Hiramatsu Yukihiro, Satho Tomomitsu, Hyakutake Mika, Irie Keiichi, Mishima Kenichi, Miake Fumio, Kashige Nobuhiro
Faculty of Pharmaceutical Sciences, Fukuoka University, 8-19-1, Nanakuma, Jonan-ku, Fukuoka 814-0180, Japan.
Faculty of Pharmaceutical Sciences, Fukuoka University, 8-19-1, Nanakuma, Jonan-ku, Fukuoka 814-0180, Japan.
Int Immunopharmacol. 2014 Nov;23(1):139-47. doi: 10.1016/j.intimp.2014.08.013. Epub 2014 Sep 3.
Genomic DNA has been identified as an anti-inflammatory component of Lactobacillus species, the effects of which are mediated through toll-like receptor (TLR) 9. In this study, we identified 14 novel anti-inflammatory oligodeoxynucleotide (ODN) from the genomic DNA of Lactobacillus casei by measuring their effects on the secretion of interleukin (IL)-8 (CXCL8) in the human epithelial colorectal adenocarcinoma cell line Caco-2 cells. The ODN TTTTGCCG strongly decreased IL-8 secretion. In the genomic DNA of Lactobacillus species, the frequency of TTTTGCCG was highest in the genomic DNA of L. casei and similar among strains of L. casei. Decreases in inducible nitric oxide synthase (iNOS) and cyclooxygenase (COX)-2 expressions in macrophage-like differentiated THP-1 cells confirmed the anti-inflammatory effect of TTTTGCCG. Furthermore, oral administration of TTTTGCCG ameliorated dextran sodium sulfate (DSS)-induced murine colitis and DSS-induced increased expression of inflammatory factor mRNAs, such as macrophage inflammatory protein (MIP)-2 (CXCL2), iNOS, and COX-2. The anti-inflammatory effect of TTTTGCCG was mainly regulated by an increase in heat shock protein (Hsp) 70 expression in the epithelium. TLR9 and Hsp90 may primarily mediate the anti-inflammatory effect of TTTTGCCG on Hsp70 signaling.
基因组DNA已被确定为乳酸杆菌属的一种抗炎成分,其作用是通过Toll样受体(TLR)9介导的。在本研究中,我们通过测量14种来自干酪乳杆菌基因组DNA的新型抗炎寡脱氧核苷酸(ODN)对人上皮性结肠腺癌细胞系Caco-2细胞中白细胞介素(IL)-8(CXCL8)分泌的影响,对其进行了鉴定。ODN TTTTGCCG可显著降低IL-8的分泌。在乳酸杆菌属的基因组DNA中,TTTTGCCG的频率在干酪乳杆菌的基因组DNA中最高,并且在干酪乳杆菌的菌株中相似。巨噬细胞样分化的THP-1细胞中诱导型一氧化氮合酶(iNOS)和环氧化酶(COX)-2表达的降低证实了TTTTGCCG的抗炎作用。此外,口服TTTTGCCG可改善葡聚糖硫酸钠(DSS)诱导的小鼠结肠炎以及DSS诱导的炎症因子mRNA表达增加,如巨噬细胞炎性蛋白(MIP)-2(CXCL2)、iNOS和COX-2。TTTTGCCG的抗炎作用主要通过上皮细胞中热休克蛋白(Hsp)70表达的增加来调节。TLR9和Hsp90可能主要介导TTTTGCCG对Hsp70信号通路的抗炎作用。