Yamashita Teruhito, Kobayashi Yasuhiro, Mizoguchi Toshihide, Yamaki Mariko, Miura Toshiki, Tanaka Sakae, Udagawa Nobuyuki, Takahashi Naoyuki
Division of Hard Tissue Research, Institute for Oral Science, Matsumoto Dental University, 1780 Gobara-Hirooka, Shiojiri, Nagano 399-0871, Japan.
Biochem Biophys Res Commun. 2008 Jan 11;365(2):252-7. doi: 10.1016/j.bbrc.2007.10.169. Epub 2007 Nov 5.
Phosphorylated p38 mitogen-activating kinase (MAPK) is observed in osteoclasts under in vivo inflammatory situations. However, the role of p38 MAPK in osteoclast function has not been elucidated, because all external stimuli tested hitherto failed to induce the phosphorylation of p38 MAPK in osteoclasts in culture. In this study, a constitutively active form of MKK6 (MKK6CA) was expressed in osteoclasts using adenoviral gene transfer in vitro. MKK6CA expressed in osteoclasts phosphorylated p38 MAPK and enhanced the survival of osteoclasts. Dentine-resorbing activity of osteoclasts was not enhanced by the MKK6CA expression. These results suggest that p38 MAPK signaling plays a critical role in the survival of osteoclasts in inflammatory diseases.
在体内炎症情况下,破骨细胞中可观察到磷酸化的p38丝裂原活化蛋白激酶(MAPK)。然而,p38 MAPK在破骨细胞功能中的作用尚未阐明,因为迄今为止测试的所有外部刺激均未能在培养的破骨细胞中诱导p38 MAPK的磷酸化。在本研究中,使用腺病毒基因转移在体外破骨细胞中表达了组成型活性形式的MKK6(MKK6CA)。破骨细胞中表达的MKK6CA使p38 MAPK磷酸化并提高了破骨细胞的存活率。MKK6CA的表达并未增强破骨细胞的牙本质吸收活性。这些结果表明,p38 MAPK信号传导在炎症性疾病中破骨细胞的存活中起关键作用。