RhoGTPases and p53 are involved in the morphological appearance and interferon-α response of hairy cells

17Citations
Citations of this article
25Readers
Mendeley users who have this article in their library.

Your institution provides access to this article.

Abstract

Hairy cell leukemia is an uncommon B-cell lympho-proliferative disease of unknown etiology in which tumor cells display characteristic microfilamentous membrane projections. Another striking feature of the disease is its exquisite sensitivity to interferon (IFN)-α. So far, none of the known IFN-α regulatory properties have explained EFN-α responsiveness nor have they taken into account the morphological characteristics of hairy cells. IFN-α profoundly alters cytoskeletal organization of hairy cells and causes reversion of the hairy appearance into a rounded morphology. Because cytoskeletal rearrangements are controlled by the Rho family of GTPases, we investigated the GTPase activation status in hairy cells and their regulation by IFN-α. Using immunolocalization techniques and biochemical assays, we demonstrate that hairy cells display high levels of active Cdc42 and Rac1 and that IFN-α down-regulates these activities. In sharp contrast, RhoA activity was low in hairy cells but was increased by IFN-α treatment. Finally, IFN-α-mediated morphological changes also implicated a p53-induced response. These observations shed light on the mechanism of action of IFN-α in hairy cell leukemia and are of potential relevance for the therapeutical applications of this cytokine. Copyright © American Society for Investigative Pathology.

Cite

CITATION STYLE

APA

Chaigne-Delalande, B., Deuve, L., Reuzeau, E., Basoni, C., Lafarge, D., Varon, C., … Génot, E. (2006). RhoGTPases and p53 are involved in the morphological appearance and interferon-α response of hairy cells. American Journal of Pathology, 168(2), 562–573. https://doi.org/10.2353/ajpath.2006.050345

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free