Vastagh Csaba, Rodolosse Annie, Solymosi Norbert, Farkas Imre, Auer Herbert, Sárvári Miklós, Liposits Zsolt
Laboratory of Endocrine Neurobiology, Institute of Experimental Medicine, Hungarian Academy of Sciences, Budapest, Hungary.
Neuroendocrinology. 2015;102(1-2):44-59. doi: 10.1159/000430818. Epub 2015 Apr 29.
Gonadotropin-releasing hormone (GnRH) neurons play a pivotal role in the regulation of the hypothalamic-pituitary gonadal axis in a sex-specific manner. We hypothesized that the differences seen in reproductive functions of males and females are associated with a sexually dimorphic gene expression profile of GnRH neurons.
We compared the transcriptome of GnRH neurons obtained from intact metestrous female and male GnRH-green fluorescent protein transgenic mice. About 1,500 individual GnRH neurons from each sex were sampled with laser capture microdissection followed by whole-transcriptome amplification for gene expression profiling. Under stringent selection criteria (fold change >1.6, adjusted p value 0.01), Affymetrix Mouse Genome 430 PM array analysis identified 543 differentially expressed genes. Sexual dimorphism was most apparent in gene clusters associated with synaptic communication, signal transduction, cell adhesion, vesicular transport and cell metabolism. To validate microarray results, 57 genes were selected, and 91% of their differential expression was confirmed by real-time PCR. Similarly, 88% of microarray results were confirmed with PCR from independent samples obtained by patch pipette harvesting and pooling of 30 GnRH neurons from each sex. We found significant differences in the expression of genes involved in vesicle priming and docking (Syt1, Cplx1), GABAergic (Gabra3, Gabrb3, Gabrg2) and glutamatergic (Gria1, Grin1, Slc17a6) neurotransmission, peptide signaling (Sstr3, Npr2, Cxcr4) and the regulation of intracellular ion homeostasis (Cacna1, Cacnb1, Cacng5, Kcnq2, Kcnc1).
The striking sexual dimorphism of the GnRH neuron transcriptome we report here contributes to a better understanding of the differences in cellular mechanisms of GnRH neurons in the two sexes.
促性腺激素释放激素(GnRH)神经元以性别特异性方式在下丘脑 - 垂体 - 性腺轴的调节中起关键作用。我们假设男性和女性生殖功能的差异与GnRH神经元的性别二态性基因表达谱有关。
我们比较了从处于动情后期的完整雌性和雄性GnRH - 绿色荧光蛋白转基因小鼠获得的GnRH神经元的转录组。通过激光捕获显微切割从每个性别中采样约1500个单独的GnRH神经元,然后进行全转录组扩增以进行基因表达谱分析。在严格的选择标准(倍数变化>1.6,校正p值<0.01)下,Affymetrix小鼠基因组430 PM阵列分析鉴定出543个差异表达基因。性别二态性在与突触通讯、信号转导、细胞粘附、囊泡运输和细胞代谢相关的基因簇中最为明显。为了验证微阵列结果,选择了57个基因,其中91%的差异表达通过实时PCR得到证实。同样,通过从每个性别中通过膜片吸管收集并合并30个GnRH神经元获得的独立样本进行PCR,88%的微阵列结果得到证实。我们发现参与囊泡启动和对接(Syt1、Cplx1)、GABA能(Gabra3、Gabrb3、Gabrg)和成(Gria1、Grin1、Slc17a6)神经传递、肽信号传导(Sstr3、Npr2、Cxcr4)以及细胞内离子稳态调节(Cacna1、Cacnb1、Cacng5、Kcnq2、Kcnc1)的基因表达存在显著差异。
我们在此报告的GnRH神经元转录组的显著性别二态性有助于更好地理解两性中GnRH神经元细胞机制的差异。