Temperature-Sensitive Amphiphilic Non-Ionic Triblock Copolymers for Enhanced In Vivo Skeletal Muscle Transfection.

LCST amphiphilic copolymers in vivo transfection poly(2-methyl-2-oxazoline) skeletal muscle

Journal

Macromolecular bioscience
ISSN: 1616-5195
Titre abrégé: Macromol Biosci
Pays: Germany
ID NLM: 101135941

Informations de publication

Date de publication:
03 2020
Historique:
received: 01 08 2019
revised: 30 10 2019
pubmed: 10 1 2020
medline: 6 1 2021
entrez: 10 1 2020
Statut: ppublish

Résumé

It is reported that low concentration of amphiphilic triblock copolymers of pMeOx-b-pTHF-b-pMeOx structure (TBCPs) improves gene expression in skeletal muscle upon intramuscular co-injection with plasmid DNA. Physicochemical studies carried out to understand the involved mechanism show that a phase transition of TBCPs under their unimer state is induced when the temperature is elevated from 25 to 37 °C, the body temperature. Several lines of evidences suggest that TBCP insertion in a lipid bilayer causes enough lipid bilayer destabilization and even pore formation, a phenomenon heightened during the phase transition of TBCPs. Interestingly, this property allows DNA translocation across the lipid bilayer model. Overall, the results indicate that TBCPs exhibiting a phase transition at the body temperature is promising to favor in vivo pDNA translocation in skeletal muscle cells for gene therapy applications.

Identifiants

pubmed: 31917515
doi: 10.1002/mabi.201900276
doi:

Substances chimiques

DNA 9007-49-2

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e1900276

Informations de copyright

© 2020 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

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Auteurs

Bazoly Rasolonjatovo (B)

LAMBE, CNRS, Université Evry, CEA, Université Paris-Saclay, 91025, Evry, France.
LAMBE, UCP, Université Paris-Seine, 91025, Evry, France.

Nicolas Illy (N)

Equipe Chimie des Polymères, Institut Parisien de Chimie Moléculaire, CNRS, Sorbonne Université, 4 Place Jussieu, 75005, Paris, France.

Véronique Bennevault (V)

Equipe Chimie des Polymères, Institut Parisien de Chimie Moléculaire, CNRS, Sorbonne Université, 4 Place Jussieu, 75005, Paris, France.
Université Evry, 91025, Evry, France.

Jérôme Mathé (J)

LAMBE, CNRS, Université Evry, CEA, Université Paris-Saclay, 91025, Evry, France.
LAMBE, UCP, Université Paris-Seine, 91025, Evry, France.

Patrick Midoux (P)

Centre de Biophysique Moléculaire, CNRS UPR4301, 45071, Orléans Cedex 02, France.

Tony Le Gall (T)

Groupe - Transfert de Gènes et Thérapie Génique, UMR 1078 - Génétique, Génomique Fonctionnelle et Biotechnologies, Université de Brest, INSERM, CHU de Brest, 22 Avenue Camille Desmoulins, 29238, Brest Cedex, France.

Thomas Haudebourg (T)

CRCINA, INSERM, University of Angers, University of Nantes, 49000 and 44000, Nantes, France.

Tristan Montier (T)

Groupe - Transfert de Gènes et Thérapie Génique, UMR 1078 - Génétique, Génomique Fonctionnelle et Biotechnologies, Université de Brest, INSERM, CHU de Brest, 22 Avenue Camille Desmoulins, 29238, Brest Cedex, France.

Pierre Lehn (P)

Groupe - Transfert de Gènes et Thérapie Génique, UMR 1078 - Génétique, Génomique Fonctionnelle et Biotechnologies, Université de Brest, INSERM, CHU de Brest, 22 Avenue Camille Desmoulins, 29238, Brest Cedex, France.

Bruno Pitard (B)

CRCINA, INSERM, University of Angers, University of Nantes, 49000 and 44000, Nantes, France.

Herve Cheradame (H)

LAMBE, CNRS, Université Evry, CEA, Université Paris-Saclay, 91025, Evry, France.
LAMBE, UCP, Université Paris-Seine, 91025, Evry, France.

Cécile Huin (C)

Equipe Chimie des Polymères, Institut Parisien de Chimie Moléculaire, CNRS, Sorbonne Université, 4 Place Jussieu, 75005, Paris, France.
Université Evry, 91025, Evry, France.

Philippe Guégan (P)

Equipe Chimie des Polymères, Institut Parisien de Chimie Moléculaire, CNRS, Sorbonne Université, 4 Place Jussieu, 75005, Paris, France.

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