Murata F, Wohltman H, Spicer S S, Nagata T
Virchows Arch B Cell Pathol. 1977 Oct 7;25(1):61-73. doi: 10.1007/BF02889421.
Lymphocytes from 6 patients with 3 types of genetic mucopolysaccharidoses (Hurler's syndrome, Hunter's syndrome and Morquio's syndrome) contained numberous vacuoles in their cytoplasm. The size of the vacuoles ranged from approximately 300 nm to 750 nm. The percentage of the lymphocytes with vacuoles varied from 10% to 38%. The vacuoles showed acid phosphatase activity, which indicated their lysosommal nature. Staining with dialyzed iron solution usually localized acid mucosubstance in the peripheral region of these vacuoles after glutaraldehyde fixation. Ferritin and horseradish peroxidase were observed in the vacuoles after incubation of the patient's lymphocytes with these tracers. This finding indicates the participation of endocytosis in the formation of these vacuoles.
6例患有3种遗传性黏多糖贮积症(Hurler综合征、Hunter综合征和Morquio综合征)患者的淋巴细胞,其细胞质中含有大量空泡。空泡大小范围约为300纳米至750纳米。有空泡的淋巴细胞百分比在10%至38%之间变化。这些空泡显示出酸性磷酸酶活性,这表明它们具有溶酶体性质。在戊二醛固定后,用透析铁溶液染色通常可将酸性黏液物质定位在这些空泡的周边区域。在用这些示踪剂孵育患者的淋巴细胞后,在空泡中观察到了铁蛋白和辣根过氧化物酶。这一发现表明内吞作用参与了这些空泡的形成。