den Hertog J, de Laat S W, Schlessinger J, Kruijer W
Hubrecht Laboratory, Netherlands Institute for Developmental Biology, Utrecht.
Cell Growth Differ. 1991 Mar;2(3):155-64.
The human epidermal growth factor receptor (hEGF-R) was introduced into murine P19 embryonal carcinoma (EC) cells, which do not express endogenous EGF-R. Undifferentiated stable P19 EC transfectants containing multiple copies of the hEGF-R complementary DNA were isolated. These cells express functional EGF-R, exhibiting characteristic biphasic EGF binding and intrinsic tyrosine protein kinase activity. Whereas normally EGF induces the expression of multiple nuclear protooncogenes, only junB expression is induced by EGF in the HER-transfected cells. This indicates that undifferentiated P19 EC cells contain at least part of a signal transduction machinery capable of coupling to the ectopically expressed hEGF-R. Interestingly, neuronal differentiation is induced in these cells in response to EGF under culture conditions resembling those during early preimplantation embryogenesis. These results indicate that neuronal differentiation of pluripotent P19 EC cells can be induced via activation of a tyrosine protein kinase signaling pathway.
将人类表皮生长因子受体(hEGF-R)导入不表达内源性EGF-R的小鼠P19胚胎癌细胞中。分离出含有多个hEGF-R互补DNA拷贝的未分化稳定P19胚胎癌细胞转染体。这些细胞表达功能性EGF-R,表现出典型的双相EGF结合和内在酪氨酸蛋白激酶活性。正常情况下,EGF可诱导多种核原癌基因的表达,但在HER转染细胞中,EGF仅诱导junB的表达。这表明未分化的P19胚胎癌细胞至少包含部分能够与异位表达的hEGF-R偶联的信号转导机制。有趣的是,在类似于植入前早期胚胎发育过程中的培养条件下,这些细胞在EGF的作用下会诱导神经分化。这些结果表明,多能P19胚胎癌细胞的神经分化可通过激活酪氨酸蛋白激酶信号通路来诱导。