Contrasting roles of E2F2 and E2F3 in endothelial cell growth and ischemic angiogenesis

Junlan Zhou, Min Cheng, Min Wu, Chan Boriboun, Kentaro Jujo, Shiyue Xu, Ting C. Zhao, Yao Liang Tang, Raj Kishore, Gangjian Qin

Research output: Contribution to journalArticle

8 Scopus citations

Abstract

The growth of new blood vessels after ischemic injury requires endothelial cells (ECs) to divide and proliferate, and the E2F transcription factors are key regulators of the genes responsible for cell-cycle progression; however, the specific roles of individual E2Fs in ECs are largely unknown. To determine the roles of E2F2 and E2F3 in EC proliferation and the angiogenic response to ischemic injury, hind-limb ischemia was surgically induced in E2F2-/- mice, endothelial-specific E2F3-knockout (EndoE2F3{increment}/{increment}) mice, and their littermates with wild-type E2F2 and E2F3 expression. Two weeks later, Laser-Doppler perfusion measurements, capillary density, and endothelial proliferation were significantly greater in E2F2-/- mice and significantly lower in EndoE2F3{increment}/{increment} mice than in their littermates, and EndoE2F3{increment}/{increment} mice also developed toe and limb necrosis. The loss of E2F2 expression was associated with increases in the proliferation and G1/S-phase gene expression of isolated ECs, while the loss of E2F3 expression led to declines in these parameters. Thus E2F2 impairs, and endothelial E2F3 promotes, the angiogenic response to peripheral ischemic injury through corresponding changes in EC cell-cycle progression.

Original languageEnglish (US)
Pages (from-to)68-71
Number of pages4
JournalJournal of molecular and cellular cardiology
Volume60
Issue number1
DOIs
StatePublished - Jul 1 2013
Externally publishedYes

Keywords

  • Angiogenesis
  • E2F
  • Endothelial cells
  • Ischemia
  • Proliferation

ASJC Scopus subject areas

  • Molecular Biology
  • Cardiology and Cardiovascular Medicine

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