Department of Pharmacology, School of Medicine, University of Maryland Baltimore, Baltimore, Maryland 21201, USA.
J Neurosci. 2013 Feb 13;33(7):2761-72. doi: 10.1523/JNEUROSCI.1268-12.2013.
Brain sexual differentiation in rodents results from the perinatal testicular androgen surge. In the preoptic area (POA), estradiol aromatized from testosterone upregulates the production of the proinflammatory molecule, prostaglandin E(2) (PGE(2)) to produce sex-specific brain development. PGE(2) produces a two-fold greater density of dendritic spines in males than in females and masculinizes adult copulatory behavior. One neonatal dose of PGE(2) masculinizes the POA and behavior, and simultaneous treatment with an inhibitor of additional prostaglandin synthesis prevents this masculinization, indicating a positive feedforward process that leads to sustained increases in PGE(2). The mechanisms underlying this feedforward process were unknown. Microglia, the primary immunocompetent cells in the brain, are active neonatally, contribute to normal brain development, and both produce and respond to prostaglandins. We investigated whether there are sex differences in microglia in the POA and whether they influence developmental masculinization. Neonatal males had twice as many ameboid microglia as females and a more activated morphological profile, and both estradiol and PGE(2) masculinized microglial number and morphology in females. Microglial inhibition during the critical period for sexual differentiation prevented sex differences in microglia, estradiol-induced masculinization of dendritic spine density, and adult copulatory behavior. Microglial inhibition also prevented the estradiol-induced upregulation of PGE(2), indicating that microglia are essential to the feedforward process through which estradiol upregulates prostaglandin production. These studies demonstrate that immune cells in the brain interact with the nervous and endocrine systems during development, and are crucial for sexual differentiation of brain and behavior.
啮齿动物的大脑性别分化源于围产期睾丸雄激素激增。在视前区(POA)中,睾丸酮转化的雌二醇上调促炎性分子前列腺素 E2(PGE2)的产生,从而产生性别特异性的大脑发育。PGE2 使雄性大脑中的树突棘密度增加一倍,而使雌性大脑中的树突棘密度增加一倍,并使成年雄性交配行为雄性化。单次新生剂量的 PGE2 可使 POA 和行为雄性化,同时用额外的前列腺素合成抑制剂进行治疗可防止这种雄性化,表明存在正向反馈过程,从而导致 PGE2 的持续增加。这种正向反馈过程的机制尚不清楚。小胶质细胞是大脑中主要的免疫活性细胞,在新生儿期活跃,有助于正常的大脑发育,并且既能产生又能对前列腺素作出反应。我们研究了 POA 中小胶质细胞是否存在性别差异,以及它们是否会影响发育中的雄性化。新生雄性的阿米巴样小胶质细胞数量是雌性的两倍,其形态更活跃,雌二醇和 PGE2 均使雌性的小胶质细胞数量和形态雄性化。在性别分化的关键时期进行小胶质细胞抑制可防止小胶质细胞、雌二醇诱导的树突棘密度雄性化以及成年雄性交配行为的性别差异。小胶质细胞抑制还阻止了雌二醇诱导的 PGE2 上调,表明小胶质细胞是雌激素上调前列腺素产生的正向反馈过程所必需的。这些研究表明,大脑中的免疫细胞在发育过程中与神经和内分泌系统相互作用,对于大脑和行为的性别分化至关重要。