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A Cardiolipin from Muribaculum intestinale Induces Antigen-Specific Cytokine Responses.


ABSTRACT: An systematic phenotypic screen of the mouse gut microbiome for metabolites with an immunomodulatory effect identified Muribaculum intestinale as one of only two members with an oversized effect on T-cell populations. Here we report the identification and characterization of a lipid, MiCL-1, as the responsible metabolite. MiCL-1 is an 18:1-16:0 cardiolipin, whose close relatives are found on concave lipid surfaces of both mammals and bacteria. MiCL-1 was synthesized to confirm the structural analysis and functionally characterized in cell-based assays. It has a highly restrictive structure-activity profile, as its chain-switched analog fails to induce responses in any of our assays. MiCL-1 robustly induces the production of pro-inflammatory cytokines like TNF-α, IL-6, and IL-23, but has no detectable effect on the anti-inflammatory cytokine IL-10. As is the case with other recently discovered immunomodulatory lipids, MiCL-1 requires functional TLR2 and TLR1 but not TLR6 in cell-based assays.

SUBMITTER: Bang S 

PROVIDER: S-EPMC10623554 | biostudies-literature | 2023 Nov

REPOSITORIES: biostudies-literature

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A Cardiolipin from <i>Muribaculum intestinale</i> Induces Antigen-Specific Cytokine Responses.

Bang Sunghee S   Shin Yern-Hyerk YH   Ma Xiao X   Park Sung-Moo SM   Graham Daniel B DB   Xavier Ramnik J RJ   Clardy Jon J  

Journal of the American Chemical Society 20231023 43


An systematic phenotypic screen of the mouse gut microbiome for metabolites with an immunomodulatory effect identified <i>Muribaculum intestinale</i> as one of only two members with an oversized effect on T-cell populations. Here we report the identification and characterization of a lipid, MiCL-1, as the responsible metabolite. MiCL-1 is an 18:1-16:0 cardiolipin, whose close relatives are found on concave lipid surfaces of both mammals and bacteria. MiCL-1 was synthesized to confirm the structu  ...[more]

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