Volume 195, Issue 3 , Pages 822-828, September 2006
Uterine transcriptomes of bacteria-induced and ovariectomy-induced preterm labor in mice are characterized by differential expression of arachidonate metabolism genes
Objective
The purpose of this study was to identify changes in gene expression that are associated with preterm labor induced by either bacteria or ovariectomy.
Study design
Pregnant mice (14.5 days of gestation) were allocated to: (1) intrauterine injection of heat-inactivated Escherichia coli; (2) media alone; (3) ovariectomy; or (4) sham operation. The uterine transcriptome was studied with photolithographic, very short oligonucleotide-based microarrays, and arachidonate metabolism genes were assayed with quantitative reverse transcriptase–polymerase chain reaction. Significance was determined by analysis of variance.
Results
Microarray-based gene expression changes in the arachidonate metabolism pathway are associated globally with bacteria-induced preterm labor (P ≤ .0031) and ovariectomy-induced preterm labor (P ≤ .00036). Quantitative real-time reverse transcriptase–polymerase chain reaction measurements demonstrated that bacteria-induced preterm labor substantially increased the expression of genes involved in prostaglandin synthesis. In contrast, ovariectomy-induced preterm labor increased the expression of genes involved in lipoxin, leukotriene, and hydroxyeicosatetraenoic acid synthesis.
Conclusion
Bacteria-induced and ovariectomy-induced preterm labor each express a different balance of genes that are required for the synthesis of prostaglandins, lipoxins, leukotrienes, and hydroxyeicosatetraenoic acids.
Key words: Mouse, Cyclooxygenase pathway, Lipoxygenase pathway, Parturition, Infection, Progesterone
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Supported in part by the Intramural Research Program of the National Institute of Child Health and Human Development, National Institutes of Health, Department of Health and Human Services.Presented at the 26th Annual Meeting of the Society for Maternal Fetal Medicine, January 30-February 4, 2006, Miami, FL.Reprints not available. Address correspondence to Roberto Romero, MD, Hutzel Women's Hospital, 3990 John R, 4th Floor, Detroit, MI 48201-2018 or Ramsi Haddad, PhD, Translational Oncogenomics Laboratory, Karmanos Cancer Institute, Detroit, MI 48201.
PII: S0002-9378(06)00808-8
doi:10.1016/j.ajog.2006.06.053
© 2006 Mosby, Inc. All rights reserved.
Volume 195, Issue 3 , Pages 822-828, September 2006
