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Sustained CREB phosphorylation by lipid-peptide liquid crystalline nanoassemblies

Cyclic-AMP-response element-binding protein (CREB) is a leucine zipper class transcription factor that is activated through phosphorylation. Ample CREB phosphorylation is required for neurotrophin expression, which is of key importance for preventing and regenerating neurological disorders, includin...

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Published in:Communications chemistry 2023-11, Vol.6 (1), p.241-241, Article 241
Main Authors: Wu, Yu, Angelov, Borislav, Deng, Yuru, Fujino, Takehiko, Hossain, Md Shamim, Drechsler, Markus, Angelova, Angelina
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container_title Communications chemistry
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creator Wu, Yu
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Angelova, Angelina
description Cyclic-AMP-response element-binding protein (CREB) is a leucine zipper class transcription factor that is activated through phosphorylation. Ample CREB phosphorylation is required for neurotrophin expression, which is of key importance for preventing and regenerating neurological disorders, including the sequelae of long COVID syndrome. Here we created lipid-peptide nanoassemblies with different liquid crystalline structural organizations (cubosomes, hexosomes, and vesicles) as innovative nanomedicine delivery systems of bioactive PUFA-plasmalogens (vinyl ether phospholipids with polyunsaturated fatty acid chains) and a neurotrophic pituitary adenylate cyclase-activating polypeptide (PACAP). Considering that plasmalogen deficiency is a potentially causative factor for neurodegeneration, we examined the impact of nanoassemblies type and incubation time in an in vitro Parkinson’s disease (PD) model as critical parameters for the induction of CREB phosphorylation. The determined kinetic changes in CREB, AKT, and ERK-protein phosphorylation reveal that non-lamellar PUFA-plasmalogen-loaded liquid crystalline lipid nanoparticles significantly prolong CREB activation in the neurodegeneration model, an effect unattainable with free drugs, and this effect can be further enhanced by the cell-penetrating peptide PACAP. Understanding the sustained CREB activation response to neurotrophic nanoassemblies might lead to more efficient use of nanomedicines in neuroregeneration. PUFA-plasmalogens show neuroprotective properties via the stimulation of CREB activation, however, their efficiency is limited by low bioavailabilities. Here, the authors develop PUFA-plasmalogen-loaded liquid crystalline lipid-peptide nanoparticles to achieve sustained CREB activation in an in vitro neurodegeneration model.
doi_str_mv 10.1038/s42004-023-01043-9
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subjects 13/31
631/154/152
639/301/54/152
639/925/352/152
Biochemistry
Biochemistry, Molecular Biology
Chemical Sciences
Chemistry
Chemistry and Materials Science
Chemistry/Food Science
Leucine
Life Sciences
Lipids
Liquid crystals
Medicinal Chemistry
Nanoparticles
Neurobiology
Neurodegeneration
Neurological diseases
Neurons and Cognition
Parkinson's disease
Peptides
Phospholipids
Phosphorylation
Polypeptides
Proteins
Vinyl ethers
title Sustained CREB phosphorylation by lipid-peptide liquid crystalline nanoassemblies
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