Corte G, Viale G, Cosulich E, Bargellesi A, Ferrarini M
Scand J Immunol. 1979;10(3):275-80. doi: 10.1111/j.1365-3083.1979.tb01350.x.
Endogenous and surface labeling techniques were used on human lymphoid cells to characterize intracytoplasmic, membrane and secreted IgD, IgD synthesized by lymphocytes and inserted into the cell membrane displayed a single molecular form with the same mobility in sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) as the previously described slow migrating serum IgDl. Plasma cells produced and secreted IgDl and another IgD corresponding to the faster-moving serum IgD2. Conversion of one molecular form into the other was never observed, thus indicating that neither molecule is a precursor or a degradation product of the other.
采用内源性和表面标记技术对人淋巴细胞进行研究,以表征细胞质内、细胞膜及分泌型IgD。淋巴细胞合成并插入细胞膜的IgD在十二烷基硫酸钠聚丙烯酰胺凝胶电泳(SDS-PAGE)中呈现单一分子形式,其迁移率与先前描述的慢速迁移血清IgD1相同。浆细胞产生并分泌IgD1以及另一种对应于快速迁移血清IgD2的IgD。从未观察到一种分子形式向另一种分子形式的转化,因此表明这两种分子都不是另一种分子的前体或降解产物。