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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 |
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creator | Wu, Yu Angelov, Borislav Deng, Yuru Fujino, Takehiko Hossain, Md Shamim Drechsler, Markus 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 |
format | article |
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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.</description><identifier>ISSN: 2399-3669</identifier><identifier>EISSN: 2399-3669</identifier><identifier>DOI: 10.1038/s42004-023-01043-9</identifier><identifier>PMID: 37932487</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>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</subject><ispartof>Communications chemistry, 2023-11, Vol.6 (1), p.241-241, Article 241</ispartof><rights>The Author(s) 2023</rights><rights>The Author(s) 2023. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>Attribution</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c552t-6486075d8baf9c00ea83dcf7a2a3e1eca28ed91e42dfbf50fb9121d5a124e4d83</citedby><cites>FETCH-LOGICAL-c552t-6486075d8baf9c00ea83dcf7a2a3e1eca28ed91e42dfbf50fb9121d5a124e4d83</cites><orcidid>0000-0002-0285-0637 ; 0000-0003-3131-4822 ; 0000-0001-7192-7821</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10628290/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2886463217?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,38516,43895,44590,53791,53793</link.rule.ids><backlink>$$Uhttps://hal.science/hal-04293969$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Wu, Yu</creatorcontrib><creatorcontrib>Angelov, Borislav</creatorcontrib><creatorcontrib>Deng, Yuru</creatorcontrib><creatorcontrib>Fujino, Takehiko</creatorcontrib><creatorcontrib>Hossain, Md Shamim</creatorcontrib><creatorcontrib>Drechsler, Markus</creatorcontrib><creatorcontrib>Angelova, Angelina</creatorcontrib><title>Sustained CREB phosphorylation by lipid-peptide liquid crystalline nanoassemblies</title><title>Communications chemistry</title><addtitle>Commun Chem</addtitle><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.</description><subject>13/31</subject><subject>631/154/152</subject><subject>639/301/54/152</subject><subject>639/925/352/152</subject><subject>Biochemistry</subject><subject>Biochemistry, Molecular Biology</subject><subject>Chemical Sciences</subject><subject>Chemistry</subject><subject>Chemistry and Materials Science</subject><subject>Chemistry/Food Science</subject><subject>Leucine</subject><subject>Life Sciences</subject><subject>Lipids</subject><subject>Liquid crystals</subject><subject>Medicinal Chemistry</subject><subject>Nanoparticles</subject><subject>Neurobiology</subject><subject>Neurodegeneration</subject><subject>Neurological diseases</subject><subject>Neurons and Cognition</subject><subject>Parkinson's disease</subject><subject>Peptides</subject><subject>Phospholipids</subject><subject>Phosphorylation</subject><subject>Polypeptides</subject><subject>Proteins</subject><subject>Vinyl ethers</subject><issn>2399-3669</issn><issn>2399-3669</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>COVID</sourceid><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNp9kktv1DAUhSMEolXpH2AViQ0sAtePJPYKlVGhlUZCvNaWY9_MeOSJUzupNP8ez6QC2gULy77X53zXsk5RvCbwngATHxKnALwCyiogwFklnxXnlElZsaaRz_85nxWXKe0AgAJhbSteFmeslYxy0Z4X337MadJuQFuuvl9_KsdtSHnFg9eTC0PZHUrvRmerEcfJWczV3exsaeIh-7zPznLQQ9Ap4b7zDtOr4kWvfcLLh_2i-PX5-ufqplp__XK7ulpXpq7pVDVcNNDWVnS6lwYAtWDW9K2mmiFBo6lAKwlyavuur6HvJKHE1ppQjtwKdlHcLlwb9E6N0e11PKignTo1QtwoHSdnPCrGgLRGCk67mhPTdjzDqWTQykb2GjPr48Ia526P1uAwRe0fQR_fDG6rNuFeEWiooBIy4d1C2D7x3Vyt1bEHPA_M4-5J1r59mBbD3YxpUnuXDHqvBwxzUlSIRrJG0DZL3zyR7sIch_yvJxVvGCVHFV1UJoaUIvZ_XkBAHdOilrSonBZ1SouS2cQWU8riYYPxL_o_rt_dwMBX</recordid><startdate>20231106</startdate><enddate>20231106</enddate><creator>Wu, Yu</creator><creator>Angelov, Borislav</creator><creator>Deng, Yuru</creator><creator>Fujino, Takehiko</creator><creator>Hossain, Md Shamim</creator><creator>Drechsler, Markus</creator><creator>Angelova, Angelina</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</general><general>Nature Research</general><general>Nature Portfolio</general><scope>C6C</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>8FE</scope><scope>8FG</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>CCPQU</scope><scope>COVID</scope><scope>D1I</scope><scope>DWQXO</scope><scope>HCIFZ</scope><scope>KB.</scope><scope>L6V</scope><scope>M7S</scope><scope>PDBOC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PTHSS</scope><scope>7X8</scope><scope>1XC</scope><scope>VOOES</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-0285-0637</orcidid><orcidid>https://orcid.org/0000-0003-3131-4822</orcidid><orcidid>https://orcid.org/0000-0001-7192-7821</orcidid></search><sort><creationdate>20231106</creationdate><title>Sustained CREB phosphorylation by lipid-peptide liquid crystalline nanoassemblies</title><author>Wu, Yu ; 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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.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>37932487</pmid><doi>10.1038/s42004-023-01043-9</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0002-0285-0637</orcidid><orcidid>https://orcid.org/0000-0003-3131-4822</orcidid><orcidid>https://orcid.org/0000-0001-7192-7821</orcidid><oa>free_for_read</oa></addata></record> |
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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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