Please use this identifier to cite or link to this item:
Scopus Web of Science® Altmetric
Type: Journal article
Title: Facilitating THP-1 macrophage studies by differentiating and investigating cell functions in polystyrene test tubes
Author: Small, A.
Lansdown, N.
Al-Baghdadi, M.
Quach, A.
Ferrante, A.
Citation: Journal of Immunological Methods, 2018; 461:73-77
Publisher: Elsevier
Issue Date: 2018
ISSN: 0022-1759
Statement of
Annabelle Small, Nikki Lansdown, Marwah Al-Baghdadi, Alex Quach, Antonio Ferrante
Abstract: Macrophage cell lines are a useful model to explore the properties of primary macrophages. However, a major limitation in the use of these cells is that when they are differentiated, they become adherent and hence present with the same limitation as natural macrophages. The cells need to be detached and are often subjected to detachment techniques such as detachment buffers containing proteolytic enzymes or scraping with a rubber 'policeman'. These steps are time-consuming, reduce cell yields as well as cell viability and function. We have therefore investigated the possibility of differentiating the human macrophage THP-1 cell line in polystyrene FACS tubes to enable cells to be directly used for investigations by flow cytometry. Here we demonstrate that when the human macrophage cell line THP-1 are cultured in FACS tubes with phorbol myristate acetate added, they undergo differentiation into macrophages, assessed morphologically and by autofluorescence expression, in a similar manner to those cultured in tissue culture dishes. The cells can be readily washed and adjusted in concentration by centrifugation in the same tubes and can be directly tested for expression of cell surface markers and function by flow cytometry. This avoids the use of either detachment reagents or physical cell scraping. Consequently, we showed that the tube culture method results in increased cell yield and viability compared to those subjected to detachment procedures. The tube method generated functional macrophages which expressed the complement receptors, CR3 and CR4, and effectively phagocytosed complement opsonised Staphylococcus aureus via these receptors.
Keywords: Complement receptors
THP-1 cell line
Rights: © 2018 Elsevier B.V. All rights reserved.
DOI: 10.1016/j.jim.2018.06.019
Published version:
Appears in Collections:Aurora harvest 3
Opthalmology & Visual Sciences publications

Files in This Item:
There are no files associated with this item.

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.