Kuo Ming-Wei, Lou Show-Wan, Chung Bon-chu
Institute of Molecular Biology, Academia Sinica, Taipei, Taiwan; Institute of Fisheries Science, National Taiwan University, Taipei, Taiwan.
Institute of Fisheries Science, National Taiwan University, Taipei, Taiwan.
PLoS One. 2014 May 30;9(5):e95545. doi: 10.1371/journal.pone.0095545. eCollection 2014.
GnRH neurons secrete GnRH that controls the development of the reproduction system. Despite many studies, the signals controlling the development of GnRH neurons from its progenitors have not been fully established. To understand the development of GnRH neurons, we examined the development of gnrh3-expressing cells using a transgenic zebrafish line that expresses green fluorescent protein (GFP) and LacZ driven by the gnrh3 promoter. GFP and LacZ expression recapitulated that of gnrh3 in the olfactory region, olfactory bulb and telencephalon. Depletion of gnrh3 by morpholinos led to a reduction of GFP- and gnrh3-expressing cells, while over-expression of gnrh3 mRNA increased the number of these cells. This result indicates a positive feed-forward regulation of gnrh3 cells by gnrh3. The gnrh3 cells were absent in embryos that lack Hedgehog signaling, but their numbers were increased in embryos overexpressing shhb. We manipulated the amounts of kinase that antagonizes the Hedgehog signaling pathway, protein kinase A (PKA), by treating embryos with PKA activator forskolin or by injecting mRNAs encoding its constitutively active catalytic subunit (PKA*) and dominant negative regulatory subunit (PKI) into zebrafish embryos. PKA* misexpression or forskolin treatment decreased GFP cell numbers, while PKI misexpression led to ectopic production of GFP cells. Our data indicate that the Hedgehog-PKA pathway participates in the development of gnrh3-expressing neurons during embryogenesis.
促性腺激素释放激素(GnRH)神经元分泌GnRH,其控制生殖系统的发育。尽管进行了许多研究,但控制GnRH神经元从其祖细胞发育的信号尚未完全明确。为了了解GnRH神经元的发育,我们使用了一种转基因斑马鱼品系来研究表达gnrh3的细胞的发育,该品系表达由gnrh3启动子驱动的绿色荧光蛋白(GFP)和LacZ。GFP和LacZ的表达在嗅觉区域、嗅球和端脑中重现了gnrh3的表达。用吗啉代寡核苷酸耗尽gnrh3会导致表达GFP和gnrh3的细胞数量减少,而gnrh3 mRNA的过表达会增加这些细胞的数量。这一结果表明gnrh3对gnrh3细胞具有正向反馈调节作用。在缺乏刺猬信号通路的胚胎中不存在gnrh3细胞,但在过表达shhb的胚胎中其数量增加。我们通过用PKA激活剂福斯可林处理胚胎或向斑马鱼胚胎中注射编码其组成型活性催化亚基(PKA*)和显性负性调节亚基(PKI)的mRNA来操纵拮抗刺猬信号通路的激酶蛋白激酶A(PKA)的量。PKA*的错误表达或福斯可林处理会减少GFP细胞数量,而PKI的错误表达会导致GFP细胞异位产生。我们的数据表明,刺猬 - PKA信号通路在胚胎发育过程中参与了表达gnrh3的神经元的发育。