Salivary gland macrophages and tissue-resident CD8 + T cells cooperate for homeostatic organ surveillance

It is well established that tissue macrophages and tissue-resident memory CD8 T cells (T ) play important roles for pathogen sensing and rapid protection of barrier tissues. In contrast, the mechanisms by which these two cell types cooperate for homeostatic organ surveillance after clearance of infe...

Celý popis

Uložené v:
Podrobná bibliografia
Vydané v:Science immunology Ročník 5; číslo 46
Hlavní autori: Stolp, Bettina, Thelen, Flavian, Ficht, Xenia, Altenburger, Lukas M, Ruef, Nora, Inavalli, V V G Krishna, Germann, Philipp, Page, Nicolas, Moalli, Federica, Raimondi, Andrea, Keyser, Kirsten A, Seyed Jafari, S Morteza, Barone, Francesca, Dettmer, Matthias S, Merkler, Doron, Iannacone, Matteo, Sharpe, James, Schlapbach, Christoph, Fackler, Oliver T, Nägerl, U Valentin, Stein, Jens V
Médium: Journal Article
Jazyk:English
Vydavateľské údaje: United States 03.04.2020
Predmet:
Animals
CD8-Positive T-Lymphocytes - immunology
Homeostasis - immunology
Macrophages - immunology
Mice
Mice, Inbred C57BL
Mice, Knockout
Mice, Transgenic
Organ Specificity - immunology
Salivary Glands - immunology
Surveys and Questionnaires
ISSN:2470-9468, 2470-9468
On-line prístup:Zistit podrobnosti o prístupe
Tagy: Pridať tag
Žiadne tagy, Buďte prvý, kto otaguje tento záznam!
Popis
Shrnutí:It is well established that tissue macrophages and tissue-resident memory CD8 T cells (T ) play important roles for pathogen sensing and rapid protection of barrier tissues. In contrast, the mechanisms by which these two cell types cooperate for homeostatic organ surveillance after clearance of infections is poorly understood. Here, we used intravital imaging to show that T dynamically followed tissue macrophage topology in noninflamed murine submandibular salivary glands (SMGs). Depletion of tissue macrophages interfered with SMG T motility and caused a reduction of interepithelial T cell crossing. In the absence of macrophages, SMG T failed to cluster in response to local inflammatory chemokines. A detailed analysis of the SMG microarchitecture uncovered discontinuous attachment of tissue macrophages to neighboring epithelial cells, with occasional macrophage protrusions bridging adjacent acini and ducts. When dissecting the molecular mechanisms that drive homeostatic SMG T motility, we found that these cells exhibit a wide range of migration modes: In addition to chemokine- and adhesion receptor-driven motility, resting SMG T displayed a remarkable capacity for autonomous motility in the absence of chemoattractants and adhesive ligands. Autonomous SMG T motility was mediated by friction and insertion of protrusions into gaps offered by the surrounding microenvironment. In sum, SMG T display a unique continuum of migration modes, which are supported in vivo by tissue macrophages to allow homeostatic patrolling of the complex SMG architecture.
Bibliografia:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:2470-9468
2470-9468
DOI:10.1126/sciimmunol.aaz4371