Restoring Akt1 Activity in Outgrowth Endothelial Cells From South Asian Men Rescues Vascular Reparative Potential. (15th September 2014)
- Record Type:
- Journal Article
- Title:
- Restoring Akt1 Activity in Outgrowth Endothelial Cells From South Asian Men Rescues Vascular Reparative Potential. (15th September 2014)
- Main Title:
- Restoring Akt1 Activity in Outgrowth Endothelial Cells From South Asian Men Rescues Vascular Reparative Potential
- Authors:
- Cubbon, Richard M.
Yuldasheva, Nadira Y.
Viswambharan, Hema
Mercer, Ben N.
Baliga, Vivek
Stephen, Sam L.
Askham, Jonathan
Sukumar, Piruthivi
Skromna, Anna
Mughal, Romana S.
Walker, Andrew M.N.
Bruns, Alexander
Bailey, Marc A.
Galloway, Stacey
Imrie, Helen
Gage, Matthew C.
Rakobowchuk, Mark
Li, Jing
Porter, Karen E.
Ponnambalam, Sreenivasan
Wheatcroft, Stephen B.
Beech, David J.
Kearney, Mark T. - Abstract:
- Abstract: Recent data suggest reduced indices of vascular repair in South Asian men, a group at increased risk of cardiovascular events. Outgrowth endothelial cells (OEC) represent an attractive tool to study vascular repair in humans and may offer potential in cell-based repair therapies. We aimed to define and manipulate potential mechanisms of impaired vascular repair in South Asian (SA) men. In vitro and in vivo assays of vascular repair and angiogenesis were performed using OEC derived from SA men and matched European controls, prior defining potentially causal molecular mechanisms. SA OEC exhibited impaired colony formation, migration, and in vitro angiogenesis, associated with decreased expression of the proangiogenic molecules Akt1 and endothelial nitric oxide synthase (eNOS). Transfusion of European OEC into immunodeficient mice after wire-induced femoral artery injury augmented re-endothelialization, in contrast with SA OEC and vehicle; SA OEC also failed to promote angiogenesis after induction of hind limb ischemia. Expression of constitutively active Akt1 (E17KAkt), but not green fluorescent protein control, in SA OEC increased in vitro angiogenesis, which was abrogated by a NOS antagonist. Moreover, E17KAkt expressing SA OEC promoted re-endothelialization of wire-injured femoral arteries, and perfusion recovery of ischemic limbs, to a magnitude comparable with nonmanipulated European OEC. Silencing Akt1 in European OEC recapitulated the functional deficits notedAbstract: Recent data suggest reduced indices of vascular repair in South Asian men, a group at increased risk of cardiovascular events. Outgrowth endothelial cells (OEC) represent an attractive tool to study vascular repair in humans and may offer potential in cell-based repair therapies. We aimed to define and manipulate potential mechanisms of impaired vascular repair in South Asian (SA) men. In vitro and in vivo assays of vascular repair and angiogenesis were performed using OEC derived from SA men and matched European controls, prior defining potentially causal molecular mechanisms. SA OEC exhibited impaired colony formation, migration, and in vitro angiogenesis, associated with decreased expression of the proangiogenic molecules Akt1 and endothelial nitric oxide synthase (eNOS). Transfusion of European OEC into immunodeficient mice after wire-induced femoral artery injury augmented re-endothelialization, in contrast with SA OEC and vehicle; SA OEC also failed to promote angiogenesis after induction of hind limb ischemia. Expression of constitutively active Akt1 (E17KAkt), but not green fluorescent protein control, in SA OEC increased in vitro angiogenesis, which was abrogated by a NOS antagonist. Moreover, E17KAkt expressing SA OEC promoted re-endothelialization of wire-injured femoral arteries, and perfusion recovery of ischemic limbs, to a magnitude comparable with nonmanipulated European OEC. Silencing Akt1 in European OEC recapitulated the functional deficits noted in SA OEC. Reduced signaling via the Akt/eNOS axis is causally linked with impaired OEC-mediated vascular repair in South Asian men. These data prove the principle of rescuing marked reparative dysfunction in OEC derived from these men. Stem Cells 2014;32:2714–2723 … (more)
- Is Part Of:
- Stem cells. Volume 32:Number 10(2014:Oct.)
- Journal:
- Stem cells
- Issue:
- Volume 32:Number 10(2014:Oct.)
- Issue Display:
- Volume 32, Issue 10 (2014)
- Year:
- 2014
- Volume:
- 32
- Issue:
- 10
- Issue Sort Value:
- 2014-0032-0010-0000
- Page Start:
- 2714
- Page End:
- 2723
- Publication Date:
- 2014-09-15
- Subjects:
- South Asian -- Endothelial -- Repair -- Akt
Cloning -- Periodicals
Clone cells -- Periodicals
Stem cells -- Periodicals
Cell Differentiation -- Periodicals
Cell Division -- Periodicals
Clone Cells -- Periodicals
Hematopoietic Stem Cells -- Periodicals
Stem Cells -- Periodicals
571.84 - Journal URLs:
- https://academic.oup.com/stmcls ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/stem.1766 ↗
- Languages:
- English
- ISSNs:
- 1066-5099
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 8464.133510
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 20849.xml