Literature search services are currently unavailable. During our hosting provider's UPS upgrade we experienced a hardware failure and are currently working to resolve the issue.

Preparing your results

Our searching services are busy right now. Your search will reload in five seconds.

Forgot Password

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

Blood vessel tubulogenesis requires Rasip1 regulation of GTPase signaling.

Cardiovascular function depends on patent blood vessel formation by endothelial cells (ECs). However, the mechanisms underlying vascular "tubulogenesis" are only beginning to be unraveled. We show that endothelial tubulogenesis requires the Ras interacting protein 1, Rasip1, and its binding partner, the RhoGAP Arhgap29. Mice lacking Rasip1 fail to form patent lumens in all blood vessels, including the early endocardial tube. Rasipl null angioblasts fail to properly localize the polarity determinant Par3 and display defective cell polarity, resulting in mislocalized junctional complexes and loss of adhesion to extracellular matrix (ECM). Similarly, depletion of either Rasip1 or Arhgap29 in cultured ECs blocks in vitro lumen formation, fundamentally alters the cytoskeleton, and reduces integrin-dependent adhesion to ECM. These defects result from increased RhoA/ROCK/myosin II activity and blockade of Cdc42 and Rac1 signaling. This study identifies Rasip1 as a unique, endothelial-specific regulator of Rho GTPase signaling, which is essential for blood vessel morphogenesis.

Pubmed ID: 21396893


  • Xu K
  • Sacharidou A
  • Fu S
  • Chong DC
  • Skaug B
  • Chen ZJ
  • Davis GE
  • Cleaver O


Developmental cell

Publication Data

April 19, 2011

Associated Grants

  • Agency: NIDDK NIH HHS, Id: DK079862
  • Agency: NIGMS NIH HHS, Id: GM007062
  • Agency: NHLBI NIH HHS, Id: HL59373
  • Agency: NIDDK NIH HHS, Id: R01 DK079862
  • Agency: NIDDK NIH HHS, Id: R01 DK079862-01
  • Agency: NIDDK NIH HHS, Id: R01 DK079862-02
  • Agency: NIDDK NIH HHS, Id: R01 DK079862-03
  • Agency: NIDDK NIH HHS, Id: R01 DK079862-04
  • Agency: NIDDK NIH HHS, Id: R01 DK079862-05
  • Agency: NHLBI NIH HHS, Id: R01 HL059373

Mesh Terms

  • Animals
  • Blood Vessels
  • Carrier Proteins
  • Cell Polarity
  • Cells, Cultured
  • Endothelial Cells
  • Humans
  • Mice
  • Mice, Transgenic
  • Neuropeptides
  • Ranidae
  • Signal Transduction
  • Zebrafish
  • cdc42 GTP-Binding Protein
  • rac GTP-Binding Proteins
  • rac1 GTP-Binding Protein