Morikawa Kazumasa, Goto Tetsuya, Tanimura Akihiko, Kobayashi Shigeru, Maki Kenshi
Division of Developmental Stomatognathic Function Science, Kyushu Dental College, Kitakyushu 803-8580, Japan.
Acta Histochem Cytochem. 2008 Apr 26;41(2):7-13. doi: 10.1267/ahc.07027.
Inositol 1,4,5-trisphosphate (IP3) receptors (IP3Rs) are Ca2+ channels that localize to intracellular Ca2+ stores such as the endoplasmic reticulum (ER). Recently, IP3Rs were found to participate in the formation of the cytoskeleton and cellular adhesions. In this study, we examined the cellular localization of type I, II, and III IP3Rs to assess their role in cellular adhesion in rat osteoclasts. Rat bone marrow cells were cultured in alpha-MEM with 10% fetal bovine serum, M-CSF, RANKL, and 1,25(OH)2D3 for 1 week to promote osteoclast formation. Type I, II, and III IP3R expression in the osteoclasts was then examined by RT-PCR. Double-staining was performed using antibodies against type I, II, and III IP3Rs and DiOC6, an ER marker, or TRITC-phalloidin, an actin filament marker. Expression of all three IP3Rs was detected in the newly formed osteoclasts; however, the localization of the type I and II IP3Rs was predominantly close to nuclear, and possibly colocalized with the ER, while the type III IP3Rs were localized to the ER and podosomes, actin-rich adhesion structures in osteoclasts. These findings suggest that type III IP3Rs are associated with osteoclast adhesion.
肌醇1,4,5-三磷酸(IP3)受体(IP3Rs)是定位于内质网(ER)等细胞内钙库的钙离子通道。最近,发现IP3Rs参与细胞骨架的形成和细胞黏附。在本研究中,我们检测了I型、II型和III型IP3Rs的细胞定位,以评估它们在大鼠破骨细胞细胞黏附中的作用。将大鼠骨髓细胞在含10%胎牛血清、M-CSF、RANKL和1,25(OH)2D3的α-MEM中培养1周以促进破骨细胞形成。然后通过RT-PCR检测破骨细胞中I型、II型和III型IP3R的表达。使用针对I型、II型和III型IP3Rs的抗体以及内质网标记物DiOC6或肌动蛋白丝标记物TRITC-鬼笔环肽进行双重染色。在新形成的破骨细胞中检测到所有三种IP3Rs的表达;然而,I型和II型IP3Rs主要定位于细胞核附近,可能与内质网共定位,而III型IP3Rs定位于内质网和足体,足体是破骨细胞中富含肌动蛋白的黏附结构。这些发现表明III型IP3Rs与破骨细胞黏附有关。