Dvorak A M, Klebanoff S J, Henderson W R, Monahan R A, Pyne K, Galli S J
Am J Pathol. 1985 Mar;118(3):425-38.
Guinea pig basophils, cloned mouse mast cells, and cloned mouse granule-containing lymphoid cells were found to utilize a vesicular transport system to internalize eosinophil peroxidase (EPO) added in vitro. Kinetic analysis indicated that EPO internalization involved the binding of EPO to the plasma membrane, the formation of complex surface invaginations, and the movement of EPO-laden vesicles, tubules, and vacuoles toward the center of the cells. EPO became associated with multivesicular bodies in granule-containing lymphoid cells and mast cells, with immature granules in mast cells, and with mature granules in basophils. In other cells, the endogenous production of granule peroxidases (neutrophils and eosinophils) or the prior uptake of exogenous peroxidatic substances (some basophils) precluded cytochemical analysis of granules for EPO. Vesicular transport of EPO provides a possible explanation for the variable detection of peroxidase activity in mast cells or basophils. It also provides a mechanism for sequestration of this potentially toxic material or for its storage for possible future use.
研究发现,豚鼠嗜碱性粒细胞、克隆的小鼠肥大细胞以及克隆的含颗粒小鼠淋巴细胞利用囊泡运输系统内化体外添加的嗜酸性粒细胞过氧化物酶(EPO)。动力学分析表明,EPO内化涉及EPO与质膜的结合、复杂表面内陷的形成,以及载有EPO的囊泡、小管和液泡向细胞中心的移动。在含颗粒淋巴细胞和肥大细胞中,EPO与多泡体相关;在肥大细胞中,EPO与未成熟颗粒相关;在嗜碱性粒细胞中,EPO与成熟颗粒相关。在其他细胞中,颗粒过氧化物酶(中性粒细胞和嗜酸性粒细胞)的内源性产生或外源性过氧化物物质的预先摄取(一些嗜碱性粒细胞)妨碍了对颗粒进行EPO的细胞化学分析。EPO的囊泡运输为肥大细胞或嗜碱性粒细胞中过氧化物酶活性的可变检测提供了一种可能的解释。它还为隔离这种潜在有毒物质或储存以备将来可能使用提供了一种机制。