Abstract

BackgroundNeutrophils are non-dividing cells with poor survival after isolation. Consequently, exogenous gene expression in neutrophils is challenging. We report here the transfection of genes and expression of active proteins in human primary peripheral neutrophils using nucleofection.ResultsExogenous gene expression in human neutrophils was achieved 2 h post-transfection. We show that neutrophils transfected by nucleofection are functional cells, able to respond to soluble and particulate stimuli. They conserved the ability to undergo physiological processes including phagocytosis. Using this technique, we were able to show that the phox homology (PX) domain of p47phox localizes to the plasma membrane in human neutrophils. We also show that RhoB, but not the PX domain of p47phox, is translocated to the membrane of mature phagosomes.ConclusionWe demonstrated that cDNA transfer and expression of exogenous protein in human neutrophils is compatible with cell viability and is no longer a limitation for the study of protein function in human neutrophils.

Highlights

  • Neutrophils are non-dividing cells with poor survival after isolation

  • We show that the electrical settings corresponding to programs U14 and Y01 resulted in higher transfection efficiency for similar experimental conditions based on flow cytometric analysis of neutrophils transfected with the vector pmaxGFP

  • We show that the second generation programs (U14 and Y01) better preserve cell viability when evaluated by propidium iodide

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Summary

Introduction

Neutrophils are non-dividing cells with poor survival after isolation. exogenous gene expression in neutrophils is challenging. We report here the transfection of genes and expression of active proteins in human primary peripheral neutrophils using nucleofection. Study of a gene product by expressing its constitutively active or dominant negative mutant in a cell is a powerful tool of investigation. Researchers have partially overcome these difficulties by performing studies in well-developed cell-free systems [1], with permeabilized neutrophils [2] and with cell lines that undergo some neutrophil functions, such as HL-60 cells or B-lymphoblasts [3,4]. We report the transfection and expression of genes into neutrophils by nucleofection. Using this technology, which delivers the vector directly into the nucleus [6], exogenous genes can be expressed in neutrophils in as short as 2 h after transfection, overcoming the difficulties associated with the short lifetime of these cells

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