TY - JOUR
T1 - Circulating Ficolin-2 and Ficolin-3 Form Heterocomplexes
AU - Jarlhelt, Ida
AU - Pilely, Katrine
AU - Clausen, Jytte Bryde
AU - Skjoedt, Mikkel-Ole
AU - Bayarri-Olmos, Rafael
AU - Garred, Peter
N1 - Copyright © 2020 by The American Association of Immunologists, Inc.
PY - 2020/4/1
Y1 - 2020/4/1
N2 - The complement system constitutes an important part of the innate immune system. The collectins and the ficolins are soluble pattern recognition molecules that contribute to complement activation via the lectin pathway. During previous experiments with ficolin-2 and ficolin-3, we have observed that the molecules may interact. We therefore hypothesized the existence of stable ficolin-2/-3 heterocomplexes. We could demonstrate ficolin-2/-3 heterocomplexes in normal human serum and plasma by ELISA using Abs specific for ficolin-2 and ficolin-3. The formation of heteromeric protein complexes were validated by coimmunoprecipitation and Western blot analysis. When recombinant ficolin-2 and recombinant ficolin-3 were mixed, no complexes were formed. However, when coexpressing ficolin-2 and ficolin-3 in Chinese hamster ovary cells, we could detect ficolin-2/-3 heterocomplexes in the supernatant. Furthermore, we measured concentration of the ficolin-2/-3 heterocomplexes in arbitrary units in 94 healthy individuals. We also established the relationship between the concentrations of ficolin-2, ficolin-3, and the ficolin-2/-3 heterocomplexes. We observed that the concentration of the ficolin-2/-3 heterocomplex correlated significantly with ficolin-2 (ρ: 0.24, p < 0.018) and ficolin-3 concentrations (ρ: 0.46, p < 0.0001). In conclusion, we describe a novel protein complex between ficolin-2 and ficolin-3 present in serum and plasma, which might be of additional biological relevance apart from the native ficolin-2 and ficolin-3 molecules.
AB - The complement system constitutes an important part of the innate immune system. The collectins and the ficolins are soluble pattern recognition molecules that contribute to complement activation via the lectin pathway. During previous experiments with ficolin-2 and ficolin-3, we have observed that the molecules may interact. We therefore hypothesized the existence of stable ficolin-2/-3 heterocomplexes. We could demonstrate ficolin-2/-3 heterocomplexes in normal human serum and plasma by ELISA using Abs specific for ficolin-2 and ficolin-3. The formation of heteromeric protein complexes were validated by coimmunoprecipitation and Western blot analysis. When recombinant ficolin-2 and recombinant ficolin-3 were mixed, no complexes were formed. However, when coexpressing ficolin-2 and ficolin-3 in Chinese hamster ovary cells, we could detect ficolin-2/-3 heterocomplexes in the supernatant. Furthermore, we measured concentration of the ficolin-2/-3 heterocomplexes in arbitrary units in 94 healthy individuals. We also established the relationship between the concentrations of ficolin-2, ficolin-3, and the ficolin-2/-3 heterocomplexes. We observed that the concentration of the ficolin-2/-3 heterocomplex correlated significantly with ficolin-2 (ρ: 0.24, p < 0.018) and ficolin-3 concentrations (ρ: 0.46, p < 0.0001). In conclusion, we describe a novel protein complex between ficolin-2 and ficolin-3 present in serum and plasma, which might be of additional biological relevance apart from the native ficolin-2 and ficolin-3 molecules.
KW - Animals
KW - CHO Cells
KW - Cell Line
KW - Collectins/metabolism
KW - Complement Activation/physiology
KW - Complement Pathway, Mannose-Binding Lectin/physiology
KW - Complement System Proteins/metabolism
KW - Cricetulus
KW - Humans
KW - Lectins/blood
KW - Mannose-Binding Protein-Associated Serine Proteases/metabolism
KW - Mice
UR - http://www.scopus.com/inward/record.url?scp=85082342360&partnerID=8YFLogxK
U2 - 10.4049/jimmunol.1900694
DO - 10.4049/jimmunol.1900694
M3 - Journal article
C2 - 32094208
VL - 204
SP - 1919
EP - 1928
JO - Journal of Immunology
JF - Journal of Immunology
SN - 0022-1767
IS - 7
ER -