4.5 Article

Vagal innervation is required for the formation of tertiary lymphoid tissue in colitis

Journal

EUROPEAN JOURNAL OF IMMUNOLOGY
Volume 46, Issue 10, Pages 2467-2480

Publisher

WILEY-BLACKWELL
DOI: 10.1002/eji.201646370

Keywords

Chemokines; Dextran sodium sulphate colitis model; Stromal cells; Tertiary lymphoid tissue; Vagus nerve

Categories

Funding

  1. VICI from the Netherlands Organization for Scientific Research [NWO 91856612, NWO 91876623]
  2. VIDI from the Netherlands Organization for Scientific Research [NWO 91796310]
  3. Dutch Digestive Disease Foundation
  4. TI Pharma [1-215]
  5. Flemish Fonds Wetenschappelijk Onderzoek (FWO) [G.0905.07]

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Tertiary lymphoid tissue (TLT) is lymphoid tissue that forms in adult life as a result of chronic inflammation in a tissue or organ. TLT has been shown to form in a variety of chronic inflammatory diseases, though it is not clear if and how TLT develops in the inflamed colon during inflammatory bowel disease. Here, we show that TLT develops as newly formed lymphoid tissue in the colon following dextran sulphate sodium induced colitis in C57BL/6mice, where it can be distinguished from the preexisting colonic patches and solitary intestinal lymphoid tissue. TLT in the inflamed colon develops following the expression of lymphoid tissue-inducing chemokines and adhesion molecules, such as CXCL13 and VCAM-1, respectively, which are produced by stromal organizer cells. Surprisingly, this process of TLT formation was independent of the lymphotoxin signaling pathway, but rather under neuronal control, as we demonstrate that selective surgical ablation of vagus nerve innervation inhibits CXCL13 expression and abrogates TLT formation without affecting colitis. Sympathetic neuron denervation does not affect TLT formation. Hence, we reveal that inflammation in the colon induces the formation of TLT, which is controlled by innervation through the vagus nerve.

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