Evidence map›Paper›PMID 30065627›Full record

ArticleFrontiers in molecular neuroscience2018

Ghrelin Through GHSR1a and OX1R Heterodimers Reveals a Gαs-cAMP-cAMP Response Element Binding Protein Signaling Pathway

Qingjie Xue, Bo Bai, Bingyuan Ji, Xiaoyu Chen, Chunmei Wang, Peixiang Wang, Chunqing Yang, Rumin Zhang, Yunlu Jiang, Yanyou Pan and 2 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in molecular neuroscience, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.8field-weighted citation impact, top 16% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

21 citing papers in PubMed, 33 citations in OpenAlex.

  1. Article
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  6. Article
  7. Review
  8. Review
  9. Review
  10. Article
  11. Ghrelin system in Alzheimer's disease.Current opinion in neurobiology · 2023
    Review
  12. Article
  13. "Sibling" battle or harmony: crosstalk between nesfatin-1 and ghrelin.Cellular and molecular life sciences : CMLS · 2022
    Review
  14. Review
  15. Prader-Willi syndrome: an update on obesity and endocrine problems.Annals of pediatric endocrinology & metabolism · 2021
    Article
  16. Review
  17. Article
  18. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors at 2 institutions in 2 countries.

Qingjie XueNeurobiology Institute, Jining Medical University, Jining, China.
Bo BaiNeurobiology Institute, Jining Medical University, Jining, China.
Bingyuan JiNeurobiology Institute, Jining Medical University, Jining, China.
Xiaoyu ChenDepartment of Physiology, Taishan Medical University, Taian, China.
Chunmei WangNeurobiology Institute, Jining Medical University, Jining, China.
Peixiang WangNeurobiology Institute, Jining Medical University, Jining, China.
Chunqing YangNeurobiology Institute, Jining Medical University, Jining, China.
Rumin ZhangNeurobiology Institute, Jining Medical University, Jining, China.
Yunlu JiangNeurobiology Institute, Jining Medical University, Jining, China.
Yanyou PanNeurobiology Institute, Jining Medical University, Jining, China.
Baohua ChengNeurobiology Institute, Jining Medical University, Jining, China.
Jing ChenNeurobiology Institute, Jining Medical University, Jining, China.
Jining Medical University · CNTaishan Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Growth hormone secretagogue receptor 1α (GHSR1a) and Orexin 1 receptor (OX1R) are involved in various important physiological processes, and have many similar characteristics in function and distribution in peripheral tissues and the central nervous system. We explored the possibility of heterodimerization between GHSR1a and OX1R and revealed a signal transduction pathway mechanism. In this study, bioluminescence and fluorescence resonance energy transfer and co-immunoprecipitation (Co-IP) analyses were performed to demonstrate the formation of functional GHSR1a/OX1R heterodimers. This showed that a peptide corresponding to the 5-transmembrane domain of OX1R impaired heterodimer construction. We found that ghrelin stimulated GHSR1a/OX1R heterodimer cells to increase the activation of Gαs protein, compared to the cells that express GHSR1a. Stimulation of GHSR1a/OX1R heterodimers with orexin-A did not alter GPCR interactions with Gα protein subunits. GHSR1a/OX1R heterodimers induced Gαs and downstream signaling pathway activity, including increase of cAMP-response element luciferase reporter activity and cAMP levels. In addition, ghrelin induced a higher proliferation rate in SH-SY5Y cells than in controls. This suggests that ghrelin GHSR1a/OX1R heterodimers promotes an upregulation of a Gαs-cAMP-cAMP-responsive element signaling pathway

Indexed as

allosteric signalinggrowth hormone secretagogue receptor 1α (GHSR1a)heterodimerizationneuroblastoma cell proliferationorexin type 1 receptor (OX1R)

Identifiers

PMID30065627
PMCPMC6056640
OpenAlexW2883406925

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.