Laboratory of Biotechnology and Genomics, Department of Swine and Small Ruminant Breeding, Agricultural University, 31-274 Krakow, Poland.
J Endocrinol. 2011 Jan;208(1):81-8. doi: 10.1677/JOE-10-0282. Epub 2010 Oct 20.
Suppressors of cytokine signalling (SOCS) negatively regulate cytokine-induced signalling pathways and may be involved in leptin and prolactin (PRL) interactions. Herein, we examined the effect of PRL on SOCS-3 mRNA expression in pituitary explants and investigated whether leptin could modify the expression of SOCS-3 mRNA in pituitary explants. In the first experiment, we used pituitaries isolated from 16 ewes decapitated in March, May, July and October (four per month). Tissues were cut into 50 mg explants, which were treated with control or medium containing PRL (100 or 300 ng/ml). Incubation was maintained for different time intervals: 0, 60, 120, 180, 240 or 300 min. Real-time PCR was used to measure SOCS-3 mRNA levels. In the second study, we used 24 ewes surgically fitted with third ventricle cannulas (12 were used during the long-day period, and 12 were used during the short-day (SD) period). Each ewe was administered an i.c.v. injection of Ringer-Locke buffer or leptin (0.5 or 1.0 μg/kg body weight). Explants of anterior pituitaries were collected and snap frozen 1 h after injection. Semi-quantitative expression of SOCS-3 mRNA was performed using reverse transcription-PCR. PRL stimulated SOCS-3 expression in the pituitaries collected in March (P<0.05) and May (P<0.01 and P<0.05 for lower and higher doses respectively), inhibited SOCS-3 expression in pituitaries collected in July (P<0.01) and had no effect in pituitaries collected in October. Treatment with leptin increased SOCS-3 expression during the SDs in a dose-dependent manner (P<0.01). The results demonstrated that photoperiod may be involved in leptin and PRL effects on SOCS-3 expression in sheep.
细胞因子信号转导抑制因子(SOCS)负调控细胞因子诱导的信号通路,可能参与瘦素和催乳素(PRL)的相互作用。在此,我们研究了 PRL 对垂体组织中 SOCS-3 mRNA 表达的影响,并探讨了瘦素是否可以调节垂体组织中 SOCS-3 mRNA 的表达。在第一个实验中,我们使用了 3 月、5 月、7 月和 10 月(每月 4 只)被断头处死的 16 只母羊的垂体。将组织切成 50mg 的小块,用对照培养基或含有 PRL(100 或 300ng/ml)的培养基处理。孵育时间不同:0、60、120、180、240 或 300min。采用实时 PCR 法测定 SOCS-3 mRNA 水平。在第二个研究中,我们使用了 24 只接受第三脑室套管手术的母羊(长日周期 12 只,短日周期 12 只)。每只母羊均接受 i.c.v. 注射林格氏液或瘦素(0.5 或 1.0μg/kg 体重)。注射后 1h 采集垂体前叶组织并迅速冷冻。采用逆转录-PCR 法检测 SOCS-3 mRNA 的半定量表达。3 月(P<0.05)和 5 月(低剂量和高剂量分别为 P<0.01 和 P<0.05)采集的垂体中 PRL 刺激 SOCS-3 表达(P<0.05),7 月采集的垂体中 PRL 抑制 SOCS-3 表达(P<0.01),10 月采集的垂体无影响。在短日周期中,瘦素以剂量依赖的方式增加 SOCS-3 表达(P<0.01)。结果表明,光照周期可能参与了瘦素和 PRL 对绵羊 SOCS-3 表达的影响。