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. Author manuscript; available in PMC: 2015 Dec 1.
Published in final edited form as: Reprod Toxicol. 2014 Oct 17;50:154–162. doi: 10.1016/j.reprotox.2014.10.005

Table 1.

Fold change of selected genes from Innate and Adaptive Immune Responses PCR Array1

PCR Array qRT-PCR Validation
Gene Name Symbol Fold changea P-value Fold change (± SE)a P-value
Heme oxygenase (decycling) 1 HMOX1 2.9 0.01 4.159 ± 0.524 <0.001
Interleukin 6 (interferon, beta 2) IL6 9.7 2.2 E-5 46.555 ± 15.197 0.016
Lipopolysaccharide binding protein LBP 3.5 0.018 2.301 ± 0.171 0.001
Triggering receptor expressed on myeloid cells 1 TREM1 115.2 0.0009 7.079 ±0.162 <0.001
Prostaglandin-endoperoxide synthase 2b PTGS2 −1.2 0.59 7.677 ± 2.128 0.018
1

HTR-8 cells were treated with DMSO (0.1 % v/v; solvent control) or 10 μM TBBPA for 24 h. The Innate and Adaptive Immune Responses PCR Array (SABiosciences; Valencia, CA) was used to explore changes in gene expression as described in the “Materials and Methods” section. Fold changes and p-values are shown for the genes with significant changes compared to the solvent control.

a

Mean fold change relative to the solvent control. PCR Array: n= 4 experiments, qRT-PCR Validation: n=3 experiments. Each experiment was performed in triplicate.

b

Although the change was not statistically significant in the array, gene expression was assessed by qRT-PCR because of this gene’s pertinence to human pregnancy.