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. 2023 Mar 17;14:1100461. doi: 10.3389/fimmu.2023.1100461

Table 4.

Key complement components and their functions.

Classical pathway
C1q Binds to Fc region of Ab
C1r Activates C1s
C1s Activates C4/C2
C2 Key component of C4b2a
C4 Key component of C4b2a
C4b2a Actives C3
C1 inhibitor Inactivates C1r and C1s
C4BP Blocks C4b2a formation
Factor I/CD46/CR1 Inactivates C4b
CD55 Prevents C4b2a formation
Lectin pathway
MASP1 Activates MASP2, MASP3, C4, and CoaC
MASP2 Activates C4
MASP3 Activates alternative pathway
MBL Binds to mannose residues on microbial surfaces
C2 Key component of C4b2a
C4 Key component of C4b2a
C4b2a Actives C3
Ficolin Binds to carbohydrates of bacterial surfaces
Collectins Binds to oligosaccharide structure or lipids of microorganic surfaces
C1 inhibitor Inactivates MASP-1 and MASP-2
C4BP Blocks C4b2a formation
Factor I/CD46/CR1 Inactivates C4b
CD55 Prevents C4b2a formation
Alternative pathway
C3(H2O) Binds to factor B
Factor B Key component of C3bBb and C3bBb3b
Factor D Activates factor B
Properdin Stabilizes C3bBb
C3bBb Activates C3
C4BP Blocks C3bBb formation
Factor H Inhibits C3bBb formation
Factor I/CD46/CR1/CRIg Inactivates C3b
CD55 Prevents C3bBb formation
Common pathway
C3 Key component of classical, lectin, and alternative pathways
Extrinsic pathway
PMN-/MΦ-derived proteases Activate C3 and C5
TF Activate C3 and C5
CoaC factors (FIIa, IXa, Xa, XIIa, etc.) Activate C3 and C5
kallikrein Activate C3 and C5
FibC (plasmin, fibrin, etc.) Activate C3 and C5
Terminal pathway
C5 The first component (C5b) of C5b-9
C6 Binds to C5b and C7
C7 Binds to C8
C8 Bonds to C9
C9 Polymerized to form C5b-9
C3bBb3b Activates C5
C4b2b3b Activates C5
CD59 Inhibits C5b-9 formation
Vitronectin/clusterin Inactivates C5b-9

C4BP, C4b binding protein; CoaC, coagulation cascade; CR1, complement receptor type 1; CRIg, complement receptor of immunoglobulin; Fib, fibrinolytic cascade; MΦ, macrophage; MASP, mannan-biding lectin serin protease; MBL, mannose binding lectin; PMN, polymorphonuclear leukocyte; TF, tissue factor.