It is the central tenant of Core B and this program project that the most appropriate method to study? MH is in murine models that expresses frequently seen human MH mutations. Mouse models can provide? sufficient tissues for molecular, biochemical, cellular, and physiological analyses by a multidiscipiinary team? whose collective goal is to understand the etiology of these myopathies. The use of mice also permits these? analyses to be performed in diverse genetic backgrounds.? Core B will perform the repetitive tasks that are necessary to support all four Projects. This core will? provide an important and integrated facility to receive gene-targeting constructs from Project 1 and Project 3.? They will transfect these constructs into ES cells and after the projects identify homologously targeted clones,? amplify these clones for blastocyst injection and inject these targeted ES cells into blastocysts to produce? chimeras. After confirmation of germline transmission by Projects 1 and 3, Core B will produce MH """"""""knock-in""""""""? mice to be studied by all four Projects.? Core B will take cDNA constructs from Projects 1, 3 and 4 and package them into HSV1 (RyRs) or? Lentivirus (DHPRs) virions to be used for expression of mutated proteins and intracellular reporters in? myotube cultures and distribute them as needed to all 4 projects. Core B will make myoblast cell lines from all? heterozygous and homozygous MH """"""""knock-in"""""""" mice and maintain dyspedic, dysgenic and dyspedic/dysgenic? cell lines to be used by all 4 projects.? Core B will receive human MHS muscle samples from Core C and maintain myoblast cell lines from? these samples to be used by projects 1 and 4.? In addition to maintaining MH """"""""knock-in"""""""" animal lines Core B will take responsibility for interbreeding? these animals with C57BL6 and BalbC mice to produce MH animals with different genetic backgrounds? The uniform and consistent supply of exactly the same study models to all four Projects by this? Core will allow a truly integrated approach to the study of Malignant Hyperthermia.

Agency
National Institute of Health (NIH)
Institute
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Type
Research Program Projects (P01)
Project #
5P01AR052354-02
Application #
7436120
Study Section
Special Emphasis Panel (ZAR1)
Project Start
2007-04-01
Project End
2011-03-31
Budget Start
2007-04-01
Budget End
2008-03-31
Support Year
2
Fiscal Year
2007
Total Cost
$87,019
Indirect Cost
Name
Brigham and Women's Hospital
Department
Type
DUNS #
030811269
City
Boston
State
MA
Country
United States
Zip Code
02115
Riazi, Sheila; Kraeva, Natalia; Hopkins, Philip M (2018) Malignant Hyperthermia in the Post-Genomics Era: New Perspectives on an Old Concept. Anesthesiology 128:168-180
Zheng, Jing; Chen, Juan; Zou, Xiaohan et al. (2018) Saikosaponin d causes apoptotic death of cultured neocortical neurons by increasing membrane permeability and elevating intracellular Ca2+ concentration. Neurotoxicology 70:112-121
Lavorato, Manuela; Loro, Emanuele; Debattisti, Valentina et al. (2018) Elongated mitochondrial constrictions and fission in muscle fatigue. J Cell Sci 131:
Glaser, Nosta; Iyer, Ramesh; Gilly, William et al. (2018) Functionally Driven Modulation of Sarcomeric Structure and Membrane Systems in the Fast Muscles of a Copepod (Gaussia princeps). Anat Rec (Hoboken) 301:2164-2176
Polster, Alexander; Nelson, Benjamin R; Papadopoulos, Symeon et al. (2018) Stac proteins associate with the critical domain for excitation-contraction coupling in the II-III loop of CaV1.1. J Gen Physiol 150:613-624
Holland, Erika B; Goldstone, Jared V; Pessah, Isaac N et al. (2017) Ryanodine receptor and FK506 binding protein 1 in the Atlantic killifish (Fundulus heteroclitus): A phylogenetic and population-based comparison. Aquat Toxicol 192:105-115
Perni, Stefano; Lavorato, Manuela; Beam, Kurt G (2017) De novo reconstitution reveals the proteins required for skeletal muscle voltage-induced Ca2+ release. Proc Natl Acad Sci U S A 114:13822-13827
Lavorato, Manuela; Iyer, V Ramesh; Dewight, Williams et al. (2017) Increased mitochondrial nanotunneling activity, induced by calcium imbalance, affects intermitochondrial matrix exchanges. Proc Natl Acad Sci U S A 114:E849-E858
Zhang, Rui; Pessah, Isaac N (2017) Divergent Mechanisms Leading to Signaling Dysfunction in Embryonic Muscle by Bisphenol A and Tetrabromobisphenol A. Mol Pharmacol 91:428-436
Linsley, Jeremy W; Hsu, I-Uen; Groom, Linda et al. (2017) Congenital myopathy results from misregulation of a muscle Ca2+ channel by mutant Stac3. Proc Natl Acad Sci U S A 114:E228-E236

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