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Table 1 High-throughput qRT-PCR of NHBE cells treated with CdSe or InP QDs

From: Quantifying engineered nanomaterial toxicity: comparison of common cytotoxicity and gene expression measurements

Cell response pathway

Gene name

Fold change (5 µg/mL, 24 h)

Fold change (80 µg/mL, 6 h)

CdSe-MUA

InP-MUA

CdSe-MUA

InP-MUA

DNA damage

CDK1

0.50 ± 0.15

0.21 ± 0.09

1.92 ± 0.10

1.15 ± 0.01

GADD45A

1.18 ± 0.02

1.00 ± 0.09

4.17 ± 0.95

4.95 ± 0.66

SFN

1.50 ± 0.04

1.75 ± 0.04

2.84 ± 0.50

0.86 ± 0.44

DNA repair

BRCA1

0.55 ± 0.07

0.18 ± 0.03

1.20 ± 0.05

0.96 ± 0.22

BRCA2

0.57 ± 0.07

0.20 ± 0.02

3.06 ± 0.48

0.43 ± 0.17

XPC

0.89 ± 0.02

0.79 ± 0.05

0.84 ± 0.15

2.29 ± 0.15

Mitochondrial function and repair

AHR

0.99 ± 0.04

1.11 ± 0.05

2.18 ± 0.29

2.35 ± 0.43

CYP1A1

1.02 ± 0.11

1.17 ± 0.17

1.38 ± 0.35

0.17 ± 0.04

CYP1B1

1.29 ± 0.02

1.16 ± 0.07

3.19 ± 0.46

0.70 ± 0.09

DHFR

0.57 ± 0.02

0.40 ± 0.02

1.10 ± 0.10

1.15 ± 0.07

UCP1

2.29 ± 0.50

2.20 ± 1.64

4.32 ± 0.87

7.20 ± 0.51

Proliferation

VEGFA

1.43 ± 0.05

1.44 ± 0.17

2.18 ± 0.48

1.21 ± 0.16

  1. Cells were incubated with 5 μg/mL CdSe or InP QDs for 24 h or with 80 μg/mL CdSe or InP QDs for 6 h. Gene expression changes for different classes of cellular functions and processes were measured by qRT-PCR. Values are expressed as fold change relative to media controls (= 1.0). Italics values indicates a twofold or greater decrease in gene expression relative to untreated cells (≤ 0.5) while bold italics highlights twofold or greater increases in gene expression relative to untreated cells (≥ 2.0). All experiments were independently repeated three times (n = 3). Errors represent one standard deviation