Research Center, C875, UMDNJ-NJ Dental School, University of Medicine and Dentistry of New Jersey, Newark, NJ 07103-2400, USA.
Inflammopharmacology. 2010 Jun;18(3):119-25. doi: 10.1007/s10787-010-0035-7. Epub 2010 Feb 13.
Recent advances in identifying the salivary constituents capable of influencing the oral mucosal inflammatory responses have brought to focus the importance of a peptide hormone, ghrelin. Here, we report on the involvement of ghrelin in controlling the apoptotic processes induced in sublingual salivary gland acinar cells by the lipopolysaccharide (LPS) of a periodontopathic bacterium, Porphyromonas gingivalis. We show that the countering effect of ghrelin on the LPS-induced acinar cell apoptosis was associated with the increase in constitutive nitric oxide synthase (cNOS) activity, and the reduction in caspase-3 and inducible nitric oxide synthase (iNOS). The loss in countering effect of ghrelin on the LPS-induced changes in apoptosis and caspase-3 activity was attained with Src kinase inhibitor, PP2, as well as Akt inhibitor, SH-5, and cNOS inhibitor, L-NAME, but not the iNOS inhibitor, 1400W. The effect of ghrelin on the LPS-induced changes in cNOS activity, moreover, was reflected in the increased cNOS phosphorylation that was sensitive to PP2 as well as SH-5. Furthermore, the ghrelin-induced up-regulation in cNOS activity was associated with the increase in caspase-3 S-nitrosylation that was susceptible to the blockage by SH-5 and L-NAME. The findings point to the involvement of ghrelin in Src/Akt kinase-mediated cNOS activation and the apoptogenic signal inhibition through the NO-induced caspase-3 S-nitrosylation.
最近在鉴定能够影响口腔黏膜炎症反应的唾液成分方面的进展,使人们关注一种肽激素——ghrelin 的重要性。在这里,我们报告 ghrelin 参与控制牙周病细菌牙龈卟啉单胞菌 LPS 诱导的舌下唾液腺腺泡细胞凋亡的过程。我们表明,ghrelin 对 LPS 诱导的腺泡细胞凋亡的拮抗作用与组成型一氧化氮合酶 (cNOS) 活性的增加以及 caspase-3 和诱导型一氧化氮合酶 (iNOS) 的减少有关。Src 激酶抑制剂 PP2 以及 Akt 抑制剂 SH-5 和 cNOS 抑制剂 L-NAME,但不是 iNOS 抑制剂 1400W,可使 ghrelin 对 LPS 诱导的凋亡和 caspase-3 活性变化的拮抗作用丧失。ghrelin 对 LPS 诱导的 cNOS 活性变化的影响,此外,反映在对 PP2 和 SH-5 敏感的 cNOS 磷酸化增加上。此外,ghrelin 诱导的 cNOS 活性增加与 caspase-3 的 S-亚硝基化增加有关,S-亚硝基化易受 SH-5 和 L-NAME 的阻断。这些发现表明 ghrelin 参与 Src/Akt 激酶介导的 cNOS 激活和通过 NO 诱导的 caspase-3 S-亚硝基化抑制促凋亡信号。