• Register
X
Forgot Password

If you have forgotten your password you can enter your email here and get a temporary password sent to your email.

X

Leaving Community

Are you sure you want to leave this community? Leaving the community will revoke any permissions you have been granted in this community.

No
Yes

miR-221 is required for endothelial tip cell behaviors during vascular development.

Angiogenesis requires coordination of distinct cell behaviors between tip and stalk cells. Although this process is governed by regulatory interactions between the vascular endothelial growth factor (Vegf) and Notch signaling pathways, little is known about the potential role of microRNAs. Through deep sequencing and functional screening in zebrafish, we find that miR-221 is essential for angiogenesis. miR-221 knockdown phenocopied defects associated with loss of the tip cell-expressed Flt4 receptor. Furthermore, miR-221 was required for tip cell proliferation and migration, as well as tip cell potential in mosaic blood vessels. miR-221 knockdown also prevented "hyper-angiogenesis" defects associated with Notch deficiency and miR-221 expression was inhibited by Notch signaling. Finally, miR-221 promoted tip cell behavior through repression of two targets: cyclin dependent kinase inhibitor 1b (cdkn1b) and phosphoinositide-3-kinase regulatory subunit 1 (pik3r1). These results identify miR-221 as an important regulatory node through which tip cell migration and proliferation are controlled during angiogenesis.

Pubmed ID: 22340502

Authors

  • Nicoli S
  • Knyphausen CP
  • Zhu LJ
  • Lakshmanan A
  • Lawson ND

Journal

Developmental cell

Publication Data

February 14, 2012

Associated Grants

  • Agency: NHLBI NIH HHS, Id: R01 HL093467
  • Agency: NHLBI NIH HHS, Id: R01 HL093467-04
  • Agency: NHLBI NIH HHS, Id: R01HL093467

Mesh Terms

  • Animals
  • Biological Markers
  • Blotting, Northern
  • Blotting, Western
  • Cell Movement
  • Cell Proliferation
  • Cells, Cultured
  • Embryo, Nonmammalian
  • Endothelium, Vascular
  • Gene Expression Profiling
  • Gene Expression Regulation, Developmental
  • MicroRNAs
  • Neovascularization, Physiologic
  • Oligonucleotide Array Sequence Analysis
  • Phosphatidylinositol 3-Kinases
  • Receptors, Notch
  • Signal Transduction
  • Vascular Endothelial Growth Factor C
  • Vascular Endothelial Growth Factor Receptor-3
  • Zebrafish
  • Zebrafish Proteins