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lantz

Chris Lantz

Associate Professor of Biology

A.A.S. - Blue Ridge Community College
B.S. - James Madison University
Ph.D. - Medical College of Virginia


E-mail - lantz2cs@jmu.edu
Phone - 540-568-2840
Fax - 540-568-3333

Office - 110 Burruss
 


Courses:   Cell and Molecular Biology (Bio 214), Immunology (BIO 442/542), Virology (BIO 444/544)


Research Interests:  Allergy and Inflammation

Mast cells are critical participants in allergic disorders (e.g. anaphylaxis, asthma, hay fever) and in host defense against certain parasites. Following immunological activation in tissues, these cells release histamine and a variety of biologically active proteins that contribute to many of the characteristic signs and symptoms of these diseases. The research activities of this laboratory are focused on the cellular and molecular biology of mast cells and on proteins that contribute to allergies and inflammation called interleukins. One of the best ways to study the biological function of proteins thought to be involved in mast cell biology and inflammation is to examine mice that have been genetically engineered to lack a functional copy of a particular gene. Accordingly, much of the research in this laboratory involves the use of 'knockout' mice deficient in interleukin-3 and/or the receptor for interleukin-4. Obviously, understanding the biology of mast cells and interleukins has therapeutic implications. From a more basic science perspective, these studies represent a powerful model system to examine fundamental mechanisms in immunobiology.


Selected Publications:

K. Kimura, C.H. Song, A. Rastogi, G. Dranoff, S.J. Galli & C.S. Lantz. 2006. Interleukin-3 and c-Kit/stem cell factor are required for normal eosinophil responses in mice infected with Strongyloides venezuelensis. Laboratory Investigation. 86: 987-996.

Neel, N.F., Creasy, B.M., Rankin, J.N., Pierce, E.M., McCoy, M.E., Daner, R.H., Fowler, J.A., Daniel, J.C., Lantz, C.S. 2004. Absence of interleukin-3 does not affect the severity of local and systemic anaphylaxis but does enhance eosinophil infliltration in a mouse model of allergic peritonitis. Immunology Letters. 95: 37-44.

Shelburne, C.P., McCoy, M.E. (JMU student), Piekorz, R., Sexl, V., Roh, K-H., Jacobs-Helber, S.M., Gillespie, S.R., Bailey, D.P., Mirmonsef, P., Mann, M.N., Kashyap, M., Wright, H.V., Chong, H.J., Bouton, L.A., Barnstein, B., Ramirez, C.D., Bunting, K.D., Sawyer, S.T., Lantz, C.S., Ryan, J.J. 2003. Stat5 expression is critical for mast cell development and survival. Blood. 102: 1290-1297.

Shelburne C.P., McCoy M.E. (JMU student), Piekorz, R., Sexl V.V., Gillespie S.R., Bailey D.P., Gharse A., Mirmonsef P., Mann M.N., Kashyap M., Wright H.V., Chong H.J., Bouton L A., Ramirez C.D., Lantz C.S., Ryan J.J. 2002. Stat5: an essential regulator of mast cell biology. Molecular Immunology. 38: 1187-1191.

Lantz, C.S., Galli, S.J. 2001. Mast cell and basophil development. In: Zon, L., ed. Hematopoiesis: A Developmental Approach. Oxford University Press, New York, pp. 461-475.




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For information contact:
Sheila Santee
540-568-6225 or 6733
Dept. Fax: 540-568-3333
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Jon Monroe
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Department of Biology
MSC 7801
James Madison University
Harrisonburg, VA  22807   USA
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Burruss Hall, Room 243
James Madison University
Harrisonburg, VA  22807   USA

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