Malignant T Cells Exhibit CD45 Resistant Stat3 Activation and Proliferation in Cutaneous T-Cell Lymphoma

CD45 is a protein tyrosine phosphatase, which is well-known for regulating antigen receptor signalling in T and B cells via its effect on Src kinases. It has recently been shown that CD45 can also dephosphorylate Janus kinases (Jaks) and thereby regulate Signal transducer and activator of transcript...

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Published inThe Open leukemia journal Vol. 3; pp. 9 - 15
Main Authors Krejsgaard, Thorbjorn, Helvad, Rikke, Ralfkiaer, Elisabeth, Astvad, Karen, Gronbaek, Kirsten, Eriksen, Karsten W, Geisler, Carsten, Kopp, Katharina, Zhang, Qian, Odum, Niels, Woetmann, Anders
Format Journal Article
LanguageEnglish
Published 01.01.2010
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Summary:CD45 is a protein tyrosine phosphatase, which is well-known for regulating antigen receptor signalling in T and B cells via its effect on Src kinases. It has recently been shown that CD45 can also dephosphorylate Janus kinases (Jaks) and thereby regulate Signal transducer and activator of transcription (Stat) activation and cytokine-induced proliferation in lymphocytes. Consequently, CD45 dysregulation could be implicated in aberrant Jak/Stat activation and proliferation in lymphoproliferative diseases. Despite high expression of the CD45 ligand, Galectin-1, in skin lesions from cutaneous T-cell lymphoma (CTCL), the malignant T cells exhibit constitutive activation of the Jak3/Stat3 signalling pathway and uncontrolled proliferation. We show that CD45 expression is down-regulated on malignant T cells when compared to non-malignant T cells established from CTCL skin lesions. Moreover, CD45 cross-linking does not suppress the constitutive activation of Stat3 in the malignant T cells and there is no correlation between the level of activated Stat3 and the level of CD45 expression on the malignant T cells. Furthermore, in contrast to non-malignant T cells, the malignant T cells are protected against CD45-mediated inhibition of proliferation. In conclusion, our data suggest that CD45 dysregulation might play a role in the aberrant proliferation and Jak3/Stat3 activation in CTCL.
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ISSN:1876-8164
DOI:10.2174/1876816401003010009