Cancer Research Infection and Cancer: Biology, Therapeutics, and Prevention
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[Cancer Research 63, 1615-1622, April 1, 2003]
© 2003 American Association for Cancer Research


Molecular Biology and Genetics

Mice Deficient for N-ras

Impaired Antiviral Immune Response and T-Cell Function1

Ignacio Pérez de Castro, Roberto Diaz, Marcos Malumbres2, María-Inmaculada Hernández3, Jaishree Jagirdar4, María Jiménez, Daniel Ahn and Angel Pellicer5

Department of Pathology and Kaplan Comprehensive Cancer Center, New York University School of Medicine, New York, New York 10016

Ras proteins have a key role in the regulation of several cellular functions, and are involved in a significant percentage of human tumors. However, the specific functions of the different Ras isoforms are poorly understood. In this work, we show for the first time a specific role for N-ras in T-cell function and development. Mice defective for N-ras have low numbers of CD8 single positive thymocytes and decreased thymocyte proliferation in vitro. In Ras signaling and activation assays, KO-N-ras thymocytes showed a defective response to T-cell activation. In turn, these deficiencies resulted in a significant reduction in the production of interleukin 2 on thymocyte activation. We have also detected in vivo the functional consequences of N-ras deficiency. KO-N-ras mice showed an increased sensitivity to influenza infection, especially when low doses of virus were used. Finally, we have detected an abnormal activation pattern of downstream Ras molecules in T-cell receptor-activated KO-N-ras thymocytes that is consistent with the defective T-cell function found in these animals. All of the results derived from this work constitute a significant contribution to the knowledge of N-ras-specific functions.




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HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
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Molecular Cancer Research Cancer Prevention Research
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Annual Meeting Education Book Meeting Abstracts Online
Copyright © 2003 by the American Association for Cancer Research.