Pregnancy-specific transcriptional changes upon endotoxin exposure in mice

Author:

Motomura Kenichiro12,Romero Roberto13456,Tarca Adi L.127,Galaz Jose12,Bhatti Gaurav12,Done Bogdan12,Arenas-Hernandez Marcia12,Levenson Dustyn12,Slutsky Rebecca1,Hsu Chaur-Dong128,Gomez-Lopez Nardhy129

Affiliation:

1. Perinatology Research Branch, Division of Obstetrics and Maternal-Fetal Medicine, Division of Intramural Research , Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, U.S. Department of Health and Human Services (NICHD/NIH/DHHS), Bethesda, MD , and Detroit, MI , USA

2. Department of Obstetrics and Gynecology , Wayne State University School of Medicine, Detroit , MI , USA

3. Department of Obstetrics and Gynecology , University of Michigan , Ann Arbor , MI , USA

4. Department of Epidemiology and Biostatistics , Michigan State University , East Lansing , MI , USA

5. Center for Molecular Medicine and Genetics , Wayne State University , Detroit , MI , USA

6. Detroit Medical Center , Detroit , MI , USA

7. Department of Computer Science , Wayne State University College of Engineering , Detroit , MI , USA

8. Department of Physiology , Wayne State University School of Medicine , Detroit , MI , USA

9. Department of Biochemistry, Microbiology and Immunology , Wayne State University School of Medicine , Detroit , MI , USA

Abstract

Abstract Objectives Pregnant women are more susceptible to certain infections; however, this increased susceptibility is not fully understood. Herein, systems biology approaches were utilized to elucidate how pregnancy modulates tissue-specific host responses to a bacterial product, endotoxin. Methods Pregnant and non-pregnant mice were injected with endotoxin or saline on 16.5 days post coitum (n=8–11 per group). The uterus, cervix, liver, adrenal gland, kidney, lung, and brain were collected 12 h after injection and transcriptomes were measured using microarrays. Heatmaps and principal component analysis were used for visualization. Differentially expressed genes between groups were assessed using linear models that included interaction terms to determine whether the effect of infection differed with pregnancy status. Pathway analysis was conducted to interpret gene expression changes. Results We report herein a multi-organ atlas of the transcript perturbations in pregnant and non-pregnant mice in response to endotoxin. Pregnancy strongly modified the host responses to endotoxin in the uterus, cervix, and liver. In contrast, pregnancy had a milder effect on the host response to endotoxin in the adrenal gland, lung, and kidney. However, pregnancy did not drastically affect the host response to endotoxin in the brain. Conclusions Pregnancy imprints organ-specific host immune responses upon endotoxin exposure. These findings provide insight into the host-response against microbes during pregnancy.

Publisher

Walter de Gruyter GmbH

Subject

Obstetrics and Gynecology,Pediatrics, Perinatology and Child Health

Reference234 articles.

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