Heine H, Schaeg G
Z Mikrosk Anat Forsch. 1980;94(1):160-8.
Phosphatase-positive and -negative multivesicular bodies (mvb) are discernable by ultrastructural and ultracytochemical findings. The phosphatase-negative mvb are actually not considered to belong to the group of lysosomes. Because, they are obviously involved in synthesizing the cell-specific lamellated bodies (i.e. multilamellated bodies of type II alveolarepithelium cells, keratinosomes, praemelanosomes). By studying the literature about ultrastructural findings in tumors we found that mvb are generally increased in number in tumor cells. The changes in structure of the tumor cell membrane might be interpreted in a way that the synthesizing ability of mvb would generally provide phospholipoproteins to adjust a structural steady state of cell membranes. Our findings suggest that the synthetical activities of the mvb are coupled with multi-enzyme complexes of the vesicle membranes. Obviously, these membranes originate fro the Golgi-apparatus being closely related to the smooth endoplasmic reticulum.
通过超微结构和超细胞化学研究结果可辨别出磷酸酶阳性和阴性多囊泡体(mvb)。磷酸酶阴性多囊泡体实际上并不被认为属于溶酶体类别。因为,它们明显参与细胞特异性板层小体(即Ⅱ型肺泡上皮细胞的多层板层小体、角质小体、前黑素小体)的合成。通过研究有关肿瘤超微结构研究结果的文献,我们发现肿瘤细胞中mvb的数量通常会增加。肿瘤细胞膜结构的变化可以这样解释,即mvb的合成能力通常会提供磷脂蛋白来调节细胞膜的结构稳态。我们的研究结果表明,mvb的合成活动与囊泡膜的多酶复合物相关。显然,这些膜起源于与滑面内质网密切相关的高尔基体。