Darmon M, Buc-Caron M H, Paulin D, Jacob F
EMBO J. 1982;1(8):901-6. doi: 10.1002/j.1460-2075.1982.tb01269.x.
1003 is a multipotential embryonal carcinoma (EC) clonal cell line which can be induced to follow different developmental pathways by altering the composition of the culture medium. When grown in serum-containing medium the great majority of 1003 cells remain undifferentiated; they express the ECMA 7 cell-surface embryonic antigen and very low amounts of vimentin. In serum-free medium, most 1003 cells differentiate into neuroepithelial cells. The majority of these cells are still labelled with ECMA 7 antibodies. They contain higher amounts of vimentin than EC cells, but no neurofilament proteins. Neuroepithelial cells then differentiate into neurons through a stage of preneurons containing both vimentin and the 70-K neurofilament protein. Fully differentiated neurons contain 70-K neurofilament protein but no vimentin. The 200-K neurofilament protein is detected later in the neurons. Mesenchymal cells (induced by re-adding serum) express high amounts of vimentin organized in networks. Preneurons , neurons, and mesenchymal cells do not express ECMA 7 antigen.
1003是一种多能性胚胎癌(EC)克隆细胞系,通过改变培养基成分可诱导其沿着不同的发育途径分化。当在含血清的培养基中培养时,绝大多数1003细胞保持未分化状态;它们表达ECMA 7细胞表面胚胎抗原和极少量波形蛋白。在无血清培养基中,大多数1003细胞分化为神经上皮细胞。这些细胞中的大多数仍能用ECMA 7抗体标记。它们所含波形蛋白的量比EC细胞多,但不含神经丝蛋白。神经上皮细胞随后通过一个同时含有波形蛋白和70-K神经丝蛋白的前神经元阶段分化为神经元。完全分化的神经元含有70-K神经丝蛋白,但不含波形蛋白。200-K神经丝蛋白在神经元中稍后被检测到。间充质细胞(通过重新添加血清诱导产生)表达大量以网络形式组织的波形蛋白。前神经元、神经元和间充质细胞不表达ECMA 7抗原。