3. Inflammation Flashcards
What is the definition of inflammation?
Tissue response to injury/infection characterised by increased blood flow and entry of leukocytes into the tissues
What is complement?
Key component of inflammation, 20-40 molecules in a system (many enzymes) which act in an amplification cascade in order to amplify a small stimulus
What are the three complement activating pathways? Describe each pathway
- Classical pathway: complement activated when antibody binds to antigen
- Lectin pathway: C/A pathway intermediate, mannose binding lectin may bind to bacterial cell walls (mannose) on surface of microbes - activates
- Alternative pathway: complement activated directly by other stuff on microbial surfaces
How many complement activating pathways will be used when infection occurs?
All of them, get activated at different points
Which complement activating pathway takes the longest to activate?
Classical
Which enzyme is common in all three complement activating pathways? What does it do?
C3 convertase - converts C3 complement component into fragments C3A and C3B - central thing that occurs when complement activated
What happens in complement when C(number) split?
They develop a function, e.g. C3 splitting creates C3A and B which both have functions
Which is produced first, C3 convertase or C5 convertase?
C3, you fuckwit
What does complement do?
- C5B to C9 produce MAC (membrane attack complex)
- C3A, C4A, C5A stimulate mast cells to release granules (
- C3B and C4B coat microorganisms and opsonise them, link organism to phagocytic cell (like glue)
- C3D activates B lymphocytes
Which complement protein is recognised by RBCs?
C3B (infection->antibody produced->complement activated->microorganism coated with C3B->recognised by RBC)
After the RBC has recognised C3B what does it do with the pathogen?
Takes pathogen to spleen and liver where lots of macrophages are present in order to destroy the pathogen
Why is opsonisation of microorganisms undertaken when Toll-like receptors recognise them relatively well anyway?
Coating microorganism with antibody and complement (phagocyte has receptors for both) provides a very strong binding
How exactly is the membrane attack complex formed?
- C5 convertase deposited on cell surface causes C5 to be split into C5A and B
- C6 and C7 recruited
- C8 recruited, punches small hole in membrane
- Several C9 molecules come and polymerise to form pore
What cells cause inflammation and how?
Mast cells
- C5A, C4A, damager triggers degranulation of mast cells, activation of phospholipase A2 and release of vasoactive amines (histamines), cytokines and chemotactic factors
- phospholipase A2 produces arachidonic acid which activates lipoxygenase/cyclooxygenase pathways producing leukotrienes and prostaglandins
- histamine enhances vascular permeability allowing neutrophils out of blood
Acute inflammatory response is reliant on getting neutrophils into tissues
Which complement molecules also act as a chemotactic factor?
C5A and C3A - attract neutrophils to site of infection