Blok J, Mulder-Stapel A A, Daems W T, Ginsel L A
Histochemistry. 1981 Dec;73(3):429-38. doi: 10.1007/BF00495657.
The effect of chloroquine on the intralysosomal degradation of cell-coat glycoproteins in cultured intestinal absorptive cell was investigated by silver proteinate staining. The results of this staining method, which is specific for carbohydrate containing macromolecules such as glycoproteins and mucopolysaccharides, showed that in the presence of the drug considerable amounts of silver proteinate-positive material accumulated in one type of lysosome-like body: the dense bodies. The staining pattern of other cell organelles was not affected by chloroquine. The presence of the drug in the culture medium also resulted in the occurrence of numerous small vesicular structures in the matrix of the dense bodies. These showed a similar size and structure to those present in the other type of lysosome-like body: the multivesicular bodies. This observation, together with earlier autoradiographical data, suggests that cell-coat material is transferred from multivesicular to dense bodies by fusion between these organelles. This study thus provides further evidence for a regulatory mechanism of cell-coat glycoprotein transport by the lysosome-like bodies in human intestinal absorptive cells.
通过蛋白银染色研究了氯喹对培养的肠吸收细胞中细胞被糖蛋白溶酶体内降解的影响。这种染色方法对含碳水化合物的大分子如糖蛋白和粘多糖具有特异性,其结果显示,在药物存在的情况下,大量蛋白银阳性物质积聚在一种溶酶体样小体即致密体内。氯喹不影响其他细胞器的染色模式。培养基中药物的存在还导致致密体基质中出现大量小泡状结构。这些小泡状结构的大小和结构与另一种溶酶体样小体即多泡体中的小泡相似。这一观察结果与早期的放射自显影数据一起表明,细胞被物质通过这些细胞器之间的融合从多泡体转移到致密体。因此,本研究为人类肠吸收细胞中溶酶体样小体对细胞被糖蛋白运输的调节机制提供了进一步的证据。