Age-related changes in the local milieu of inflamed tissues cause aberrant 
neutrophil trafficking and subsequent remote organ damage

Barkaway, Anna; Rolas, Loïc; Joulia, Régis; Bodkin, Jennifer; Lenn, Tchern; Owen-Woods, Charlotte; Reglero-Real, Natalia; Stein, Monja; Vázquez-Martínez, Laura; Girbl, Tamara; Poston, Robin N; Golding, Matthew; Saleeb, Rebecca S; Thiriot, Aude; von Andrian, Ulrich H; Duchene, Johan; Voisin, Mathieu-Benoit; Bishop, Cleo L; Voehringer, David; Roers, Axel; Rot, Antal; Lämmermann, Tim; Nourshargh, Sussan

doi:10.1016/j.immuni.2021.04.025

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Age-related changes in the local milieu of inflamed tissues cause aberrant neutrophil trafficking and subsequent remote organ damage

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Lämmermann, Tim
Max Planck Institute of Immunobiology and Epigenetics, Max Planck Society;

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https://www.sciencedirect.com/science/article/pii/S1074761321001874?via%3Dihub
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Zitation

Barkaway, A., Rolas, L., Joulia, R., Bodkin, J., Lenn, T., Owen-Woods, C., et al. (2021). Age-related changes in the local milieu of inflamed tissues cause aberrant neutrophil trafficking and subsequent remote organ damage. Immunity, 54, 1494-1510. doi:10.1016/j.immuni.2021.04.025.

Zitierlink: https://hdl.handle.net/21.11116/0000-0008-96AE-B

Zusammenfassung

Aging is associated with dysregulated immune functions. Here, we investigated the impact of age on neutrophil diapedesis. Using confocal intravital microscopy, we found that in aged mice, neutrophils adhered to vascular endothelium in inflamed tissues but exhibited a high frequency of reverse transendothelial migration (rTEM). This retrograde breaching of the endothelium by neutrophils was governed by enhanced production of the chemokine CXCL1 from mast cells that localized at endothelial cell (EC) junctions. Increased EC expression of the atypical chemokine receptor 1 (ACKR1) supported this pro-inflammatory milieu in aged venules. Accumulation of CXCL1 caused desensitization of the chemokine receptor CXCR2 on neutrophils and loss of neutrophil directional motility within EC junctions. Fluorescent tracking revealed that in aged mice, neutrophils undergoing rTEM re-entered the circulation and disseminated to the lungs where they caused vascular leakage. Thus, neutrophils stemming from a local inflammatory site contribute to remote organ damage, with implication to the dysregulated systemic inflammation associated with aging.