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Speaker
P.RAMESH
Ph.D. SCHOLAR
(ABC)
IMMUNITY
Immunity refers to, reactions by an human body to
foreign substances such as microbes and various
macro molecules

( Abbas et al.,1991)
IMMUNITY

INNATE IMMUNITY

ACQUIRED IMMUNITY
Anatomical Barriers
Physiological Barriers
Inflammatory Barriers

Phagocytic/endocytic Barriers
 Phagocytosis is an Innate defense mechanism is
ingestion of extracellular particles

It is conducted by specialized cells such as
Blood Monocytes
Neutrophils and
Tissue Macrophages
 Recognition
 Adherence
 Ingestion using Pseudopodia
 Phagosome
 Phagolysosome
 Destruction of Microbes
Oxygen Dependent Killing Mechanisms
Oxygen Independent Killing
Mechanisms
Activation of Macrophages synthesizes
Lysozyme
Defensins
Tumor necrosis factor-α (TNF-α) and
Other hydrolytic enzymes
Activated phagocytes produce a number of Reactive
Oxygen Intermediates & Reactive Nitrogen
Intermediate

When exposed to certain stimuli, phagocytes
(Neutrophils, Eosinophils & Macrophages)

Oxygen uptake increase greatly, some times more
than 50 fold; undergoes a series of changes
“Respiratory Burst”
“Respiratory Burst” occurs during:
 Activation of macrophages during phagocytosis
 Abrupt rise in Oxygen consumption
 Increase Glucose consumption (HMP pathway)
 Large amount of ROI
 Activation of NADPH oxidase/Phagocyte oxidase
“NADPH Oxidase:
It is also called as Respiratory burst
oxidase/Phagocyte oxidase

Present in membrane associated of phagocytic cells
Catalyzes one-electron reduction of oxygen to O2202 + NADPH
202- + 2H+

202- + NADP+ + H+
H202- + 02

Glucose is metabolized through HMP to generate
NADPH
“NADPH Oxidase:

 Originally it is discovered by Babior in 1973
 It is having five major components in its structure
 2 Membrane components

 3 Cytosolic components
 Guanine nucleotide binding proteins
Membrane Components:

It is having 2 subuints:

(p22PHOX & gp91PHOX)
Distributed in membrane of secretory vesicles &
specific granules, associated with a heterodimeric
flavohemoprotein

FlavoCytochromeb558 (1 FAD & 2 Hemes)

Rac2 in resting cell is located in cytoplasm in a dimeric
complex with Rho-GDI & Rac1 located in membrane
PHagocyte
Oxidase
Cytosolic Components:

It is having 3 subuints:

p40PHOX, p47PHOX & p67PHOX
Guanine nucleotide binding proteins: Rac2 & Rac1
Rac2 in resting cell is located in cytoplasm in a dimeric
complex with Rho-GDI

Rac1 located in membrane
Guanine nucleotide Dissociation
Inhibitor

PHagocyte
Oxidase
Sequences
of Events:
External Stimuli:

LPS in Bacteria

Phosphorylation of p47PHOX

p47PHOX:p67PHOX:p40PHOX migrates to
membrane

Association with Cytochromeb558 to assemble
active Oxidase
Cell membrane

gp91

p22

gp91

Rap1A

p22

Rap1A

Rac2
Rac2
OPO3

p67

OH

p67

p47
p47

OPO3

OH
p40

OH

p40
ACTIVATED

RESTING
Cytosol

OPO3
Action of NADPH oxidase during
Properties & Functions of Oxidase components:

 Cytochromeb558:
 It is a heterodimer containing one of each kind of subunit
& contains 1 FAD & 2 Heme groups

 In enzyme bound FAD having Isoalloxazine act as
electron carrier/donar

 Cytosolic components:
 p40PHOX is responsible for transporting cytosolic
components from cytosol to membrane during Oxidase
activation
 Function of p67PHOX has been mystery
 p67PHOX facilitates e- transfer from flavin of
cytochromeb558 in absence of P40phox

 In the presence of p40PHOX, p67PHOX transfer ebeyond the flavin centre to heme in cytochrome & then
transfers to oxygen

 p67PHOX in oxidase shows it is having catalytically
essential binding site for NADPH
Small Guanine nucleotide binding proteins:

 Rac2, Rap1A are low m.w of G-proteins

 Rac2 is a member of Rho family where as Rap1A
Ras family, it regulates cell proliferation

 Rac2 having effector region (residues 26-45) &
insert region (residue 125-145) is bind to p67PHOX
but not p47PHOX
 Superoxide (O2¯• ) –


No direct effects on targets



Penetrates important sites



Subsequently converted to other ROI

 Hydrogen Peroxide (H2O2) –


Dismutation of superoxide radical
2H + + 2O2¯•

SOD

H2O2 + O2
(SuperOxide Dismutase)



Reacts with thiols



Bacteriocidal only at higher concentrations



Secondary oxidants from H2O2 responsible for killing
 Hydroxyl Radicals (OH•) – Fenton Reaction
Fe 2+ +H2O2


