: Overview: The proposed projects involve altering glycosylation and lectin ligand formation in studies of the vascular and immune systems. In several instances, it is not possible to precisely predict the outcome in terms of alterations of vascular physiology or innate immune responses. Therefore genetically altered mice will be analyzed by this Core facility using standardized assays for the presence and function of cells and systems operating in immune and immunerelated vascular physiology. The goal is to ensure that subtle alterations in immune development and responses are not missed. Data obtained will provide essential baseline findings for use by the Project personnel, other Cores, as well as their collaborators. The Immune Cell Evaluation Core E (ICEC or Core E) consists of two personnel with experience in defining alterations in immune cell development, function, and the roles of leukocytes and other cells in processes involving the innate immune system and vasculature. The ICEC is fully equipped for the studies to be carried out. The Core Director has approximately 1,500 square feet of laboratory space available on the UCSD campus in the CMM-West and CMM-East buildings. The buildings are adjacent to each other, separated by approximately 200 feet of courtyard. The Core Director also has adequate animal containment space within the pathogen-free vivarium (mouse-only) on the first floor of the Cellular and Molecular Medicine (CMM)-East building. The CMM-E vivarium barrier facility includes a surgical and microinjection procedures room in addition to animal containment rooms and rooms dedicated to cage washing and reagent sterilization. This barrier houses the mice to be analyzed by Core E, as supplied by Core A and project personnel. The Core Director has IBM and Macintosh computer workstations present in the laboratory and offices with a connecting office immediately adjacent to his laboratory in CMM-W. The Core Director further maintains a two laser Becton Dickinson FACScalibur Flow Cytometer with a computer station and cell quest software for use by the Staff Research Associate of Core E, as well as tissue culture facilities for analyses of cell function as necessary. Supporting facilities of relevance to Core E include a darkroom, a cold room, and a meeting room. All Projects will make use of Core E for one or more of the analyses.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Program Projects (P01)
Project #
2P01HL057345-06
Application #
6704466
Study Section
Heart, Lung, and Blood Initial Review Group (HLBP)
Project Start
2003-02-01
Project End
2007-11-30
Budget Start
2003-02-01
Budget End
2003-11-30
Support Year
6
Fiscal Year
2003
Total Cost
$131,176
Indirect Cost
Name
University of California San Diego
Department
Type
DUNS #
804355790
City
La Jolla
State
CA
Country
United States
Zip Code
92093
Sato, Emi; Zhang, Ling-Juan; Dorschner, Robert A et al. (2017) Activation of Parathyroid Hormone 2 Receptor Induces Decorin Expression and Promotes Wound Repair. J Invest Dermatol 137:1774-1783
Johns, Scott C; Yin, Xin; Jeltsch, Michael et al. (2016) Functional Importance of a Proteoglycan Coreceptor in Pathologic Lymphangiogenesis. Circ Res 119:210-21
Mooij, Hans L; Bernelot Moens, Sophie J; Gordts, Philip L S M et al. (2015) Ext1 heterozygosity causes a modest effect on postprandial lipid clearance in humans. J Lipid Res 56:665-73
Yin, Xin; Johns, Scott C; Kim, Daniel et al. (2014) Lymphatic specific disruption in the fine structure of heparan sulfate inhibits dendritic cell traffic and functional T cell responses in the lymph node. J Immunol 192:2133-42
Chang, Yung-Chi; Olson, Joshua; Beasley, Federico C et al. (2014) Group B Streptococcus engages an inhibitory Siglec through sialic acid mimicry to blunt innate immune and inflammatory responses in vivo. PLoS Pathog 10:e1003846
Schommer, Nina N; Muto, Jun; Nizet, Victor et al. (2014) Hyaluronan breakdown contributes to immune defense against group A Streptococcus. J Biol Chem 289:26914-21
Kawamura, Tetsuya; Stephens, Bryan; Qin, Ling et al. (2014) A general method for site specific fluorescent labeling of recombinant chemokines. PLoS One 9:e81454
Muto, Jun; Morioka, Yasuhide; Yamasaki, Kenshi et al. (2014) Hyaluronan digestion controls DC migration from the skin. J Clin Invest 124:1309-19
Mooij, H L; Cabrales, P; Bernelot Moens, S J et al. (2014) Loss of function in heparan sulfate elongation genes EXT1 and EXT 2 results in improved nitric oxide bioavailability and endothelial function. J Am Heart Assoc 3:e001274
Xu, Ding; Young, Jeffrey H; Krahn, Juno M et al. (2013) Stable RAGE-heparan sulfate complexes are essential for signal transduction. ACS Chem Biol 8:1611-20

Showing the most recent 10 out of 140 publications