| Project/Area Number |
02670291
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| Research Category |
Grant-in-Aid for General Scientific Research (C)
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| Allocation Type | Single-year Grants |
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| Research Field |
内科学一般
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| Research Institution | Kanazawa Medical University |
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Principal Investigator |
SHIMIZU Shiro Kanazawa Med. Univ. Internal Med. Associate Prof., 医学部, 助教授 (50097432)
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| Co-Investigator(Kenkyū-buntansha) |
FUKUTOKU Masaaki Kanazawa Med. Univ., Internal Med. Assistant Prof., 医学部, 助手 (20218944)
YOSHIOKA Ritshko Kanazawa Med. Univ., Internal Med. Assistant Prof., 医学部, 助手 (30200950)
TACHIBANA Junko Kanazawa Med. Univ., Internal Med. Assistant Prof., 医学部, 助手 (70163475)
SAWADA Makoto Kanazawa Med. Univ., Internal Med. Assistant Prof., 医学部, 助手 (50170824)
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| Project Period (FY) |
1990 – 1991
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| Project Status |
Completed (Fiscal Year 1991)
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| Budget Amount *help |
¥2,100,000 (Direct Cost: ¥2,100,000)
Fiscal Year 1991: ¥700,000 (Direct Cost: ¥700,000)
Fiscal Year 1990: ¥1,400,000 (Direct Cost: ¥1,400,000)
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| Keywords | Multiple Myeloma / Paracrine Growth / Autocrine Growth / Factor-independent Growth / IL-6 / Macrophage / Adhesion Receptors / パラクリン機構 / オ-トクリン機構 / 白血球接着分子 |
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| Research Abstract |
The growth mechanisms of multipje myeloma cells were studied utilizing ten estabhshed human multiple myeloma cell lines and molecular biological methods.
1. Ten human multiple myeloma cell lines were established using macrophages as a feeder layer. Four of them were derived from bone marrow and the other 6 from extrarnedullary lesions.
2. Bone marrow-derived ceU. 1ines grew dependently on a macrophage feeder layer or in response to interleuldn-6(IL-6). In contrast, extrameduffary lesion-derived cell lines grew independent of any feeder layers or cytokines.
3. All cell lines constitutively expressed IL-6 receptor (IL-6R) mRNA and cell surface IL-6R.
4. All cell lines except for AMO1 prolfferated in response to IL-6. Bone marrow-derived cell lines proliferated absolutely dependently on IL-6. Spontaneously proliferating extramedullary-lesion derived cell lines additively proliferated in response to IL-6.
5. No cell lines constitutively expressed IL-6 mRNA nor secreted IL-6.
6. The anti-IL-6 antibody or anti-IL-6R antibody inhibited only IL-6-induced proliferation, but did not inhibit the spontaneous proliferation of extramedullary lesion-derived cell lines.
These results indicate that the IL-6 paracrine mechanism plays the central role in the growth of bone marrow-derived cell lines. In contrast, the factor-independent mechanism plays a primary role in the growth of extra meduffary lesion-derived cell lines, that also additively proliferate in response to IL-6 (paracrine mechanisms). Because no IL-6 mRNA was detected in any cell lines, the intracellular autocrine mechanism or autocrine mechanisim appeared not to be operating in any of the cell lines.
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