Fe 3+ + OH¯ + OH•

OH• as a major component of neutrophil bacteriocidal
arsenal is controversial



Limited radius of action



Secondary radicals from bicarbonate and chloride,
which may have biological activity

 Singlet Oxygen (O21) –


Electronically excited state of oxygen



Thought to be produced from reaction of H2O2 with
HOCl
Myeloperoxidase (MPO) mediated Halogenation
 Present in cytoplasmic granules at very high
concentrations

 Most H2O2 consumed by MPO
 Heme Peroxidase, uses H2O2 to oxidize variety of
compounds

 Unique property – oxidizes Cl ¯to HOCl
MPO

H2O2 + HCl

HOCl¯ + H2O
 Hypochlorous acid (HOCl)


Most bacteriocidal oxidant known to be produced



Bacterial targets – Fe-S proteins, membrane
transport proteins, ATP generating system

 Chloramines


Generated indirectly through reactions of HOCl with
amines



Highly bacteriocidal



H+ + OCl¯ + R-NH2

RNHCl + OH¯
 Activated macrophages express high levels of Nitric oxide
synthase (NOS)

 NOS catalyzes:
L-arginine + O2 + NADPH

NO + L-citrulline +NADP+

 NO has potent antimicrobial activity

 Can combine with O2¯• to yield more potent antimicrobial
substances (Peroxynitrites)
NO + 2O2¯•

ONOO¯
 Microbial killing mainly ROI dependent in phagocytic cells

 RNI may play role in cells with deficiencies of NADPH
oxidase/MPO pathways

 NO can react with ROI to give more potent cytotoxic
species

 May facilitate migration of phagocytic cells from blood
vessels to surrounding tissues by causing vasodilation
 O2- generated by oxidase, serves as a starting material
for production of Reactive Oxygen Species (ROS)

Production has to be tightly regulated to make sure they
are only generated when & where required
Oxygen Dependent Myeloperoxidase
Independent Reactions
Glucose +NADP+
G-6-P-dehydrogenase
NADPH + O2
Cytochrome b558

Pentose-P
+ NADPH
+

NADP + O2

-

-

2O2 + 2H+
Superoxide dismutase
-

2O2 + H2O2

H2 O2 + 1 O2

.OH + OH- + 1O2
Oxygen Dependent Myeloperoxidase
dependent reactions
H2 O2 + Cl-

-

OCl + H2O

myeloperoxidase
-

OCL + H2O

1

O2 + Cl- + H2O

-

2O2 + 2H+
Superoxide dismutase
2 H2 O2
catalase

H2 O2 + 1 O2

H2 O + O 2
Phagocytosis Innate Immunity Mechanisms
Phagocytosis Innate Immunity Mechanisms

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Phagocytosis Innate Immunity Mechanisms

