Miyake M, Zenita K, Tanaka O, Okada Y, Kannagi R
Department of Clinical Science, Kyoto University, School of Medicine, Japan.
Cancer Res. 1988 Dec 15;48(24 Pt 1):7150-8.
The localization of three carbohydrate antigens, Lex, Ley, and sialylated Lex-i, which are closely related to stage-specific embryonic antigen 1, in the lung of developing human embryos was investigated using specific monoclonal antibodies. In the 38-day-old embryo, when the primitive lung bud has appeared and developed into two lung sacs, only Ley antigen was specifically positive in the proliferating cells in the terminal portion of lung bud. In the 50-53-day-old embryos, the future bronchi were actively developing from the bronchial buds. At this stage, the Ley antigen was maximally expressed and the Lex antigen appeared in the bud cells. In the lung of the 12-week-old embryo, buds for the future bronchioles were lined by simple cuboidal epithelial cells, which were strongly positive for Lex antigen, weakly positive for Ley antigen, and still completely negative for sialylated Lex-i antigen. Sialylated Lex-i antigen finally appeared in 18-week-old embryos, in the cells of the terminal buds for the future alveoli. At this stage, the Lex and Ley antigens were already beginning to disappear and were only weakly positive in cells of terminal buds. At 20 weeks, only sialylated Lex-i antigen was weakly detected in the cells in the terminal buds; after 8 months, all three antigens were essentially not detected in the respiratory cells in most of the embryos examined in this study. Formation of bronchial glands was detected at 18 weeks, where the developing gland cells were specifically positive for sialylated Lex-i antigen. Ciliation of the bronchial epithelial cells started at 12 weeks and propagated thereafter. The ciliation was accompanied by the reappearance of Ley and Lex antigen in the epithelial cells. These findings collectively indicated that the three antigens all have a physiological significance as stage-specific developmental antigens of the human lung; those antigens were specifically present in the bud cells at each important step of the morphogenesis of the human lung, such as cells in the lung buds, bronchial buds, and terminal buds for the formation of the alveolus, and cells differentiating into bronchial gland cells. The three antigens gradually disappear in the later stage of development along with the maturation process of the lung. Stage-specific embryonic antigen 1 and related antigens are known to be associated with various human cancers, including lung cancers. We suggest that the expression of these antigens in the lung cancer cells is the result of the retrodifferentiation of the cancer cells to the stages of immature embryonic lung cells.
利用特异性单克隆抗体,研究了三种与阶段特异性胚胎抗原1密切相关的碳水化合物抗原Lex、Ley和唾液酸化Lex-i在发育中的人胚胎肺中的定位。在38天大的胚胎中,当原始肺芽出现并发育成两个肺囊时,只有Ley抗原在肺芽末端的增殖细胞中呈特异性阳性。在50 - 53天大的胚胎中,未来的支气管正从支气管芽积极发育。在此阶段,Ley抗原表达最高,Lex抗原出现在芽细胞中。在12周大的胚胎肺中,未来细支气管的芽由单层立方上皮细胞排列,这些细胞对Lex抗原呈强阳性,对Ley抗原呈弱阳性,对唾液酸化Lex-i抗原仍完全阴性。唾液酸化Lex-i抗原最终出现在18周大的胚胎中,存在于未来肺泡的终末芽细胞中。在此阶段,Lex和Ley抗原已经开始消失,在终末芽细胞中仅呈弱阳性。在20周时,仅在终末芽细胞中微弱检测到唾液酸化Lex-i抗原;8个月后,在本研究中检测的大多数胚胎的呼吸细胞中基本上未检测到所有三种抗原。在18周时检测到支气管腺的形成,此时发育中的腺细胞对唾液酸化Lex-i抗原呈特异性阳性。支气管上皮细胞的纤毛形成始于12周并随后扩展。纤毛形成伴随着Ley和Lex抗原在上皮细胞中的重新出现。这些发现共同表明,这三种抗原作为人肺的阶段特异性发育抗原均具有生理意义;这些抗原在人肺形态发生的每个重要步骤中特异性存在于芽细胞中,如肺芽、支气管芽和形成肺泡的终末芽中的细胞,以及分化为支气管腺细胞的细胞。随着肺的成熟过程,这三种抗原在发育后期逐渐消失。已知阶段特异性胚胎抗原1及相关抗原与包括肺癌在内的各种人类癌症有关。我们认为这些抗原在肺癌细胞中的表达是癌细胞逆向分化到未成熟胚胎肺细胞阶段的结果。