Ptprf is the conserved receptor for Asprosin’s glucogenic effects in vertebrates

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Authors: Zhiquan Liu, Pengyu Wang, Yixuan Hu, Nan Zhang, Liting Xu, Tao Kang, Shengyou Zhao, Deping Zhao, Chibun Chan, Jianzhen Li
Cited by: 3
References: 22

Abstract

Asprosin, a fasting-induced glucogenic hormone, plays a crucial role in maintaining glucose homeostasis; however, its receptor remains elusive. This study identifies protein tyrosine phosphatase receptor F (Ptprf) as the receptor mediating Asprosin's metabolic functions. Using zebrafish models, we demonstrate the evolutionary conservation of Asprosin's role in glucose metabolism. Through binding assays, we determined Ptprf as Asprosin's interacting receptor in zebrafish liver. Zebrafish possess two Ptprf paralogs (Ptprfa/b), both hepatically expressed and binding Asprosin with high affinity. The genetic ablation of ptprfa/b reduced basal glucose levels and eliminated Asprosin-induced hyperglycemia. Conversely, the overexpression of soluble Ptprf ligand-binding domains neutralized Asprosin's glucogenic effects. These findings were validated in mammals: Asprosin binds PTPRF in mice and humans, and Ptprf knockout mice showed a blunted response to Asprosin. Our results establish Ptprf as an evolutionarily conserved Asprosin receptor across vertebrates, providing mechanistic insights for developing therapies targeting this pathway for diabetes and obesity.

Fields of Study & Subjects

Protein Tyrosine Phosphatases Glycogen Storage Diseases and Myoclonus Diabetes and associated disorders

Publication details

Journal / source
Cell Reports
Publisher
Elsevier BV
Volume
45
Issue
2
Pages
116974–116974
Publication date
1 February 2026
Language
EN