The Experimental Animal Core has been established to address the unique issues associated with gene therapy studies involving animals. The use of high titers of potentially infectious agents as gene transfer vectors in animal models requires that both the investigative and animal husbandry stuff have access to specialized knowledge and equipment in order to safely and effectively conduct research. The Experimental Animal Core functions as a resource to provide centralized expert services in the design and implementation of gene therapy studies involving experimental animals in accordance with the Institutional Animal Care and Use Committee (IACUC) guidelines. The Core centralizes experimental animal studies to a pathogen-free, strictly regulated facility from which animals are never removed for the duration of each study. The facility is secured by individually coded, magnetic card locks and contains 4 animal housing rooms, 2 fully equipped procedure rooms for rodents, one surgical suite for higher mammals, a cage wash center, and support facilities. The detailed knowledge and training of the Core staff with regard to experimental animal models for gene therapy greatly improve the ability of investigative staff to conduct research, freeing investigative staff to concentrate on the generation and analysis of experimental data, greatly enhancing the continuity and quality of the research. The Core provides expertise in a wide variety of animal related, gene transfer techniques as well as in depth knowledge of tissue and fluid harvest and analysis. The Core supports all aspects of gene therapy research involving animals including drafting of animal use protocols, training investigators, conducting animal surgical procedures, generating and breeding transgenic animals, post-operative veterinary care, and harvest procedures. In addition, the Core provides to investigators stocks of syringes, sutures, catheters, and other supplies necessary for surgical procedures, sees to the maintenance of all equipment in the facility, and monitors the Core facility to insure that all standard operating procedures for the use of the Core facility are followed. The Core provides written standard operating procedures (SOP) for all experimental procedures it supports.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Program Projects (P01)
Project #
5P01HL059312-08
Application #
7575022
Study Section
Heart, Lung, and Blood Initial Review Group (HLBP)
Project Start
Project End
Budget Start
2004-09-01
Budget End
2005-08-31
Support Year
8
Fiscal Year
2004
Total Cost
$290,389
Indirect Cost
Name
Weill Medical College of Cornell University
Department
Type
DUNS #
060217502
City
New York
State
NY
Country
United States
Zip Code
10065
Ding, Bi-Sen; Nolan, Daniel J; Butler, Jason M et al. (2010) Inductive angiocrine signals from sinusoidal endothelium are required for liver regeneration. Nature 468:310-5
Kobayashi, Hideki; Butler, Jason M; O'Donnell, Rebekah et al. (2010) Angiocrine factors from Akt-activated endothelial cells balance self-renewal and differentiation of haematopoietic stem cells. Nat Cell Biol 12:1046-56
Rabbany, Sina Y; James, Daylon; Rafii, Shahin (2010) New dimensions in vascular engineering: opportunities for cancer biology. Tissue Eng Part A 16:2157-9
Rafii, Shahin; Nolan, Daniel (2010) Cholesterol activates vascular niche and hematopoiesis. Blood 115:3857-8
Yamamoto, Masaya; James, Daylon; Li, Hui et al. (2010) Generation of stable co-cultures of vascular cells in a honeycomb alginate scaffold. Tissue Eng Part A 16:299-308
Butler, Jason M; Kobayashi, Hideki; Rafii, Shahin (2010) Instructive role of the vascular niche in promoting tumour growth and tissue repair by angiocrine factors. Nat Rev Cancer 10:138-46
Butler, Jason M; Nolan, Daniel J; Vertes, Eva L et al. (2010) Endothelial cells are essential for the self-renewal and repopulation of Notch-dependent hematopoietic stem cells. Cell Stem Cell 6:251-64
James, Daylon; Nam, Hyung-song; Seandel, Marco et al. (2010) Expansion and maintenance of human embryonic stem cell-derived endothelial cells by TGFbeta inhibition is Id1 dependent. Nat Biotechnol 28:161-6
Kiuru, Maija; Hidaka, Chisa; Hubner, Ralf-Harto et al. (2009) Sonic hedgehog expands diaphyseal trabecular bone altering bone marrow niche and lymphocyte compartment. Mol Ther 17:1442-52
Hooper, Andrea T; Shmelkov, Sergey V; Gupta, Sunny et al. (2009) Angiomodulin is a specific marker of vasculature and regulates vascular endothelial growth factor-A-dependent neoangiogenesis. Circ Res 105:201-8

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