Fleischman L F, Holtzclaw L, Russell J T, Mavrothalassitis G, Fisher R J
Laboratory of Molecular Oncology, National Cancer Institute, Frederick, Maryland.
Mol Cell Biol. 1995 Feb;15(2):925-31. doi: 10.1128/MCB.15.2.925.
The ets-1 protein has been primarily studied as a sequence-specific transcriptional regulator that is predominately expressed in lymphoid cells. In this report, we show that ets-1 is also expressed in astrocytes and astrocytoma cells and is regulated during both signal transduction and differentiation. Both isoforms of ets-1, p51 and p42, were found in astrocytes and astrocytoma cells, but whereas expression of p51 was strong, p42, the alternate splice product previously shown to lack the phosphorylation domain, was difficult to detect and was present at a level 10- to 40-fold lower than that of p51. This differed by roughly an order of magnitude from the ratio generally observable in T cells and thymocytes. In two astrocytoma lines of human origin, CCF and 1321N1, ets-1 phosphorylation was stimulated by bradykinin and carbachol, respectively. Glutamate, norepinephrine, and bradykinin elicited phosphorylation of p51 in cultures of primary rat type 1 astrocytes. ets-1 phosphorylation was dramatically blocked by KT5926, an inhibitor of myosin light-chain kinase, suggesting that this kinase may be involved in phosphorylation of ets-1 in vivo. Investigations of retinoic acid-induced differentiation in P19 cells provided further support for a strong correlation of ets-1 with the pathway for astrocyte differentiation.
ets - 1蛋白主要作为一种序列特异性转录调节因子进行研究,其在淋巴细胞中大量表达。在本报告中,我们表明ets - 1也在星形胶质细胞和星形细胞瘤细胞中表达,并且在信号转导和分化过程中受到调节。在星形胶质细胞和星形细胞瘤细胞中发现了ets - 1的两种同工型,p51和p42,但p51表达强烈,而p42(先前显示缺乏磷酸化结构域的可变剪接产物)难以检测到,其水平比p51低10至40倍。这与在T细胞和胸腺细胞中通常观察到的比例大致相差一个数量级。在两个人源星形细胞瘤细胞系CCF和1321N1中,缓激肽和卡巴胆碱分别刺激ets - 1磷酸化。谷氨酸、去甲肾上腺素和缓激肽在原代大鼠1型星形胶质细胞培养物中引起p51磷酸化。ets - 1磷酸化被肌球蛋白轻链激酶抑制剂KT5926显著阻断,这表明该激酶可能在体内参与ets - 1的磷酸化。对维甲酸诱导P19细胞分化的研究进一步支持了ets - 1与星形胶质细胞分化途径密切相关。