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Detargeting Lentiviral-Mediated CFTR Expression in Airway Basal Cells Using miR-106b.

Genes | 2020

Lentiviral-mediated integration of a CFTR transgene cassette into airway basal cells is a strategy being considered for cystic fibrosis (CF) cell-based therapies. However, CFTR expression is highly regulated in differentiated airway cell types and a subset of intermediate basal cells destined to differentiate. Since basal stem cells typically do not express CFTR, suppressing the CFTR expression from the lentiviral vector in airway basal cells may be beneficial for maintaining their proliferative capacity and multipotency. We identified miR-106b as highly expressed in proliferating airway basal cells and extinguished in differentiated columnar cells. Herein, we developed lentiviral vectors with the miR-106b-target sequence (miRT) to both study miR-106b regulation during basal cell differentiation and detarget CFTR expression in basal cells. Given that miR-106b is expressed in the 293T cells used for viral production, obstacles of viral genome integrity and titers were overcome by creating a 293T-B2 cell line that inducibly expresses the RNAi suppressor B2 protein from flock house virus. While miR-106b vectors effectively detargeted reporter gene expression in proliferating basal cells and following differentiation in the air-liquid interface and organoid cultures, the CFTR-miRT vector produced significantly less CFTR-mediated current than the non-miR-targeted CFTR vector following transduction and differentiation of CF basal cells. These findings suggest that miR-106b is expressed in certain airway cell types that contribute to the majority of CFTR anion transport in airway epithelium.

Pubmed ID: 33036232 RIS Download

Research resources used in this publication

None found

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Associated grants

  • Agency: NIEHS NIH HHS, United States
    Id: P30 ES005605
  • Agency: NIH HHS, United States
    Id: T32 HL007638
  • Agency: NIDDK NIH HHS, United States
    Id: P30 DK054759
  • Agency: NIDDK NIH HHS, United States
    Id: R01 DK047967
  • Agency: NHLBI NIH HHS, United States
    Id: P01 HL152960
  • Agency: NIH HHS, United States
    Id: R01 DK047967
  • Agency: NIGMS NIH HHS, United States
    Id: T32 GM007337
  • Agency: NIH HHS, United States
    Id: P01 HL152960

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