Palmiter R D, Wrenn J T
J Cell Biol. 1971 Sep;50(3):598-615. doi: 10.1083/jcb.50.3.598.
Administration of estrogen (E) to immature chicks triggers the cytodifferentiation of tubular gland cells in the magnum portion of the oviduct epithelium; these cells synthesize the major egg-white protein, ovalbumin. Electron microscopy and immunoprecipitation of ovalbumin from oviduct explants labeled with radioactive amino acids in tissue culture were used to follow and measure the degree of tubular gland cell cytodifferentiation. Ovalbumin is undetectable in the unstimulated chick oviduct and in oviducts of chicks treated with progesterone (P) for up to 5 days. Ovalbumin synthesis is first detected 24 hr after E administration, and by 5 days it accounts for 35% of the soluble protein being synthesized. Tubular gland cells begin to synthesize ovalbumin before gland formation which commences after 36 hr of E treatment. When E + P are administered together there is initially a synergistic effect on ovalbumin synthesis, however, after 2 days ovalbumin synthesis slows and by 5 days there is only 1/20th as much ovalbumin per magnum as in the E-treated controls. Whereas the magnum wet weight doubles about every 21 hr with E alone, growth stops after 3 days of E + P treatment. Histological and ultrastructural observations show that the partially differentiated tubular gland cells resulting from E + P treatment never invade the stroma and form definitive glands, as they would with E alone. Instead, these cells appear to transform into other cell types-some with cilia and some with unusual flocculent granules. We present a model of tubular gland cell cytodifferentiation and suggest that a distinct protodifferentiated stage exists. P appears to interfere with the normal transition from the protodifferentiated state to the mature tubular gland cell.
给未成熟的雏鸡施用雌激素(E)会引发输卵管上皮蛋白分泌部管状腺细胞的细胞分化;这些细胞合成主要的蛋清蛋白——卵清蛋白。利用电子显微镜以及从组织培养中用放射性氨基酸标记的输卵管外植体中免疫沉淀卵清蛋白的方法,来追踪和测量管状腺细胞的细胞分化程度。在未受刺激的雏鸡输卵管以及用孕酮(P)处理长达5天的雏鸡输卵管中,检测不到卵清蛋白。在施用E后24小时首次检测到卵清蛋白合成,到5天时,其占正在合成的可溶性蛋白的35%。管状腺细胞在腺体形成之前就开始合成卵清蛋白,而腺体形成在E处理36小时后开始。当同时施用E + P时,最初对卵清蛋白合成有协同作用,然而,2天后卵清蛋白合成减缓,到5天时,每个蛋白分泌部的卵清蛋白含量只有单独用E处理的对照组的1/20。单独使用E时,蛋白分泌部的湿重大约每21小时增加一倍,而在E + P处理3天后生长停止。组织学和超微结构观察表明,E + P处理导致的部分分化的管状腺细胞从未侵入基质并形成成熟腺体,而单独使用E时它们会这样。相反,这些细胞似乎会转化为其他细胞类型——一些有纤毛,一些有异常的絮状颗粒。我们提出了一个管状腺细胞细胞分化模型,并认为存在一个独特的原分化阶段。P似乎会干扰从原分化状态到成熟管状腺细胞的正常转变。