Fibroblastic reticular cells initiate immune responses in visceral adipose tissues and secure peritoneal immunity
abstract
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Immune protection of the body cavities depends on the swift
activation of innate and adaptive immune responses in nonclassical
secondary lymphoid organs known as fat-associated lymphoid clusters
(FALCs). Compared with classical secondary lymphoid organs such as
lymph nodes and Peyer's patches, FALCs develop along distinct
differentiation trajectories and display a reduced structural
complexity. Although it is well established that fibroblastic
reticular cells (FRCs) are an integral component of the
immune-stimulating infrastructure of classical secondary lymphoid
organs, the role of FRCs in FALC-dependent peritoneal immunity
remains unclear. Using FRC-specific gene targeting, we found that
FRCs play an essential role in FALC-driven immune responses.
Specifically, we report that initiation of peritoneal immunity was
governed through FRC activation in a myeloid differentiation primary
response 88 (MYD88)-dependent manner. FRC-specific ablation of MYD88
blocked recruitment of inflammatory monocytes into FALCs and
subsequent CD4 T cell-dependent B-cell activation and IgG class
switching. Moreover, containment of infection was compromised in
mice lacking MYD88 expression in FRCs, indicating that FRCs in FALCs
function as an initial checkpoint in the orchestration of protective
immune responses in the peritoneal cavity.
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citation
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Perez Shibayama C, Gil Cruz C, Cheng H W, Onder L, Printz A, Mörbe
U, Novkovic M, Li C, Lopez-Macias C, Buechler M B, Turley S J, Mack
M, Soneson C, Robinson M D, Scandella E, Gommerman J, Ludewig B.
Fibroblastic reticular cells initiate immune responses in visceral
adipose tissues and secure peritoneal immunity. Sci Immunol 2018;
3:.
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type
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journal paper/review (English)
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date of publishing
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10-8-2018
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journal title
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Sci Immunol (3/26)
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ISSN electronic
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2470-9468
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PubMed
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30097537
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DOI
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10.1126/sciimmunol.aar4539
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