Sun Fen, Nguyen Trinh, Jin Xin, Huang Renqi, Chen Zhenglan, Cunningham Rebecca L, Singh Meharvan, Su Chang
Department of Pharmacology and Neuroscience, University of North Texas Health Science Center, Fort Worth, Texas 76107.
Endocrinology. 2016 May;157(5):2067-79. doi: 10.1210/en.2015-1610. Epub 2016 Mar 18.
Progesterone (P4) exerts robust cytoprotection in brain slice cultures (containing both neurons and glia), yet such protection is not as evident in neuron-enriched cultures, suggesting that glia may play an indispensable role in P4's neuroprotection. We previously reported that a membrane-associated P4 receptor, P4 receptor membrane component 1, mediates P4-induced brain-derived neurotrophic factor (BDNF) release from glia. Here, we sought to determine whether glia are required for P4's neuroprotection and whether glia's roles are mediated, at least partially, via releasing soluble factors to act on neighboring neurons. Our data demonstrate that P4 increased the level of mature BDNF (neuroprotective) while decreasing pro-BDNF (potentially neurotoxic) in the conditioned media (CMs) of cultured C6 astrocytes. We examined the effects of CMs derived from P4-treated astrocytes (P4-CMs) on 2 neuronal models: 1) all-trans retinoid acid-differentiated SH-SY5Y cells and 2) mouse primary hippocampal neurons. P4-CM increased synaptic marker expression and promoted neuronal survival against H2O2. These effects were attenuated by Y1036 (an inhibitor of neurotrophin receptor [tropomysin-related kinase] signaling), as well as tropomysin-related kinase B-IgG (a more specific inhibitor to block BDNF signaling), which pointed to BDNF as the key protective component within P4-CM. These findings suggest that P4 may exert its maximal protection by triggering a glia-neuron cross talk, in which P4 promotes mature BDNF release from glia to enhance synaptogenesis as well as survival of neurons. This recognition of the importance of glia in mediating P4's neuroprotection may also inform the design of effective therapeutic methods for treating diseases wherein neuronal death and/or synaptic deficits are noted.
孕酮(P4)在脑片培养物(包含神经元和神经胶质细胞)中具有强大的细胞保护作用,但这种保护在富含神经元的培养物中并不明显,这表明神经胶质细胞可能在P4的神经保护作用中发挥不可或缺的作用。我们之前报道过,一种膜相关的P4受体,即P4受体膜成分1,介导P4诱导的神经胶质细胞释放脑源性神经营养因子(BDNF)。在此,我们试图确定神经胶质细胞是否是P4神经保护作用所必需的,以及神经胶质细胞的作用是否至少部分是通过释放可溶性因子作用于邻近神经元来介导的。我们的数据表明,P4增加了培养的C6星形胶质细胞条件培养基(CMs)中成熟BDNF(具有神经保护作用)的水平,同时降低了前体BDNF(可能具有神经毒性)的水平。我们研究了来自P4处理的星形胶质细胞的CMs(P4-CMs)对两种神经元模型的影响:1)全反式视黄酸分化的SH-SY5Y细胞和2)小鼠原代海马神经元。P4-CM增加了突触标记物的表达,并促进神经元抵抗H2O2的存活。这些作用被Y1036(神经营养因子受体[原肌球蛋白相关激酶]信号抑制剂)以及原肌球蛋白相关激酶B-IgG(一种更特异性的阻断BDNF信号的抑制剂)减弱,这表明BDNF是P4-CM中的关键保护成分。这些发现表明,P4可能通过触发神经胶质细胞-神经元的相互作用来发挥其最大保护作用,其中P4促进神经胶质细胞释放成熟BDNF,以增强突触形成以及神经元的存活。认识到神经胶质细胞在介导P4神经保护作用中的重要性,也可能为设计治疗出现神经元死亡和/或突触缺陷疾病的有效治疗方法提供思路。