Evidence map›Paper›PMID 35298903›Full record

ArticleCell metabolism2022

Protein tyrosine phosphatase receptor δ serves as the orexigenic asprosin receptor.

Ila Mishra, Wei Rose Xie, Juan C Bournat, Yang He, Chunmei Wang, Elizabeth Sabath Silva, Hailan Liu, Zhiqiang Ku, Yinghua Chen, Bernadette O Erokwu and 7 more

Open access · greenAbstract read
In one paragraph

Article in Cell metabolism, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
5.1field-weighted citation impact, top 3% 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

35 citing papers in PubMed, 51 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Asprosin activates multiple placental pathwaysMolecular medicine reports · 2025
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. The cerebellum modulates thirst.Nature neuroscience · 2024
    Article
  19. Review
  20. Article
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

17 authors at 4 institutions in 1 country.

Ila MishraHarrington Discovery Institute, Cleveland, OH, USA.
Wei Rose XieHarrington Discovery Institute, Cleveland, OH, USA.
Juan C BournatDepartment of Molecular and Cellular Biology, Baylor College of Medicine, Houston, TX, USA.
Yang HeDepartment of Molecular and Cellular Biology, Baylor College of Medicine, Houston, TX, USA; USDA-ARS Children's Nutrition Research Center, Department of Pediatrics, Baylor College of Medicine, Houston, TX, USA.
Chunmei WangDepartment of Molecular and Cellular Biology, Baylor College of Medicine, Houston, TX, USA; USDA-ARS Children's Nutrition Research Center, Department of Pediatrics, Baylor College of Medicine, Houston, TX, USA.
Elizabeth Sabath SilvaHarrington Discovery Institute, Cleveland, OH, USA.
Hailan LiuDepartment of Molecular and Cellular Biology, Baylor College of Medicine, Houston, TX, USA; USDA-ARS Children's Nutrition Research Center, Department of Pediatrics, Baylor College of Medicine, Houston, TX, USA.
Zhiqiang KuBrown Foundation Institute of Molecular Medicine, The University of Texas Health Science Center at Houston, Houston, TX, USA.
Yinghua ChenDepartment of Physiology and Biophysics, Case Western Reserve University, Cleveland, OH, USA.
Bernadette O ErokwuDepartments of Radiology, Biomedical Engineering, and Pediatrics, Case Western Reserve University, Cleveland, OH, USA.
Peilin JiaCenter for Precision Health, School of Biomedical Informatics, The University of Texas Health Science Center at Houston, Houston, TX, USA.
Zhongming ZhaoCenter for Precision Health, School of Biomedical Informatics, The University of Texas Health Science Center at Houston, Houston, TX, USA.
Zhiqiang AnBrown Foundation Institute of Molecular Medicine, The University of Texas Health Science Center at Houston, Houston, TX, USA.
Chris A FlaskDepartments of Radiology, Biomedical Engineering, and Pediatrics, Case Western Reserve University, Cleveland, OH, USA.
Yanlin HeDepartment of Molecular and Cellular Biology, Baylor College of Medicine, Houston, TX, USA; USDA-ARS Children's Nutrition Research Center, Department of Pediatrics, Baylor College of Medicine, Houston, TX, USA; Pennington Biomedical Research Center, Louisiana State University, Baton Rouge, LA, USA.
Yong XuDepartment of Molecular and Cellular Biology, Baylor College of Medicine, Houston, TX, USA; USDA-ARS Children's Nutrition Research Center, Department of Pediatrics, Baylor College of Medicine, Houston, TX, USA.
Atul R ChopraHarrington Discovery Institute, Cleveland, OH, USA; Department of Medicine, Case Western Reserve University, Cleveland, OH, USA; Department of Genetics and Genome Sciences, Case Western Reserve University, Cleveland, OH, USA. Electronic address: atul.chopra@case.edu.
Case Western Reserve University · USBrown Foundation · USThe University of Texas Health Science Center at Houston · USBaylor College of Medicine · US

Funding

Research BaseP30DK072476 · NIDDK · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI ROBERT A KESTERSON · 2005 to 2026
$26.5M
The CNS Receptor For AsprosinR01DK130931 · NIDDK · CASE WESTERN RESERVE UNIVERSITY · PI CHOPRA, ATUL · 2022 to 2025
$2.2M
Asprosin, body weight, and risk of type 2 diabetes in U.S. men and womenR01DK125403 · NIDDK · UNIVERSITY OF CALIFORNIA-IRVINE · PI CHOPRA, ATUL, LIU, SIMIN · 2020 to 2022
$2.1M
ASPROSIN NEUTRALIZATION AS A NOVEL ANTI-OBESITY TREATMENTR01DK118290 · NIDDK · CASE WESTERN RESERVE UNIVERSITY · PI CHOPRA, ATUL · 2018 to 2022
$2.0M
The Role of FBN1 in mammalian energy balanceK08DK102529 · NIDDK · CASE WESTERN RESERVE UNIVERSITY · PI CHOPRA, ATUL · 2014 to 2018
$761k
NIDDK NIH HHS K08 DK102529NIDDK NIH HHS P30 DK072476NIDDK NIH HHS R01 DK118290NIDDK NIH HHS R01 DK125403NIDDK NIH HHS R01 DK130931
6 · The paper itself

Abstract

Asprosin is a fasting-induced glucogenic and centrally acting orexigenic hormone. The olfactory receptor Olfr734 is known to be the hepatic receptor for asprosin that mediates its effects on glucose production, but the receptor for asprosin's orexigenic function has been unclear. Here, we have identified protein tyrosine phosphatase receptor δ (Ptprd) as the orexigenic receptor for asprosin. Asprosin functions as a high-affinity Ptprd ligand in hypothalamic AgRP neurons, regulating the activity of this circuit in a cell-autonomous manner. Genetic ablation of Ptprd results in a strong loss of appetite, leanness, and an inability to respond to the orexigenic effects of asprosin. Ablation of Ptprd specifically in AgRP neurons causes resistance to diet-induced obesity. Introduction of the soluble Ptprd ligand-binding domain in the circulation of mice suppresses appetite and blood glucose levels by sequestering plasma asprosin. Identification of Ptprd as the orexigenic asprosin receptor creates a new avenue for the development of anti-obesity therapeutics.

Indexed as

Peptide HormonesReceptor-Like Protein Tyrosine Phosphatases, Class 2AdipokinesAgouti-Related ProteinAnimalsFibrillin-1GlucoseLigandsMiceObesityPeptide FragmentsAdipokinesAgouti-Related ProteinFbn1 protein, mouseFibrillin-1GlucoseLigandsPeptide FragmentsPeptide HormonesPtprd protein, mouseReceptor-Like Protein Tyrosine Phosphatases, Class 2AgRPappetiteasprosinhypothalamusmetabolismobesityPtprdreceptor

Identifiers

PMID35298903
PMCPMC8986618
OpenAlexW4221086066

What OpenQuestion holds

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Registered trials

None linked

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.