Glass J, Fischer S, Lavidor L M, Nunez T
Cancer Res. 1977 May;37(5):1497-501.
The development pattern of one class of plasma membrane proteins, the external surface proteins, was examined in neoplastic and nonneoplastic differentiating murine erythroid cells. Neoplastic erythroid precusor cells were obtained from spleens of CD-1 mice after infection with Friend erythroleukemia virus while the nonneoplastic ellls were obtained from spleens of mice with phenylhydrazine-stimulated erythroid hyperplasia. Erythroid precursors at different stages of development were isolated from these erythroid cell populations by sedimentation at unit gravity. The surface proteins were labeled by lactoperoxidase-catalyzed iodination, solubilized in sodium dodecyl sulfate, and separated by sodium dodecyl sulfate gradient gel electrophoresis. Multiple labeled bands were found at all stages of neoplastic and nonneoplastic erythroid differentiation examined. The pattern of external membrane proteins labeled in nonneoplastic erythrocytes and in reticulocytes from peripheral blood were qualitatively similar and not altered by infection with Friend virus. The nucleated precursor cells from noninfected mice exhibited distinct differences from erythrocytes, and with increaseing differentiation an evolutionary pattern of several minor proteins was seen. Clear-cut differences in lactoperoxidast-reactive proteins were also observed between neoplastic and nonneoplastic precursors. The most marked differences were observed between the most immature cells. The youngest neoplastic cells from CD-1 mice possessed a protein with a molecular weight of 8000 not seen in normal erythroid cells. Additionally, there was an absence of a normally occurring protein with a molecular weight of 13,000 and increased amounts of a protein with a molecular weight of 140,000. With increasing maturation of the neoplastic cells, labeling of the protein with a molecular weight of 8,000 decreased while the protein with a molecular weight of 13,000 became apparent, so that a labeling pattern similar to that of nonneoplastic cells was obtained. These studies deomnstrate both distinct alterations of lactoperoxidase-reactive surface membrane proteins in nonneoplastic erythroid cells druring cell maturation in neoplastic erythroid cells as compared with nonneoplastic erythroid cells at similar stages of development.
在肿瘤性和非肿瘤性分化的小鼠红细胞中,研究了一类质膜蛋白即外表面蛋白的发育模式。肿瘤性红细胞前体细胞是从感染了Friend红白血病病毒的CD-1小鼠脾脏中获得的,而非肿瘤性细胞则是从苯肼刺激引起红细胞增生的小鼠脾脏中获得的。通过单位重力沉降从这些红细胞群体中分离出不同发育阶段的红细胞前体。表面蛋白通过乳过氧化物酶催化碘化进行标记,在十二烷基硫酸钠中溶解,并通过十二烷基硫酸钠梯度凝胶电泳进行分离。在所研究的肿瘤性和非肿瘤性红细胞分化的所有阶段都发现了多条标记带。非肿瘤性红细胞和外周血网织红细胞中标记的外膜蛋白模式在质量上相似,并且不受Friend病毒感染的影响。未感染小鼠的有核前体细胞与红细胞表现出明显差异,随着分化程度的增加,可观察到几种次要蛋白的演变模式。在肿瘤性和非肿瘤性前体之间也观察到乳过氧化物酶反应性蛋白的明显差异。在最不成熟的细胞之间观察到最显著的差异。来自CD-1小鼠的最年轻肿瘤性细胞拥有一种分子量为8000的蛋白,而正常红细胞中未见该蛋白。此外,一种分子量为13000的正常存在的蛋白缺失,而一种分子量为140000的蛋白含量增加。随着肿瘤性细胞的成熟,分子量为8000的蛋白标记减少,而分子量为13000的蛋白变得明显,从而获得了与非肿瘤性细胞相似的标记模式。这些研究表明,与处于相似发育阶段的非肿瘤性红细胞相比,肿瘤性红细胞在细胞成熟过程中,非肿瘤性红细胞中乳过氧化物酶反应性表面膜蛋白存在明显改变。