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C1q/TNF-Related Protein 6 Is a Pattern Recognition Molecule That Recruits Collectin-11 from the Complement System to Ligands
The Journal of Immunology ( IF 3.6 ) Pub Date : 2020-02-10 , DOI: 10.4049/jimmunol.1901316 Nikolaj Kirketerp-Møller 1 , Rafael Bayarri-Olmos 1 , Karen Angeliki Krogfelt 2, 3 , Peter Garred 1
The Journal of Immunology ( IF 3.6 ) Pub Date : 2020-02-10 , DOI: 10.4049/jimmunol.1901316 Nikolaj Kirketerp-Møller 1 , Rafael Bayarri-Olmos 1 , Karen Angeliki Krogfelt 2, 3 , Peter Garred 1
Affiliation
Key Points CTRP6 binds selectively to ligands, carbohydrates, and live bacteria. CTRP6 guides collectin-11 to surfaces and facilitates complement activation. Visual Abstract C1q/TNF-related protein (CTRP) 6 is a member of the CTRP protein family associated with the regulation of cellular and endocrine processes. CTRP6 contains collagen and globular structures, resembling the pattern recognition molecules (PRMs) of the classical and lectin complement pathways. We expressed human CTRP6 in Chinese hamster ovary cells and investigated the binding to different putative ligands (acetylated BSA [AcBSA], zymosan, mannan, and LPS from Escherichia coli and Salmonella as well as to the monosaccharides l-fucose, d-mannose, N-acetylglucosamine, N-acetylgalactosamine, and galactose). Furthermore, we investigated the binding of CTRP6 to various Gram-negative bacteria as well as PRMs and enzymes of the lectin complement pathway. We found that CTRP6 bound to AcBSA and to a lesser extent to zymosan. Using EDTA as chelating agent, we observed an increased binding to AcBSA, zymosan and the two strains of LPS. We detected no binding to mannan and BSA. We identified l-fucose as a ligand for CTRP6 and that it bound to certain enteroaggregative Escherichia coli and Pseudomonas aeruginosa isolates, whereas to other bacterial isolates, no binding was observed. CTRP6 did not appear to interact directly with the activating enzymes of the lectin pathway; however, we could show the specific recruitment of collectin-11 and subsequent initiation of the complement cascade through deposition of C4. In conclusion, our results demonstrate the binding of CTRP6 to a variety of microbial and endogenous ligands identifying CTRP6 as a novel human lectin and PRM of importance for complement recognition and innate immunity.
更新日期：2020-02-10
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