Chemerin attracts neutrophil reverse migration by interacting with C–C motif chemokine receptor-like 2

• Published in: Cell death & disease Vol. 15; no. 6; pp. 425 - 10
• Main Authors: Ji, Jingjing, Zhong, Hanhui, Wang, Yawen, Liu, Jinghua, Tang, Jing, Liu, Zhifeng
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 18.06.2024; Springer Nature B.V; Nature Publishing Group
• Subjects: 13; 13/31; 14; 14/34; 38; 38/91; 631/250/98; 631/80; 64; 64/60; 82; 82/1; Acute Lung Injury - metabolism; Acute Lung Injury - pathology; Animals; Antibodies; Biochemistry; Biomedical and Life Sciences; Cell Biology; Cell Culture; Cell Movement; Chemokine receptors; Chemokines; Chemokines - metabolism; Gene expression; Humans; Immunology; Inflammation; Inflammation - metabolism; Inflammation - pathology; Intercellular Signaling Peptides and Proteins - metabolism; Leukocyte migration; Leukocytes (neutrophilic); Life Sciences; Male; Mice; Mice, Inbred C57BL; Neutrophils; Neutrophils - metabolism; Receptors, CCR - metabolism
• ISSN: 2041-4889; 2041-4889
• DOI: 10.1038/s41419-024-06820-5

Neutrophil reverse migration (rM) is a recently identified phenomenon in which neutrophils migrate away from the inflammatory site back into the vasculature following initial infiltration, which involved in the resolution of loci inflammatory response or dissemination of inflammation. Present study was aimed to explore the mechanisms in neutrophil rM. By scRNA-seq on the white blood cells in acute lung injury model, we found rM-ed neutrophils exhibited increased gene expression of C–C motif chemokine receptor-like 2 (Ccrl2), an atypical chemokine receptor. Furthermore, an air pouch model was established to directly track rM-ed neutrophils in vivo. Air pouches were generated by 3 ml filtered sterile air injected subcutaneously for 3 days, and then LPS (2 mg/kg) was injected into the pouches to mimic the inflammatory state. For the rM-ed neutrophil tracking system, cell tracker CMFDA were injected into the air pouch to stain the inflammatory loci cells, and after 6 h, stained cells in blood were regarded as the rM-ed neutrophil. Based on this tracking system, we confirmed that rM-ed neutrophils showed increased CCRL2. We also found that the concentrations of the CCRL2 ligand chemerin in plasma was increased in the late stage. Neutralizing chemerin decreased the rM-ed neutrophil ratio in the blood. These results suggest that circulating chemerin attracts neutrophils to leave inflammatory sites by interacting with CCRL2, which might involve in the dissemination of inflammation.