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2010 (PDF) - The College of Veterinary Medicine at Cornell University

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Daniel Woodburn, Virginia-Maryland Regional <strong>College</strong> <strong>of</strong> <strong>Veterinary</strong> <strong>Medicine</strong><br />

Characteriz<strong>at</strong>ion <strong>of</strong> Microparticle-Derived Thrombin Gener<strong>at</strong>ion in Hypocoagulable<br />

Dogs<br />

I fi rst learned <strong>of</strong> the Leadership Program when Dr. Philip Carter, a program<br />

facilit<strong>at</strong>or, visited Virginia Tech and gave a brief recruitment present<strong>at</strong>ion. I<br />

submitted my applic<strong>at</strong>ion on somewh<strong>at</strong> <strong>of</strong> a whim. Thankfully I was accepted and<br />

could not have been more impressed with the experience I’ve had <strong>at</strong> <strong>Cornell</strong>.<br />

My research focused largely on the gener<strong>at</strong>ion <strong>of</strong> thrombin in canine plasma.<br />

Thrombin is produced by the cleavage <strong>of</strong> prothrombin in the penultim<strong>at</strong>e reaction <strong>of</strong><br />

the coagul<strong>at</strong>ion cascade; its primary function is the activ<strong>at</strong>ion <strong>of</strong> fi brinogen, leading<br />

to the form<strong>at</strong>ion <strong>of</strong> a fi brin clot. Reactions leading to the form<strong>at</strong>ion <strong>of</strong> thrombin<br />

occur largely on neg<strong>at</strong>ively charged phospholipid surfaces, including pl<strong>at</strong>eletderived<br />

microparticles. During the course <strong>of</strong> the summer, I prepared pl<strong>at</strong>elet-free<br />

plasma as well as plasma free <strong>of</strong> both pl<strong>at</strong>elets and microparticles in order to<br />

study the effects <strong>of</strong> microparticles on thrombin gener<strong>at</strong>ion in a variety <strong>of</strong> dogs<br />

with hypocoagulability disorders. Surprisingly, I observed th<strong>at</strong> microparticles from<br />

Factor IX defi cient (Hemophilia B) plasma possessed gre<strong>at</strong>er thrombin gener<strong>at</strong>ing<br />

potential than those from normal plasma. I found the research fascin<strong>at</strong>ing because it has signifi cant implic<strong>at</strong>ions for<br />

understanding the p<strong>at</strong>hophisiology <strong>of</strong> coagul<strong>at</strong>ion disorders and possibly developing future tre<strong>at</strong>ments.<br />

I would like to thank the following individuals: Dr. McGregor, Dr. Fraser, and all <strong>of</strong> the facilit<strong>at</strong>ors for providing such a<br />

wonderful learning experience; Dr. C<strong>at</strong>alfamo, Dr. Brooks, and their team <strong>at</strong> the Coagul<strong>at</strong>ion lab for putting up with<br />

me; the other students in the program for the fun times; and lastly Henry, Quanta, and Ned, without whom none <strong>of</strong><br />

this would be possible.<br />

Sirima Yaemsiri, North Carolina St<strong>at</strong>e <strong>University</strong>, Reproductive Biology<br />

Organiz<strong>at</strong>ion and Possible Functional Role <strong>of</strong> GM1-Enriched Membrane Domains in<br />

Murine Epididymis<br />

After an in-fi eld research project with World Wildlife Fund on the migr<strong>at</strong>ion p<strong>at</strong>terns<br />

<strong>of</strong> forest elephants in Cameroon, I realized the potential impact <strong>of</strong> research on<br />

wildlife conserv<strong>at</strong>ion efforts, human popul<strong>at</strong>ions, and ecosystem dynamics. I hope<br />

to apply inform<strong>at</strong>ion gained from basic science research to clinically relevant issues<br />

facing thre<strong>at</strong>ened and endangered species in order to help improve both veterinary<br />

care and conserv<strong>at</strong>ion management str<strong>at</strong>egies. <strong>The</strong> Leadership Program has<br />

helped me broadened my labor<strong>at</strong>ory skill set and introduced me to leaders in the<br />

research fi eld <strong>of</strong> my interest.<br />

<strong>The</strong> Travis Lab studies male germ cell biology in the hopes <strong>of</strong> improving human<br />

reproductive health as well as preserving genetic diversity in wildlife. My project<br />

<strong>at</strong>tempts to understand the mechanism through which mammalian sperm become<br />

transl<strong>at</strong>ionally active and competent during epididymal transit. Membrane rafts are<br />

functional membrane domains, highly enriched in sterols and sphingolipids such as<br />

ganglioside GM1 and are currently hypothesized to play a role in the m<strong>at</strong>ur<strong>at</strong>ional<br />

process <strong>of</strong> sperm. Immunohistological experiments with murine epididymis showed localiz<strong>at</strong>ion <strong>of</strong> GM1 in epithelial<br />

cells <strong>of</strong> the initial segment and distal caput segment. Using several markers, we found th<strong>at</strong> in the initial segment,<br />

GM1 was specifi cally localized in narrow cells, which are known to contribute to the modul<strong>at</strong>ion <strong>of</strong> the intraluminal<br />

microenvironment. This evidence suggests th<strong>at</strong> GM1-enriched membrane domains might be involved in epididymal<br />

sperm m<strong>at</strong>ur<strong>at</strong>ion.<br />

I would like to thank Drs. Alex Travis and Atsushi Asano for their guidance and mentorship throughout the project, as<br />

well as the entire Travis Lab for their continued support and good humor.<br />

34 www.vet.cornell.edu/oge/leadership

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