2018
DOI: 10.1002/jcp.27890
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Serum‐reduced media impacts on cell viability and protein expression in human lung epithelial cells

Abstract: Serum starvation is a widely used condition in molecular biology experiments. Opti‐MEM is a serum‐reduced media used during transfection of genetic molecules into mammalian cells. However, the impact of such media on cell viability and protein synthesis is unknown. A549 human lung epithelial cell viability and morphology were adversely affected by growing in Opti‐MEM. The cellular protein levels of chloride intracellular channel protein 1, proteasome subunit alpha Type 2, and heat shock 70 kDa protein 5 were d… Show more

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Cited by 69 publications
(54 citation statements)
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“…The CAFs were suspended in DMEM containing 10% fetal bovine serum (FBS) with 1% penicillin/ streptomycin and cultured in a constant temperature incubator at 37ºC with 5% carbon dioxide. 29…”
Section: Methods Isolation Cell Sorting and Culturementioning
confidence: 99%
“…The CAFs were suspended in DMEM containing 10% fetal bovine serum (FBS) with 1% penicillin/ streptomycin and cultured in a constant temperature incubator at 37ºC with 5% carbon dioxide. 29…”
Section: Methods Isolation Cell Sorting and Culturementioning
confidence: 99%
“…Reduction of the viability of HeLa cells upon exposure to capsules was measured using different incubation procedures: (i) first 4 h of incubation in cell growth medium without fetal bovine serum (FBS), and then 20 h of incubation in the medium supplemented with FBS; (ii) 24 h of incubation in the cell growth medium supplemented with FBS. The two conditions were used as the transfection of cells varies upon the presence/absence of FBS [ 53 , 54 ]. The capsule concentration was quantified in terms of delivered encapsulated DEX-blue m DEX-blue [pg/cell].…”
Section: Resultsmentioning
confidence: 99%
“…This may be convenient for some applications because growing cells in low serum media (which is recommended for transfection by lipofection) can decrease cell viability and protein expression. [54] Recent studies indicate that ratiometric control of Cas9 and sgRNA is important in CRISPR/Cas9 gene editing. [55] Hence, establishing a universal transfection method that exploits delivery mechanisms in which dosage control can be achieved, at the single-cell level, is a high priority.…”
Section: Discussionmentioning
confidence: 99%