Literature DB >> 21504098

Gene delivery into mammalian cells: an overview on existing approaches employed in vitro and in vivo.

Peter Hahn1, Elizabeth Scanlan.   

Abstract

Delivery of nucleic acids into cells is one of the central techniques underpinning molecular biology research and is also a critical process for in vivo applications such as gene therapy, vaccination, and drug development. Delivery of plasmid DNA enables expression of recombinant genes, while delivery of siRNA is used to downregulate gene expression. Over the last 40 years, multiple different methods of nucleic acid delivery have been developed. These include viral methods and non-viral methods, which can be further subdivided into mechanical, physical, and chemical methods. Here we describe the principal delivery methods, including their advantages, disadvantages, and suitability for particular applications.

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Year:  2010        PMID: 21504098     DOI: 10.1007/128_2010_71

Source DB:  PubMed          Journal:  Top Curr Chem        ISSN: 0340-1022


  9 in total

1.  Optimization of PAMAM-gold nanoparticle conjugation for gene therapy.

Authors:  Elizabeth R Figueroa; Adam Y Lin; Jiaxi Yan; Laureen Luo; Aaron E Foster; Rebekah A Drezek
Journal:  Biomaterials       Date:  2013-11-26       Impact factor: 12.479

2.  Asymmetric partitioning of transfected DNA during mammalian cell division.

Authors:  Xuan Wang; Nhung Le; Annina Denoth-Lippuner; Yves Barral; Ruth Kroschewski
Journal:  Proc Natl Acad Sci U S A       Date:  2016-06-13       Impact factor: 11.205

3.  Spatial and Temporal Control of Cavitation Allows High In Vitro Transfection Efficiency in the Absence of Transfection Reagents or Contrast Agents.

Authors:  Kamel Chettab; Stéphanie Roux; Doriane Mathé; Emeline Cros-Perrial; Maxime Lafond; Cyril Lafon; Charles Dumontet; Jean-Louis Mestas
Journal:  PLoS One       Date:  2015-08-14       Impact factor: 3.240

4.  A combined approach of hollow microneedles and nanocarriers for skin immunization with plasmid DNA encoding ovalbumin.

Authors:  Boonnada Pamornpathomkul; Adisak Wongkajornsilp; Wanida Laiwattanapaisal; Theerasak Rojanarata; Praneet Opanasopit; Tanasait Ngawhirunpat
Journal:  Int J Nanomedicine       Date:  2017-01-27

5.  A mechanistic investigation exploring the differential transfection efficiencies between the easy-to-transfect SK-BR3 and difficult-to-transfect CT26 cell lines.

Authors:  Elizabeth Figueroa; Pallavi Bugga; Vishwaratn Asthana; Allen L Chen; J Stephen Yan; Emily Reiser Evans; Rebekah A Drezek
Journal:  J Nanobiotechnology       Date:  2017-05-02       Impact factor: 10.435

6.  Modeling vanishing white matter disease with patient-derived induced pluripotent stem cells reveals astrocytic dysfunction.

Authors:  Ling Zhou; Peng Li; Na Chen; Li-Fang Dai; Kai Gao; Yi-Nan Liu; Li Shen; Jing-Min Wang; Yu-Wu Jiang; Ye Wu
Journal:  CNS Neurosci Ther       Date:  2019-02-05       Impact factor: 5.243

7.  Higher Order Architecture of Designer Peptides Forms Bioinspired 10 nm siRNA Delivery System.

Authors:  Alicia Gamboa; Selina F Urfano; Katrina Hernandez; Deborah A Fraser; Luladey Ayalew; Katarzyna Slowinska
Journal:  Sci Rep       Date:  2019-11-14       Impact factor: 4.379

8.  GPI-anchored glutathione S-transferase as marker allows affinity sorting of transfection-positive cells.

Authors:  Shumin Ma; Lele Yang; Qingqing Zuo; Qilai Huang
Journal:  Front Mol Biosci       Date:  2022-09-29

9.  Avians as a Model System of Vascular Development.

Authors:  Rieko Asai; Michael Bressan; Takashi Mikawa
Journal:  Methods Mol Biol       Date:  2021
  9 in total

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