Comprehensive Analysis of the Expression and Functions of Pattern Recognition Receptors in Differentiated Cytotrophoblasts Derived from Term Human Placentas

Author:

Motomura Kenichiro12ORCID,Morita Hideaki1ORCID,Okada Naoko13ORCID,Matsuda Akio1,Nakae Susumu4ORCID,Fujieda Mikiya5,Sago Haruhiko2ORCID,Saito Hirohisa1,Matsumoto Kenji1ORCID

Affiliation:

1. *Department of Allergy and Clinical Immunology, National Research Institute for Child Health and Development, Tokyo, Japan

2. †Center for Maternal-Fetal, Neonatal and Reproductive Medicine, National Center for Child Health and Development, Tokyo, Japan

3. ‡Department of Pharmaceutical Sciences, Nihon Pharmaceutical University, Saitama, Japan

4. §Graduate School of Integrated Sciences for Life, Hiroshima University, Hiroshima, Japan

5. ¶Department of Pediatrics, Kochi Medical School, Kochi, Japan

Abstract

Abstract Pregnant women are exposed to various microbes, some of which can harm the mother and/or fetus and can lead to life-long morbidity and even death. The syncytiotrophoblast (STB) covers the placental villi and comes into direct contact with pathogens contained in the maternal blood and plays a key role in placental host defense. However, the precise mechanisms whereby the STB recognizes and responds to pathogenic microbes remain unclear. In this study, we comprehensively analyzed the expression of functional pattern recognition receptors, which are responsible for tissue defense against pathogens, in a primary STB model differentiated from highly purified human term cytotrophoblasts (CTBs). Screening for mRNA expression and multiplex cytokine/chemokine production demonstrated that differentiated CTBs (dCTBs) predominantly expressed dsRNA receptors, including TLR3, MDA5, and RIG-I. We confirmed that term human placentas also expressed TLR3. Transcriptome analysis revealed common and unique responses of dCTBs to a synthetic dsRNA (polyinosinic-polycytidylic acid) compared with human peripheral mononuclear cells. Moreover, polyinosinic-polycytidylic acid induced the release of type I and type III IFNs (IFN-β, IFN-λ1, IFN-λ2, IFN-λ3), as well as mRNA expression of IFN-stimulated genes (IFIT1, MX1, and OAS1). dCTBs underwent apoptosis via the mitochondrial pathway in response to dsRNA stimulation. These results suggest that dsRNA receptors expressed on the STB are key players in antiviral defense in the placenta. Elucidation of the underpinnings of these defense processes can help us better understand the pathophysiology of viral infections during pregnancy.

Funder

MEXT | Japan Society for the Promotion of Science

National research institute for child health and development

Nipponham Foundation

Kanzawa Medical Research Foundation

Publisher

The American Association of Immunologists

Subject

Immunology,Immunology and Allergy

Reference100 articles.

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