Tbx1 regulates Vegfr3 and is required for lymphatic vessel development

Li Chen, Annalisa Mupo, Tuong Huynh, Sara Cioffi, Matthew Woods, Chengliu Jin, Wallace McKeehan, Luann Thompson-Snipes, Antonio Baldini, Elizabeth Illingworth

Research output: Contribution to journalArticle

Abstract

Lymphatic dysfunction causes several human diseases, and tumor lymphangiogenesis is implicated in cancer spreading. TBX1 is the major gene for DiGeorge syndrome, which is associated with multiple congenital anomalies. Mutation of Tbx1 in mice recapitulates the human disease phenotype. In this study, we use molecular, cellular, and genetic approaches to show, unexpectedly, that Tbx1 plays a critical role in lymphatic vessel development and regulates the expression of Vegfr3, a gene that is essential for lymphangiogenesis. Tbx1 activates Vegfr3 transcription in endothelial cells (ECs) by binding to an enhancer element in the Vegfr3 gene. Conditional deletion of Tbx1 in ECs causes widespread lymphangiogenesis defects in mouse embryos and perinatal death. Using the mesentery as a model tissue, we show that Tbx1 is not required for lymphatic EC differentiation; rather, it is required for the growth and maintenance of lymphatic vessels. Our findings reveal a novel pathway for the development of the lymphatic vessel network.

Original languageEnglish
Pages (from-to)417-424
Number of pages8
JournalJournal of Cell Biology
Volume189
Issue number3
DOIs
Publication statusPublished - May 3 2010

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ASJC Scopus subject areas

  • Cell Biology

Cite this

Chen, L., Mupo, A., Huynh, T., Cioffi, S., Woods, M., Jin, C., McKeehan, W., Thompson-Snipes, L., Baldini, A., & Illingworth, E. (2010). Tbx1 regulates Vegfr3 and is required for lymphatic vessel development. Journal of Cell Biology, 189(3), 417-424. https://doi.org/10.1083/jcb.200912037