Note to users. If you're seeing this message, it means that your browser cannot find this page's style/presentation instructions -- or possibly that you are using a browser that does not support current Web standards. Find out more about why this message is appearing, and what you can do to make your experience of our site the best it can be.
Sci. Signal., 29 September 2009
Vol. 2, Issue 90, p. ra58
[DOI: 10.1126/scisignal.2000213]
RESEARCH ARTICLES
Editor's Summary
Exploiting the Hosts Phosphatases
Leishmaniasis is a globally important infectious disease caused by the parasite Leishmania. Gomez et al. show that infection of macrophages with Leishmania alters the activity of multiple protein tyrosine phosphatases (PTPs) through cleavage mediated by the parasite protein GP63. The activated PTPs inhibit macrophage inflammatory immune responses through dephosphorylation of Janus kinases. In addition to the PTP SHP-1, previously reported to be activated in response to Leishmania infection, Gomez et al. show that the PTPs TCPTP and PTP1B are also activated and that PTP1B serves a key role in the initial stages of disease progression in mice.
Citation: M. A. Gomez, I. Contreras, M. Hallé, M. L. Tremblay, R. W. McMaster, M. Olivier, Leishmania GP63 Alters Host Signaling Through Cleavage-Activated Protein Tyrosine Phosphatases. Sci. Signal.2, ra58 (2009).
The editors suggest the following Related Resources on Science sites:
In Science Signaling
EDITORIAL GUIDES
Nancy R. Gough and John F. Foley (31 August 2010) Sci. Signal.3 (137), eg6.
[DOI: 10.1126/scisignal.3137eg6] |Abstract »|Full Text »|PDF »
PERSPECTIVES
Jonathan C. Kagan (4 May 2010) Sci. Signal.3 (120), pe15.
[DOI: 10.1126/scisignal.3120pe15] |Abstract »|Full Text »|PDF »
PODCASTS
George Hajishengallis and Annalisa M. VanHook (16 February 2010) Sci. Signal.3 (109), pc4.
[DOI: 10.1126/scisignal.3109pc4] |Abstract »|Full Text »|Podcast »
RESEARCH ARTICLES
Min Wang, Jennifer L. Krauss, Hisanori Domon, Kavita B. Hosur, Shuang Liang, Paola Magotti, Martha Triantafilou, Kathy Triantafilou, John D. Lambris, and George Hajishengallis (16 February 2010) Sci. Signal.3 (109), ra11.
[DOI: 10.1126/scisignal.2000697] |Editor's Summary »|Abstract »|Full Text »|PDF »|Supplementary Materials »
EDITORIAL GUIDES
John F. Foley and Nancy R. Gough (19 January 2010) Sci. Signal.3 (105), eg2.
[DOI: 10.1126/scisignal.3105eg2] |Abstract »|Full Text »|PDF »
EDITORS' CHOICE
Wei Wong (1 December 2009) Sci. Signal.2 (99), ec384.
[DOI: 10.1126/scisignal.299ec384] |Abstract »
Deficiency in Hematopoietic Phosphatase Ptpn6/Shp1 Hyperactivates the Innate Immune System and Impairs Control of Bacterial Infections in Zebrafish Embryos.
Z. Kanwal, A. Zakrzewska, J. den Hertog, H. P. Spaink, M. J. M. Schaaf, and A. H. Meijer (2013)
J. Immunol.
190, 1631-1645
|Abstract »|Full Text »|PDF »
The Protein Tyrosine Phosphatase SHP-1 Regulates Phagolysosome Biogenesis.
C. P. Gomez, M. Tiemi Shio, P. Duplay, M. Olivier, and A. Descoteaux (2012)
J. Immunol.
189, 2203-2210
|Abstract »|Full Text »|PDF »
Secreted virulence factors and immune evasion in visceral leishmaniasis.
U. Lambertz, J. M. Silverman, D. Nandan, W. R. McMaster, J. Clos, L. J. Foster, and N. E. Reiner (2012)
J. Leukoc. Biol.
91, 887-899
|Abstract »|Full Text »|PDF »
Genome sequencing of the lizard parasite Leishmania tarentolae reveals loss of genes associated to the intracellular stage of human pathogenic species.
F. Raymond, S. Boisvert, G. Roy, J.-F. Ritt, D. Legare, A. Isnard, M. Stanke, M. Olivier, M. J. Tremblay, B. Papadopoulou, et al. (2012)
Nucleic Acids Res.
40, 1131-1147
|Abstract »|Full Text »|PDF »
Chromosome and gene copy number variation allow major structural change between species and strains of Leishmania.
M. B. Rogers, J. D. Hilley, N. J. Dickens, J. Wilkes, P. A. Bates, D. P. Depledge, D. Harris, Y. Her, P. Herzyk, H. Imamura, et al. (2011)
Genome Res.
21, 2129-2142
|Abstract »|Full Text »|PDF »
Leishmania donovani Amastigotes Impair Gamma Interferon-Induced STAT1{alpha} Nuclear Translocation by Blocking the Interaction between STAT1{alpha} and Importin-{alpha}5.