Yuan D, Tucker P W
J Immunol. 1984 Mar;132(3):1561-5.
Although IgD is expressed on the surface of resting B cells at a higher density than IgM, we determined that both the steady-state level and the biosynthetic rate of mu m-mRNA is higher than that of delta m-mRNA, suggesting that translational or post-translational processing of the Ig heavy chains may modulate the expression of cell surface Ig. After B cell activation by LPS, delta m-mRNA decreases drastically, accounting for the observed decrease in expression of IgD. Concomitantly, a dramatic increase in the level of mu s- and gamma s-mRNA corresponds to the observed increase in secretion of these Ig isotypes in LPS-stimulated cells.
尽管IgD在静息B细胞表面的表达密度高于IgM,但我们确定μm -mRNA的稳态水平和生物合成速率均高于δm -mRNA,这表明Ig重链的翻译或翻译后加工可能会调节细胞表面Ig的表达。在LPS激活B细胞后,δm -mRNA急剧下降,这解释了所观察到的IgD表达下降。与此同时,μm -和γs -mRNA水平的显著增加与LPS刺激细胞中这些Ig同种型分泌的增加相对应。