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39 Cards in this Set
- Front
- Back
alternative pathway of complement
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pathway initiated by C3b, associated with innate immunity
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anaphylatoxin
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C3a, C4a, C5a; binding to their receptors on mast cells and basophils induces cell degranulation
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anaphylatoxin inhibitor
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protein that inactivates the anaphylatoxins
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Ba and Bb
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proteolytic fragments of Factor B following cleavage by Factor D; Bb forms part of the AP C3 convertase
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C1 INH
C1 inhibitor protein |
protein that binds to C1 preventing its activation (C1 cleaves C4 and C2)
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C1 through C9
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proteins of the classical pathway
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C2b
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proteolytic fragment of C2 that is also a weak kinin (increases vascular permeability)
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alternative pathway C3 convertase
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C3bBb
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classical pathway C3 convertase
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C4b2a
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C3 tickover
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refers to the spontaneous production of C3b which activates complement AP
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C3a, C4a, C5a
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proteolytic fragments of C3, C4, C5, respectively that are also anaphylatoxins
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C3b
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an opsonin that activates AP; a component of both AP and CP
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C4bp
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a regulatory protein that binds C4b, preventing its attachment to cells and also promotes the dissociation of AP C3 convertase
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AP C5 convertase
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C3bBbC3b
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CP C5 convertase
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C4b2a3b
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CD59
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MAC inhibitor
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classical pathway of complement
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pathway initiated by IgM or IgG immune complexes
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CR1
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complement receptor 1 for C3b
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CR2
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complement receptor 2 for C3bi
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CR3a/4a
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complement receptor for anaphylatoxins C3a and C4a
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DAF
decay accelerating factor |
prevents formation of, or causes dissociation of C3 convertases by binding to C4b and C3b
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CR5a
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complement receptor of the anaphylatoxin C5a
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Factor B
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binds to deposited C3b
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Factor D
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enzyme that cleave bound Factor B
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Factor H
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binds C3b which prevents binding of Factor B to C3b and causes dissociation of C3bBb
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Factor I
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regulatory protein that cleaves soluble forms of C3b and C4b in the presence of one of several cofactors
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GPI
glycosyl-phosphatidyl-inositol |
molecule that serves to attach some proteins to the cell in lieu of a transmembrane domain
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HAE
hereditary angioedema |
complement disorder caused by genetic deficiency of C1 INH
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HRF
homologous restriction factor |
MAC inhibitor
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kallikrein
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formed during intrinsic coagulation pathway activation
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kininogen
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cleaved by kallikrein to create bradykinin
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MAC
membrane attack complex |
complex made up of C5b, C6, C7, C8, and C9; inserts into membranes to induce cell lysis
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Neisseria species
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MAC protein deficiencies (esp. C8) results in recurrent infections with these particular bacterial species
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paroxysmal nocturnal haemoglobulinuria
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genetic disorder that manifests as hemolytic anemia due to defect in GPI linkages
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properdin
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protein that stabilizes AP C3 convertase
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S protein
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MAC inhibitor
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terminal pathway
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convergence of AP and CP leading to MAC formation
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vitronectin
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MAC inhibitor
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xenograft
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graft from another species
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