Oshima R G, Howe W E, Klier F G, Adamson E D, Shevinsky L H
Dev Biol. 1983 Oct;99(2):447-55. doi: 10.1016/0012-1606(83)90294-4.
The synthesis of two extraembryonic endodermal cytoskeletal proteins (Endo B, Mr = 50,000; Endo A, Mr = 55,000) was detected by immunoprecipitation at the 4- to 8-cell stage of preimplantation mouse development. The first detectable synthesis of both proteins occurs at about the same time as the earliest allocation of cells to the trophectodermal lineage. Both Endo A and B were identified in the two-dimensional gel pattern of blastocyst cytoskeletal proteins prepared by nonionic detergent and high-salt extraction. Endo A and B were identified as the y and x blastocyst cytoskeletal proteins, respectively, previously described by other investigators. Antibodies to Endo B are shown to react with intermediate filaments at the electron microscopic level, confirming that Endo B is an authentic intermediate filament protein. Previously, the TROMA 1 monoclonal antibody prepared by other investigators was shown to react specifically with Endo A and to decorate trophoblast cytoskeletons but did not react with the inner cell mass of blastocysts. Endo B antibodies are now also shown to decorate trophoblast cytoskeletons.
通过免疫沉淀法在植入前小鼠发育的4至8细胞阶段检测到两种胚外内胚层细胞骨架蛋白(Endo B,分子量50,000;Endo A,分子量55,000)的合成。这两种蛋白质最早可检测到的合成发生时间与细胞最早分配到滋养外胚层谱系的时间大致相同。通过非离子去污剂和高盐提取制备的囊胚细胞骨架蛋白的二维凝胶图谱中鉴定出了Endo A和B。Endo A和B分别被鉴定为先前其他研究者描述的囊胚细胞骨架蛋白y和x。Endo B抗体在电子显微镜水平上显示与中间丝反应,证实Endo B是一种真正的中间丝蛋白。先前,其他研究者制备的TROMA 1单克隆抗体显示与Endo A特异性反应并修饰滋养层细胞骨架,但不与囊胚的内细胞团反应。现在还显示Endo B抗体也能修饰滋养层细胞骨架。