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Selective expression of c-mas proto-oncogene in rat cerebral endothelial cells

M Kumar1, P Grammas, F Giacomelli

  • 1Department of Pathology, University of Oklahoma Health Sciences Center, Oklahoma City 73104, USA.

Neuroreport
|December 20, 1996
PubMed

Insights

Researchers found mas messenger RNA (mRNA) selectively in rat brain endothelial cells, not in aorta or mesenteric vessels. This proto-oncogene does not appear to regulate cell proliferation in these brain endothelial cells.

Area of Science:

  • Molecular Biology
  • Cell Biology
  • Neuroscience

Background:

  • The mas proto-oncogene has been implicated in regulating cellular responses.
  • Endothelial cells form the blood-brain barrier and play crucial roles in brain function.
  • Previous research suggested a role for mas in angiotensin-mediated proliferation.

Purpose of the Study:

  • To investigate the expression of c-mas mRNA in different vascular endothelial cells.
  • To determine if c-mas expression influences endothelial cell proliferation, particularly in response to angiotensin.

Main Methods:

  • Northern blot analysis was used to detect c-mas mRNA in cultured endothelial cells from rat cerebral resistance vessels, aorta, and mesenteric resistance vessels.
  • Cell proliferation assays were performed on these endothelial cell cultures, both under basal conditions and when stimulated with angiotensin.

Main Results:

  • c-mas mRNA was detected in endothelial cells from rat cerebral resistance vessels.
  • c-mas mRNA was not detectable in endothelial cells from rat aorta or mesenteric resistance vessels.
  • No significant differences in basal or angiotensin-stimulated cell growth were observed among the three endothelial cell types.

Conclusions:

  • c-mas is selectively expressed in rat brain endothelial cells.
  • The presence of c-mas in brain endothelial cells does not appear to regulate their proliferation in response to angiotensin.

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