Department of Periodontology, School of Dentistry, Ege University, Izmir, Turkey.
Oral Dis. 2011 Jan;17(1):60-7. doi: 10.1111/j.1601-0825.2010.01704.x.
To investigate the levels of antimicrobial peptide hCAP-18/LL-37 protein and mRNA expression in gingival tissues with different periodontal disease.
Ten patients with generalized aggressive periodontitis, 10 patients with chronic periodontitis, and 10 healthy controls were included in this study. Periodontal parameters including probing depth, clinical attachment level, plaque index, and papilla bleeding index were assessed in study subjects. hCAP-18/LL-37 mRNA analysis by RT-PCR and immunohistochemistry were performed in 19 samples provided enough RNA in terms of concentration and integrity.
This study demonstrated that hCAP-18/LL-37 was a product of neutrophils. Tissue samples of chronic periodontitis patients had significantly higher immunostaining of hCAP-18/LL-37 on neutrophils infiltrating in both epithelium and connective tissue compared with controls. hCAP-18/LL-37 mRNA expression levels in tissue samples of chronic periodontitis patients seemed to be upregulated compared with controls. While two generalized aggressive periodontitis patients showed downregulated hCAP-18/LL-37 mRNA expression levels, one generalized aggressive periodontitis patient showed slightly increased hCAP-18/LL-37 mRNA level compared with controls.
hCAP-18/LL-37 has an important role in innate response during periodontal inflammation. Local deficiency in hCAP-18/LL-37 might be a confounding effect in the pathogenesis of generalized aggressive periodontitis.
研究不同牙周病患者牙龈组织中抗菌肽 hCAP-18/LL-37 蛋白和 mRNA 的表达水平。
本研究纳入了 10 例广泛性侵袭性牙周炎患者、10 例慢性牙周炎患者和 10 例健康对照者。研究对象的牙周参数包括探诊深度、临床附着水平、菌斑指数和牙龈出血指数。采用 RT-PCR 和免疫组织化学法对 19 例 RNA 浓度和完整性足够的样本进行 hCAP-18/LL-37 mRNA 分析。
本研究表明 hCAP-18/LL-37 是中性粒细胞的产物。与对照组相比,慢性牙周炎患者组织样本中浸润上皮和结缔组织的中性粒细胞 hCAP-18/LL-37 的免疫染色明显更高。慢性牙周炎患者组织样本中的 hCAP-18/LL-37 mRNA 表达水平似乎上调。两名广泛性侵袭性牙周炎患者的 hCAP-18/LL-37 mRNA 表达水平下调,一名患者的 hCAP-18/LL-37 mRNA 水平略高于对照组。
hCAP-18/LL-37 在牙周炎症的固有反应中具有重要作用。局部缺乏 hCAP-18/LL-37 可能是广泛性侵袭性牙周炎发病机制中的一个混杂因素。