Neovascularization of injured tissue is fundamental for its regeneration. Recent studies have indicated an intimate relationship between angiogenesis, vasculogenesis and the repair of injured nerves. Our preliminary data indicate that repair of injured nerves is accompanied by active growth or restoration of the blood supply of the nerves. The growth of new vessels, commonly known as angiogenesis, appears to be a critical component of the healing process of nerves. Our preliminary studies also indicate that sonic hedgehog, a protein previously thought to be important primarily during embryonic life, is also capable of participating in the repair of damaged or ischemic tissues, including nerves. The effect of sonic hedgehog appears to be mediated in part by the restoration of blood vessels which supply nerves, but may also involve effects on endothelial progenitor cells that contribute not only to new blood vessel growth, but perhaps also to the reconstitution of the nerve tissue itself. In this Proposal we will investigate the potential for sonic hedgehog to improve the neovascularization and thereby the healing process of injured nerves and will investigate some of the underlying mechanisms responsible for these effects. Our preliminary data suggests that this may represent a novel therapeutic approach for accelerating recovery of damaged peripheral nerves,. Accordingly, these studies will provide basic mechanistic insights, as well as insights into potentially important novel therapeutics.

Public Health Relevance

impairment of peripheral nerve function leads to significant disability. The repair and regeneration of injured nerves involves coordinated angiogenesis and neurogenesis. This application seeks to extend our preliminary investigations into the role of the Hedgehog signaling pathway during functional nerve recovery and to evaluate the potential use of Sonic Hedgehog therapy for accelerating the repair of injured nerves.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
5R01HL053354-12
Application #
7851329
Study Section
Clinical Neuroplasticity and Neurotransmitters Study Section (CNNT)
Program Officer
Gao, Yunling
Project Start
1995-01-01
Project End
2011-06-30
Budget Start
2010-07-01
Budget End
2011-06-30
Support Year
12
Fiscal Year
2010
Total Cost
$455,842
Indirect Cost
Name
Northwestern University at Chicago
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
005436803
City
Chicago
State
IL
Country
United States
Zip Code
60611
Cheng, Zhongjian; Shen, Xinggui; Jiang, Xiaohua et al. (2018) Hyperhomocysteinemia potentiates diabetes-impaired EDHF-induced vascular relaxation: Role of insufficient hydrogen sulfide. Redox Biol 16:215-225
Gupta, Rajesh; Mackie, Alexander R; Misener, Sol et al. (2018) Endothelial smoothened-dependent hedgehog signaling is not required for sonic hedgehog induced angiogenesis or ischemic tissue repair. Lab Invest 98:682-691
Cheng, Zhongjian; Verma, Suresh K; Losordo, Douglas W et al. (2017) Reprogrammed Human Endothelial Cells: A Novel Cell Source for Regenerative Vascular Medicine. Circ Res 120:756-758
Srikanth Garikipati, Venkata Naga; Kishore, Raj (2017) Young Hearts Run Free: Therapeutic Potential of Neonatal Human Cardiac Progenitor Cells Secretome. Circ Res 120:751-752
Verma, Suresh Kumar; Garikipati, Venkata Naga Srikanth; Kishore, Raj (2017) Mitochondrial dysfunction and its impact on diabetic heart. Biochim Biophys Acta Mol Basis Dis 1863:1098-1105
Verma, Suresh K; Garikipati, Venkata N S; Krishnamurthy, Prasanna et al. (2017) Interleukin-10 Inhibits Bone Marrow Fibroblast Progenitor Cell-Mediated Cardiac Fibrosis in Pressure-Overloaded Myocardium. Circulation 136:940-953
Morishita, Yoshihiro; Kobayashi, Koichi; Klyachko, Ekaterina et al. (2016) Wnt11 Gene Therapy with Adeno-associated Virus 9 Improves Recovery from Myocardial Infarction by Modulating the Inflammatory Response. Sci Rep 6:21705
Kishore, Raj; Khan, Mohsin (2016) More Than Tiny Sacks: Stem Cell Exosomes as Cell-Free Modality for Cardiac Repair. Circ Res 118:330-43
Kishore, Raj; Garikipati, Venkata Naga Srikanth; Gumpert, Anna (2016) Tiny Shuttles for Information Transfer: Exosomes in Cardiac Health and Disease. J Cardiovasc Transl Res 9:169-75
Jeyabal, Prince; Thandavarayan, Rajarajan A; Joladarashi, Darukeshwara et al. (2016) MicroRNA-9 inhibits hyperglycemia-induced pyroptosis in human ventricular cardiomyocytes by targeting ELAVL1. Biochem Biophys Res Commun 471:423-9

Showing the most recent 10 out of 141 publications