Fitz-Gibbon L, Shematek G, Sullivan A K
Leuk Res. 1985;9(1):123-34. doi: 10.1016/0145-2126(85)90026-8.
Specialized internal granules are a major feature of myeloid differentiation and are deficient in most acute myeloid leukemia cells. Although they arise from the same synthetic apparatus as does the plasma membrane, their relationship to it is not well characterized in human tissues. Using murine monoclonal antibodies, we have identified myeloid-related structures that illustrate three possible modes of antigen expression in these organelles. Immunocytochemical studies with the light microscope have shown that the first (D51) was restricted to the surface of neutrophils, monocytes, megakaryocytes and platelets; a second (D46) was found on the surface of blastic cell lines but on only internal components of mature granulocytes; the third (H36/71) appeared on both the surface and internal particles of promyelocytes, myelocytes and polymorphs. These model antigens may be used to study the control of granule synthesis in normal and leukemic cells.
特殊的内部颗粒是髓系分化的主要特征,且在大多数急性髓系白血病细胞中缺乏。尽管它们与质膜起源于相同的合成装置,但在人体组织中它们与质膜的关系尚未得到充分表征。利用鼠单克隆抗体,我们鉴定出了与髓系相关的结构,这些结构说明了这些细胞器中三种可能的抗原表达模式。光学显微镜下的免疫细胞化学研究表明,第一种(D51)仅限于中性粒细胞、单核细胞、巨核细胞和血小板的表面;第二种(D46)见于原始细胞系的表面,但仅见于成熟粒细胞的内部成分;第三种(H36/71)出现在早幼粒细胞、中幼粒细胞和多形核细胞的表面和内部颗粒上。这些模型抗原可用于研究正常细胞和白血病细胞中颗粒合成的调控。