Literature DB >> 27572655

Promoter optimisation of lentiviral vectors for efficient insulin gene expression in canine mesenchymal stromal cells: potential surrogate beta cells.

Pratigya Gautam1, Asha Recino2, Robert D Foale3, Jing Zhao1, Shu Uin Gan4, Maja Wallberg3, Roy Calne5, Andrew M L Lever6.   

Abstract

BACKGROUND: The lack of an ideal cell type that can be easily acquired, modified to produce insulin, and re-implanted has been a limitation for ex vivo insulin gene therapy. Canine diabetes is currently treated with human insulin and is a good model for human diabetes. Mesenchymal stromal cells (MSCs) are a promising candidate cell type for gene therapy. In the present study, we optimised insulin production using lentiviral transduced canine MSCs (cMSCs), aiming to evaluate their ability for use as surrogate beta cells.
METHODS: Canine MSCs were derived from bone marrow and validated by measuring the expression of MSC lineage specific markers. Lentivirus vectors encoding the proinsulin gene (with or without a Kozak sequence) under the control of spleen focus forming virus, cytomegalovirus, elongation factor 1α and simian virus 40 promotors were generated and used to transduce primary cMSCs and a hepatocyte cell line. The insulin-producing capacity of transduced primary cMSCs was assessed by measuring the concentration of C-peptide produced.
RESULTS: Primary cMSC could be readily expanded in culture and efficiently transduced using lentiviral vectors encoding proinsulin. Increasing the multiplicity of infection from 3 to 20 led to an increase in C-peptide secretion (from 1700 to 4000 pmol/l). The spleen focus forming virus promoter conferred the strongest transcriptional ability.
CONCLUSIONS: The results of the present study suggest that optimised lentiviral transduction of the insulin gene into primary cMSCs renders these cells capable of secreting insulin over both the short- and long-term, in sufficient quantities in vitro to support their potential use in insulin gene therapy.
© 2016 The Authors. The Journal of Gene Medicine Published by John Wiley & Sons, Ltd.

Entities:  

Keywords:  diabetes; gene therapy; insulin; lentivirus; mesenchymal stromal cells

Mesh:

Substances:

Year:  2016        PMID: 27572655     DOI: 10.1002/jgm.2900

Source DB:  PubMed          Journal:  J Gene Med        ISSN: 1099-498X            Impact factor:   4.565


  2 in total

1.  Immunosuppression overcomes insulin- and vector-specific immune responses that limit efficacy of AAV2/8-mediated insulin gene therapy in NOD mice.

Authors:  Asha Recino; Shu Uin Gan; Kian Chuan Sia; Yvonne Sawyer; Jenny Trendell; Richard Kay; Fiona M Gribble; Frank Reimann; Rob Foale; Maria Notaridou; Nick Holmes; Andrew Lever; Kok Onn Lee; Amit Nathwani; Anne Cooke; Roy Calne; Maja Wallberg
Journal:  Gene Ther       Date:  2018-12-04       Impact factor: 5.250

Review 2.  Gene Therapy - Can it Cure Type 1 Diabetes?

Authors:  Mirra Srinivasan; Santhosh Raja Thangaraj; Hadia Arzoun
Journal:  Cureus       Date:  2021-12-19
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.