Dahlstrand Rudin Agnes, Khamzeh Arsham, Venkatakrishnan Vignesh, Persson Tishana, Gabl Michael, Savolainen Otto, Forsman Huamei, Dahlgren Claes, Christenson Karin, Bylund Johan
Department of Oral Microbiology and Immunology, Institute of Odontology, The Sahlgrenska Academy at University of Gothenburg, Gothenburg, Sweden.
Department of Rheumatology and Inflammation Research, Institute of Medicine, The Sahlgrenska Academy at University of Gothenburg, Gothenburg, Sweden.
Front Cell Infect Microbiol. 2021 Jan 19;10:620681. doi: 10.3389/fcimb.2020.620681. eCollection 2020.
Neutrophil migration from blood to tissue-residing microbes is governed by a series of chemoattractant gradients of both endogenous and microbial origin. Periodontal disease is characterized by neutrophil accumulation in the gingival pocket, recruited by the subgingival biofilm consisting mainly of gram-negative, anaerobic and proteolytic species such as . The fact that neutrophils are the dominating cell type in the gingival pocket suggests that neutrophil-specific chemoattractants are released by subgingival bacteria, but characterization of chemoattractants released by subgingival biofilm species remains incomplete. In the present study we characterized small (< 3 kDa) soluble chemoattractants released by growing , and show that these are selective for neutrophils. Most neutrophil chemoattractant receptors are expressed also by mononuclear phagocytes, the free fatty acid receptor 2 (FFAR2) being an exception. In agreement with the selective neutrophil recruitment, the chemotactic activity found in supernatants was mediated in part by a mixture of short chain fatty acids (SCFAs) that are recognized by FFAR2, and other leukocytes (including monocytes) did not respond to SCFA stimulation. Although SCFAs, produced by bacterial fermentation of dietary fiber in the gut, has previously been shown to utilize FFAR2, our data demonstrate that the pronounced proteolytic metabolism employed by (and likely also other subgingival biofilm bacteria associated with periodontal diseases) may result in the generation of SCFAs that attract neutrophils to the gingival pocket. This finding highlights the interaction between SCFAs and FFAR2 in the context of colonization during periodontal disease, but may also have implications for other inflammatory pathologies involving proteolytic bacteria.
中性粒细胞从血液迁移到组织驻留微生物受一系列内源性和微生物源性趋化因子梯度的调控。牙周病的特征是中性粒细胞在牙龈沟积聚,这是由主要由革兰氏阴性、厌氧和蛋白水解菌组成的龈下生物膜招募所致。中性粒细胞是牙龈沟中的主要细胞类型,这一事实表明龈下细菌会释放中性粒细胞特异性趋化因子,但对龈下生物膜菌种释放的趋化因子的表征仍不完整。在本研究中,我们对生长中的[具体菌种未给出]释放的小分子(<3 kDa)可溶性趋化因子进行了表征,并表明这些趋化因子对中性粒细胞具有选择性。大多数中性粒细胞趋化因子受体在单核吞噬细胞中也有表达,游离脂肪酸受体2(FFAR2)是个例外。与中性粒细胞的选择性募集一致,在[具体菌种未给出]培养上清液中发现的趋化活性部分是由FFAR2识别的短链脂肪酸(SCFAs)混合物介导的,其他白细胞(包括单核细胞)对SCFA刺激无反应。虽然肠道中膳食纤维细菌发酵产生的SCFAs此前已被证明可利用FFAR2,但我们的数据表明,[具体菌种未给出](以及可能与牙周病相关的其他龈下生物膜细菌)所采用的显著蛋白水解代谢可能导致产生吸引中性粒细胞到牙龈沟的SCFAs。这一发现突出了牙周病期间[具体菌种未给出]定植背景下SCFAs与FFAR2之间的相互作用,但也可能对涉及蛋白水解菌的其他炎症性疾病有影响。