Luís Rafael, Volkman Brian F, Szpakowska Martyna, Chevigné Andy
Immuno-Pharmacology and Interactomics, Department of Infection and Immunity, Luxembourg Institute of Health (LIH), 29, rue Henri Koch, L-4354 Esch-sur-Alzette, Luxembourg.
Faculty of Science, Technology and Medicine, University of Luxembourg, 2, place de l'Université, L-4365 Esch-sur-Alzette, Luxembourg.
J Leukoc Biol. 2025 Apr 23;117(4). doi: 10.1093/jleuko/qiaf013.
Atypical chemokine receptors are a subfamily of important regulators of chemokine functions. Among them, ACKR2 has long been considered a scavenger of multiple inflammatory chemokines exclusively from the CC family. Recently, we demonstrated the ability of ACKR2 to scavenge the CXC chemokine CXCL10, previously reported to bind solely the classical receptor CXCR3. This discovery emphasized the need for systematic reassessments of chemokine-receptor pairings. In this work, we established a highly sensitive NanoBRET-based competition binding assay using a novel proprietary ACKR2 modulator (LIH222) and applied it in a comprehensive reassessment of the pairings between human and murine chemokines and their respective ACKR2 orthologs. We confirmed CXCL10 as a ligand for the human but also the mouse ACKR2. We also identified CXCL5, CXCL11, and CXCL12 as new CXC chemokines for both ACKR2 orthologs. Furthermore, we showed that CXCL2 is a ligand for the human but not the mouse ACKR2, whereas CXCL1 binds the mouse but not the human receptor. Finally, we found that N-terminally truncated CXCL5 (CXCL58-78) loses its capacity to bind ACKR2, whereas the removal of the first 2 residues of CXCL11 (CXCL113-73) enhances its antagonist potency, showing a tendency toward a reduction of the receptor basal interactions with β-arrestins. Altogether, this study demonstrates that ACKR2 is not exclusive to CC chemokines, and although with a weaker affinity, it can also bind and scavenge a subset of inflammatory and homeostatic CXC chemokines important for the regulation of the immune system.
非典型趋化因子受体是趋化因子功能的重要调节因子亚家族。其中,ACKR2长期以来一直被认为是一种专门清除CC家族多种炎症趋化因子的清道夫受体。最近,我们证明了ACKR2具有清除CXC趋化因子CXCL10的能力,此前报道CXCL10仅与经典受体CXCR3结合。这一发现强调了对趋化因子-受体配对进行系统重新评估的必要性。在这项工作中,我们使用一种新型专利ACKR2调节剂(LIH222)建立了一种基于NanoBRET的高灵敏度竞争结合测定法,并将其应用于对人和小鼠趋化因子及其各自的ACKR2直系同源物之间配对的全面重新评估。我们证实CXCL10是人类和小鼠ACKR2的配体。我们还确定CXCL5、CXCL11和CXCL12是两种ACKR2直系同源物的新CXC趋化因子。此外,我们表明CXCL2是人类而非小鼠ACKR2的配体,而CXCL1与小鼠而非人类受体结合。最后,我们发现N端截短的CXCL5(CXCL58 - 78)失去了与ACKR2结合的能力,而去除CXCL11的前2个残基(CXCL113 - 73)可增强其拮抗效力,显示出受体与β - 抑制蛋白的基础相互作用有降低的趋势。总之,这项研究表明ACKR2并非仅限于CC趋化因子,尽管亲和力较弱,但它也能结合并清除对免疫系统调节重要的一部分炎症和稳态CXC趋化因子。