Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2019 Jun;234(6):7718-7724.
doi: 10.1002/jcp.27890. Epub 2018 Dec 4.

Serum-reduced media impacts on cell viability and protein expression in human lung epithelial cells

Affiliations

Serum-reduced media impacts on cell viability and protein expression in human lung epithelial cells

Mahamud-Ur Rashid et al. J Cell Physiol. 2019 Jun.

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 dysregulated in A549 cells after growing in serum-reduced media. Small interfering RNA transfection was done in Dulbecco's modified Eagle's medium (DMEM) with 10% fetal bovine serum, and knockdown efficacy was determined compared with Opti-MEM. Similar amounts of knockdown of the target proteins were achieved in DMEM, and cell viability was higher compared with Opti-MEM after transfection. Careful consideration of the impact of Opti-MEM media during the culture or transfection is important for experimental design and results interpretation.

Keywords: Dulbecco's modified Eagle's medium (DMEM); cellular protein expression; opti-MEM; serum starvation; transfection.

PubMed Disclaimer

Conflict of interest statement

The authors declare that they have no conflicts of interest.

Figures

Figure 1
Figure 1
Impact of Opti‐MEM on A549 cells viability, morphology, and protein expression. (a) Observation of cells under microscope in Opti‐MEM and DMEM for 4 days (200×). Scale bar is 100 μm. (b) A549 cell viability in Opti‐MEM and DMEM media, determined by the WST‐1 assay. (c) Expression of cellular proteins in Opti‐MEM and DMEM by western blot. (d) Quantification of PSMA2, CLIC1, HSPA5, and GAPDH expression in Opti‐MEM compared with DMEM from western blot. ***p < 0.001, **p  < 0.01, and *p < 0.05. CLIC1: chloride intracellular channel protein 1; DMEM: Dulbecco's modified Eagle's medium; HSPA5: heat shock 70 kDa protein 5; PSMA2: proteasome subunit alpha Type 2
Figure 2
Figure 2
CLIC1 knockdown efficacy in DMEM media compared with Opti‐MEM. (a) A549 cell morphology under microscope (200×) after knockdown of CLIC1 protein. Scale bar is 100 μm. (b) A549 cell viability after CLIC1 knockdown in DMEM and Opti‐MEM media determined by the WST‐1 assay. (c) Knockdown efficacy of CLIC1 siRNA in DMEM and Opti‐MEM media determined by western blot. (d) Quantification of CLIC1 knockdown efficacy siRNA in Opti‐MEM from western blot. ***p < 0.001, **p < 0.01, and *p < 0.05. CLIC1: chloride intracellular channel protein 1; DMEM: Dulbecco's modified Eagle's medium; KD: knockdown; NSC: nonsilencing control (scrambled siRNA); siRNA: small interfering RNA
Figure 3
Figure 3
PSMA2 knockdown efficacy in DMEM media compared with Opti‐MEM. (a) A549 cell morphology under microscope (200×) after knockdown of PSMA2 protein. Scale bar is 100 μm. (b) A549 cell viability after PSMA2 knockdown in DMEM and Opti‐MEM media determined by WST‐1 assay. (c) Knockdown efficacy of PSAM2 siRNA in DMEM and Opti‐MEM media determined by western blot. (d) Quantification of PSMA2 knockdown efficacy siRNA in Opti‐MEM from western blot. ***p < 0.001, **p < 0.01, and *p < 0.05. DMEM: Dulbecco's modified Eagle's medium; KD: knockdown; NSC: nonsilencing control (scrambled siRNA); PSMA2: proteasome subunit alpha Type 2; siRNA: small interfering RNA

References

    1. http://dharmacon.gelifesciences.com/uploadedFiles/Resources/basic‐dharma.... Date 10 August 2018.
    1. https://cellculturedish.com/ask‐the‐expert/transfection‐optimization‐imp.... Date 10 August 2018.
    1. https://www.thermofisher.com/order/catalog/product/31985070. Date 10 August 2018.
    1. Arrington, D. D. , & Schnellmann, R. G. (2008). Targeting of the molecular chaperone oxygen‐regulated protein 150 (ORP150) to mitochondria and its induction by cellular stress. American Journal of Physiology‐Cell Physiology, 294(2), C641–C650. - PubMed
    1. Bhutia, S. K. , Kegelman, T. P. , Das, S. K. , Azab, B. , Su, Z. , Lee, S. G. , … Fisher, P. B. (2010). Astrocyte elevated gene‐1 induces protective autophagy. Proceedings of the National Academy of Sciences, 107(51), 22243–22248. - PMC - PubMed

Publication types

Grants and funding