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The posterior pituitary expresses the serotonin receptor 2C

机译:后脑后脑脊液表达血清素受体2C

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摘要

The serotonin receptor 2C (5HT2C) is an important drug target to treat obesity and depression. Its pre-mRNA undergoes alternative splicing, encoding a short RNA1 isoform that is localized intracellularly and a full-length isoform (RNA2) that can reach the cell membrane. These splicing isoforms are deregulated in Prader-Willi syndrome (PWS), due to the loss of a trans-acting regulatory RNA, SNORD115. Here we show that the 5HT2C mRNA is expressed in the posterior pituitary, suggesting that 5HT2C mRNA is generated in the hypothalamus and subsequently conveyed by axonal transport. In the pituitary, the ratio of 5HT2C isoforms is regulated by feeding, and can be manipulated using a splice-site changing oligonucleotide injected into the blood. The pituitary expression of the 5HT2C mRNA may constitute a previously unknown mechanism whereby serotonin in the circulation or drugs targeting the 5HT2C might induce side-effects. Finally, the deregulation of 5HT2C splicing isoforms in PWS could contribute to the known hormonal imbalances.
机译:血清素受体2C(5HT2C)是治疗肥胖和抑郁的重要药物靶标。其前mRNA经历替代剪接,编码局部化的短RNA1同种型,其可以到达细胞膜的全长同种型(RNA2)。这些拼接同种型在PRADER-WILLI综合征(PWS)中都是管制的,由于失效调节RNA,SnORD115的丧失。在这里,我们表明5HT2C mRNA在后脑后表达,表明5HT2C mRNA在下丘脑中产生,随后通过轴突运输传达。在垂体中,通过进料来调节5HT2C同种型的比例,并且可以使用注入血液中的剪接部位改变的寡核苷酸来操纵。 5HT2C mRNA的垂体表达可以构成先前未知的机制,其中靶向5HT2C的循环或药物中的血清素可能会诱导副作用。最后,PWS中5HT2C剪接同种型的放松管制可能有助于已知的激素失衡。

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