| Project/Area Number |
12670431
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| Research Category |
Grant-in-Aid for Scientific Research (C)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
内科学一般
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| Research Institution | Sapporo Medical University School of Medicin |
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Principal Investigator |
ISHIDA Sadao Sapporo Medical University School of Medicine, First department of internal medicine, instructor, 医学部, 講師 (20305220)
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| Co-Investigator(Kenkyū-buntansha) |
SASAKI Shigeru Sapporo Medical University School of Medicine, First department of internal medicine instructor, 医学部, 助手 (10305229)
ADACHI Masaaki Sapporo Medical University School of Medicine, First department of internal medicine, Association professor, 医学部, 助教授 (70240926)
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| Project Period (FY) |
2000 – 2001
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| Project Status |
Completed (Fiscal Year 2001)
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| Budget Amount *help |
¥3,400,000 (Direct Cost: ¥3,400,000)
Fiscal Year 2001: ¥1,600,000 (Direct Cost: ¥1,600,000)
Fiscal Year 2000: ¥1,800,000 (Direct Cost: ¥1,800,000)
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| Keywords | dendritic cells / LPS / PSMA3 / NAIP / IAP / immune complex / gene analysis / アポトーシス / キメラ抗体 / JNK / ERK / モノクローナル抗体 / erbB-2 |
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| Research Abstract |
Dendritic cells (DCs), are the most important antigen presenting cells. Many recent studies have compared the function of immature and mature DCs, but there have been few reports of the molecular changes that occur in DCs during maturation. Here we report differential gene expression in immature DCs generated from peripheral blood monocytes compared with mature DCs. Gene expression was evaluated using the differential display method after activation of immature DCs with a low concentration of lipopolysaccaride to induce maturation. Proteasome subunit (PSMA3), TFEC isoform, and BTK region clone 2f10-rpi were transiently up-regulated. Tryptophanyl-tRNA synthetase and CD63 antigen were up-regulated for at least 24 hours. Neuronal apoptosis inhibitory protein (NAIP) and transforming growth factor beta-induced 68 kD protein were down-regulated. This is the first report of NAIP expression in human DCs, Comparing the expression of NAIP with that of other members of the inhibitor of apoptosis protein (IAP) family and the bcl-2 family, only NAIP was strongly expressed in immature DCs before stimulation by LPS. PSMA3 was also induced in DCs stimulated with immune complex. These findings might contribute to our understanding of DC maturation and the effectiveness of DC-based vaccines.
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