Selective Phosphorylation of Akt/Protein-Kinase B Isoforms in Response to Dietary Cues.

Selective Phosphorylation of Akt/Protein-Kinase B Isoforms in Response to Dietary Cues.

Trautenberg, Laura Christin;Prince, Elodie;Maas, Cornelia;Beier, Nora;Honold, Freya;Grzybek, Michal;Brankatschk, Marko;
Frontiers in cell and developmental biology 2019 Vol. 7 pp. 206
347
trautenberg2019selectivefrontiers

Abstract

A calorie-rich diet is one reason for the continuous spread of metabolic syndromes in western societies. Smart food design is one powerful tool to prevent metabolic stress, and the search for suitable bioactive additives is a continuous task. The nutrient-sensing insulin pathway is an evolutionary conserved mechanism that plays an important role in metabolism, growth and development. Recently, lipid cues capable to stimulate insulin signaling were identified. However, the mechanistic base of their activity remains obscure to date. We show that specific Akt/Protein-kinase B isoforms are responsive to different calorie-rich diets, and potentiate the activity of the cellular insulin cascade. Our data add a new dimension to existing models and position as a powerful tool to study the relation between dietary lipid cues and the insulin-induced cellular signal pathway.

Citation

ID: 63626
Ref Key: trautenberg2019selectivefrontiers
Use this key to autocite in SciMatic or Thesis Manager

References

Blockchain Verification

Account:
NFT Contract Address:
0x95644003c57E6F55A65596E3D9Eac6813e3566dA
Article ID:
63626
Unique Identifier:
10.3389/fcell.2019.00206
Network:
Scimatic Chain (ID: 481)
Loading...
Blockchain Readiness Checklist
Authors
Abstract
Journal Name
Year
Title
5/5
Creates 1,000,000 NFT tokens for this article
Token Features:
  • ERC-1155 Standard NFT
  • 1 Million Supply per Article
  • Transferable via MetaMask
  • Permanent Blockchain Record
Blockchain QR Code
Scan with Saymatik Web3.0 Wallet

Saymatik Web3.0 Wallet