Shimizu Keiko, Noro Nobuhiro, Matsuda Ryoichi
Department of Biology, Tokyo Metropolitan University, Setagaya, Tokyo 158, Japan.
Department of Microbiology, Tokyo Metropolitan Institute for Neurosciences, Fuchu, Tokyo 183, Japan.
Dev Growth Differ. 1988 Feb;30(1):35-47. doi: 10.1111/j.1440-169X.1988.00035.x.
The temporal and spatial expression of antigen specific for primary mesenchyme cell (PMC) lineage cells during early development of the sea urchins Hemicentrotus pulcherrimus and Stronglyocentrotus nudus was studied with a monoclonal antibody (P4). P4 was produced by a hybridoma cell line prepared by fusion of myeloma cells and spleen cells from a mouse immunized with cultured spicule-forming cells. Immunofluorescence studies demonstrated that P4 antibody reacted strongly with the surfaces of PMC's and spicule-forming cells of both species. Immunoblot analysis showed that P4 antibody reacted with several proteins including those of 140-kDa, 120-kDa, 53-kDa, 43-kDa, and 41-kDa in H. pulcherrimus and with those of 130-kDa, 110-kDa, 51-kDa, and 43-kDa in S. nudus. These proteins appeared sequentially after the hatching blastula stage. Tunicamycin inhibited the expressions of these P4 antigens as well as spicule formation. Two of the P4-reactive antigens, the 140-kDa and 43-kDa proteins, in H. pulcherrimus were synthesized de novo and shown to be identical to micromere differentiation specific proteins. These results suggest that P4 binds to specific molecules that are important in spicule formation in developing sea urchin embryos.
利用单克隆抗体(P4)研究了光棘球海胆和虾夷马粪海胆早期发育过程中初级间充质细胞(PMC)谱系细胞特异性抗原的时空表达。P4由杂交瘤细胞系产生,该杂交瘤细胞系是通过将骨髓瘤细胞与用培养的造骨针细胞免疫的小鼠脾细胞融合制备而成。免疫荧光研究表明,P4抗体与两种海胆的PMC和造骨针细胞表面均发生强烈反应。免疫印迹分析显示,P4抗体与光棘球海胆中的几种蛋白质发生反应,包括140-kDa、120-kDa、53-kDa、43-kDa和41-kDa的蛋白质,以及虾夷马粪海胆中的130-kDa、110-kDa、51-kDa和43-kDa的蛋白质。这些蛋白质在囊胚孵化阶段后依次出现。衣霉素抑制这些P4抗原的表达以及造骨针的形成。光棘球海胆中两种与P4反应的抗原,即140-kDa和43-kDa蛋白质,是重新合成的,并且显示与小分裂球分化特异性蛋白质相同。这些结果表明,P4与在海胆胚胎发育过程中对造骨针形成重要的特定分子结合。