دورية أكاديمية
Characterization of the Kaposi's sarcoma-associated herpesvirus K1 signalosome
| العنوان: | Characterization of the Kaposi's sarcoma-associated herpesvirus K1 signalosome |
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| المؤلفون: | Lee, Bok-Soo, Lee, Sun-Hwa, Feng, Pinghui, Chang, Heesoon, Cho, Nam-Hyuk, Jung, Jae U. |
| المساهمون: | 이복수, 이선화, 장희순, 조남혁, 정재유 |
| بيانات النشر: | American Society for Microbiology |
| سنة النشر: | 2005 |
| المجموعة: | Seoul National University: S-Space |
| مصطلحات موضوعية: | Amino Acid Motifs, Calcium/analysis, Cell Cycle Proteins/metabolism, Cell Line, Cytokines/analysis, Cytoplasm/chemistry, DNA Mutational Analysis, DNA-Binding Proteins/metabolism, Enzyme Precursors/metabolism, Herpesvirus 8, Human/*physiology, Humans, Intracellular Signaling Peptides and Proteins, NFATC Transcription Factors, Nuclear Proteins/metabolism, Phospholipase C gamma, Phosphorylation, Protein Binding, Protein Phosphatase 1, Protein Tyrosine Phosphatases/metabolism, Protein-Tyrosine Kinases/metabolism, Proto-Oncogene Proteins/metabolism, Proto-Oncogene Proteins c-vav, Transcription Factor AP-1/metabolism, Transcription Factors/metabolism, Type C Phospholipases/metabolism, Tyrosine/metabolism, Viral Proteins/genetics/metabolism/*physiology, src-Family Kinases/metabolism, Signal Transduction |
| الوصف: | Kaposi's sarcoma (KS) is a multifocal angiogenic tumor and appears to be a hyperplastic disorder caused, in part, by local production of inflammatory cytokines. The K1 lymphocyte receptor-like protein of KS-associated herpesvirus (KSHV) efficiently transduces extracellular signals to elicit cellular activation events through its cytoplasmic immunoreceptor tyrosine-based activation motif (ITAM). To further delineate K1-mediated signal transduction, we purified K1 signaling complexes and identified its cellular components. Upon stimulation, the K1 ITAM was efficiently tyrosine phosphorylated and subsequently interacted with cellular Src homology 2 (SH2)-containing signaling proteins Lyn, Syk, p85, PLCgamma2, RasGAP, Vav, SH2 domain-containing protein tyrosine phosphatase 1/2, and Grab2 through its phosphorylated tyrosine residues. Mutational analysis demonstrated that each tyrosine residue of K1 ITAM contributed to the interactions with cellular signaling proteins in distinctive ways. Consequently, these interactions led to the marked augmentation of cellular signal transduction activity, evidenced by the increase of cellular tyrosine phosphorylation and intracellular calcium mobilization, the activation of NF-AT and AP-1 transcription factor activities, and the production of inflammatory cytokines. These results demonstrate that KSHV K1 effectively recruits a set of cellular SH2-containing signaling molecules to form the K1 signalosome, which elicits downstream signal transduction and induces inflammatory cytokine production. |
| نوع الوثيقة: | article in journal/newspaper |
| اللغة: | English |
| العلاقة: | J Virol. 2005 Oct;79(19):12173-84.; 0022-538X (Print); http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&dopt=Citation&list_uids=16160144Test; https://hdl.handle.net/10371/29617Test |
| DOI: | 10.1128/JVI.79.19.12173-12184.2005 |
| الإتاحة: | https://doi.org/10.1128/JVI.79.19.12173-12184.2005Test https://hdl.handle.net/10371/29617Test http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&dopt=Citation&list_uids=16160144Test |
| رقم الانضمام: | edsbas.56FF25FA |
| قاعدة البيانات: | BASE |
| DOI: | 10.1128/JVI.79.19.12173-12184.2005 |
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