|
|
||||||||
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Symposium Reports |
1 Vascular Biology Program and Institute for Cell Engineering, Departments of Pediatrics, Medicine, Oncology and Radiation Oncology; and McKusick-Nathans Institute of Genetic Medicine, The Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA
Abstract
The regulation of tissue perfusion is a major mechanism by which oxygen homeostasis is maintained. Hypoxia-inducible factor 1 (HIF-1) is a transcriptional regulator that mediates adaptive responses to reduced partial pressure of O2 in all metazoan species. In mammals, HIF-1 promotes angiogenesis, arteriogenesis and vasculogenesis through the production of multiple angiogenic growth factors in ischaemic tissue and by cell-autonomous effects on endothelial cells and bone marrow-derived angiogenic cells. Administration of viral vectors encoding constitutively active forms of the HIF-1
subunit results in increased tissue perfusion in animal models of ischaemic cardiovascular disease.
(Received 17 May 2007;
accepted after revision 14 August 2007; first published online 24 August 2007)
Corresponding author G. L. Semenza: Broadway Research Building, Suite 671, 733 North Broadway, Baltimore, MD 21205, USA. Email: gsemenza{at}jhmi.edu
This article has been cited by other articles:
![]() |
L. M Ellis Resistance to Anti-VEGF Therapy Am. Assoc. Cancer Res. Educ. Book, April 12, 2008; 2008(1): 203 - 207. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. R. Dwinell Physiological genomics: from bench to bedside Exp Physiol, November 1, 2007; 92(6): 987 - 987. [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |