The Murine Hematology/Coagulation Core's primary function is to check for hematological and related metabolic abnormalities in the different mouse strains produced by different Projects. The following tasks will be carried out by this core: 1) Identifying abnormalities in blood cell number and morphology, and abnormalities in hemostasis. Measurements will include: a) Hematological parameters: quantitation of red blood cells, white blood cells (including subsets), and platelets in whole blood. b) Hemostatic parameters: bleeding time, prothrombin time (PT), activated partial thromboplastin time (APTT), and thrombin time. c) Fibrinolytic parameters: dilute whole blood clot lysis time. d) Anticoagulation parameters: protein C, protein S and antithrombin activities. 2) Identifying abnormalities in endothelial cell function with respect to hemostasis. The effect of genetically altered endothelial cell surface glycosaminoglycans (project #5) upon blood coagulation and fibrinolysis will be assessed by use of endothelial cell cultures derived from different tissues of control and transgenic mice. Cell surface related activities of tissue factor/VIIa, antithrombin, TFPI, and plasminogen will be measured. If the endothelium-targeted transgenic mice produced in projects #1 and 4 show evidence of thrombosis, similar studies will be carried out with the corresponding tissue cell cultures. 3) Screening for abnormalities of liver function and other metabolic derangements. A panel of chemistry tests will be established to evaluate the overall function of the liver and the metabolic status of control and transgenic mice. When abnormal test results are found in one of these screening tests, further studies will be performed as needed, in close co- operation with the individual project leaders.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Program Projects (P01)
Project #
5P01HL057345-02
Application #
6110814
Study Section
Project Start
1998-09-01
Project End
1999-08-31
Budget Start
1997-10-01
Budget End
1998-09-30
Support Year
2
Fiscal Year
1998
Total Cost
Indirect Cost
Name
University of California San Diego
Department
Type
DUNS #
077758407
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

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