Angiogenesis is an important repair process in response to ischemia and therapeutic angiogenesis has been the most promising therapy for treating ischemic diseases. However, it appears that delivery of a single growth factor or cell type does not support angiogenesis sufficiently to prevent the ischemic damage. Thus, a better understanding of the biology of angiogenesis is necessary to identify new targets for treating ischemia diseases. Our preliminary data show that there are markedly increased mRNA and protein levels of sucrose non-fermenting 1 (Snf1)-related kinase (SNRK), a serine/threonine kinase, a novel member of the AMP-activated protein kinase (AMPK)-related superfamily, in the patients with myocardial infarction. Further, upregulated SNRK correlated with increased levels of neovascular formation in human ischemic myocardium. Similarly, hind limb ischemia upregulates SNRK levels and increased neovessel formation in the vasculature of skeletal muscles. The most conclusive evidence for the essential role of SNRK in vascular genesis and angiogenesis is that global heterozygous deletion of SNRK impaired new vessel formation in both physiological and pathological conditions and exacerbated ischemic injury in several murine models of angiogenesis including hind limb ischemia and left anterior descending coronary artery (LAD) ligation in hearts. Thus, our central hypothesis is that SNRK promotes angiogenesis by activating ITGB1-mediated EC migration and cell adhesion. This hypothesis will be tested using gain-/loss-of-function strategies in both animal models and cultured cells.
Aim 1 will determine the role of SNRK in regulating angiogenesis, using EC-specific snrk knockout (snrkf/f/VE-cad-Cre+/?) mice and SNRK EC-specific transgenic (snrk-TG) mice and define the mechanism by which ischemia/hypoxia increases SNRK expression. In addition, the role of SNRK in regulating angiogenesis will be determined using gain- and loss-of-function approaches in cultured aortic rings and ECs.
Aim 2 is to delineate the mechanism by which SNRK increases EC migration, leading to angiogenesis by testing the hypothesis that SNRK promotes angiogenesis by activating ITGB1-mediates EC migration and cell adhesion. The successful completion of the proposed study will demonstrate that SNRK upregulation and its related activation of ?1 integrin (ITGB1)-mediated EC migration and adhesion is a new avenue to treat ischemic vascular diseases. Since the formation of new blood vessels also contributes to malignant, inflammatory, infectious and immune disorders, our proposed research may have implications beyond ischemic vascular disease.

Public Health Relevance

Therapeutic angiogenesis is one of the most promising therapies for ischemic vascular diseases, a leading cause of mortality and disability worldwide but our limited understanding on molecular mechanisms of angiogenesis impedes the development of effective therapies to prevent ischemic damages. This application has addressed this critical gap of knowledge by proposing studies to establish indispensable roles for SNRK in angiogenesis, which will demonstrate that SNRK-promoting angiogenesis is a new avenue to cure ischemic vascular diseases, an unmet clinical need.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
5R01HL142287-02
Application #
9673203
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Gao, Yunling
Project Start
2018-04-01
Project End
2022-02-28
Budget Start
2019-03-01
Budget End
2020-02-29
Support Year
2
Fiscal Year
2019
Total Cost
Indirect Cost
Name
Georgia State University
Department
Miscellaneous
Type
Organized Research Units
DUNS #
837322494
City
Atlanta
State
GA
Country
United States
Zip Code
30302