Multiple Sclerosis Program, Department of Neurology, School of Medicine, University of California, Los Angeles, CA 90095, USA.
Neuroscience. 2013 Aug 15;245:166-78. doi: 10.1016/j.neuroscience.2013.04.017. Epub 2013 Apr 15.
In addition to androgen differences between males and females, there are genetic differences that are caused by unequal dosage of sex chromosome genes. Using the cuprizone-induced demyelination model, we recently showed that surgical gonadectomy of adult mice resulted in decreased normal myelination and remyelination compared to gonadally intact animals, suggesting a supporting role for sex hormones in the maintenance of myelination. However, inherent sex differences in normal myelination and remyelination persisted even after gonadectomy, with males consistently remyelinating to a lesser extent relative to normal myelination as assayed by axon conduction and immunohistochemistry. This suggests a potential role for the sex chromosome complement in mediating the differential rates of remyelination observed in males and females. The present study focuses on the impact that sex chromosomes might have on these myelination differences. Making use of the four core-genotype mice and cuprizone-diet induced demyelination/remyelination paradigm, our results demonstrate sex chromosome-mediated asymmetry between XX and XY mice. The rate of functional remyelination following cuprizone diet-induced callosal demyelination in four core-genotype mice is attenuated in XY compared to XX animals of both gonadal sexes. Importantly, this difference arises only in the absence of circulating sex hormones following gonadectomy and confirms the role of sex hormones in the remyelination process reported earlier by our group. Because a genotype-mediated difference only arises following gonadectomy, the chromosomal contribution to myelination and remyelination is subtle yet significant. To explain this difference, we propose a possible asymmetry in the expression of myelination-related genes in XX vs. XY mice that needs to be investigated in future studies.
除了男性和女性之间的雄激素差异外,还有由性染色体基因剂量不均等引起的遗传差异。我们最近使用杯状醇诱导的脱髓鞘模型表明,与性腺完整的动物相比,成年小鼠的性腺切除术导致正常髓鞘形成和髓鞘再生减少,这表明性激素在维持髓鞘形成中起支持作用。然而,即使在性腺切除术后,正常髓鞘形成和髓鞘再生也存在固有的性别差异,与正常髓鞘形成相比,雄性的髓鞘再生程度始终较小,这可以通过轴突传导和免疫组织化学来评估。这表明性染色体组成在介导雄性和雌性观察到的髓鞘再生率差异方面具有潜在作用。本研究侧重于性染色体可能对这些髓鞘差异产生的影响。利用四种核心基因型小鼠和杯状醇饮食诱导的脱髓鞘/髓鞘再生范式,我们的研究结果表明性染色体介导了 XX 和 XY 小鼠之间的不对称性。在四种核心基因型小鼠中,在环枕带脱髓鞘后用杯状醇饮食诱导的功能再髓鞘化的速度在 XY 中比 XX 动物的性腺性别都要慢。重要的是,这种差异仅在性腺切除术后没有循环性激素时才会出现,这证实了性激素在我们小组之前报道的髓鞘再生过程中的作用。由于只有在性腺切除术后才会出现基因型介导的差异,因此染色体对髓鞘形成和髓鞘再生的贡献是微妙而显著的。为了解释这种差异,我们提出了 XX 与 XY 小鼠中与髓鞘形成相关的基因表达可能存在不对称性的假设,这需要在未来的研究中进行调查。