Show simple item record

dc.contributor.advisorLeibson, Paul J.
dc.contributor.authorBoos, Markus D.
dc.date.accessioned2011-10-26T13:13:37Z
dc.date.available2011-10-26T13:13:37Z
dc.date.issued1999
dc.identifier.urihttp://hdl.handle.net/10920/23813
dc.descriptioniv, 33 p.en_US
dc.description.abstractNatural killer (NK) cells represent a unique hematopoietic lineage in their ability to destroy tumors and virally infected cells without prior sensitization, yet details of the dual forms of NK cytotoxicity (antibody-dependent and natural cytotoxicity) remain poorly characterized. Extracellular signal related kinase (ERK) is a member of the mitogen activated protein (MAP) kinase family of enzymes that has been shown to be a necessary component of the signal cascades employed during the NK cytotoxic response. Like ERK, p38 is another MAP kinase that has been shown to regulate immune responses in assorted hematopoietic cell lines and thus also has the potential to influence NK activation. In order to test whether p38 and ERK are necessary regulators ofNK cytotoxicity, NK cells were stimulated with both free antibody and target cells, after which biochemical and functional analyses were performed. Increased MAP kinase phosphorylation after NK stimulation suggested that ERK. and p38 are involved in signal transduction associated with NK cytotoxicity. This was further supported by evidence demonstrating that NK killing decreased following selective inhibition of either kinase. Also vital to the understanding of NK cells and the role of MAP kinases in NK-mediated immunity is knowledge of upstream regulators in the biochemical pathway whose function couples surface receptor stimulation to kinase activation. Using gene transfer techniques, it was observed that the guanosine-triphosphate (GTP) binding proteins rac and rho regulate p38 and ERK in the antibody-dependent NK cytotoxic signal pathway. Experimental results reinforce previous findings concerning ERK and support the hypothesis that p38 critically influences NK cell-mediated cytotoxicity. By incorporating this information into existing knowledge of NK signal transduction and function, it will be possible to develop pharmacological strategies that increase NK activation, leading to a greater therapeutic role for the cells in the treatment of cancer and infection.en_US
dc.description.sponsorshipDepartment of Immunology. Mayo Clinic Foundation. Rochester, Minnesota.
dc.format.mimetypeapplication/pdf
dc.language.isoen_USen_US
dc.publisherKalamazoo Collegeen_US
dc.relation.ispartofKalamazoo College Biology Senior Individualized Projects Collection
dc.relation.ispartofseriesSenior Individualized Projects. Biology;
dc.rightsU.S. copyright laws protect this material. Commercial use or distribution of this material is not permitted without prior written permission of the copyright holder.
dc.titleNatural Killer Cell Cytotoxitcity is Dependent upon the MAP Kinases p38 and ERKen_US
dc.typeThesisen_US
KCollege.Access.ContactIf you are not a current Kalamazoo College student, faculty, or staff member, email dspace@kzoo.edu to request access to this thesis.


Files in this item

Thumbnail

This item appears in the following Collection(s)

  • Biology Senior Individualized Projects [1489]
    This collection includes Senior Individualized Projects (SIP's) completed in the Biology Department. Abstracts are generally available to the public, but PDF files are available only to current Kalamazoo College students, faculty, and staff.

Show simple item record