The Role of Lactic Acid on Wound Healing, Cell Growth, Cell Cycle Kinetics, and Gene Expression of Cultured Junctional Epithelium Cells in the Pathophysiology of Periodontal Disease

• Published in: Pathogens (Basel) Vol. 10; no. 11; p. 1507
• Main Authors: Ishikawa, Taichi, Sasaki, Daisuke, Aizawa, Ryo, Yamamoto, Matsuo, Yaegashi, Takashi, Irié, Tarou, Sasaki, Minoru
• Format: Journal Article
• Language: English
• Published: Basel MDPI AG 18.11.2021; MDPI
• Subjects: Alveolar bone; Bacteria; Bone loss; Butyric acid; Cell adhesion; Cell adhesion & migration; Cell cycle; Cell growth; Disease; Epithelial cells; Epithelium; Fatty acids; Fibroblasts; Gene expression; Inflammation; Intercellular adhesion molecule 1; Interleukin 8; junctional epithelium; Kinetics; Lactic acid; Lactic acid bacteria; Metabolites; Pathophysiology; Periodontal disease; Periodontal diseases; Propionic acid; Proteins; short-chain fatty acids; Stimulation; Wound healing
• ISSN: 2076-0817; 2076-0817
• DOI: 10.3390/pathogens10111507

Lactic acid (LA) is short-chain fatty acid, such as butyric acid and propionic acid, that is produced as a metabolite of lactic acid bacteria, including periodontopathic bacteria. These short-chain fatty acids have positive effects on human health but can also have negative effects, such as the promotion of periodontal disease (PD), which is caused by periodontal pathogens present in the gingival sulcus. PD is characterized by apical migration of junctional epithelium, deepening of pockets, and alveolar bone loss. Thus, the junctional epithelial cells that form the bottom of the gingival sulcus are extremely important in investigating the pathophysiology of PD. The aim of this study was to investigate the effect of LA on wound healing, cell growth, cell cycle kinetics, and gene expression of cultured junctional epithelium cells. The results showed that stimulation with 10 mM LA slowed wound healing of the junctional epithelial cell layer and arrested the cell cycle in the G0/G1 (early cell cycle) phase, thereby inhibiting cell growth. However, cell destruction was not observed. LA also enhanced mRNA expression of integrin α5, interleukin (IL)-6, IL-8, intercellular adhesion molecule-1, and receptor activator of nuclear factor kappa-B ligand. The results of this study suggest that stimulation of junctional epithelial cells with high concentrations of LA could exacerbate PD, similarly to butyric acid and propionic acid.