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Sukhbir Kaur
 First line of defense – innate immunity.
 Ability to discriminate between self and
foreign pathogen relies on TLRs.
 Discovered in Drosophila melanogaster as a
receptor for establishing dorsoventral polarity
during embryogenesis and component of
innate immunity in adult flies.
 TLRs : first PRR to be identified .
 Recognize different features (PAMPs) of
bacteria, viruses and other microbes.
 TLRs are type I transmembrane proteins having:
• Ectodomain :amino terminal domain composed
of repeated motifs rich in leucine and known as
lecine rich repeats(LRRs).
• Transmembrane region
• Cytosolic domain: called as Toll/Interleukin I
receptor (TIR) domain.
 TIR domain has 3 regions, highly conserved
among all family members, called boxes 1,2 in
and 3. these serve as binding site for intra
cellular proteins that participate in signalling
pathway.
 TLRs are expressed on cell surface and within
intracellular vesicles( ER, endosomes, lysosomes
etc.)
 TLRs on cell surface recognize components of
microbial membrane while those expressed
within intracellular vesicles recognize foreign
nucleic acids.
 Protein PRAT4A regulates exit of TLR1,
TLR2,TLR4, TLR7 and TLR9 from ER to respective
places.
 Gp96 – ER resident heat shock protein 90 family
acts as chaperone for most TLRs .
 TLR1, TLR2 and TLR6
 Structurally related.
 TLR2 recognizes:
 Lipoproteins from various pathogens
• Peptidoglycan and techoic acid (Gram + ve
bacteria)
• Lipoarabinomanan (mycobacterium)
• Glycophosphatidyl inositol (Trypanosoma cruzi).
• Zymosan (fungi)
• Glycolipids (Treponema)
 TLR1, TLR2 and TLR6
 Heterodimer of TLR2 and TLR6 recognize
diacyl lipopeptides from mycoplasma.
 Heterodimer of TLR2 and TLR1 recognize
triacyl lipopeptides from Gram –ve bacteria.
 TLR2 and Dectin1( lectin family receptor)
recognize β-glucan (component of fungal cell
wall)
 TLR3
 Recognizes:
 Genomic RNA from dsRNA virus (reovirus).
 dsRNA (Influenza A, West Nile virus)
 dsDNA (Herpes Simplex Virus)
 TLR4
 Essential for LPS recognition
 LPS binds to soluble LPS binding protein
(LBP), then LPS transferred to CD14 and
finally TLR4 is activated.
 TLR4
 Also recognizes endogenous ligands such as:
 Heat shock protein ( HSP 60 and 70)
 Extra domain A of fibronectin, heparan
sulfate and fibrinogen.
 Heterodimer of TLR4 and TLR6 enhances the
activity of TLR4 while its dimerisation with
TLR1 inhibits its activity.
 TLR5
 Recognize flagellin
 Expressed where?
 Mucosal surface of intestinal epithelial cells
 Epithelial cells of lungs.
 TLR7 and TLR8
 Recognize imidazoquinoline (anti-viral
compound).
 TLR8 active in humans not in mouse.
 Also recognize nucleoside guanosine or uridine
rich ssRNA from viruses such as HIV and
Influenza virus.
 TLR9
• Receptor for CpGDNA
• Bacterial DNA has unmethylated CpG motifs.
 TLR11
• Active in mouse.
• Expressed in urinary bladdedr epithelial cells.
• Recognizes uropathogenic bacteria.
Toll like receptors

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Toll like receptors

  • 2.  First line of defense – innate immunity.  Ability to discriminate between self and foreign pathogen relies on TLRs.  Discovered in Drosophila melanogaster as a receptor for establishing dorsoventral polarity during embryogenesis and component of innate immunity in adult flies.  TLRs : first PRR to be identified .  Recognize different features (PAMPs) of bacteria, viruses and other microbes.
  • 3.  TLRs are type I transmembrane proteins having: • Ectodomain :amino terminal domain composed of repeated motifs rich in leucine and known as lecine rich repeats(LRRs). • Transmembrane region • Cytosolic domain: called as Toll/Interleukin I receptor (TIR) domain.  TIR domain has 3 regions, highly conserved among all family members, called boxes 1,2 in and 3. these serve as binding site for intra cellular proteins that participate in signalling pathway.
  • 4.
  • 5.  TLRs are expressed on cell surface and within intracellular vesicles( ER, endosomes, lysosomes etc.)  TLRs on cell surface recognize components of microbial membrane while those expressed within intracellular vesicles recognize foreign nucleic acids.  Protein PRAT4A regulates exit of TLR1, TLR2,TLR4, TLR7 and TLR9 from ER to respective places.  Gp96 – ER resident heat shock protein 90 family acts as chaperone for most TLRs .
  • 6.
  • 7.
  • 8.  TLR1, TLR2 and TLR6  Structurally related.  TLR2 recognizes:  Lipoproteins from various pathogens • Peptidoglycan and techoic acid (Gram + ve bacteria) • Lipoarabinomanan (mycobacterium) • Glycophosphatidyl inositol (Trypanosoma cruzi). • Zymosan (fungi) • Glycolipids (Treponema)
  • 9.  TLR1, TLR2 and TLR6  Heterodimer of TLR2 and TLR6 recognize diacyl lipopeptides from mycoplasma.  Heterodimer of TLR2 and TLR1 recognize triacyl lipopeptides from Gram –ve bacteria.  TLR2 and Dectin1( lectin family receptor) recognize β-glucan (component of fungal cell wall)
  • 10.  TLR3  Recognizes:  Genomic RNA from dsRNA virus (reovirus).  dsRNA (Influenza A, West Nile virus)  dsDNA (Herpes Simplex Virus)  TLR4  Essential for LPS recognition  LPS binds to soluble LPS binding protein (LBP), then LPS transferred to CD14 and finally TLR4 is activated.
  • 11.  TLR4  Also recognizes endogenous ligands such as:  Heat shock protein ( HSP 60 and 70)  Extra domain A of fibronectin, heparan sulfate and fibrinogen.  Heterodimer of TLR4 and TLR6 enhances the activity of TLR4 while its dimerisation with TLR1 inhibits its activity.
  • 12.  TLR5  Recognize flagellin  Expressed where?  Mucosal surface of intestinal epithelial cells  Epithelial cells of lungs.  TLR7 and TLR8  Recognize imidazoquinoline (anti-viral compound).  TLR8 active in humans not in mouse.  Also recognize nucleoside guanosine or uridine rich ssRNA from viruses such as HIV and Influenza virus.
  • 13.  TLR9 • Receptor for CpGDNA • Bacterial DNA has unmethylated CpG motifs.  TLR11 • Active in mouse. • Expressed in urinary bladdedr epithelial cells. • Recognizes uropathogenic bacteria.