? ? This revised proposal describes a five year training program for the development of an academic career in basic science and medicine. The principal investigator (PI) has completed training in Pediatric hematology-oncology at the University of Michigan and is in the first year of his appointment as Lecturer. The mentor will be David Ginsburg, an internationally recognized leader in the fields of molecular hematology and the genetics of blood clotting diseases. In addition, an advisory committee of successful senior faculty members will provide scientific and career development advice. ? ? The experiments presented focus on the roles that von Willebrand Factor (VWF) and the newly described metalloprotease ADAMTS13 play in pathogenesis of the disease thrombotic thrombocytopenic purpura (TTP). ADAMTS13 deficiency in humans causes TTP. In preliminary experiments disruption of the murine ADAMTS13 gene interestingly did not result in TTP, demonstrating additional environmental and/or genetic factors are required to induce TTP in the setting of murine ADAMTS 13 deficiency. In support of this, TTP-like finding were induced with a combination of environmental factors (shigatoxin administration) and genetic crosses (to the CASA/Rk mouse strain).
Specific aim #1 will investigate the hypothesis that ADAMTS 13 regulates VWF-mediated interactions between platelets and endothelial cells;
specific aim #2 investigates the hypothesis that environmental triggers (e.g. infection) or genetic modifiers (e.g. VWF) may trigger TTP or alter the phenotype seen in the ADAMTS13 deficient mice;
specific aim #3 investigates the hypothesis that differences in VWF physiology underlie the variable susceptibility to TTP among different mouse strains;
and specific aim #4 investigates the mechanism of action of shigatoxin in the induction of TTP-like findings. ? ? These studies have the potential to further our understanding of TTP, a complex and important disease in humans. This training will build upon the applicant's prior research experience and it is anticipated that it will lead ultimately to his transition to independent investigator. The applicant's goal is to run a successful laboratory in an academic setting and continue to develop his expertise in clinical Pediatric hematology. (End of Abstract) ? ? ? ?

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Clinical Investigator Award (CIA) (K08)
Project #
5K08HL076539-02
Application #
7278612
Study Section
Special Emphasis Panel (ZHL1-CSR-B (O1))
Program Officer
Mondoro, Traci
Project Start
2006-08-22
Project End
2011-07-31
Budget Start
2007-08-01
Budget End
2008-07-31
Support Year
2
Fiscal Year
2007
Total Cost
$126,387
Indirect Cost
Name
University of Iowa
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
062761671
City
Iowa City
State
IA
Country
United States
Zip Code
52242
Khan, M M; Motto, D G; Lentz, S R et al. (2012) ADAMTS13 reduces VWF-mediated acute inflammation following focal cerebral ischemia in mice. J Thromb Haemost 10:1665-71
Khan, Mohammad Moshahid; Gandhi, Chintan; Chauhan, Neelam et al. (2012) Alternatively-spliced extra domain A of fibronectin promotes acute inflammation and brain injury after cerebral ischemia in mice. Stroke 43:1376-82
Gandhi, Chintan; Motto, David G; Jensen, Melissa et al. (2012) ADAMTS13 deficiency exacerbates VWF-dependent acute myocardial ischemia/reperfusion injury in mice. Blood 120:5224-30
Motto, David (2012) Endothelial cells and thrombotic microangiopathy. Semin Nephrol 32:208-14
Huang, Jing; Motto, David G; Bundle, David R et al. (2010) Shiga toxin B subunits induce VWF secretion by human endothelial cells and thrombotic microangiopathy in ADAMTS13-deficient mice. Blood 116:3653-9
Chauhan, Anil K; Walsh, Meghan T; Zhu, Guojing et al. (2008) The combined roles of ADAMTS13 and VWF in murine models of TTP, endotoxemia, and thrombosis. Blood 111:3452-7