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SFB 670 TP6: Role of p47 (IRG) GTPases in cell-autonomous resistance to protozoal pathogens

Project

Risks

This project contributes to the research aim 'Risks'. Which funding institutions are active for this aim? What are the sub-aims? Take a look:
Risks


Project code: DFG SFB 670
Contract period: 01.01.2006 - 31.12.2010
Purpose of research: Basic research

The interferon-inducible p47 (IRG) GTPases are major effectors of cell-autonomous immunity in mice against vacuolar pathogens. Little is known about their mechanism of action. We have proposed that the action of the p47 GTPases in Toxoplasma immunity is mediated through the vesiculation and ultimately the destruction of the parasitophorous vacuole membrane. Our work is designed to examine this hypothesis experimentally, and to see whether it can be extended to account for our unpublished finding that loss of one p47 GTPase, IIGP1 Irga6, results in heightened susceptibility in mice to the malarial pathogen, Plasmodium berghei.

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Subjects

Collaborative Project

SFB 670: Cell-autonomous Immunity

Excutive institution

Institute for Genetics

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