Normal cardiac neural crest function is essential for normal structural and functional development of the heart and great arteries. We have shown that development of myocardial function is critically dependent on the earliest phase of cardiac neural crest development which occurs several days before the neural crest cells migrate into the outflow tract. While it is apparent that myocardial excitation-contraction coupling is depressed, we still do not understand the full extent of the functional deficit or its genesis. The alteration in myocardial function is not due to hemodynamic abnormalities present in the peripheral circulation or aortic arch arteries. Our collective data indicate that extracardiac signaling coordinated by the cardiac neural crest is required for normal myocardial maturation. The overall goal during the next funding period is to elucidate the molecular nature of myocardial dysfunction, establish the mechanism of signal coordination by neural crest cells, and determine factors that alter neural crest function. Project 1 will examine the modulation of an FGF-like signal originating form pharyngeal endoderm by neural crest cells, and the effect of excess retinoic acid on neural crest's ability to modulate this signal. Dr. Creazzo's project will establish the molecular and functional consequences of altered signal modulation in myocardial will establish the molecular and functional consequences of altered signal modulation in myocardial maturation. Dr. Lo's project will elucidate the cardiovascular consequences of Cx43 gap junction dysfunction in neural crest cells during migration into the pharyngeal region and outflow tract. The hypotheses to be tested by this application proposes a dramatic revision in the classical form-function hypothesis that has driven most earlier studies of cardiovascular development.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Program Projects (P01)
Project #
7P01HL036059-15
Application #
6388999
Study Section
Heart, Lung, and Blood Initial Review Group (HLBP)
Program Officer
Wang, Lan-Hsiang
Project Start
1986-04-01
Project End
2005-03-31
Budget Start
2001-04-01
Budget End
2002-03-31
Support Year
15
Fiscal Year
2001
Total Cost
$1,708,608
Indirect Cost
Name
Duke University
Department
Pediatrics
Type
Schools of Medicine
DUNS #
071723621
City
Durham
State
NC
Country
United States
Zip Code
27705
Palatinus, Joseph A; O'Quinn, Michael P; Barker, Ralph J et al. (2011) ZO-1 determines adherens and gap junction localization at intercalated disks. Am J Physiol Heart Circ Physiol 300:H583-94
Evans, Sylvia M; Yelon, Deborah; Conlon, Frank L et al. (2010) Myocardial lineage development. Circ Res 107:1428-44
Kirby, Margaret L; Hutson, Mary R (2010) Factors controlling cardiac neural crest cell migration. Cell Adh Migr 4:609-21
Hutson, Mary Redmond; Zeng, Xiaopei Lily; Kim, Andrew J et al. (2010) Arterial pole progenitors interpret opposing FGF/BMP signals to proliferate or differentiate. Development 137:3001-11
Hutson, Mary Redmond; Sackey, Faustina N; Lunney, Katherine et al. (2009) Blocking hedgehog signaling after ablation of the dorsal neural tube allows regeneration of the cardiac neural crest and rescue of outflow tract septation. Dev Biol 335:367-73
Gurjarpadhye, Abhijit; Hewett, Kenneth W; Justus, Charles et al. (2007) Cardiac neural crest ablation inhibits compaction and electrical function of conduction system bundles. Am J Physiol Heart Circ Physiol 292:H1291-300
Graham, Victoria; Zhang, Hengtao; Willis, Shannon et al. (2006) Expression of a two-pore domain K+ channel (TASK-1) in developing avian and mouse ventricular conduction systems. Dev Dyn 235:143-51
Hutson, Mary R; Zhang, Ping; Stadt, Harriett A et al. (2006) Cardiac arterial pole alignment is sensitive to FGF8 signaling in the pharynx. Dev Biol 295:486-97
Lindsey, Merry L; Escobar, G Patricia; Mukherjee, Rupak et al. (2006) Matrix metalloproteinase-7 affects connexin-43 levels, electrical conduction, and survival after myocardial infarction. Circulation 113:2919-28
Gourdie, Robert G; Ghatnekar, Gautam S; O'Quinn, Michael et al. (2006) The unstoppable connexin43 carboxyl-terminus: new roles in gap junction organization and wound healing. Ann N Y Acad Sci 1080:49-62

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