Genetic Modification of Primary Human Myeloid Cells to Study Cell Migration, Activation, and Organelle Dynamics. Issue 8 (26th August 2022)

• Record Type: Journal Article
• Authors: Greiner, Daniel; Scott, Tiana M.; Olson, Gregory S.; Aderem, Alan; Roh‐Johnson, Minna; Johnson, Jarrod S.
• Is Part Of: Current protocols. Volume 2:Issue 8(2022)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2022-08-26
• Subjects: gene delivery -- innate immunity -- viral vectors; Life sciences -- Laboratory manuals -- Periodicals; Biology -- Laboratory manuals -- Periodicals; Life sciences -- Technique -- Periodicals; Biology -- Technique -- Periodicals; 570.028
• DOI: 10.1002/cpz1.514
• Languages: English
• ISSNs: 2691-1299

Abstract

Abstract: Myeloid dendritic cells (DCs) and macrophages are mononuclear phagocytes with key roles in the immune system. As antigen‐presenting cells, they link innate detection of microbes with programming adaptive immune responses. Myeloid DCs and macrophages also play critical roles in development, promote tissue homeostasis, and direct repair in response to injury and inflammation. As cellular migration and organelle dynamics are intimately connected with these processes, it is necessary to develop tools to track myeloid cell behavior and function. Here, we build on previously established protocols to isolate primary human myeloid cells from peripheral blood and report an optimized method for their genetic modification with lentiviral vectors to study processes related to cell migration, activation, and organelle dynamics. Specifically, we provide a protocol for delivering genetically encoded fluorescent markers into primary monocyte‐derived DCs (MDDCs) and monocyte‐derived macrophages (MDMs) to label mitochondria, peroxisomes, and whole cells. We describe the isolation of primary CD14+ monocytes from peripheral blood using positive selection with magnetic beads and, alternatively, isolation based on plastic adherence. Isolated CD14+ cells can be transduced with lentiviral vectors and subsequently cultured in the presence of cytokines to derive MDDCs or MDMs. This protocol is highly adaptable for cotransduction with vectors to knock down or overexpress genes of interest. These tools enable mechanistic studies of genetically modified myeloid cells through flow cytometry, fluorescence microscopy, and other downstream assays. © 2022 Wiley Periodicals LLC. Basic Protocol : Transduction of MDDCs and MDMs with lentiviral vectors encoding fluorescent markers Alternate Protocol 1 : Isolation of monocytes by plastic adhesion Alternate Protocol 2 : Transduction of MDDCs and MDMs with lentiviral vectors to knock down or overexpress genes of interest Support Protocol 1 : Production and purification of lentiviral vectors for transduction into primary human myeloid cells Support Protocol 2 : Flow cytometry of MDDCs and MDMs Support Protocol 3 : Fixed and live‐cell imaging of fluorescent markers in MDMs and MDDCs