  • 2. IMMUNITY Immunity refers to, reactions by an human body to foreign substances such as microbes and various macro molecules ( Abbas et al.,1991)
  • 4. Anatomical Barriers Physiological Barriers Inflammatory Barriers Phagocytic/endocytic Barriers
  • 5.
  • 6.  Phagocytosis is an Innate defense mechanism is ingestion of extracellular particles It is conducted by specialized cells such as Blood Monocytes Neutrophils and Tissue Macrophages
  • 7.  Recognition  Adherence  Ingestion using Pseudopodia  Phagosome  Phagolysosome  Destruction of Microbes
  • 8.
  • 9. Oxygen Dependent Killing Mechanisms Oxygen Independent Killing Mechanisms
  • 10. Activation of Macrophages synthesizes Lysozyme Defensins Tumor necrosis factor-α (TNF-α) and Other hydrolytic enzymes
  • 11. Activated phagocytes produce a number of Reactive Oxygen Intermediates & Reactive Nitrogen Intermediate When exposed to certain stimuli, phagocytes (Neutrophils, Eosinophils & Macrophages) Oxygen uptake increase greatly, some times more than 50 fold; undergoes a series of changes “Respiratory Burst”
  • 12. “Respiratory Burst” occurs during:  Activation of macrophages during phagocytosis  Abrupt rise in Oxygen consumption  Increase Glucose consumption (HMP pathway)  Large amount of ROI  Activation of NADPH oxidase/Phagocyte oxidase
  • 13.
  • 14. “NADPH Oxidase: It is also called as Respiratory burst oxidase/Phagocyte oxidase Present in membrane associated of phagocytic cells Catalyzes one-electron reduction of oxygen to O2202 + NADPH 202- + 2H+ 202- + NADP+ + H+ H202- + 02 Glucose is metabolized through HMP to generate NADPH
  • 15. “NADPH Oxidase:  Originally it is discovered by Babior in 1973  It is having five major components in its structure  2 Membrane components  3 Cytosolic components  Guanine nucleotide binding proteins
  • 16. Membrane Components: It is having 2 subuints: (p22PHOX & gp91PHOX) Distributed in membrane of secretory vesicles & specific granules, associated with a heterodimeric flavohemoprotein FlavoCytochromeb558 (1 FAD & 2 Hemes) Rac2 in resting cell is located in cytoplasm in a dimeric complex with Rho-GDI & Rac1 located in membrane PHagocyte Oxidase
  • 17. Cytosolic Components: It is having 3 subuints: p40PHOX, p47PHOX & p67PHOX Guanine nucleotide binding proteins: Rac2 & Rac1 Rac2 in resting cell is located in cytoplasm in a dimeric complex with Rho-GDI Rac1 located in membrane Guanine nucleotide Dissociation Inhibitor PHagocyte Oxidase
  • 18. Sequences of Events: External Stimuli: LPS in Bacteria Phosphorylation of p47PHOX p47PHOX:p67PHOX:p40PHOX migrates to membrane Association with Cytochromeb558 to assemble active Oxidase
  • 20. Action of NADPH oxidase during
  • 21. Properties & Functions of Oxidase components:  Cytochromeb558:  It is a heterodimer containing one of each kind of subunit & contains 1 FAD & 2 Heme groups  In enzyme bound FAD having Isoalloxazine act as electron carrier/donar  Cytosolic components:  p40PHOX is responsible for transporting cytosolic components from cytosol to membrane during Oxidase activation
  • 22.  Function of p67PHOX has been mystery  p67PHOX facilitates e- transfer from flavin of cytochromeb558 in absence of P40phox  In the presence of p40PHOX, p67PHOX transfer ebeyond the flavin centre to heme in cytochrome & then transfers to oxygen  p67PHOX in oxidase shows it is having catalytically essential binding site for NADPH
  • 23. Small Guanine nucleotide binding proteins:  Rac2, Rap1A are low m.w of G-proteins  Rac2 is a member of Rho family where as Rap1A Ras family, it regulates cell proliferation  Rac2 having effector region (residues 26-45) & insert region (residue 125-145) is bind to p67PHOX but not p47PHOX
  • 24.  Superoxide (O2¯• ) –  No direct effects on targets  Penetrates important sites  Subsequently converted to other ROI  Hydrogen Peroxide (H2O2) –  Dismutation of superoxide radical 2H + + 2O2¯• SOD H2O2 + O2 (SuperOxide Dismutase)  Reacts with thiols  Bacteriocidal only at higher concentrations  Secondary oxidants from H2O2 responsible for killing
  • 25.  Hydroxyl Radicals (OH•) – Fenton Reaction Fe 2+ +H2O2  Fe 3+ + OH¯ + OH• OH• as a major component of neutrophil bacteriocidal arsenal is controversial  Limited radius of action  Secondary radicals from bicarbonate and chloride, which may have biological activity  Singlet Oxygen (O21) –  Electronically excited state of oxygen  Thought to be produced from reaction of H2O2 with HOCl
  • 26. Myeloperoxidase (MPO) mediated Halogenation  Present in cytoplasmic granules at very high concentrations  Most H2O2 consumed by MPO  Heme Peroxidase, uses H2O2 to oxidize variety of compounds  Unique property – oxidizes Cl ¯to HOCl MPO H2O2 + HCl HOCl¯ + H2O
  • 27.  Hypochlorous acid (HOCl)  Most bacteriocidal oxidant known to be produced  Bacterial targets – Fe-S proteins, membrane transport proteins, ATP generating system  Chloramines  Generated indirectly through reactions of HOCl with amines  Highly bacteriocidal  H+ + OCl¯ + R-NH2 RNHCl + OH¯
  • 28.  Activated macrophages express high levels of Nitric oxide synthase (NOS)  NOS catalyzes: L-arginine + O2 + NADPH NO + L-citrulline +NADP+  NO has potent antimicrobial activity  Can combine with O2¯• to yield more potent antimicrobial substances (Peroxynitrites) NO + 2O2¯• ONOO¯
  • 29.  Microbial killing mainly ROI dependent in phagocytic cells  RNI may play role in cells with deficiencies of NADPH oxidase/MPO pathways  NO can react with ROI to give more potent cytotoxic species  May facilitate migration of phagocytic cells from blood vessels to surrounding tissues by causing vasodilation
  • 30.
  • 31.
  • 32.
  • 33.
  • 34.
  • 35.
  • 36.  O2- generated by oxidase, serves as a starting material for production of Reactive Oxygen Species (ROS) Production has to be tightly regulated to make sure they are only generated when & where required
  • 37.
  • 38. Oxygen Dependent Myeloperoxidase Independent Reactions Glucose +NADP+ G-6-P-dehydrogenase NADPH + O2 Cytochrome b558 Pentose-P + NADPH + NADP + O2 - - 2O2 + 2H+ Superoxide dismutase - 2O2 + H2O2 H2 O2 + 1 O2 .OH + OH- + 1O2
  • 39. Oxygen Dependent Myeloperoxidase dependent reactions H2 O2 + Cl- - OCl + H2O myeloperoxidase - OCL + H2O 1 O2 + Cl- + H2O - 2O2 + 2H+ Superoxide dismutase 2 H2 O2 catalase H2 O2 + 1 O2 H2 O + O 2