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神经肽 W 作为一种生理性促肾上腺皮质素释放因子在雄性小鸡中的作用证据。

Evidence for Neuropeptide W Acting as a Physiological Corticotropin-releasing Inhibitory Factor in Male Chickens.

机构信息

Key Laboratory of Bio-resources and Eco-environment of Ministry of Education, College of Life Sciences, Sichuan University, Chengdu, China.

College of Life Science, Sichuan Agricultural University, Ya'an, China.

出版信息

Endocrinology. 2022 Jul 1;163(7). doi: 10.1210/endocr/bqac073.

DOI:10.1210/endocr/bqac073
PMID:35583189
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9170129/
Abstract

In vertebrates, adrenocorticotropin (ACTH), released by the pituitary gland, is a critical part of the stress axis and stress response. Generally, the biosynthesis and secretion of ACTH are controlled by both hypothalamic stimulatory factors and inhibitory factors [eg, ACTH-releasing inhibitory factor (CRIF)], but the identity of this CRIF remains unrevealed. We characterized the neuropeptide B (NPB)/neuropeptide W (NPW) system in chickens and found that NPW could directly target the pituitary to inhibit growth hormone (GH) and prolactin (PRL) secretion via neuropeptide B/W receptor 2 (NPBWR2), which is completely different from the mechanism in mammals. The present study first carried out a series of assays to investigate the possibility that NPW acts as a physiological CRIF in chickens. The results showed that (1) NPW could inhibit ACTH synthesis and secretion by inhibiting the 3',5'-cyclic adenosine 5'-monophosphate/protein kinase A signaling cascade in vitro and in vivo; (2) NPBWR2 was expressed abundantly in corticotrophs (ACTH-producing cells), which are located mainly in cephalic lobe of chicken pituitary, as demonstrated by single-cell RNA-sequencing, immunofluorescent staining, and fluorescence in situ hybridization; (3) dexamethasone could stimulate pituitary NPBWR2 and hypothalamic NPW expression in chicks, which was accompanied by the decease of POMC messenger RNA levels, as revealed by in vitro and subcutaneous injection assays; and (4) the temporal expression profiles of NPW-NPBWR2 pair in hypothalamus-pituitary axis and POMC in pituitary were almost unanimous in chicken. Collectively, these findings provide comprehensive evidence for the first time that NPW is a potent physiological CRIF in chickens that plays a core role in suppressing the activity of the stress axis.

摘要

在脊椎动物中,脑垂体分泌的促肾上腺皮质激素(ACTH)是应激轴和应激反应的关键部分。一般来说,ACTH 的生物合成和分泌受下丘脑刺激因子和抑制因子的控制[例如,ACTH 释放抑制因子(CRIF)],但这种 CRIF 的身份仍未被揭示。我们对鸡的神经肽 B(NPB)/神经肽 W(NPW)系统进行了表征,发现 NPW 可以通过神经肽 B/W 受体 2(NPBWR2)直接靶向垂体,抑制生长激素(GH)和催乳素(PRL)的分泌,这与哺乳动物的机制完全不同。本研究首先进行了一系列实验,以研究 NPW 是否可以作为鸡的一种生理性 CRIF。结果表明:(1)NPW 可以通过抑制 3',5'-环磷酸腺苷/蛋白激酶 A 信号级联反应,在体外和体内抑制 ACTH 的合成和分泌;(2)NPBWR2 在促皮质素细胞(产生 ACTH 的细胞)中大量表达,这一点通过单细胞 RNA 测序、免疫荧光染色和荧光原位杂交得到证实,这些细胞主要位于鸡垂体的头部;(3)地塞米松可以刺激小鸡垂体 NPBWR2 和下丘脑 NPW 的表达,同时伴有 POMC 信使 RNA 水平的降低,这一点通过体外和皮下注射实验得到证实;(4)NPW-NPBWR2 对在鸡的下丘脑-垂体轴和垂体中的 POMC 的表达时间谱几乎完全一致。综上所述,这些发现首次提供了全面的证据,证明 NPW 是鸡中一种有效的生理性 CRIF,在抑制应激轴的活性方面发挥着核心作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/36d1/9170129/b0eb982a6586/bqac073_fig10.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/36d1/9170129/db0d1e48914f/bqac073_fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/36d1/9170129/45e9f178e1ab/bqac073_fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/36d1/9170129/7aff1f907cd0/bqac073_fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/36d1/9170129/aa09939e339c/bqac073_fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/36d1/9170129/5b627322e44e/bqac073_fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/36d1/9170129/34637884baef/bqac073_fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/36d1/9170129/fb6f9510050c/bqac073_fig7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/36d1/9170129/b00284b53e83/bqac073_fig8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/36d1/9170129/b1559b5732ef/bqac073_fig9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/36d1/9170129/b0eb982a6586/bqac073_fig10.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/36d1/9170129/db0d1e48914f/bqac073_fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/36d1/9170129/45e9f178e1ab/bqac073_fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/36d1/9170129/7aff1f907cd0/bqac073_fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/36d1/9170129/aa09939e339c/bqac073_fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/36d1/9170129/5b627322e44e/bqac073_fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/36d1/9170129/34637884baef/bqac073_fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/36d1/9170129/fb6f9510050c/bqac073_fig7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/36d1/9170129/b00284b53e83/bqac073_fig8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/36d1/9170129/b1559b5732ef/bqac073_fig9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/36d1/9170129/b0eb982a6586/bqac073_fig10.jpg

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