pNaSS-Grafted PCL Film-Guided rAAV TGF-β Gene Therapy Activates the Chondrogenic Activities in Human Bone Marrow Aspirates.


Journal

Human gene therapy
ISSN: 1557-7422
Titre abrégé: Hum Gene Ther
Pays: United States
ID NLM: 9008950

Informations de publication

Date de publication:
09 2021
Historique:
pubmed: 13 2 2021
medline: 1 2 2022
entrez: 12 2 2021
Statut: ppublish

Résumé

Scaffold-guided viral gene therapy is a novel, powerful tool to enhance the processes of tissue repair in articular cartilage lesions by the delivery and overexpression of therapeutic genes in a noninvasive, controlled release manner based on a procedure that may protect the gene vehicles from undesirable host immune responses. In this study, we examined the potential of transferring a recombinant adeno-associated virus (rAAV) vector carrying a sequence for the highly chondroregenerative transforming growth factor beta (TGF-β), using poly(ɛ-caprolactone) (PCL) films functionalized by the grafting of poly(sodium styrene sulfonate) (pNaSS) in chondrogenically competent bone marrow aspirates as future targets for therapy in cartilage lesions. Effective overexpression of TGF-β in the aspirates by rAAV was achieved upon delivery using pNaSS-grafted and ungrafted PCL films for up to 21 days (the longest time point evaluated), with superior levels using the grafted films, compared with respective conditions without vector coating. The production of rAAV-mediated TGF-β by pNaSS-grafted and ungrafted PCL films significantly triggered the biological activities and chondrogenic processes in the samples (proteoglycan and type-II collagen deposition and cell proliferation), while containing premature mineralization and hypertrophy relative to the other conditions, with overall superior effects supported by the pNaSS-grafted films. These observations demonstrate the potential of PCL film-assisted rAAV TGF-β gene transfer as a convenient, off-the-shelf technique to enhance the reparative potential of the bone marrow in patients in future approaches for improved cartilage repair.

Identifiants

pubmed: 33573471
doi: 10.1089/hum.2020.329
doi:

Substances chimiques

Transforming Growth Factor beta 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

895-906

Auteurs

Jagadeesh K Venkatesan (JK)

Center of Experimental Orthopaedics, Université Sorbonne Paris Nord, Villetaneuse, France.

Xiaoyu Cai (X)

Center of Experimental Orthopaedics, Université Sorbonne Paris Nord, Villetaneuse, France.

Weikun Meng (W)

Center of Experimental Orthopaedics, Université Sorbonne Paris Nord, Villetaneuse, France.

Ana Rey-Rico (A)

Center of Experimental Orthopaedics, Université Sorbonne Paris Nord, Villetaneuse, France.

Gertrud Schmitt (G)

Center of Experimental Orthopaedics, Université Sorbonne Paris Nord, Villetaneuse, France.

Susanne Speicher-Mentges (S)

Center of Experimental Orthopaedics, Université Sorbonne Paris Nord, Villetaneuse, France.

Céline Falentin-Daudré (C)

LBPS/CSPBAT UMR CNRS 7244, Université Sorbonne Paris Nord, Villetaneuse, France.

Amélie Leroux (A)

LBPS/CSPBAT UMR CNRS 7244, Université Sorbonne Paris Nord, Villetaneuse, France.

Henning Madry (H)

Center of Experimental Orthopaedics, Université Sorbonne Paris Nord, Villetaneuse, France.
Department of Orthopaedic Surgery, Saarland University Medical Center, Homburg/Saar, Germany.

Véronique Migonney (V)

LBPS/CSPBAT UMR CNRS 7244, Université Sorbonne Paris Nord, Villetaneuse, France.

Magali Cucchiarini (M)

Center of Experimental Orthopaedics, Université Sorbonne Paris Nord, Villetaneuse, France.

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Classifications MeSH