CDK6 kinase activity is required for thymocyte development

Miaofen G. Hu, Amit Deshpande, Nicolette Schlichting, Elisabeth A. Hinds, Changchuin Mao, Marei Dose, Guo Fu Hu, Richard A. Van Etten, Fotini Gounari, Philip W. Hinds

Research output: Contribution to journalArticlepeer-review

50 Scopus citations

Abstract

Cyclin-dependent kinase-6 (CDK6) is required for early thymocyte development and tumorigenesis. To mechanistically dissect the role of CDK6 in thymocyte development, we generated and analyzed mutant knock-in mice and found that mice expressing a kinase-dead Cdk6 allele (Cdk6K43M) had a pronounced reduction in thymocytes and hematopoietic stem cells and progenitor cells (Lin-Sca-1+c-Kit- [LSK]). In contrast, mice expressing the INK4-insensitive, hyperactive Cdk6R31C allele displayed excess proliferation in LSK and thymocytes. However, this is countered at least in part by increased apoptosis, which may limit progenitor and thymocyte expansion in the absence of other genetic events. Our mechanistic studies demonstrate that CDK6 kinase activity contributes to Notch signaling because inactive CDK6 kinase disrupts Notchdependent survival, proliferation, and differentiation of LSK, with concomitant alteration of Notch target gene expression, such as massive up-regulation of CD25. Further, knockout of CD25 in Cdk6K43M mice rescued most defects observed inyoungmice. These results illustrate an important role for CDK6 kinase activity in thymocyte development that operates partially through modulating Notch target gene expression. This role of CDK6 as a downstream mediator of Notch identifiesCDK6kinase activity as a potential therapeutic target inhumanlymphoid malignancies.

Original languageEnglish
Pages (from-to)6120-6131
Number of pages12
JournalBlood
Volume117
Issue number23
DOIs
StatePublished - 9 Jun 2011
Externally publishedYes

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