Cytomegalovirus-induced embryopathology: mouse submandibular salivary gland epithelial-mesenchymal ontogeny as a model
Open Access
- 7 September 2006
- journal article
- research article
- Published by Springer Nature in BMC Developmental Biology
- Vol. 6 (1) , 42
- https://doi.org/10.1186/1471-213x-6-42
Abstract
Human studies suggest, and mouse models clearly demonstrate, that cytomegalovirus (CMV) is dysmorphic to early organ and tissue development. CMV has a particular tropism for embryonic salivary gland and other head mesenchyme. CMV has evolved to co-opt cell signaling networks so to optimize replication and survival, to the detriment of infected tissues. It has been postulated that mesenchymal infection is the critical step in disrupting organogenesis. If so, organogenesis dependent on epithelial-mesenchymal interactions would be particularly vulnerable. In this study, we chose to model the vulnerability by investigating the cell and molecular pathogenesis of CMV infected mouse embryonic submandibular salivary glands (SMGs). We infected E15 SMG explants with mouse CMV (mCMV). Active infection for up to 12 days in vitro results in a remarkable cell and molecular pathology characterized by atypical ductal epithelial hyperplasia, apparent epitheliomesenchymal transformation, oncocytic-like stromal metaplasia, β-catenin nuclear localization, and upregulation of Nfkb2, Relb, Il6, Stat3, and Cox2. Rescue with an antiviral nucleoside analogue indicates that mCMV replication is necessary to initiate and maintain SMG dysmorphogenesis. mCMV infection of embryonic mouse explants results in dysplasia, metaplasia, and, possibly, anaplasia. The molecular pathogenesis appears to center around the activation of canonical and, perhaps more importantly, noncanonical NFκB. Further, COX-2 and IL-6 are important downstream effectors of embryopathology. At the cellular level, there appears to be a consequential interplay between the transformed SMG cells and the surrounding extracellular matrix, resulting in the nuclear translocation of β-catenin. From these studies, a tentative framework has emerged within which additional studies may be planned and performed.Keywords
This publication has 100 references indexed in Scilit:
- Morphogen gradient interpretation by a regulated trafficking step during ligand–receptor transductionGenes & Development, 2005
- α5β1 integrin stimulates Bcl‐2 expression and cell survival through Akt, focal adhesion kinase, and Ca2+/calmodulin‐dependent protein kinase IVJournal of Cellular Biochemistry, 2005
- Synergistic activation of the CMV promoter by NF-κB P50 and PKGBiochemical and Biophysical Research Communications, 2004
- Fibronectin stimulates human lung carcinoma cell growth by inducing cyclooxygenase‐2 (COX‐2) expressionInternational Journal of Cancer, 2004
- FGF8 dose-dependent regulation of embryonic submandibular salivary gland morphogenesisDevelopmental Biology, 2004
- Sonic hedgehog signaling plays an essential role during embryonic salivary gland epithelial branching morphogenesisDevelopmental Dynamics, 2004
- EGF‐stimulated signaling by means of PI3K, PLCγ1, and PKC isozymes regulates branching morphogenesis of the fetal mouse submandibular glandDevelopmental Dynamics, 2003
- Prenatal diagnosis of congenital cytomegalovirus infectionObstetrics & Gynecology, 2001
- The Immediate Early Gene 1 Product of Human Cytomegalovirus Is Sufficient for Up-Regulation of Interleukin-8 Gene ExpressionBiochemical and Biophysical Research Communications, 2000
- Demonstration of Developmental Anomalies in Mouse Fetuses by Transfer of Murine Cytomegalovirus DNA-Injected Eggs to Surrogate MothersThe Journal of Infectious Diseases, 1993