The long term objective of this project is to understand the signaling pathways which regulate the activity of heme oxygenase-2 (HO2), which catalyzes the conversion of carbon monoxide (CO), biliverdin. and iron. CO formed by the action of H02 has been proposed to function as a neurotransmitter. Furthermore, bilirubin (rapidly formed from biliverdin by the enzyme biliverdin reductase) has been shown to be a potent antioxidant which confers neuroprotection against oxidative damage. However, the role of CO as a neurotransmitter remains controversial because H02 has not been shown to be activated by a signal transduction pathway.
The specific aims of this project are as follows: 1) We will determine the functional effects of various protein kinases on the enzymatic activity of H02 and determine the molecular mechanisms by which H02 is activated in vivo by signal transduction pathways. 2) We will develop a novel assay to measure H02 activity in real time in intact cells by exploiting recently developed iron-sensitive dyes. Once developed this assay will then be used to monitor H02 activity in neuronal cultures in response to multiple stimuli including membrane depolarization and agonist stimulation. 3) We will elucidate the signaling pathways responsible for the activation of H02 response to oxidative damage. This will be accomplished by the combination of the use of phospho-specific H02 antibodies, phannacological agents, and real-time monitoring of H02 activity in primary neuronal cultures.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
5F32NS043850-02
Application #
6626152
Study Section
Special Emphasis Panel (ZRG1-F03B (20))
Program Officer
Kleitman, Naomi
Project Start
2002-06-01
Project End
Budget Start
2003-06-01
Budget End
2004-05-31
Support Year
2
Fiscal Year
2003
Total Cost
$46,420
Indirect Cost
Name
Johns Hopkins University
Department
Neurosciences
Type
Schools of Medicine
DUNS #
001910777
City
Baltimore
State
MD
Country
United States
Zip Code
21218
Boehning, Darren; van Rossum, Damian B; Patterson, Randen L et al. (2005) A peptide inhibitor of cytochrome c/inositol 1,4,5-trisphosphate receptor binding blocks intrinsic and extrinsic cell death pathways. Proc Natl Acad Sci U S A 102:1466-71
Boehning, Darren; Sedaghat, Leela; Sedlak, Thomas W et al. (2004) Heme oxygenase-2 is activated by calcium-calmodulin. J Biol Chem 279:30927-30
van Rossum, Damian B; Patterson, Randen L; Kiselyov, Kirill et al. (2004) Agonist-induced Ca2+ entry determined by inositol 1,4,5-trisphosphate recognition. Proc Natl Acad Sci U S A 101:2323-7
Watkins, Crystal C; Boehning, Darren; Kaplin, Adam I et al. (2004) Carbon monoxide mediates vasoactive intestinal polypeptide-associated nonadrenergic/noncholinergic neurotransmission. Proc Natl Acad Sci U S A 101:2631-5
Patterson, Randen L; Boehning, Darren; Snyder, Solomon H (2004) Inositol 1,4,5-trisphosphate receptors as signal integrators. Annu Rev Biochem 73:437-65
Boehning, Darren; Moon, Cheil; Sharma, Sumit et al. (2003) Carbon monoxide neurotransmission activated by CK2 phosphorylation of heme oxygenase-2. Neuron 40:129-37
Boehning, Darren; Patterson, Randen L; Sedaghat, Leela et al. (2003) Cytochrome c binds to inositol (1,4,5) trisphosphate receptors, amplifying calcium-dependent apoptosis. Nat Cell Biol 5:1051-61
Boehning, Darren; Snyder, Solomon H (2003) Novel neural modulators. Annu Rev Neurosci 26:105-31