GBPs: Immunity to intracellular pathogens

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GBPs: Immunity to intracellular pathogens Juliana Ueda Thais Herrero Claudia Polli GBP

description

GBPs: Immunity to intracellular pathogens. GBP. Juliana Ueda Thais Herrero Claudia Polli. IFN- γ : Central in host resistance to infection. WT. IFN KO. IFN- γ regulates the expression of more than 1.200 genes Products: Only a fraction: Mediators of host immune responses - PowerPoint PPT Presentation

Transcript of GBPs: Immunity to intracellular pathogens

Page 1: GBPs: Immunity to intracellular pathogens

GBPs: Immunity to intracellular pathogens

Juliana UedaThais HerreroClaudia Polli

GBP

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IFN-γ : Central in host resistance to infection

WT

IFN KO

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IFN-γ regulates the expressionof more than 1.200 genes

Products:Only a fraction:Mediators of host immune responsesRemainder: little is known

Mainly produced by:

GTPases GTPases: GTP-binding proteins

NRAMP1: natural-resistance associated macrophage protein 1

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Cellular functions of GTPases

Two conformations:

• Bound to GTP: active Hydrolisis GTP GDP and GMP

• Bound t GDP: inactiveGEF (guanine exchange factor)GDP GTPActive GTPase

Cellular functions:Activation of cell-surface receptorsto modulation of membrane-fusion eventsMembrane taffickingCell signaling and migrationTranslation and protein translocationNuclear transport

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Families of GTPases• 4 major families:

- Mx family (type I and II IFN antiviral activity )

- Very large inducible GTPases (type II IFN ???) - p47 immunity-related GTPases (IRGs) antimicrobial activity - Guanylate-binding proteins (GBPs) ??? Type I IFN and IFN-γ

* Mice: IRGs against intracellular pathogens Human: lack IRGs GBPs

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11 mGBPs

7 hGBPs

GBPs: Guanylate-binding proteins

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GBPs: Guanylate-binding proteins

Induced by: type I IFN, IL-1β, LPS, IFN-γ65-KDa

GTP-binding domain(G domain)

Isoprenylation:Addition of either a C15 farnesyl orC20 geranygeranyl lipid to the C-terminus of the GBPs

Isoprenylation is important in targeting proteinsto intracellular membranes and/or to facilitate protein/protein interactions

GBPs are predominantly cytosolic and have,at most, a relatively small portion of the totalamount associated with membranes.

leucine

serine

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Functions of GBPs

Regulation of vasculogenesis by proinflammatory cytokines

Mutant GTPase active site

These are strinking phenomena but seem unlike to constitute

the adaptative function of hGBP because the G domain was not required

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Functions of GBPs

Regulation of MMP1 production

MMP1: Matrix metalloprotease 1 is required for the breakdown of extracellular colagen, enabling endothelial cells to form vessels in vivo

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Functions of GBPs

Since GBPs are induced by both type I and type II IFNs, it seemed logical to examine whether they are involved in host defense

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Functions of GBPs

Antiviral activity

HeLa cellshGBP-1SVS, EMCV m.o.i 1

mGBP-2S52N: single point mutation GTP binding regionSVS, EMCV m.o.i 0.1

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Functions of GBPs

Antiviral activity

The basis of antiviral effects is unknown. The antiproliferative activity might help to limit the cell-to-cell spread of vírus.

Control

Clone 1GBP-2

Clone 2 GBP-2

SN52

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Functions of GBPs

Response to Protozoan infections

MEFs

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Functions of GBPs

Response to Bacterial infections

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Functions of GBPs

Antibacterial activity

Thais

Claudia

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NADPH oxidase complex is a cluster of proteins that donate an electron from NADPH to molecular oxygen (O2) to produce superoxide anion (O2

-). This initiates the respiratory burst, a key step in immune defense against bacterial and fungal pathogens

Neutrophil

NADPH oxidase

http://www.clinsci.org

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http://www.caymanchem.com

Gp91phox large glycosylated proteinp22phoxsmaller adapter proteinFAD:cofactor

Soluble components:p47phox

P67phox

p40phox

PKC-mediated phosphorylation p47phox

Translocation to the membrane47phox binding to p22phox

Electrons from NADPH are donated to O2 to produce superoxide O2

-

Protons dissociated from NADPH proton channels interact with O2

- to produce H2O2

Phagosome acidification

Also engulfed with the bacterium will be membrane proteins, including gp91/p22 and FAD

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Second antimicrobial pathway…Nonoxidative mechanisms:

http://www.fbs.osaka-u.ac.jp

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Microtubule-associated protein light-chain 3 (LC3)

Antioxid Redox Signal. 2009 August; 11(8): 1975–1988.