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The cytoskeletal protein ezrin regulates EC proliferation and angiogenesis via TNF-α–induced transcriptional repression of cyclin A
Raj Kishore, … , David Goukassain, Douglas W. Losordo
Raj Kishore, … , David Goukassain, Douglas W. Losordo
Published July 1, 2005
Citation Information: J Clin Invest. 2005;115(7):1785-1796. https://doi.org/10.1172/JCI22849.
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Research Article Vascular biology

The cytoskeletal protein ezrin regulates EC proliferation and angiogenesis via TNF-α–induced transcriptional repression of cyclin A

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Abstract

TNF-α modulates EC proliferation and thereby plays a central role in new blood vessel formation in physiologic and pathologic circumstances. TNF-α is known to downregulate cyclin A, a key cell cycle regulatory protein, but little else is known about how TNF-α modulates EC cell cycle and angiogenesis. Using primary ECs, we show that ezrin, previously considered to act primarily as a cytoskeletal protein and in cytoplasmic signaling, is a TNF-α–induced transcriptional repressor. TNF-α exposure leads to Rho kinase–mediated phosphorylation of ezrin, which translocates to the nucleus and binds to cell cycle homology region repressor elements within the cyclin A promoter. Overexpression of dominant-negative ezrin blocks TNF-α–induced modulation of ezrin function and rescues cyclin A expression and EC proliferation. In vivo, blockade of ezrin leads to enhanced transplanted EC proliferation and angiogenesis in a mouse hind limb ischemia model. These observations suggest that TNF-α regulates angiogenesis via Rho kinase induction of a transcriptional repressor function of the cytoskeletal protein ezrin and that ezrin may represent a suitable therapeutic target for processes dependent on EC proliferation.

Authors

Raj Kishore, Gangjian Qin, Corinne Luedemann, Evelyn Bord, Allison Hanley, Marcy Silver, Mary Gavin, David Goukassain, Douglas W. Losordo

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Figure 8

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Overexpression of DN ezrin enhances the proliferation of transplanted HU...
Overexpression of DN ezrin enhances the proliferation of transplanted HUVECs and enhances capillary density. (A) Proliferating ECs in the hind limb tissues were identified by BrdU incorporation and were counted in 8 randomly selected microscope fields from randomly selected sections of tissue from each animal and quantified. (B) Mice receiving control or spent medium after hind limb surgery were perfused with FITC–BS-1 lectin. Fluorescent capillaries were identified by confocal microscopy, counted, and quantified. (C) Tissue sections from indicated animals were subjected to confocal microscopy to visualize BS-1 lectin–perfused capillaries (green) and DiI-labeled HUVECs (red) and quantified. The merge images on the right show capillaries double-positive for BS-1 lectin and DiI (yellow). hvf, high visual field. *P < 0.01; **P < 0.001.

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