Physical association of G(i2)alpha with interleukin-8 receptors

被引:74
|
作者
Damaj, BB
McColl, SR
Mahana, W
Crouch, MF
Naccache, PH
机构
[1] CHU LAVAL,CTR RECH RHUMATOL & IMMUNOL,CTR RECH,ST FOY,PQ G1V 4G2,CANADA
[2] UNIV LAVAL,FAC MED,DEPT MED,ST FOY,PQ G1V 4G2,CANADA
[3] UNIV ADELAIDE,DEPT MICROBIOL & IMMUNOL,ADELAIDE,SA 5001,AUSTRALIA
[4] NIAID,IMMUNOGENET LAB,NIH,ROCKVILLE,MD 20852
[5] AUSTRALIAN NATL UNIV,JOHN CURTIN SCH MED RES,DIV NEUROSCI,CANBERRA,ACT 2601,AUSTRALIA
关键词
D O I
10.1074/jbc.271.22.12783
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
Interleukin-8 (IL-8), one of the major mediators of the inflammatory response, belongs to a family of chemokines that includes NAP-2 (neutrophil-activating peptide-2) and Gro-alpha and whose biological activities are directed to a great extent toward neutrophils. Two distinct receptors have been described with overlapping, but not identical, binding affinities for IL-8, NAP-2, and Gro-alpha. This study was designed to examine the intracellular pathways activated upon the occupation of each of the IL-8 receptors (IL-8R). The formation of a physical coupling between IL-8 receptors and the alpha-subunit of heterotrimeric G proteins was tested in neutrophils by examining the presence of the former in anti-G alpha immune precipitates. The addition of IL-8 to a suspension of human neutrophils led to a time-dependent detection of IL-8 in anti-G(i2)alpha (raised against amino acids 159-168 (LERIAQSDYI) of G(i2)alpha) and anti-G(t) alpha (raised against the COOH-terminal 10 amino acids (KENLKDCGLF) of G(t) alpha), but not anti-G(q), immunoprecipitates. Similar results were obtained in human 293 cells stably transfected with IL-8RA or IL-8RB. The peptide derived from the COOH-terminal sequence of G(t) inhibited the co-immunoprecipitation of IL-8R and G(i) observed in response to the anti-G(t) alpha and anti-G(i2)alpha antibodies. On the other hand, the G(i2)alpha peptide only inhibited the immunoprecipitation induced by the anti-G(i2)alpha antibody. Peptides derived from G(i1)alpha or G(i3)alpha had no effect in this assay. The introduction of the anti-G(i2)alpha or anti-(t) alpha antibodies or their neutralizing peptides, but not the G(i1)alpha or G(i3)alpha peptides, into 293 IL-8RA or 293 IL-8RB cells completely blocked the calcium responses obtained upon stimulation with IL-8. These results demonstrate that the occupation of either type of IL-8 receptor leads to a physical coupling to the alpha-subunit of G(i2). In addition, the use of the subunit-specific peptides identified two functionally important but distinct regions of G(i) alpha, one involved in receptor/G(i) alpha interaction (KENLKDCGLF) and the other mediating downstream signal transmission (LERIAQSDYI). Finally, the results of this study also validate the use of the transfected 293 cell line as a model for the study of the signal transduction pathway(s) initiated by IL-8.
引用
收藏
页码:12783 / 12789
页数:7
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