The role of extracellular vesicles throughout normal pregnancy and in relation to oral bacteria.

BACKGROUND: Recently, the relationship between the maternal oral environment and complicated pregnancies has been discussed in depth. The depletion of all bacterial flora, including oral bacteria, significantly decreased the size of the maternal placenta and suppressed fetal bone reabsorption. Furthermore, bacterial flora DNA of the host placenta has been reported to be remarkably similar to that of oral flora DNA. These findings indicate that maternal oral flora has a considerable effect on the formation of the placenta and fetus. HIGHLIGHT: Placenta is a sophisticated tissue, in which the fetus and mother exchange substance. Placental homeostasis affects the maternal and fetal health; therefore, any disorder in this context is directly linked to serious health issues for the mother and developmental inhibition of the fetus. Extracellular vesicles (EVs) possess and deliver various factors (i.e., nucleic acids, proteins, and lipids) to distant organs through intercellular crosstalk. EVs are released during natural physiological events as well as under stress conditions. EVs derived from reproductive tissues, such as the placenta, are deeply involved in all stages of pregnancy, including the maturation and survival of sperm and egg, various events during fertilization, implantation, spiral artery remodeling, and immunomodulation. CONCLUSION: To date, the precise role of EVs in oral diseases, including periodontal disease, is not well understood. Nonetheless, placental EVs are likely to attract attention, in the future, to objectively evaluate the effects of periodontal disease on maternal and fetal health. Therefore, the role of EVs throughout normal pregnancy will be discussed in this review.

Outer membrane vesicles of Porphyromonas gingivalis: Novel communication tool and strategy.

Extracellular vesicles (EVs) have been recognized as a universal method of cellular communications and are reportedly produced in bacteria, archaea, and eukaryotes. Bacterial EVs are often called "Outer Membrane Vesicles" (OMVs) as they were the result of a controlled blebbing of the outer membrane of gram-negative bacteria such as Porphyromonas gingivalis (P. gingivalis). Bacterial EVs are natural messengers, implicated in intra- and inter-species cell-to-cell communication among microorganism populations present in microbiota. Bacteria can incorporate their pathogens into OMVs; the content of OMVs differs, depending on the type of bacteria. The production of distinct types of OMVs can be mediated by different factors and routes. A recent study highlighted OMVs ability to carry crucial molecules implicated in immune modulation, and, nowadays, they are considered as a way to communicate and transfer messages from the bacteria to the host and vice versa. This review article focuses on the current understanding of OMVs produced from major oral bacteria, P. gingivalis: generation, characteristics, and contents as well as the involvement in signal transduction of host cells and systemic diseases. Our recent study regarding the action of P. gingivalis OMVs in the living body is also summarized.

O-GlcNAcylation drives calcium signaling toward osteoblast differentiation: A bioinformatics-oriented study.

This study aimed to reveal the possible mechanisms by which O-linked-N-acetylglucosaminylation (O-GlcNAcylation) regulates osteoblast differentiation using a series of bioinformatics-oriented experiments. To examine the influence of O-GlcNAcylation levels on osteoblast differentiation, osteoblastic MC3T3-E1 cells were treated with O-GlcNAc transferase (OGT) and O-GlcNAcase (OGA) inhibitors. Correlations between the levels of O-GlcNAcylation and the expression of osteogenic markers as well as OGT were evaluated by qPCR and western blotting. The O-GlcNAcylated proteins assumed to correlate with Runx2 expression were retrieved from several public databases and used for further bioinformatics analysis. Following the findings of the bioinformatics analysis, intracellular calcium ([Ca2+ ]i ) was monitored in the cells treated with OGT and OGA inhibitors using a confocal laser-scanning microscope (CLS). The interaction effect between O-GlcNAcylation and [Ca2+ ]i on osteogenic marker expression was determined using stable OGT knockdown MC3T3-E1 cells. O-GlcNAcylation was positively associated with osteoblast differentiation. The time-course profile of global O-GlcNAcylated proteins showed a distinctive pattern with different molecular weights during osteoblast differentiation. The expression pattern of several O-GlcNAcylated proteins was significantly similar to that of Runx2 expression. Bioinformatic analysis of the retrieved Runx2-related-O-GlcNAcylated-proteins revealed the importance of [Ca2+ ]i . CLS showed that alteration of O-GlcNAcylation rapidly changed [Ca2+ ]i in MC3T3-E1 cells. O-GlcNAcylation and [Ca2+ ]i showed an interaction effect on the expression of osteogenic markers. OGT knockdown disrupted the [Ca2+ ]i -induced expression changes of osteogenic markers. O-GlcNAcylation interacts with [Ca2+ ]i and elicits osteoblast differentiation by regulating the expression of osteogenic markers.