Wongdee Kannikar, Pandaranandaka Jantarima, Teerapornpuntakit Jarinthorn, Tudpor Kukiat, Thongbunchoo Jirawan, Thongon Narongrit, Jantarajit Walailak, Krishnamra Nateetip, Charoenphandhu Narattaphol
Consortium for Calcium and Bone Research, Faculty of Science, Mahidol University, Rama VI Road, Bangkok, 10400, Thailand.
Histochem Cell Biol. 2008 Jul;130(1):79-90. doi: 10.1007/s00418-008-0419-6. Epub 2008 Mar 26.
Osteoblasts were previously reported to form tight junctions, which may play an important role in the regulation of ion transport across the epithelial-like bone membrane. However, the evidence for the presence of tight junction-associated proteins in osteoblasts is lacking. We therefore studied the expression of tight junction-associated genes in primary rat osteoblasts and bone tissues. Quantitative real-time PCR showed that osteoblasts expressed ZO-1, -2, -3, cingulin, occludin, claudin-1 to -12, -14 to -20, -22 and -23. By using western blot analyses of selected claudins, expression of claudin-5, -11, -14 and -15, but not claudin-3, were identified in osteoblasts. A confocal immunofluorescent study in undecalcified tibial sections confirmed that claudin-16 was localized on the trabecular surface, normally covered by osteoblasts and bone-lining cells. In addition, immunohistochemical studies in decalcified tibial sections demonstrated the expression of claudin-5, -11, -14, -15 and -16 in bone-lining cells (inactive osteoblasts). Primary osteoblasts cultured in the Snapwell for 19-26 days were found to form a monolayer with measurable transepithelial resistance of approximately 110-180 Omegacm(2), confirming the presence of barrier functions of the tight junction. It was concluded that osteoblasts expressed several tight junction-associated proteins, which possibly regulated ion transport across the bone membrane.
以前有报道称成骨细胞可形成紧密连接,这可能在调节离子跨上皮样骨膜运输中发挥重要作用。然而,缺乏成骨细胞中存在紧密连接相关蛋白的证据。因此,我们研究了原代大鼠成骨细胞和骨组织中紧密连接相关基因的表达。定量实时PCR显示,成骨细胞表达ZO-1、-2、-3、cingulin、occludin、claudin-1至-12、-14至-20、-22和-23。通过对选定的claudin进行蛋白质印迹分析,在成骨细胞中鉴定出了claudin-5、-11、-14和-15的表达,但未检测到claudin-3的表达。对未脱钙胫骨切片进行的共聚焦免疫荧光研究证实,claudin-16定位于小梁表面,通常被成骨细胞和骨衬细胞覆盖。此外,对脱钙胫骨切片进行的免疫组织化学研究表明,骨衬细胞(静止的成骨细胞)中存在claudin-5、-11、-14、-15和-16的表达。在Snapwell中培养19至26天的原代成骨细胞形成了单层,其跨上皮电阻约为110 - 180Ω·cm²,证实了紧密连接具有屏障功能。研究得出结论,成骨细胞表达多种紧密连接相关蛋白,这些蛋白可能调节离子跨骨膜的运输。