Department of Spine Surgery, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Bone. 2010 May;46(5):1328-35. doi: 10.1016/j.bone.2009.11.017. Epub 2009 Nov 18.
LIM mineralization protein-1 (LMP-1) is an intracellular regulator of bone formation and has been shown to be osteoinductive in vitro and in vivo. The effect of LMP-1 on other aspects of bone homeostasis has not been previously studied. In a pilot study we observed that LMP-1 decreased nitric oxide (NO) production in pre-osteoclasts. Here we report a new anti-inflammatory effect of LMP-1 and define its mechanism of action in lipopolysaccharide (LPS)-stimulated RAW 264.7 pre-osteoclasts. We found that LMP-1 significantly inhibited LPS-induced NO production. LMP-1 also effectively inhibited the expression of inducible nitric oxide synthase (iNOS), potently suppressed the transcriptional activity and nuclear translocation of nuclear factor kappa B (NF-kappaB), and prevented the phosphorylation of inhibitor of kappa B (IkappaB). Interestingly, LMP-1 had no effect on Receptor-Activator of Nuclear Factor B Ligand (RANKL)-induced activation of NF-kappaB. Furthermore, LMP-1 had no effect on the LPS-induced phosphorylation of extracellular signal-regulated kinase 1/2 (ERK1/2), whereas it did attenuate the phosphorylation of c-Jun NH2-terminal kinase (JNK) while enhancing phosphorylation of p38 mitogen-activated protein kinases (p38 MAPK). These results suggest that LMP-1 has an anti-inflammatory effect, and this effect is, at least in part, due to the inhibition of NO production by the suppression of NF-kappaB activation and selective regulation of mitogen-activated protein kinase (MAPK) pathways.
LMP-1 是一种细胞内骨形成的调节剂,已被证明在体外和体内具有成骨诱导作用。LMP-1 对骨稳态的其他方面的影响尚未被研究过。在一项初步研究中,我们观察到 LMP-1 减少了破骨前体细胞中的一氧化氮(NO)的产生。在这里,我们报道了 LMP-1 的一种新的抗炎作用,并定义了其在脂多糖(LPS)刺激的 RAW 264.7 前破骨细胞中的作用机制。我们发现 LMP-1 显著抑制 LPS 诱导的 NO 产生。LMP-1 还能有效抑制诱导型一氧化氮合酶(iNOS)的表达,强烈抑制核因子 kappa B(NF-kappaB)的转录活性和核转位,并防止 I kappa B 的磷酸化。有趣的是,LMP-1 对核因子 B 受体激活剂配体(RANKL)诱导的 NF-kappaB 激活没有影响。此外,LMP-1 对 LPS 诱导的细胞外信号调节激酶 1/2(ERK1/2)的磷酸化没有影响,而它确实抑制了 c-Jun NH2-末端激酶(JNK)的磷酸化,同时增强了丝裂原激活蛋白激酶(MAPK)的磷酸化(p38 MAPK)。这些结果表明 LMP-1 具有抗炎作用,这种作用至少部分是由于抑制 NF-kappaB 激活和选择性调节丝裂原激活蛋白激酶(MAPK)通路导致的 NO 产生的抑制。