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• W2983444734 endingPage "e1008163" @default.
• W2983444734 startingPage "e1008163" @default.
• W2983444734 abstract "Macrophages mediate the elimination of pathogens by phagocytosis resulting in the activation of specific signaling pathways that lead to the production of cytokines, chemokines and other factors. Borrelia burgdorferi, the causative agent of Lyme disease, causes a wide variety of pro-inflammatory symptoms. The proinflammatory capacity of macrophages is intimately related to the internalization of the spirochete. However, most receptors mediating this process are largely unknown. We have applied a multiomic approach, including the proteomic analysis of B. burgdorferi-containing phagosome-enriched fractions, to identify surface receptors that are involved in the phagocytic capacity of macrophages as well as their inflammatory output. Sucrose gradient protein fractions of human monocyte-derived macrophages exposed to B. burgdorferi contained the phagocytic receptor, CR3/CD14 highlighting the major role played by these proteins in spirochetal phagocytosis. Other proteins identified in these fractions include C-type lectins, scavenger receptors or Siglecs, of which some are directly involved in the interaction with the spirochete. We also identified the Fc gamma receptor pathway, including the binding receptor, CD64, as involved both in the phagocytosis of, and TNF induction in response to B. burgdorferi in the absence of antibodies. The common gamma chain, FcγR, mediates the phagocytosis of the spirochete, likely through Fc receptors and C-type lectins, in a process that involves Syk activation. Overall, these findings highlight the complex array of receptors involved in the phagocytic response of macrophages to B. burgdorferi." @default.
• W2983444734 created "2019-11-22" @default.
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• W2983444734 date "2019-11-18" @default.
• W2983444734 modified "2023-10-17" @default.
• W2983444734 title "Regulation of macrophage activity by surface receptors contained within Borrelia burgdorferi-enriched phagosomal fractions" @default.
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• W2983444734 doi "https://doi.org/10.1371/journal.ppat.1008163" @default.
• W2983444734 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/6886865" @default.
• W2983444734 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/31738806" @default.
• W2983444734 hasPublicationYear "2019" @default.
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