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Published May 2011 | Accepted Version
Journal Article Open

Activation of the maternal immune system induces endocrine changes in the placenta via IL-6


Activation of the maternal immune system in rodent models sets in motion a cascade of molecular pathways that ultimately result in autism- and schizophrenia-related behaviors in offspring. The finding that interleukin-6 (IL-6) is a crucial mediator of these effects led us to examine the mechanism by which this cytokine influences fetal development in vivo. Here we focus on the placenta as the site of direct interaction between mother and fetus and as a principal modulator of fetal development. We find that maternal immune activation (MIA) with a viral mimic, synthetic double-stranded RNA (poly(I:C)), increases IL-6 mRNA as well as maternally-derived IL-6 protein in the placenta. Placentas from MIA mothers exhibit increases in CD69+ decidual macrophages, granulocytes and uterine NK cells, indicating elevated early immune activation. Maternally-derived IL-6 mediates activation of the JAK/STAT3 pathway specifically in the spongiotrophoblast layer of the placenta, which results in expression of acute phase genes. Importantly, this parallels an IL-6-dependent disruption of the growth hormone-insulin-like growth factor (GH-IGF) axis that is characterized by decreased GH, IGFI and IGFBP3 levels. In addition, we observe an IL-6-dependent induction in pro-lactin-like protein-K (PLP-K) expression as well as MIA-related alterations in other placental endocrine factors. Together, these IL-6-mediated effects of MIA on the placenta represent an indirect mechanism by which MIA can alter fetal development.

Additional Information

© 2010 Elsevier Inc. Received 22 November 2010; Received in revised form 21 December 2010; Accepted 22 December 2010; Available online 30 December 2010. The authors acknowledge the kind assistance of B. Deverman and A. Bonnin with reviewing the manuscript; A. Colon, L. Sandoval and R. Sauza with caring for and maintaining the animals; and N. Tetreault and D. Anderson with providing the LMD and qPCR equipment. This research was supported by an Autism Speaks Dennis Weatherstone Pre-Doctoral Fellowship and by a Caltech training grant from the National Institutes of Health (NIH/NRSA 5 T32 GM07737).

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