Plasma derived chemical mediators of inflammation - ttylim

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CHEMICAL MEDIATORS OF INFLAMMATION ( PLASMA PROTEIN DERIVED ) BY : Izatty Lim (0308188)

description

describing clotting cascade, complement system, fibrinolytic system and their interrelations.

Transcript of Plasma derived chemical mediators of inflammation - ttylim

Page 1: Plasma derived chemical mediators of inflammation - ttylim

CHEMICAL MEDIATORS OF INFLAMMATION

( PLASMA PROTEIN DERIVED )

BY : Izatty Lim (0308188)

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LEARNING OUTCOMES Able to describe the 3 systems of the plasma

protein-derived mediator of inflammation. Identify the plasma protein-derived mediator in

the 3 systems and their actions.

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CHEMICAL MEDIATORS OF INFLAMMATION

Definition : any messenger that acts on blood vessels, inflammatory cells or other cells to contribute to an inflammatory response.

MEDIATORS

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PLASMA PROTEIN-DERIVED MEDIATORS

Circulating protein of 3 interrelated system :o Complement systemo Kinin systemo Coagulation system

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COMPLEMENT SYSTEM

Consist of plasma protein that play important role in host defense & inflammation. C1 – C9 Activated by proteolysis to acquire their own proteolytic activity, thus setting up an

enzymatic cascade. Critical step : activation of 3rd component, C3, by

o Classical pathway • By fixation of C1 to antigen-antibody complexes

o Alternative pathway• Triggered by bacterial polysaccharides (eg. Endotoxin) & other bacterial cell

wall component• Involving distinct set of plasma protein including properdin & factors B and D.

o Lectin pathway• Plasma lectin bind to mannose residues on microbes & activates the early

component of classical pathway

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COMPLEMENT SYSTEM

CLASSICAL PATHWAY

ALTERNATIVE PATHWAY

LECTIN PATHWAY

Formation of C3 Convertase

C 3 a C 3 b

C6 – C9

Formation of C5 Convertase

C 5 bC 5 a

Deposit on cell/microbial surface & bind with C3 convertase

(4) MAC (made up of multiple copies of final component C9) create pores disrupt osmotic balance cell lysis

(1) VASCULAR EFFECTS:-C3a & C5a induce release of histamine-↑ vascular permeability & cause vasodilation-C5a also activates lipoxygenase pathway of AA

(2) LEUKOCYTE ACTIVATION, ADHESION & CHEMOTAXIS:-C5a, C3a & C4a (lesser extent)-potent chemotatic agent for neutrophils, monocytes, eosinophil & basophil.

(3) PHAGOCYTOSIS:-C3b & iC3b act as opsonins- ↑ phagocytosis

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Vascular effects (C3a & C5a) Leukocyte activation, adhesion, chemotaxis

(C5a) Phagocytosis (C3b,iC3b) MAC ( C9)

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COAGULATION & KININ SYSTEM

Hageman factor ( Factor XII )o A protein synthesized by the livero Circulate in inactive form in plasmao Activated by collagen, basement membrane or activated

plateletso Activated Hageman factor (factor XIIa) further actives:

• Kinin system (vasoactive kinins)• Clotting system (activation of thrombin, fibrinopeptides & factor

X)• Fibrinolytic system (plasmin production & inactivating thrombin)• Complement system (anaphylatoxins C3a & C5a)

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(High molecular-weight kininogen)

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KININ SYSTEM

Bradykinino ↑ vascular permeabilityo Arteriolar dilationo Branchial smooth muscle contractiono Pain

Kallikreino Chemotatic activityo Potent activator of Hageman factor link with clotting

system

HMW KININOGEN BRADYKININ

KALLIKREIN

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CLOTTING SYSTEM

Activated thrombino Fibrin cloto Enhance leukocytes adhesiono Cleave C5 C5a ( link with complement system )

Fibrinopeptideo ↑ vascular permeabilityo Chemotatic for leukocytes

Factor Xa (intermediate in clotting cascade)o ↑ vascular permeability & leukocyte emigration

Fibrinogen

Activated thrombin

Thrombin

Fibrin Clot

Fibrinopeptide

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FIBRINOLYTIC SYSTEM

Plasmin o Multifunctional protease that cleaves fibrino Fibrin degradation product will ↑ permeabilityo Cleaves C3 C3a (vasodilation & ↑ vascular permeability)o Activate Hageman factor, thus amplify the entire set of

responses

• Activated concurrently with activation of clotting system

• Serve to limit clotting

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The end.