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  3. Non-viral Gene Delivery Methods for Bone and Joints.
 

Non-viral Gene Delivery Methods for Bone and Joints.

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BORIS DOI
10.48350/149902
Publisher DOI
10.3389/fbioe.2020.598466
PubMed ID
33330428
Description
Viral carrier transport efficiency of gene delivery is high, depending on the type of vector. However, viral delivery poses significant safety concerns such as inefficient/unpredictable reprogramming outcomes, genomic integration, as well as unwarranted immune responses and toxicity. Thus, non-viral gene delivery methods are more feasible for translation as these allow safer delivery of genes and can modulate gene expression transiently both in vivo, ex vivo, and in vitro. Based on current studies, the efficiency of these technologies appears to be more limited, but they are appealing for clinical translation. This review presents a summary of recent advancements in orthopedics, where primarily bone and joints from the musculoskeletal apparatus were targeted. In connective tissues, which are known to have a poor healing capacity, and have a relatively low cell-density, i.e., articular cartilage, bone, and the intervertebral disk (IVD) several approaches have recently been undertaken. We provide a brief overview of the existing technologies, using nano-spheres/engineered vesicles, lipofection, and in vivo electroporation. Here, delivery for microRNA (miRNA), and silencing RNA (siRNA) and DNA plasmids will be discussed. Recent studies will be summarized that aimed to improve regeneration of these tissues, involving the delivery of bone morphogenic proteins (BMPs), such as BMP2 for improvement of bone healing. For articular cartilage/osteochondral junction, non-viral methods concentrate on targeted delivery to chondrocytes or MSCs for tissue engineering-based approaches. For the IVD, growth factors such as GDF5 or GDF6 or developmental transcription factors such as Brachyury or FOXF1 seem to be of high clinical interest. However, the most efficient method of gene transfer is still elusive, as several preclinical studies have reported many different non-viral methods and clinical translation of these techniques still needs to be validated. Here we discuss the non-viral methods applied for bone and joint and propose methods that can be promising in clinical use.
Date of Publication
2020
Publication Type
Article
Subject(s)
600 Technology > 610 Medicine & health
500 Science > 570 Life sciences; biology
600 Technology > 620 Engineering
600 Technology > 660 Chemical engineering
Keyword(s)
BMP2 FOXF1 GDF5 bone cartilage intervertebral disk non-viral gene delivery tendon
Language(s)
en
Contributor(s)
Gantenbein, Benjaminorcid-logo
Department for BioMedical Research, Forschungsgruppe Tissue Engineering für Orthopädie & Mechanobiologie (TOM)
Universitätsklinik für Orthopädische Chirurgie und Traumatologie
Tang, Shirley
Guerrero, Julien Paul
Universitätsklinik für Orthopädische Chirurgie und Traumatologie
Department for BioMedical Research, Forschungsgruppe Tissue Engineering für Orthopädie & Mechanobiologie (TOM)
Higuita-Castro, Natalia
Salazar-Puerta, Ana I
Croft, Andreas Shaun
Universitätsklinik für Orthopädische Chirurgie und Traumatologie
Department for BioMedical Research, Forschungsgruppe Tissue Engineering für Orthopädie & Mechanobiologie (TOM)
Gazdhar, Amiq
Universitätsklinik für Pneumologie
Purmessur, Devina
Additional Credits
Universitätsklinik für Orthopädische Chirurgie und Traumatologie
Universitätsklinik für Pneumologie
Department for BioMedical Research, Forschungsgruppe Tissue Engineering für Orthopädie & Mechanobiologie (TOM)
Series
Frontiers in Bioengineering and Biotechnology
Publisher
Frontiers Media
ISSN
2296-4185
Access(Rights)
open.access
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