The functional basis of granulocyte-macrophage colony stimulating factor, interleukin-3 and interleukin-5 receptor activation, basic and clinical implications
被引:14
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作者:
Woodcock, JM
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h-index: 0
机构:
Inst Med & Vet Sci, Hanson Ctr Canc Res, Adelaide, SA 5000, AustraliaInst Med & Vet Sci, Hanson Ctr Canc Res, Adelaide, SA 5000, Australia
Woodcock, JM
[1
]
Bagley, CJ
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机构:
Inst Med & Vet Sci, Hanson Ctr Canc Res, Adelaide, SA 5000, AustraliaInst Med & Vet Sci, Hanson Ctr Canc Res, Adelaide, SA 5000, Australia
Bagley, CJ
[1
]
Lopez, AF
论文数: 0引用数: 0
h-index: 0
机构:
Inst Med & Vet Sci, Hanson Ctr Canc Res, Adelaide, SA 5000, AustraliaInst Med & Vet Sci, Hanson Ctr Canc Res, Adelaide, SA 5000, Australia
Lopez, AF
[1
]
机构:
[1] Inst Med & Vet Sci, Hanson Ctr Canc Res, Adelaide, SA 5000, Australia
来源:
INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY
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1999年
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31卷
/
10期
关键词:
inflammation;
cytokines;
receptors;
dimerization;
D O I:
10.1016/S1357-2725(99)00084-9
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
The cytokines granulocyte-macrophage colony stimulating factor, interleukin-3 and interleukin-5 have overlapping activities on cells expressing their receptors. This is explained by their sharing a receptor signal transduction subunit, beta(c). This communal signaling subunit is also required for high affinity binding of all three cytokines. Therapeutic approaches attempting to interfere or modulate haemopoietic cells using cytokines or their analogues can in some instances be limited due to functional redundancy amongst cytokines using shared receptor signaling subunits. Therefore, a better approach would be to develop therapeutics against the shared subunit. Studies examining the GM-CSF, IL-3 and IL-5 receptors have identified the key events leading to functional receptor activation. With this knowledge, it is now possible to identify new targets for the development of a new class of antagonist that blocks the biological activity of all the cytokines utilizing beta(c). This approach may be extended to other receptor systems such as IL-4 and IL-13 where receptor activation is dependent on a common signaling and binding subunit. (C) 1999 Elsevier Science Ltd. All rights reserved.
机构:
INST MED & VET SCI,HANSON CTR CANC RES,DEPT IMMUNOL,ADELAIDE,SA 5000,AUSTRALIAINST MED & VET SCI,HANSON CTR CANC RES,DEPT IMMUNOL,ADELAIDE,SA 5000,AUSTRALIA
Bagley, CJ
Woodcock, JM
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INST MED & VET SCI,HANSON CTR CANC RES,DEPT IMMUNOL,ADELAIDE,SA 5000,AUSTRALIAINST MED & VET SCI,HANSON CTR CANC RES,DEPT IMMUNOL,ADELAIDE,SA 5000,AUSTRALIA
Woodcock, JM
Stomski, FC
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机构:
INST MED & VET SCI,HANSON CTR CANC RES,DEPT IMMUNOL,ADELAIDE,SA 5000,AUSTRALIAINST MED & VET SCI,HANSON CTR CANC RES,DEPT IMMUNOL,ADELAIDE,SA 5000,AUSTRALIA
Stomski, FC
Lopez, AF
论文数: 0引用数: 0
h-index: 0
机构:
INST MED & VET SCI,HANSON CTR CANC RES,DEPT IMMUNOL,ADELAIDE,SA 5000,AUSTRALIAINST MED & VET SCI,HANSON CTR CANC RES,DEPT IMMUNOL,ADELAIDE,SA 5000,AUSTRALIA
机构:
TEL AVIV UNIV,SACKLER FAC MED,DEPT HISTOL & CELL BIOL,IL-69978 TEL AVIV,ISRAELTEL AVIV UNIV,SACKLER FAC MED,DEPT HISTOL & CELL BIOL,IL-69978 TEL AVIV,ISRAEL
RIKLIS, I
KLETTER, Y
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机构:
TEL AVIV UNIV,SACKLER FAC MED,DEPT HISTOL & CELL BIOL,IL-69978 TEL AVIV,ISRAELTEL AVIV UNIV,SACKLER FAC MED,DEPT HISTOL & CELL BIOL,IL-69978 TEL AVIV,ISRAEL
KLETTER, Y
BLEIBERG, I
论文数: 0引用数: 0
h-index: 0
机构:
TEL AVIV UNIV,SACKLER FAC MED,DEPT HISTOL & CELL BIOL,IL-69978 TEL AVIV,ISRAELTEL AVIV UNIV,SACKLER FAC MED,DEPT HISTOL & CELL BIOL,IL-69978 TEL AVIV,ISRAEL
BLEIBERG, I
FABIAN, I
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机构:
TEL AVIV UNIV,SACKLER FAC MED,DEPT HISTOL & CELL BIOL,IL-69978 TEL AVIV,ISRAELTEL AVIV UNIV,SACKLER FAC MED,DEPT HISTOL & CELL BIOL,IL-69978 TEL AVIV,ISRAEL