Montreekachon Pattanin, Nongparn Sirikul, Sastraruji Thanapat, Khongkhunthian Sakornrat, Chruewkamlow Nuttapol, Kasinrerk Watchara, Krisanaprakornkit Suttichai
Department of Restorative Dentistry and Periodontology, Faculty of Associated Medical Sciences, Chiang Mai University, Chiang Mai 50200, Thailand.
Asian Pac J Allergy Immunol. 2014 Sep;32(3):251-60. doi: 10.12932/AP0404.32.3.2014.
LL-37, the only member of the antimicrobial peptide cathelicidin family in humans, exerts a variety of biological activities, especially immunomodulation through either direct chemotactic activity or up-regulation of several cytokines and chemokines in various cell types. In this study, we aimed to determine the immunoregulatory effect of LL-37 on Th1/Th2 cytokine expression and production in human gingival epithelial cells (HGECs).
Cultured HGECs were treated with different concentrations of LL-37 for different numbers of times. The cytotoxicity of LL-37 was determined by an MTT assay. Total RNA was isolated for RT-PCR and real-time PCR analyses of cytokine expression. Cell-free culture supernatants were assayed for Th1/Th2 cytokine levels by a cytokine bead array.
Out of eleven Th1/Th2 cytokines tested, treatment of HGECs with non-toxic doses of LL-37 (2-6 μM) significantly raised only IL-8 levels in the cell-free culture supernatants, when compared to control untreated cells (P <0.05). Consistent with the elevated IL-8 levels, IL-8 mRNA expression was remarkably and significantly induced by LL-37 treatment (P < 0.05), when compared to the modest mRNA induction of other three cytokines, including IL-1β, IL-6, and TNF-α. The time-course study demonstrated a cumulative IL-8 mRNA induction by LL-37 treatment within a 24-hour interval.
These findings indicate that LL-37 favorably induces IL-8 expression and secretion in HGECs, suggesting both direct and indirect involvement of LL-37 in neutrophil recruitment into an inflammatory site within diseased periodontal tissues.
LL-37是人类抗菌肽cathelicidin家族的唯一成员,具有多种生物学活性,特别是通过直接趋化活性或上调多种细胞类型中的几种细胞因子和趋化因子来发挥免疫调节作用。在本研究中,我们旨在确定LL-37对人牙龈上皮细胞(HGECs)中Th1/Th2细胞因子表达和产生的免疫调节作用。
用不同浓度的LL-37对培养的HGECs进行不同次数的处理。通过MTT法测定LL-37的细胞毒性。分离总RNA用于细胞因子表达的RT-PCR和实时PCR分析。通过细胞因子微珠阵列检测无细胞培养上清液中的Th1/Th2细胞因子水平。
在测试的11种Th1/Th2细胞因子中,与未处理的对照细胞相比,用无毒剂量的LL-37(2-6μM)处理HGECs仅显著提高了无细胞培养上清液中的IL-8水平(P<0.05)。与IL-8水平升高一致,与包括IL-1β、IL-6和TNF-α在内的其他三种细胞因子的适度mRNA诱导相比,LL-37处理显著诱导了IL-8 mRNA表达(P<0.05)。时间进程研究表明,LL-37处理在24小时间隔内累积诱导IL-8 mRNA。
这些发现表明LL-37有利地诱导HGECs中IL-8的表达和分泌,表明LL-37直接和间接参与中性粒细胞募集到患病牙周组织内的炎症部位。