Lentiviral transduction [Neurosurgery Wiki]

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====== Lentiviral transduction ======


[[Lentiviral]] [[transduction]] is an efficient method for the delivery of [[transgene]]s to mammalian cells and unifies the ease of use and speed of transient [[transfection]] with the robust expression of stable [[cell line]]s.
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Uhlmann et al. from the [[University Hospital of Düsseldorf]], described a [[protocol]] for the alteration of [[gene expression]] in [[human induced pluripotent stem cell]]s (hiPSCs) via [[overexpression]] of a mutant form of the [[TP53]] ([[R249S]]) gene using [[lentiviral transduction]]. A high amount of TP53 protein is detected 1 week after transduction and [[antibiotic]] selection. Differentiation of transduced hiPSCs gives insight into a better understanding of cancer formation in different tissues and may be a useful tool for genetic or pharmacologic screening assays. 

Basic Protocol 1: Production and concentration of third-generation lentivirus Support Protocol 1: Cloning of gene of interest into modulation vector Support Protocol 2: Preparation of DMEM GlutaMAX™ with 10% fetal bovine serum and 1% penicillin-streptomycin Basic Protocol 2: Transduction of human-induced pluripotent stem cells and selection of positively transfected cells Support Protocol 3: Preparation of Matrigel® -coated plates Support Protocol 4: Preparation of mTeSR™1 medium
((Uhlmann C, Kuhn LM, Tigges J, Fritsche E, Kahlert UD. Efficient Modulation of 
TP53 Expression in Human Induced Pluripotent Stem Cells. Curr Protoc Stem Cell
Biol. 2020 Mar;52(1):e102. doi: 10.1002/cpsc.102. PubMed PMID: 31883435.
)).