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10.1371/journal.pone.0132571

http://scihub22266oqcxt.onion/10.1371/journal.pone.0132571
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suck abstract from ncbi


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pmid26161475      PLoS+One 2015 ; 10 (7): ä
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  • Entry of Francisella tularensis into Murine B Cells: The Role of B Cell Receptors and Complement Receptors #MMPMID26161475
  • Plzakova L; Krocova Z; Kubelkova K; Macela A
  • PLoS One 2015[]; 10 (7): ä PMID26161475show ga
  • Francisella tularensis, the etiological agent of tularemia, is an intracellular pathogen that dominantly infects and proliferates inside phagocytic cells but can be seen also in non-phagocytic cells, including B cells. Although protective immunity is known to be almost exclusively associated with the type 1 pathway of cellular immunity, a significant role of B cells in immune responses already has been demonstrated. Whether their role is associated with antibody-dependent or antibody-independent B cell functions is not yet fully understood. The character of early events during B cell?pathogen interaction may determine the type of B cell response regulating the induction of adaptive immunity. We used fluorescence microscopy and flow cytometry to identify the basic requirements for the entry of F. tularensis into B cells within in vivo and in vitro infection models. Here, we present data showing that Francisella tularensis subsp. holarctica strain LVS significantly infects individual subsets of murine peritoneal B cells early after infection. Depending on a given B cell subset, uptake of Francisella into B cells is mediated by B cell receptors (BCRs) with or without complement receptor CR1/2. However, F. tularensis strain FSC200 ?iglC and ?ftdsbA deletion mutants are defective in the ability to enter B cells. Once internalized into B cells, F. tularensis LVS intracellular trafficking occurs along the endosomal pathway, albeit without significant multiplication. The results strongly suggest that BCRs alone within the B-1a subset can ensure the internalization process while the BCRs on B-1b and B-2 cells need co-signaling from the co receptor containing CR1/2 to initiate F. tularensis engulfment. In this case, fluidity of the surface cell membrane is a prerequisite for the bacteria?s internalization. The results substantially underline the functional heterogeneity of B cell subsets in relation to F. tularensis.
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