PMID- 38160652 OWN - NLM STAT- MEDLINE DCOM- 20240112 LR - 20240112 IS - 1872-9142 (Electronic) IS - 0161-5890 (Linking) VI - 165 DP - 2024 Jan TI - Lipoproteins are key immunostimulatory components of Bacillus species for dendritic cell maturation and activation. PG - 82-91 LID - S0161-5890(23)00248-1 [pii] LID - 10.1016/j.molimm.2023.12.009 [doi] AB - Dendritic cells (DCs) play an important role in immunity by sensing and responding to invasive microbes. Bacillus species are rod-shaped sporulating bacteria that include the pathogenic Bacillus cereus and commensal Bacillus subtilis. Although the interaction between DC and these two Bacillus species has been studied, their key structural component that prompts DC activation is poorly understood. Here, we investigated the two Bacillus species in DC activation by whole cells and their representative microbe-associated molecular patterns (MAMPs). MAMPs including lipoteichoic acid (LTA), lipoprotein (LPP), and peptidoglycan (PGN) were purified from the two Bacillus species. Among the MAMPs, LPP from both species most potently induced the maturation and activation of DCs while PGN, but not LTA, moderately stimulated DCs. LPPs from both Bacillus species enhanced the expression of DC maturation markers including CCR7, CD40, CD80, CD83, CD86, CD205, MHC-I, and MHC-II. Among the MAMPs from B. cereus, PGN most considerably lowered the endocytic capacity of DCs implying DC maturation whereas PGN from B. subtilis lowered it to a similar degree to its LPP. Furthermore, DCs sensitized with LPPs from both Bacillus species and PGN from B. subtilis moderately induced TNF-alpha and IL-6 production. Notably, a combination of MAMPs did not show any synergistic effect on DC activation. Taken together, our results demonstrate that LPP is the key structural component in B. cereus and B. subtilis that leads to DC activation. CI - Copyright (c) 2023 Elsevier Ltd. All rights reserved. FAU - Jeong, Sungho AU - Jeong S AD - Department of Oral Microbiology and Immunology, and Dental Research Institute, School of Dentistry, Seoul National University, Seoul 08826, Republic of Korea. FAU - Im, Jintaek AU - Im J AD - Department of Oral Microbiology and Immunology, and Dental Research Institute, School of Dentistry, Seoul National University, Seoul 08826, Republic of Korea. FAU - Lee, Dongwook AU - Lee D AD - Department of Oral Microbiology and Immunology, and Dental Research Institute, School of Dentistry, Seoul National University, Seoul 08826, Republic of Korea. FAU - Ko, Kwang Hyun AU - Ko KH AD - Department of Oral Microbiology and Immunology, and Dental Research Institute, School of Dentistry, Seoul National University, Seoul 08826, Republic of Korea. FAU - Yun, Cheol-Heui AU - Yun CH AD - Department of Agricultural Biotechnology, and Research Institute of Agriculture and Life Sciences, Seoul National University, Seoul 08826, Republic of Korea. FAU - Han, Seung Hyun AU - Han SH AD - Department of Oral Microbiology and Immunology, and Dental Research Institute, School of Dentistry, Seoul National University, Seoul 08826, Republic of Korea. Electronic address: shhan-mi@snu.ac.kr. LA - eng PT - Journal Article DEP - 20231230 PL - England TA - Mol Immunol JT - Molecular immunology JID - 7905289 RN - 0 (Tumor Necrosis Factor-alpha) RN - 0 (Transcription Factors) RN - 0 (Lipoproteins) RN - 0 (Cytokines) SB - IM MH - *Bacillus/metabolism MH - Cell Differentiation MH - Tumor Necrosis Factor-alpha/metabolism MH - Transcription Factors/metabolism MH - Dendritic Cells MH - Lipoproteins/metabolism MH - Cytokines/metabolism OTO - NOTNLM OT - Bacillus cereus OT - Bacillus subtilis OT - Dendritic cells OT - Lipoproteins COIS- Declaration of Competing Interest The authors declared that they have no conflicts of interest to this work. We declare that we do not have any commercial or associative interest that represents a conflict of interest in connection with the work submitted. EDAT- 2024/01/02 11:43 MHDA- 2024/01/12 06:43 CRDT- 2023/12/31 18:09 PHST- 2023/06/09 00:00 [received] PHST- 2023/12/11 00:00 [revised] PHST- 2023/12/22 00:00 [accepted] PHST- 2024/01/12 06:43 [medline] PHST- 2024/01/02 11:43 [pubmed] PHST- 2023/12/31 18:09 [entrez] AID - S0161-5890(23)00248-1 [pii] AID - 10.1016/j.molimm.2023.12.009 [doi] PST - ppublish SO - Mol Immunol. 2024 Jan;165:82-91. doi: 10.1016/j.molimm.2023.12.009. Epub 2023 Dec 30.