Saleh M, Barlett P F
Walter and Eliza Hall Institute of Medical Research, Royal Melbourne Hospital, Victoria, Australia.
J Neuroimmunol. 1989 Aug;23(3):203-14. doi: 10.1016/0165-5728(89)90052-0.
We have investigated the tissue specificity of a trans-acting regulatory factor observed to suppress Thy-1 expression during normal neuronal differentiation. Heterokaryons were constructed between Thy-1.1+ expressing mouse T cell lymphoma cells and Thy-1.2- mouse sensory neurons and their surface phenotypes determined by immunofluorescence histochemistry 16 h after fusion. Thy-1.1 expression was observed to be specifically suppressed in such heterokaryons whilst the expression of the lymphoma cell surface marker, Ly-1, was not altered. As the nuclei did not fuse in the heterokaryons, it appears that the developmentally regulated diffusible suppressor factor active in sensory neurons is not tissue specific and can down-regulate Thy-1 expression in lymphoma cells. We also report the suppression of the H-2Kk surface antigen in heterokaryons by a similar but independent regulatory mechanism.
我们研究了一种反式作用调节因子的组织特异性,该因子在正常神经元分化过程中可抑制Thy-1表达。在表达Thy-1.1的小鼠T细胞淋巴瘤细胞与Thy-1.2阴性的小鼠感觉神经元之间构建异核体,并在融合16小时后通过免疫荧光组织化学确定其表面表型。观察到在这种异核体中Thy-1.1表达被特异性抑制,而淋巴瘤细胞表面标志物Ly-1的表达未改变。由于异核体中的细胞核未融合,似乎在感觉神经元中起作用的发育调控可扩散抑制因子并非组织特异性的,并且可以下调淋巴瘤细胞中Thy-1的表达。我们还报道了通过类似但独立的调节机制,异核体中H-2Kk表面抗原受到抑制。