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Asprosin, a Fasting-Induced Glucogenic Protein Hormone

  • Chase Romere
  • , Clemens Duerrschmid
  • , Juan Bournat
  • , Petra Constable
  • , Mahim Jain
  • , Fan Xia
  • , Pradip K. Saha
  • , Maria Del Solar
  • , Bokai Zhu
  • , Brian York
  • , Poonam Sarkar
  • , David A. Rendon
  • , M. Waleed Gaber
  • , Scott A. LeMaire
  • , Joseph S. Coselli
  • , Dianna M. Milewicz
  • , V. Reid Sutton
  • , Nancy F. Butte
  • , David D. Moore
  • , Atul R. Chopra
  • Baylor College of Medicine
  • Department of Molecular and Human Genetics
  • Icahn School of Medicine at Mount Sinai
  • University of Texas Health Science Center at Houston

Research output: Contribution to journalArticlepeer-review

518 Scopus citations

Abstract

Hepatic glucose release into the circulation is vital for brain function and survival during periods of fasting and is modulated by an array of hormones that precisely regulate plasma glucose levels. We have identified a fasting-induced protein hormone that modulates hepatic glucose release. It is the C-terminal cleavage product of profibrillin, and we name it Asprosin. Asprosin is secreted by white adipose, circulates at nanomolar levels, and is recruited to the liver, where it activates the G protein-cAMP-PKA pathway, resulting in rapid glucose release into the circulation. Humans and mice with insulin resistance show pathologically elevated plasma asprosin, and its loss of function via immunologic or genetic means has a profound glucose- and insulin-lowering effect secondary to reduced hepatic glucose release. Asprosin represents a glucogenic protein hormone, and therapeutically targeting it may be beneficial in type II diabetes and metabolic syndrome.

Original languageEnglish
Pages (from-to)566-579
Number of pages14
JournalCell
Volume165
Issue number3
DOIs
StatePublished - 21 Apr 2016

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