Pulsatile and Sustained Gonadotropin-releasing Hormone (GnRH) Receptor Signaling DOES THE Ca2+/NFAT SIGNALING PATHWAY DECODE GnRH PULSE FREQUENCY?

被引:37
|
作者
Armstrong, Stephen P. [1 ]
Caunt, Christopher J. [1 ]
Fowkes, Robert C. [2 ]
Tsaneva-Atanasova, Krasimira [3 ]
McArdle, Craig A. [1 ]
机构
[1] Univ Bristol, Dept Clin Sci S Bristol, Labs Integrat Neurosci & Endocrinol, Bristol BS1 3NY, Avon, England
[2] Univ London Royal Vet Coll, Endocrine Signalling Grp, London NW1 0TU, England
[3] Univ Bristol, Dept Engn Math, Bristol Ctr Appl Nonlinear Math, Bristol BS8 1TR, Avon, England
基金
英国惠康基金; 英国生物技术与生命科学研究理事会;
关键词
DYNAMIN-DEPENDENT INTERNALIZATION; DUAL-SPECIFICITY PHOSPHATASES; SUBUNIT GENE-TRANSCRIPTION; C-TERMINAL TAIL; LUTEINIZING-HORMONE; DIFFERENTIAL REGULATION; PULSE-FREQUENCY; SPATIOTEMPORAL REGULATION; ALPHA-T3-1; GONADOTROPES; RECOMBINANT ADENOVIRUS;
D O I
10.1074/jbc.M109.063917
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
Gonadotropin-releasing hormone (GnRH) acts via 7 transmembrane region receptors on gonadotrophs to stimulate synthesis and secretion of the luteinizing hormone and follicle-stimulating hormone. It is secreted in pulses, and its effects depend on pulse frequency, but decoding mechanisms are unknown. Here we have used (nuclear factor of activated T-cells 2 (NFAT2)-emerald fluorescent protein) to monitor GnRH signaling. Increasing [Ca2+](i) causes calmodulin/calcineurin-dependent nuclear NFAT translocation, a response involving proteins (calmodulins and NFATs) that decode frequency in other systems. Using live cell imaging, pulsatile GnRH caused dose- and frequency-dependent increases in nuclear NFAT2-emerald fluorescent protein, and at low frequency, translocation simply tracked GnRH exposure (albeit with slower kinetics). At high frequency (30-min intervals), failure to return to basal conditions before repeat stimulation caused integrative tracking, illustrating how the relative dynamics of up- and downstream signals can increase efficiency of GnRH action. Mathematical modeling predicted desensitization of GnRH effects on [Ca2+](i) and that desensitization would increase with dose, frequency, and receptor number, but no such desensitization was seen in HeLa and/or L beta T2 cells possibly because pulsatile GnRH did not reduce receptor expression (measured by immunofluorescence). GnRH also caused dose-and frequency-dependent activation of alpha GSU, luteinizing hormone beta, and follicle-stimulating hormone beta luciferase reporters, effects that were blocked by calcineurin inhibition. Pulsatile GnRH also activated an NFAT-responsive luciferase reporter, but this response was directly related to cumulative pulse duration. This together with the lack of desensitization of translocation responses suggests that NFAT may mediate GnRH action but is not a genuine decoder of GnRH pulse frequency.
引用
收藏
页码:35746 / 35757
页数:12
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