? Cell and Tissue Engineering Core The Cell and Tissue Engineering Core operates within the Division of Regenerative Medicine. The goal for regenerative medicine is to restore structure and function to diseases/damaged tissues and organs using stem cells alone or in combination with gene therapy, tissue engineering and/or artificial organs. The major research focus for the DRM is to develop and test novel therapeutic interventions and understand basic mechanisms of cellular and humoral immunity using several different nonhuman primate models of disease. To assist researchers focused on Regenerative Medicine research the Division of Regenerative Medicine is home to the Cell and Tissue Engineering Core Laboratory. The mission for the Core is to provide stem cell and tissue engineering products, techniques and scientific expertise to Core and Affiliate Scientists that use the resources of the TNPRC for the performance of regenerative medicine studies the NHP model. Since the last base grant submission in 2011, the efforts of the Core have focused on the generation of effective stem cell isolation protocols, defining the requirements for the expansion and characterization of rhesus macaque MSCs isolated from either the bone marrow, adipose tissue or lung. The Core has also generated a bank of viable rhesus stem cells from animals of bone or adipose tissue from animals of different ages and sexes that are routinely used for research studies. During the next funding period, the core will broaden the services it offers to include tissue engineering focus, while maintaining a focus stem cells. The core will provide services that will collect tissue samples and even generate decellularized tissue scaffolds for research projects, as needed. Currently, the core staff are routinely collecting and processing samples of nipple areolar complex, skin, lung, adipose tissue and bone. The Core has had a large impact not only on the Regenerative Medicine Program, but on other divisions such as Immunology, Microbiology and Comparative Pathology within the TNPRC, and Departments and Centers within the Tulane Health Sciences Center and other research labs nationally.

Agency
National Institute of Health (NIH)
Institute
Office of The Director, National Institutes of Health (OD)
Type
Primate Research Center Grants (P51)
Project #
5P51OD011104-58
Application #
9741861
Study Section
Special Emphasis Panel (ZRG1)
Project Start
Project End
Budget Start
2019-05-01
Budget End
2020-04-30
Support Year
58
Fiscal Year
2019
Total Cost
Indirect Cost
Name
Tulane University
Department
Type
DUNS #
053785812
City
New Orleans
State
LA
Country
United States
Zip Code
70118
Sherrill-Mix, Scott; McCormick, Kevin; Lauder, Abigail et al. (2018) Allometry and Ecology of the Bilaterian Gut Microbiome. MBio 9:
Langsjoen, Rose M; Haller, Sherry L; Roy, Chad J et al. (2018) Chikungunya Virus Strains Show Lineage-Specific Variations in Virulence and Cross-Protective Ability in Murine and Nonhuman Primate Models. MBio 9:
Kumar, Vinay; Mansfield, Joshua; Fan, Rong et al. (2018) miR-130a and miR-212 Disrupt the Intestinal Epithelial Barrier through Modulation of PPAR? and Occludin Expression in Chronic Simian Immunodeficiency Virus-Infected Rhesus Macaques. J Immunol 200:2677-2689
Sestak, Karol; Dufour, Jason P; Liu, David X et al. (2018) Beneficial Effects of Human Anti-Interleukin-15 Antibody in Gluten-Sensitive Rhesus Macaques with Celiac Disease. Front Immunol 9:1603
Ramsey, J; Martin, E C; Purcell, O M et al. (2018) Self-injurious behaviours in rhesus macaques: Potential glial mechanisms. J Intellect Disabil Res 62:1008-1017
Magnani, Diogo M; Rogers, Thomas F; Maness, Nicholas J et al. (2018) Fetal demise and failed antibody therapy during Zika virus infection of pregnant macaques. Nat Commun 9:1624
Dufour, Jason P; Russell-Lodrigue, Kasi E; Blair, Robert V (2018) Pseudoaneurysm and Arteriovenous Fistula in a Rhesus Macaque (Macaca mulatta). Comp Med 68:74-79
Parthasarathy, Geetha; Philipp, Mario T (2018) Intracellular TLR7 is activated in human oligodendrocytes in response to Borrelia burgdorferi exposure. Neurosci Lett 671:38-42
He, Ziyuan; Allers, Carolina; Sugimoto, Chie et al. (2018) Rapid Turnover and High Production Rate of Myeloid Cells in Adult Rhesus Macaques with Compensations during Aging. J Immunol 200:4059-4067
Pan, Diganta; Das, Arpita; Srivastav, Sudesh K et al. (2018) Lack of T-cell-mediated IL-2 and TNF? production is linked to decreased CD58 expression in intestinal tissue during acute simian immunodeficiency virus infection. J Gen Virol :

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