Growth hormone augments superoxide anion secretion of human neutrophils by binding to the prolactin receptor.
Growth hormone augments superoxide anion secretion of human neutrophils by binding to the prolactin receptor.
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生长激素通过与催乳素受体结合来增强人中性粒细胞的超氧阴离子分泌。
DOI:
10.1172/jci115605
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发表时间:
1992
期刊:
影响因子:
--
通讯作者:
Kelley,KW
中科院分区:
文献类型:
--
作者:
Fu,YK;Arkins,S;Fuh,G;Cunningham,BC;Wells,JA;Fong,S;Cronin,MJ;Dantzer,R;Kelley,KW
Recombinant human growth hormone (HuGH) and human prolactin (HuPRL), but not GH of bovine or porcine origin, prime human neutrophils for enhanced superoxide anion (O2-) secretion. Since HuGH, but not GH of other species, effectively binds to the HuPRL receptor (HuPRL-R), we used a group of HuGH variants created by site-directed mutagenesis to identify the receptor on human neutrophils responsible for HuGH priming. A monoclonal antibody (MAb) directed against the HuPRL-R completely abrogated O2- secretion by neutrophils incubated with either HuGH or HuPRL, whereas a MAb to the HuGH-R had no effect. The HuGH variant K172A/F176A, which has reduced affinity for both the HuGH-binding protein (BP) and the HuPRL-BP, was unable to prime human neutrophils. This indicates that priming is initiated by a ligand-receptor interaction, the affinity of which is near that defined for receptors for PRL and GH. Another HuGH variant, K168A/E174A, which has relatively low affinity for the HuPRL-BP but slightly increased affinity for the HuGH-BP, had much reduced ability to prime neutrophils. In contrast, HuGH variant E56D/R64M, which has a similar affinity as wild-type HuGH for the HuPRL-BP but a lower affinity for the HuGH-BP, primed neutrophils as effectively as the wild-type HuGH. Finally, binding of HuGH to the HuPRL-BP but not to the HuGH-BP has been shown to be zinc dependent, and priming of neutrophils by HuGH was also responsive to zinc. Collectively, these data directly couple the binding of HuGH to the HuPRL-R with one aspect of functional activation of human target cells.Images
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影响因子:
4.8
作者:
É. Nagy;I. Bérczi
通讯作者:
I. Bérczi
影响因子:
4.4
作者:
I. Bérczi;É. Nagy;S. M. de Toledo;R. Matusik;H. Friesen
通讯作者:
H. Friesen
DOI:
--
发表时间:
1984
期刊:
Journal of immunology (Baltimore, Md. : 1950)
影响因子:
--
作者:
Winchurch,RA;Thomas,DJ;Adler,WH;Lindsay,TJ
通讯作者:
Lindsay,TJ
影响因子:
4.8
作者:
Freemark,M;Comer,M;Korner,G;Handwerger,S
通讯作者:
Handwerger,S
DOI:
--
发表时间:
1991
期刊:
Journal of immunology (Baltimore, Md. : 1950)
影响因子:
--
作者:
Fu,YK;Arkins,S;Wang,BS;Kelley,KW
通讯作者:
Kelley,KW