Marchetti Luigi, Sabbieti Maria G, Agas Dimitrios, Menghi Maura, Materazzi Giovanni, Menghi Giovanna, Hurley Marja M
Department of Comparative Morphology and Biochemistry, University of Camerino, Camerino (MC)/Italy.
J Cell Biochem. 2006 Apr 15;97(6):1379-92. doi: 10.1002/jcb.20746.
Previous studies showed that prostaglandin F2alpha (PGF2alpha) stimulated fibroblast growth factor-2 (FGF-2) and fibroblast growth factor receptor 2 (FGFR2) cytosolic and nuclear accumulation, however, the endocytic pathway has not been elucidated. This study demonstrates that although PGF2alpha increased the formation of clathrin-coated structures in Py1a rat osteoblasts, they were not involved in FGF-2 and FGFR2 trafficking. PGF2alpha increased binding of FGF-2 and FGFR2 and co-localization of reactive sites in addition to nuclear translocation at the nuclear pore complex level. FGF-2 and FGFR2 were in close spatial correlation with importin beta, further supporting nuclear import of the FGF-2/FGFR2 complex. Immunogold and immunofluorescence techniques as well as Western blotting demonstrated increased importin beta protein labeling in response to PGF2alpha. Similar to PGF2alpha, phorbol 12-myristate 13-acetate (PMA) also increased importin beta protein. These data strongly suggest that prostaglandins may regulate osteoblast metabolism via FGF-2/FGFR2/importin beta nuclear trafficking.
先前的研究表明,前列腺素F2α(PGF2α)可刺激成纤维细胞生长因子-2(FGF-2)和成纤维细胞生长因子受体2(FGFR2)在细胞溶质和细胞核中的积累,然而,内吞途径尚未阐明。本研究表明,尽管PGF2α增加了Py1a大鼠成骨细胞中网格蛋白包被结构的形成,但它们并不参与FGF-2和FGFR2的转运。PGF2α除了在核孔复合体水平上增加FGF-2和FGFR2的结合以及反应位点的共定位外,还增加了核转位。FGF-2和FGFR2与输入蛋白β在空间上密切相关,进一步支持了FGF-2/FGFR2复合物的核输入。免疫金标和免疫荧光技术以及蛋白质印迹法表明,响应PGF2α,输入蛋白β蛋白标记增加。与PGF2α类似,佛波酯12-肉豆蔻酸酯13-乙酸酯(PMA)也增加了输入蛋白β蛋白。这些数据强烈表明,前列腺素可能通过FGF-2/FGFR2/输入蛋白β核转运调节成骨细胞代谢。