<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:creator>Dimova, Ivanka</dc:creator>
  <dc:creator>Hlushchuk, Ruslan</dc:creator>
  <dc:creator>Makanya, Andrew N.</dc:creator>
  <dc:creator>Styp-Rekowska, Beata</dc:creator>
  <dc:creator>Ceausu, Amalia</dc:creator>
  <dc:creator>Flueckiger, Stefanie</dc:creator>
  <dc:creator>Lang, Sonja</dc:creator>
  <dc:creator>Semela, David</dc:creator>
  <dc:creator>Le Noble, Ferdinand</dc:creator>
  <dc:creator>Chatterjee, Suvro</dc:creator>
  <dc:creator>Djonov, Valentin</dc:creator>
  <dc:date>2013</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">Notch is an intercellular signaling pathway related mainly to sprouting neo-  angiogenesis. The objective of our study was to evaluate the angiogenic mechanisms  involved in the vascular augmentation (sprouting/intussusception) after Notch  inhibition within perfused vascular beds using the chick area vasculosa and  MxCreNotch1(lox/lox) mice. In vivo monitoring combined with morphological  investigations demonstrated that inhibition of Notch signaling within perfused vascular  beds remarkably induced intussusceptive angiogenesis (IA) with resultant dense  immature capillary plexuses. The latter were characterized by 40 % increase in  vascular density, pericyte detachment, enhanced vessel permeability, as well as  recruitment and extravasation of mononuclear cells into the incipient transluminal  pillars (quintessence of IA). Combination of Notch inhibition with injection of bone  marrow-derived mononuclear cells dramatically enhanced IA with 80 % increase in  vascular density and pillar number augmentation by 420 %. Additionally, there was  down-regulation of ephrinB2 mRNA levels consequent to Notch inhibition. Inhibition of  ephrinB2 or EphB4 signaling induced some pericyte detachment and resulted in up-  regulation of VEGFRs but with neither an angiogenic response nor recruitment of  mononuclear cells. Notably, Tie-2 receptor was down-regulated, and the chemotactic  factors SDF-1/CXCR4 were up-regulated only due to the Notch inhibition. Disruption  of Notch signaling at the fronts of developing vessels generally results in massive  sprouting. On the contrary, in the already existing vascular beds, down-regulation of  Notch signaling triggered rapid augmentation of the vasculature predominantly by IA.  Notch inhibition disturbed vessel stability and led to pericyte detachment followed by  extravasation of mononuclear cells. The mononuclear cells contributed to formation of  transluminal pillars with sustained IA resulting in a dense vascular plexus without  concomitant vascular remodeling and maturation.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://folia.unifr.ch/global/documents/303097</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/303097/files/10456_2013_Article_9366.pdf</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1007/s10456-013-9366-5</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>License undefined</dc:rights>
  <dc:source>Angiogenesis. - 2013, p. 1-17</dc:source>
  <dc:subject>info:eu-repo/classification/udc/57</dc:subject>
  <dc:title xmlns:ns1="xml" ns1:lang="en">Inhibition of Notch signaling induces extensive intussusceptive neo-angiogenesis by recruitment of mononuclear cells</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
