Functional analysis of KSHV GPCR in human lymphocytes
Project Number5K08AI053971-02
Former Number1K08CA083406-01A1
Contact PI/Project LeaderCANNON, MARK L
Awardee OrganizationWEILL MEDICAL COLL OF CORNELL UNIV
Description
Abstract Text
DESCRIPTION (provided by applicant): Kaposi?s sarcoma-associated herpesvirus
(KSHV/HHV-8) is closely associated with Kaposi?s sarcoma (KS), primary
effusion lymphoma (PEL), and multicentric Castleman?s disease, disorders
associated with HIV infection. KSHV encodes a G protein-coupled receptor
(GPCR) most homologous to the human IL-8 receptors CXCR1 and CXCR2.
Transcription of vGPCR has been shown in KS and PEL, and evidence in
transfected animal cell lines suggests that KSHV GPCR may be involved in KSHVmediated
angiogenesis and oncogenesis. vGPCR has not, however, been studied
in the context of PEL cell lines or any other human cell of hematopoietic
origin. Since signaling molecules behave differently in different cellular
contexts, such work will be fundamental in understanding the role of vGPCR in
KSHV-mediated disease. To this end, Dr. Cannon designed a novel single
plasmid construct that permitted development of PEL cell lines that can be
made to over-express vGPCR in a dose-dependent manner using tetracycline.
Preliminary data in these cell lines already show that vGPCR has quite
different downstream effects than in other cell lines. Namely, vGPCR causes
activation of the mitogen-activated ERK2, downregulation of stress-related
p38, and decreased cell viability. Furthermore, vGPCR upregulates NFkB and
AP-1 activity, two transcription factors intimately involved in B cell
physiology. Importantly, other KSHV genes have been shown to have AP-1 and
NFkB-responsive promoters. These cell lines are ideal tools to study the
following: 1) vGPCR signaling mechanisms and downstream effects on PEL cell
proliferation, cell cycle and apoptosis, 2) vGPCR-mediated autocrine/paracrine
effects including secretion of VEGF, bFGF, IL-6 and other cytokines known to
play a role in angiogenesis and PEL/KS biology, 3) vGPCR-mediated effects on
KSHV gene transcription and life cycle. Another major aim of the proposal is
to provide didactic and research components in a phased manner to provide the
applicant with effective training as a physician-scientist. Dr. Cannon will
be studying at the Weill Medical College and School of Medical Sciences of
Cornell University and working in the lab under the mentorship of Dr. Ethel
Cesarman of the Department of Pathology.
Public Health Relevance Statement
Data not available.
NIH Spending Category
No NIH Spending Category available.
Project Terms
G proteinKaposi's sarcomaangiogenesisapoptosisbiological signal transductioncell cyclecell linecell migrationcell proliferationclinical researchcytokinecytokine receptorsflow cytometryhuman genetic material taghuman herpesvirus 8human tissuehyperplasialymph nodeslymphomaneoplastic cellphenotypepostdoctoral investigatorprotein structure functionreceptor couplingreceptor expressionvirus protein
National Institute of Allergy and Infectious Diseases
CFDA Code
856
DUNS Number
060217502
UEI
YNT8TCJH8FQ8
Project Start Date
01-August-2002
Project End Date
30-April-2007
Budget Start Date
01-May-2003
Budget End Date
30-April-2004
Project Funding Information for 2003
Total Funding
$114,480
Direct Costs
$106,000
Indirect Costs
$8,480
Year
Funding IC
FY Total Cost by IC
2003
National Institute of Allergy and Infectious Diseases
$114,480
Year
Funding IC
FY Total Cost by IC
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