分析性细胞分级分离研究SP-A和溶菌酶的亚细胞定位时,鉴定出了两群含有SP-A或溶菌酶的细胞器。较轻的一群约占SP-A的32%和细胞内总溶菌酶的33%,并在梯度的同一区域中与分泌性板层小体一起回收。密度更大的一群与溶酶体共定位,约占回收的SP-A和溶菌酶的67%。细胞分级分离物的蛋白质免疫印迹显示所有细胞分级分离物中均有完整的溶菌酶。这些实验结果表明,在ATII细胞中,溶菌酶的细胞内分布与表面活性蛋白A相似。溶菌酶存在于含有板层小体的分级分离物中,在那里它被包装用于分泌,也存在于溶酶体分级分离物中,在那里它可能会被降解。