UMR 788 INSERM and University Paris-Sud, 94276 Kremlin-Bicêtre, France.
Neuroscience. 2013 Feb 12;231:111-24. doi: 10.1016/j.neuroscience.2012.11.039. Epub 2012 Dec 2.
Progesterone has been shown to exert pleiotropic actions in the brain of both male and females. In particular, after traumatic brain injury (TBI), progesterone has important neuroprotective effects. In addition to intracellular progesterone receptors, membrane receptors of the hormone such as membrane progesterone receptor (mPR) may also be involved in neuroprotection. Three mPR subtypes (mPRα, mPRβ, and mPRγ) have been described and mPRα is best characterized pharmacologically. In the present study we investigated the distribution, cellular localization and the regulation of mPRα in male mouse and rat brain. We showed by reverse transcription-PCR that mPRα is expressed at similar levels in the male and female mouse brain suggesting that its expression may not be influenced by steroid levels. Treatment of males by estradiol or progesterone did not modify the level of expression of mPRα as shown by Western blot analysis. In situ hybridization and immunohistochemistry analysis showed a wide expression of mPRα in particular in the olfactory bulb, striatum, cortex, thalamus, hypothalamus, septum, hippocampus and cerebellum. Double immunofluorescence and confocal microscopy analysis showed that mPRα is expressed by neurons but not by oligodendrocytes and astrocytes. In the rat brain, the distribution of mPRα was similar to that observed in mouse brain; and after TBI, mPRα expression was induced in oligodendrocytes, astrocytes and reactive microglia. The wide neuroanatomical distribution of mPRα suggests that this receptor may play a role beyond neuroendocrine and reproductive functions. However, in the absence of injury its role might be restricted to neurons. The induction of mPRα after TBI in microglia, astrocytes and oligodendrocytes, points to a potential role in mediating the modulatory effects of progesterone in inflammation, ion and water homeostasis and myelin repair in the injured brain.
孕激素在雄性和雌性动物的大脑中表现出多种作用。特别是在创伤性脑损伤(TBI)后,孕激素具有重要的神经保护作用。除了细胞内孕激素受体外,激素的膜受体,如膜孕激素受体(mPR),也可能参与神经保护。已经描述了三种 mPR 亚型(mPRα、mPRβ和 mPRγ),并且 mPRα 在药理学上得到了最好的描述。在本研究中,我们研究了 mPRα 在雄性小鼠和大鼠大脑中的分布、细胞定位和调节。通过逆转录-PCR 显示,mPRα 在雄性和雌性小鼠大脑中的表达水平相似,表明其表达可能不受类固醇水平的影响。用雌二醇或孕酮处理雄性小鼠不会改变 mPRα 的表达水平,如 Western blot 分析所示。原位杂交和免疫组织化学分析显示 mPRα 在特定的嗅球、纹状体、皮质、丘脑、下丘脑、隔室、海马体和小脑中有广泛的表达。双免疫荧光和共聚焦显微镜分析显示 mPRα 由神经元表达,但不由少突胶质细胞和星形胶质细胞表达。在大鼠大脑中,mPRα 的分布与在小鼠大脑中观察到的相似;并且在 TBI 后,mPRα 在少突胶质细胞、星形胶质细胞和反应性小胶质细胞中被诱导。mPRα 在神经解剖学上的广泛分布表明,该受体的作用可能超出神经内分泌和生殖功能。然而,在没有损伤的情况下,其作用可能仅限于神经元。mPRα 在小胶质细胞、星形胶质细胞和少突胶质细胞中的诱导表明,它在调节孕激素在炎症、离子和水稳态以及损伤大脑中的髓鞘修复中的调节作用方面可能发挥作用。