Macrophages and nociceptor neurons form a sentinel unit around fenestrated capillaries to defend the synovium from circulating immune challenge

A wide variety of systemic pathologies, including infectious and autoimmune diseases, are accompanied by joint pain or inflammation, often mediated by circulating immune complexes (IC). How such stimuli access joints and trigger inflammation is unclear. Whole mount synovial imaging revealed PV1+ fenestrated capillaries at the periphery of the synovium in the lining-sublining interface. Circulating IC extravasated from these PV1+ capillaries, and nociceptor neurons and three distinct macrophage subsets formed a sentinel unit around them. Macrophages showed subset-specific responses to systemic IC challenge; Lyve1+CX3CR1+ macrophages orchestrated neutrophil recruitment according to FcγR signal strength and activated CGRP+ nociceptor neurons via IL-1β. In contrast, MHCII+CD11c+ and MHCII+CD11cneg interstitial macrophages formed tight clusters around PV1+ capillaries in response to systemic immune stimuli, a feature enhanced by nociceptor-derived CGRP. Altogether, we identify the anatomical location of synovial PV1+ capillaries, and subset-specific macrophage-nociceptor crosstalk that forms a blood-joint barrier protecting the synovium from circulating immune challenges.