THE INTERLEUKIN-1 FAMILY - 10 YEARS OF DISCOVERY

被引:719
作者
DINARELLO, CA [1 ]
机构
[1] TUFTS UNIV, SCH MED, DEPT MED, BOSTON, MA 02111 USA
关键词
CYTOKINES; TUMOR NECROSIS FACTOR; RECEPTOR ANTAGONIST; APOPTOSIS; INFLAMMATION;
D O I
10.1096/fasebj.8.15.8001745
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Ten years ago the cloning of two interleukin-l molecules (IL-1 alpha and IL-1 beta) resolved the question of whether a single polypeptide could evoke a wide variety of biological effects. During the past decade, the biology of IL-1 has greatly expanded our understanding of how the host responds to external challenges, such as injury and infection, as well as its role in several diseases. We learned of the remarkable potency of IL-1 in the femtomolar range and of its ability to induce a response by triggering only one or two receptors per cell. Unexpectedly, the IL-1 family of genes, receptors and associated molecules have been linked to those of Drosophila, nematodes, and microorganisms and IL-1 signal transduction is similar to that observed after cellular stress. The cloning of IL-1 opened other avenues of fundamental biological interest. For example, in addition to the two agonist molecules IL-1 alpha and IL-1 beta, a third member of the IL-1 gene family is a specific, high affinity receptor antagonist (IL-I receptor antagonist). That this third member of the IL-1 family inhibits the other two is characteristic of the tight control over production and activity exerted on IL-1. Although IL-1 contributes to the pathogenesis of many diseases, a small amount appears to be needed to combat infection and inititate healing processes. This article highlights 10 years of discoveries on IL-1.-Dinarello, C.A. The interleukin-l family: 10 years of discovery.
引用
收藏
页码:1314 / 1325
页数:12
相关论文
共 128 条
[1]
INTERLEUKIN-1 STIMULATES ITS OWN RECEPTOR EXPRESSION ON HUMAN-FIBROBLASTS THROUGH THE ENDOGENOUS PRODUCTION OF PROSTAGLANDIN(S) [J].
AKAHOSHI, T ;
OPPENHEIM, JJ ;
MATSUSHIMA, K .
JOURNAL OF CLINICAL INVESTIGATION, 1988, 82 (04) :1219-1224
[2]
A SOLUBLE RECEPTOR FOR INTERLEUKIN-1-BETA ENCODED BY VACCINIA VIRUS - A NOVEL MECHANISM OF VIRUS MODULATION OF THE HOST RESPONSE TO INFECTION [J].
ALCAMI, A ;
SMITH, GL .
CELL, 1992, 71 (01) :153-167
[3]
ANTONI G, 1986, J IMMUNOL, V137, P3201
[4]
CYTOKINES AND CYTOKINE INHIBITORS OR ANTAGONISTS IN RHEUMATOID-ARTHRITIS [J].
AREND, WP ;
DAYER, JM .
ARTHRITIS AND RHEUMATISM, 1990, 33 (03) :305-315
[5]
INTERLEUKIN-1 RECEPTOR ANTAGONIST [J].
AREND, WP .
ADVANCES IN IMMUNOLOGY, VOL 54, 1993, 54 :167-227
[6]
NUCLEOTIDE-SEQUENCE OF HUMAN MONOCYTE INTERLEUKIN-1 PRECURSOR CDNA [J].
AURON, PE ;
WEBB, AC ;
ROSENWASSER, LJ ;
MUCCI, SF ;
RICH, A ;
WOLFF, SM ;
DINARELLO, CA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1984, 81 (24) :7907-7911
[7]
BAKOUCHE O, 1987, J IMMUNOL, V138, P4249
[8]
BELIZARIO JE, 1991, CANCER RES, V51, P2379
[9]
CYTOTOXICITY OF HUMAN PI-7 INTERLEUKIN-1 FOR PANCREATIC-ISLETS OF LANGERHANS [J].
BENDTZEN, K ;
MANDRUPPOULSEN, T ;
NERUP, J ;
NIELSEN, JH ;
DINARELLO, CA ;
SVENSON, M .
SCIENCE, 1986, 232 (4757) :1545-1547
[10]
ALTERNATIVE PROMOTER USAGE OF THE FOS-RESPONSIVE GENE FIT-1 GENERATES MESSENGER-RNA ISOFORMS CODING FOR EITHER SECRETED OR MEMBRANE-BOUND PROTEINS RELATED TO THE IL-1 RECEPTOR [J].
BERGERS, G ;
REIKERSTORFER, A ;
BRASELMANN, S ;
GRANINGER, P ;
BUSSLINGER, M .
EMBO JOURNAL, 1994, 13 (05) :1176-1188