Universidade de Sao Paulo, Instituto de Ciencias Biomedicas, Departamento de Fisiologia e Biofísica, Sao Paulo 05508000, Brazil.
Edison Biotechnology Institute and Heritage College of Osteopathic Medicine, Ohio University, Athens, OH 45701, USA.
Neurosci Lett. 2022 Jan 23;770:136402. doi: 10.1016/j.neulet.2021.136402. Epub 2021 Dec 17.
Growth hormone (GH) receptor (GHR) signaling induces the phosphorylation of the signal transducer and activator of transcription 5 (pSTAT5) in the cells of several tissues including in the hypothalamus. During pregnancy, several STAT5-recruiting hormones (e.g., prolactin, GH and placental lactogens) are highly secreted. However, the precise contribution of GHR signaling to the surge of pSTAT5 immunoreactive neurons that occurs in the hypothalamus of pregnant mice is currently unknown. Thus, the objective of the present study was to determine whether GHR expression in neurons is required for inducing pSTAT5 expression in several hypothalamic nuclei during pregnancy. Initially, we demonstrated that late pregnant C57BL/6 mice (gestational day 14 to 18) exhibited increased pulsatile GH secretion compared to virgin females. Next, we confirmed that neuron-specific GHR ablation robustly reduces hypothalamic Ghr mRNA levels and prevents GH-induced pSTAT5 in the arcuate, paraventricular and ventromedial hypothalamic nuclei. Subsequently, the number of pSTAT5 immunoreactive cells was determined in the hypothalamus of late pregnant mice. Although neuron-specific GHR ablation did not affect the number of pSTAT5 immunoreactive cells in the paraventricular nucleus of the hypothalamus, reduced pSTAT5 expression was observed in the arcuate and ventromedial nuclei of pregnant neuron-specific GHR knockouts, compared to control pregnant mice. In summary, a subset of hypothalamic neurons requires GHR signaling to express pSTAT5 during pregnancy. These findings contribute to the understanding of the endocrine factors that affect the activation of transcription factors in the brain during pregnancy.
生长激素 (GH) 受体 (GHR) 信号在包括下丘脑在内的几种组织的细胞中诱导信号转导和转录激活物 5(pSTAT5) 的磷酸化。在怀孕期间,几种 STAT5 募集激素(例如,催乳素、GH 和胎盘催乳素)高度分泌。然而,目前尚不清楚 GHR 信号对怀孕小鼠下丘脑中发生的 pSTAT5 免疫反应性神经元激增的确切贡献。因此,本研究的目的是确定神经元中的 GHR 表达是否需要在怀孕期间诱导几个下丘脑核中的 pSTAT5 表达。最初,我们证明了晚孕 C57BL/6 小鼠(妊娠第 14 至 18 天)与处女雌性相比表现出增加的脉冲式 GH 分泌。接下来,我们证实神经元特异性 GHR 缺失强烈降低下丘脑 Ghr mRNA 水平并防止 GH 诱导的弓状核、室旁核和腹内侧核中的 pSTAT5。随后,确定了晚孕小鼠下丘脑内 pSTAT5 免疫反应性细胞的数量。尽管神经元特异性 GHR 缺失不影响下丘脑室旁核中 pSTAT5 免疫反应性细胞的数量,但与对照孕鼠相比,怀孕神经元特异性 GHR 敲除小鼠的弓状核和腹内侧核中 pSTAT5 表达减少。总之,一些下丘脑神经元需要 GHR 信号在怀孕期间表达 pSTAT5。这些发现有助于了解在怀孕期间影响大脑中转录因子激活的内分泌因素。