Abstract

BackgroundHuman cytomegalovirus (HCMV) infection in utero is very common during pregnancy, which can lead to adverse outcomes in both pregnancy and progeny, but its pathogenesis has not been fully clarified. The decrease of extravillous cytotrophoblasts (EVT) invasion is an essential pathophysiological process of some pregnancy complications. Hippo-YAP signaling pathway plays an important role in regulating cell proliferation and apoptosis. However, whether YAP is involved in HCMV uterine infection remains to be studied.MethodsThe primary EVT was cultured and infected by the HCMV strain AD169 virus in vitro. Immunofluorescence staining of HCMVpp65 antigen was conducted afterward to confirm the establishment of an infection model. The optimal virus infection dose was determined by the EVT proliferation status in vitro. Real-time PCR was performed to examine the mRNA level of major genes involved in the Hippo pathway in EVT after HCMV infection. The effect of HCMV on the expression of YAP protein in EVT was evaluated by Immunofluorescence staining and Western blot. An in vitro cell invasion assay was carried out to analyze the influence of HCMV on EVT invasion. The changes of EVT invasion was accessed by establishing YAP silencing and over-expression models using YAP1 specific siRNA and plasmid pcDH.ResultsThe optimal HCMV infection dose was 282.5TCID50/ml. Compared to the control group, the infection of HCMV significantly reduced the mRNA expression of Mst1, Mst2, SAV, Lats1, Lats2, Mob1, YAP1, TAZ, TEAD1-4 genes and YAP protein expression in the Hippo-YAP pathway. HCMV infection also decreased the EVT invasion. In non-infected EVT, the number of transmembrane EVT cells was significantly reduced when YAP1 gene was silenced, while it was significantly increased when YAP1 gene was over-expressed. In the HCMV-infected EVT, the number of transmembrane EVT cells significantly increased when over-expressed and eventually recovered to the level of NC.ConclusionsHCMV may decrease EVT invasion by inhibiting the expression of mRNA and protein of YAP in the Hippo-YAP signaling pathway. HCMV eventually reduces the invasion ability of EVT by inhibiting multiple genes in the Hippo-YAP signaling pathway, especially inhibiting YAP which serves as the downstream effector.

Highlights

  • Human cytomegalovirus (HCMV), known as human herpesvirus 5 (HHV-5), belongs to the Herpesviridae family, subfamily Betaherpesviridae

  • The purity of isolated extravillous cytotrophoblasts (EVT) Immunocytochemistry staining showed that isolated primary EVTs were mononuclear, triangular or irregular in shape and almost all of the cells were positively stained for CK7 (Fig. 1A) and c-erbB-2 (Fig. 1C), indicating the high purity of primary EVT isolated from human chorionic villi

  • In vitro HCMV infection of EVT Immunofluorescence staining showed that a large number of red HCMVpp65 antigen signals were expressed in the cytoplasm of the HCMV-infected EVT (Fig. 2A); while it was not seen in the control group (Fig. 2A)

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Summary

Introduction

Human cytomegalovirus (HCMV), known as human herpesvirus 5 (HHV-5), belongs to the Herpesviridae family, subfamily Betaherpesviridae. It is the virus with the largest nucleic acid molecular weight in the Betaherpesvirinae subfamily. HCMV is considered as the most common pathogen causing active infections, intrauterine infections of embryos or fetuses in pregnant women. Intrauterine transmission after HCMV infection in pregnant women can lead to congenital infections of embryos and fetuses, causing abnormal pregnancy outcomes such as embryo suspension, abortion, retardation of fetal growth, microcephaly and stillbirth. Human cytomegalovirus (HCMV) infection in utero is very common during pregnancy, which can lead to adverse outcomes in both pregnancy and progeny, but its pathogenesis has not been fully clarified. Whether YAP is involved in HCMV uterine infection remains to be studied

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