Regulation of Ghrelin Production and Food Intake by Gastric Adenylyl Cyclase Type 8

IF 4 2区 生物学 Q2 CELL BIOLOGY
Shaohong Wu, Handan Deng, Ruili Yu, Quan Yu, Wei Li, Yawen Zhao, Ke Yang, Luyang Gao, Geyang Xu
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Abstract

Ghrelin is a peptide hormone primarily produced by ghrelin cells in the stomach, playing a vital role in the regulation of eating behavior. Adenyl cyclase 8 (ADCY8), a key downstream signaling factor of G protein-coupled receptors, is essential for maintaining energy homeostasis by modulating levels of cyclic adenosine monophosphate (cAMP). Nevertheless, how ADCY8 modulates ghrelin levels and affects food intake is not well understood. Our findings demonstrated that Adcy8−/− mice exhibited elevated levels of ghrelin and increased food consumption under both normal and high-fat diet conditions. These changes were associated with a reduction in the activity of the cAMP-PKA-mTOR signaling pathway within the gastric mucosa. The administration of the ghrelin receptor antagonist d-Lys-3-GH-releasing peptide-6 significantly decreased calorie intake in both wild-type and Adcy8−/− mice. Furthermore, forskolin was shown to inhibit ghrelin and calorie intake in normal mice, an effect that was absent in Adcy8−/− mice. Treatment with forskolin or overexpression of Adcy8 in both primary ghrelin-producing cells and mHypoE-42 cells resulted in decreased ghrelin levels, accompanied by activation of the cAMP-PKA-mTOR signaling pathway. Conversely, the use of the inhibitor SQ22536 or knockdown of Adcy8 produced opposing effects. In conclusion, gastric ADCY8 regulates the expression and secretion of ghrelin via the cAMP-PKA-mTOR signaling pathway, thereby influencing food intake.

Abstract Image

胃腺苷酸环化酶8型对胃饥饿素产生和摄食的调节
胃饥饿素是一种主要由胃饥饿素细胞产生的肽激素,在调节饮食行为中起着至关重要的作用。腺苷环化酶8 (ADCY8)是G蛋白偶联受体的关键下游信号因子,通过调节环磷酸腺苷(cAMP)的水平来维持能量稳态。然而,ADCY8如何调节胃饥饿素水平和影响食物摄入还不是很清楚。我们的研究结果表明,Adcy8 - / -小鼠在正常和高脂肪饮食条件下均表现出ghrelin水平升高和食物消耗增加。这些变化与胃粘膜内cAMP-PKA-mTOR信号通路活性的降低有关。ghrelin受体拮抗剂d- lys -3- gh -释放肽-6显著降低了野生型和Adcy8 - / -小鼠的卡路里摄入量。此外,在正常小鼠中,forskolin被证明可以抑制胃饥饿素和卡路里的摄入,而在Adcy8 - / -小鼠中没有这种作用。用forskolin或Adcy8在原代生长素产生细胞和mHypoE-42细胞中过表达导致生长素水平下降,并伴有cAMP-PKA-mTOR信号通路的激活。相反,使用抑制剂SQ22536或敲低Adcy8会产生相反的效果。综上所述,胃ADCY8通过cAMP-PKA-mTOR信号通路调节胃饥饿素的表达和分泌,从而影响食物摄入。
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来源期刊
CiteScore
14.70
自引率
0.00%
发文量
256
审稿时长
1 months
期刊介绍: The Journal of Cellular Physiology publishes reports of high biological significance in areas of eukaryotic cell biology and physiology, focusing on those articles that adopt a molecular mechanistic approach to investigate cell structure and function. There is appreciation for the application of cellular, biochemical, molecular and in vivo genetic approaches, as well as the power of genomics, proteomics, bioinformatics and systems biology. In particular, the Journal encourages submission of high-interest papers investigating the genetic and epigenetic regulation of proliferation and phenotype as well as cell fate and lineage commitment by growth factors, cytokines and their cognate receptors and signal transduction pathways that influence the expression, integration and activities of these physiological mediators. Similarly, the Journal encourages submission of manuscripts exploring the regulation of growth and differentiation by cell adhesion molecules in addition to the interplay between these processes and those induced by growth factors and cytokines. Studies on the genes and processes that regulate cell cycle progression and phase transition in eukaryotic cells, and the mechanisms that determine whether cells enter quiescence, proliferate or undergo apoptosis are also welcomed. Submission of papers that address contributions of the extracellular matrix to cellular phenotypes and physiological control as well as regulatory mechanisms governing fertilization, embryogenesis, gametogenesis, cell fate, lineage commitment, differentiation, development and dynamic parameters of cell motility are encouraged. Finally, the investigation of stem cells and changes that differentiate cancer cells from normal cells including studies on the properties and functions of oncogenes and tumor suppressor genes will remain as one of the major interests of the Journal.
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