The goal of the Cell Biology Core is to provide investigators in all the projects with preparations of cardiac myocytes for their work. As described in the Research Plans, cardiac myocytes will be used in a variety of experimental protocols from electrophysiology, where acutely dissociated cells are used, to 'molecular physiology' with viral-mediated gene transfer, which demands preparations of cultured cardiac myocytes. Considerable expertise exists within the PPG as all of the Project Leaders are experienced with a diverse range of cardiac myocyte preparations. However, we have found in the past, during our collaborative efforts, that considerable inefficiency exists in the preparation and use of cells. For example, different groups may be preparing acutely dissociated cells on the same day that could have been shared. One group might invest time establishing a new preparation, for example, of cultured neonatal mouse cells, only to find that another group has prepared them for months. Thus, this Core will streamline the production and use of cardiac cells for all the projects in this PPG by centralizing the expertise and functioning as a 'centralized warehouse.' Thus, this Core will provide a framework of enhanced communication and organization that will result in a major cost savings for all of the projects. NOTE: The Core will be responsible for the ordering and maintenance of normal mice and rats that will be used in the preparation of normal cells. Each project in the program will be responsible for the maintenance of specialized transgenic animals. Thus, costs associated with such animals are included in the budget of individual projects. The Core can provide expertise in the preparation of isolated cells from diseased hearts as warranted.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Program Projects (P01)
Project #
5P01HL070709-05
Application #
7283014
Study Section
Heart, Lung, and Blood Initial Review Group (HLBP)
Project Start
Project End
Budget Start
2006-09-01
Budget End
2007-08-31
Support Year
5
Fiscal Year
2006
Total Cost
$250,426
Indirect Cost
Name
University of Maryland Baltimore
Department
Type
DUNS #
188435911
City
Baltimore
State
MD
Country
United States
Zip Code
21201
Yokota, Tomohiro; Wang, Yibin (2016) p38 MAP kinases in the heart. Gene 575:369-376
Lam, Maggie P Y; Wang, Ding; Lau, Edward et al. (2014) Protein kinetic signatures of the remodeling heart following isoproterenol stimulation. J Clin Invest 124:1734-44
Wang, Yibin (2014) Blind dates in sciences: dealing with rejection in peer review. Circ Res 114:944-6
Ma, Donghui; Taneja, Tarvinder Kaur; Hagen, Brian M et al. (2011) Golgi export of the Kir2.1 channel is driven by a trafficking signal located within its tertiary structure. Cell 145:1102-15
Zhang, Yinghua; Resneck, Wendy G; Lee, Pervis C et al. (2010) Characterization and expression of a heart-selective alternatively spliced variant of alpha II-spectrin, cardi+, during development in the rat. J Mol Cell Cardiol 48:1050-9
Ota, Asuka; Zhang, Jun; Ping, Peipei et al. (2010) Specific regulation of noncanonical p38alpha activation by Hsp90-Cdc37 chaperone complex in cardiomyocyte. Circ Res 106:1404-12
Goodall, Mariah H; Wardlow 2nd, Robert D; Goldblum, Rebecca R et al. (2010) Novel function of cardiac protein kinase D1 as a dynamic regulator of Ca2+ sensitivity of contraction. J Biol Chem 285:41686-700
Vargas, Noelle B; Brewer, Brandy Y; Rogers, Terry B et al. (2009) Protein kinase C activation stabilizes LDL receptor mRNA via the JNK pathway in HepG2 cells. J Lipid Res 50:386-97
Lu, Gang; Sun, Haipeng; Korge, Paavo et al. (2009) Functional characterization of a mitochondrial Ser/Thr protein phosphatase in cell death regulation. Methods Enzymol 457:255-73
Salnikov, V; Lukyanenko, Y O; Lederer, W J et al. (2009) Distribution of ryanodine receptors in rat ventricular myocytes. J Muscle Res Cell Motil 30:161-70

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