Cell derived inflammatory mediators

Cell derived inflammatory mediators


INFLAMMATORY MEDIATORS

  • Inflammatory mediators are of 2 types-
  1. Cell derived mediators (present in cells)
  2. Plasma derived mediators (synthesized in liver)

Cell Derived inflammatory mediators

 

I) Vasoactive amines-

II) Arachidonic acid metabolites (Eicosanoids)

  • Most potent mediators of inflammation.
  • They are formed by 2 pathways-

A) Via cyclo- oxygenase pathway- includes

B) Via- lipooxygenase pathway-

    

III) Lysosomal components- 2 types

 A) Granules of neutrophils- 3 types

1. Primary granules (azurophil granules)

  • Develop at promyelocytic stage.
  • More destructive
  • These are-
  1. Myeloperoxidase (MPO)
  2. Cathepsin
  3. Non- specific collagenase

2. Secondary granules (specific granules)

  • Develop at myelocytic stage.
  • These are-
  1. Lactoferrin
  2. Lysozyme
  3. Type IV collagenase
  4. Vitamin B12 binding proteins

3. Tertiary granules (C- particles)

  • Involved in chemotaxis
  • Contains gelatinase

IV) Platelet activating factor (PAF)

    

V) Cytokines

  • They are soluble polypeptide.
  • Source- lymphocytes & monocytes.
  • They are highly specific.
  • Important cytokines are-

a) Interleukines

  1. IL1- fever
  2. IL4- anti-inflammatory
  3. IL6- synthesis of acute phase proteins

b) Tumour necrosis factor (TNF)

  • TNF- α- acute inflammatory, septic & shock, systemic inflammatory response syndrome & cachexia.

c) INF- γ- granuloma formation 

VI)  Chemokines

  • Action- leukocyte movement, chemotaxis
  1. Alpha chemokines (C-X-C)- IL-8
  2. Beta- chemokines- Ecotaxin, RANTES, MIP1- alpha
  3. Gamma- chemokines- lymphotactin 

VII) Nitric oxide-

  • Derived- endothelial cells
  • Now synthsized from arginine amino acid
  • Action- Vasodilation, anti platelet aggregation, microbicidal action

Exam Important

I) Vasoactive amines-

 

II) Arachidonic acid metabolites (Eicosanoids)

A) Via cyclo- oxygenase pathway- includes

III) Lysosomal components

1. Primary granules (azurophil granules)

  • Develop at promyelocytic stage.
  • More destructive
  • These are-
  1. Myeloperoxidase (MPO)
  2. Cathepsin
  3. Non- specific collagenase

2. Secondary granules (specific granules)

  1. Lactoferrin
  2. Lysozyme
  3. Type IV collagenase
  4. Vitamin B12 binding proteins

3. Tertiary granules (C- particles)

  • Involved in chemotaxis
  • Contains gelatinase
IV) Platelet activating factor (PAF)

    

V) Cytokines

  • They are soluble polypeptide.
  • Source- lymphocytes & monocytes.
  • They are highly specific.
  • Important cytokines are-

a) Interleukines

  1. IL1- fever
  2. IL4- anti-inflammatory
  3. IL6- synthesis of acute phase proteins

b) Tumour necrosis factor (TNF)

  • TNF- α- acute inflammatory, septic & shock, systemic inflammatory response syndrome & cachexia.

c) INF- γ- granuloma formation

VI)  Chemokines

  • Action- leukocyte movement, chemotaxis
  1. Alpha chemokines (C-X-C)- IL-8
  2. Beta- chemokines- Ecotaxin, RANTES, MIP1- alpha
  3. Gamma- chemokines- lymphotactin 

VII) Nitric oxide-

  • Now synthsized from arginine amino acid
  • Action- Vasodilation, anti platelet aggregation, microbicidal action
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