Elleder M, Drahota Z, Lisá V, Mares V, Mandys V, Müller J, Palmer D N
Hlava's 1st Institute of Pathology, Prague, Czech Republic.
Am J Med Genet. 1995 Jun 5;57(2):213-21. doi: 10.1002/ajmg.1320570220.
Storage granules (SGs) from ovine and canine models of Batten disease were found to be easily phagocytosed by four cell types studied. The cell types tested were human fibroblasts and peripheral monocytes (control and from a late infantile Batten disease patient), rat C6 cell line, and neonatal cardiomyocytes. The phagocytosed SGs elicited an increase in acid phosphatase activity which was localized in the phagolysosome. After phagocytosis SGs were followed for various times ranging from 7 to 21 days and were found to be of unchanged density (phase contrast), autofluorescence, and ultrastructural appearance. These findings point to their undergradability, or very low degree of degradability, in phagolysosomes in both normal or Batten cultured cells. The Batten disease SGs are not toxic and did not cause any adverse affect on the host cells. Either the normal clearance rate from lysosomes is too slow to be measured by this technique or subunit c accumulation in lysosomes need not result from a primary lysosomal protease defect. Subunit c may aggregate, because of the lack of some normally preventive factor, resulting in a physical barrier to the degradation of this highly apolar molecule.
在研究的四种细胞类型中,发现来自绵羊和犬类巴滕病模型的储存颗粒(SGs)很容易被吞噬。所测试的细胞类型包括人成纤维细胞和外周单核细胞(对照以及一名晚发性婴儿型巴滕病患者的样本)、大鼠C6细胞系和新生心肌细胞。被吞噬的SGs引起了酸性磷酸酶活性的增加,该酶定位于吞噬溶酶体中。吞噬后,对SGs进行了7至21天的不同时间跟踪,发现其密度(相差显微镜观察)、自发荧光和超微结构外观均未改变。这些发现表明,在正常或巴滕病培养细胞的吞噬溶酶体中,它们难以被降解,或降解程度非常低。巴滕病SGs无毒,对宿主细胞没有任何不良影响。要么是溶酶体的正常清除率太慢,以至于无法用该技术测量,要么是溶酶体中亚基c的积累不一定是由原发性溶酶体蛋白酶缺陷导致的。由于缺乏一些正常的预防因子,亚基c可能会聚集,从而对这种高度非极性分子的降解形成物理屏障。