RRC ID 73658
著者 Ishihata K, Seong CH, Kibe T, Nakazono K, Mardiyantoro F, Tada R, Nishimura M, Matsuguchi T, Nakamura N.
タイトル Lipoteichoic Acid and Lipopolysaccharides Are Affected by p38 and Inflammatory Markers and Modulate Their Promoting and Inhibitory Effects on Osteogenic Differentiation.
ジャーナル Int J Mol Sci
Abstract Lipoteichoic acid (LTA) and lipopolysaccharide (LPS) are cell wall components of Gram-positive and Gram-negative bacteria, respectively. Notably, oral microflora consists of a variety of bacterial species, and osteomyelitis of the jaw caused by dental infection presents with symptoms of bone resorption and osteosclerosis. However, the effects of LTA and LPS on osteogenic differentiation have not yet been clarified. We examined the effects of LTA and LPS on osteoblasts and found that LTA alone promoted alizarin red staining at low concentrations and inhibited it at high concentrations. Additionally, gene expression of osteogenic markers (ALP, OCN, and OPG) were enhanced at low concentrations of LTA. High concentrations of LPS suppressed calcification potential, and the addition of low concentrations of LTA inhibited calcification suppression, restoring the gene expression levels of suppressed bone differentiation markers (ALP, BSP, and OCN). Moreover, the suppression of p38, a signaling pathway associated with bone differentiation, had opposing effects on gene-level expression of tumor necrosis factor-α (TNF-α) and interleukin-6 (IL-6), suggesting that mixed LTA and LPS infections have opposite effects on bone differentiation through concentration gradients, involving inflammatory markers (TNF-α and IL-6) and the p38 pathway.
巻・号 23(20)
公開日 2022-10-20
DOI 10.3390/ijms232012633
PII ijms232012633
PMID 36293485
PMC PMC9604490
MeSH Anti-Bacterial Agents Biomarkers Gram-Negative Bacteria / metabolism Gram-Positive Bacteria / metabolism Interleukin-6 / genetics Lipopolysaccharides* / pharmacology Osteogenesis Tumor Necrosis Factor-alpha* / genetics Tumor Necrosis Factor-alpha* / metabolism
IF 4.556
リソース情報
ヒト・動物細胞 MC3T3-E1(RCB1126)