Osteogenic microenvironment affects palatal development through glycolysis.

Palate development involves various events, including proliferation, osteogenic differentiation, and epithelial-mesenchymal transition. Disruption of these processes can result in the cleft palate (CP). Mouse embryonic palatal mesenchyme (MEPM) cells are commonly used to explore the mechanism of palatal development and CP. However, the role of the microenvironment in the biological properties of MEPM cells, which undergoes dynamic changes during palate development, is rarely reported. In this study, we investigated whether there were differences between the palatal shelf mesenchyme at different developmental stages. Our results found that the palatal shelves facilitate proliferation at the early palate stage at mouse embryonic day (E) 13.5 and the tendency towards osteogenesis at E15.5, the late palate development stage. And the osteogenic microenvironment, which was mimicked by osteogenic differentiation medium (OIM), affected the biological properties of MEPM cells when compared to the routine medium. Specifically, MEPM cells showed slower proliferation, shorter S phase, increased apoptosis, and less migration distance after osteogenesis. E15.5 MEPM cells were more sensitive than E13.5, showing an earlier change. Moreover, E13.5 MEPM cells had weaker osteogenic ability than E15.5, and both MEPM cells exhibited different Lactate dehydrogenase A (LDHA) and Cytochrome c (CytC) expressions in OIM compared to routine medium, suggesting that glycolysis might be associated with the influence of the osteogenic microenvironment on MEPM cells. By comparing the stemness of the two cells, we investigated that the stemness of E13.5 MEPM cells was stronger than that of E15.5 MEPM cells, and E15.5 MEPM cells were more like differentiated cells than stem cells, as their capacity to differentiate into multiple cell fates was reduced. E13.5 MEPM cells might be the precursor cells of E15.5 MEPM cells. Our results enriched the understanding of the effect of the microenvironment on the biological properties of E13.5 and E15.5 MEPM cells, which should be considered when using MEPM cells as a model for palatal studies in the future.

Pleiotrophin inhibited chondrogenic differentiation potential of dental pulp stem cells.

OBJECTIVE: Studies have shown that the levels of pleiotrophin (PTN) are greatly elevated in the synovial fluid and cartilage in osteoarthritis. Therefore, the purpose of this study was to investigate the effect and mechanism of PTN on the chondrogenic differentiation of DPSCs in inflammatory and normal microenvironments. MATERIALS AND METHODS: A lentiviral vector was used to deplete or overexpress PTN in DPSCs. The inflammatory microenvironment was simulated in vitro by the addition of IL-1ß to the culture medium. The chondrogenic differentiation potential was assessed using Alcian Blue staining and the main chondrogenic markers. A dual-luciferase reporter assay was used to explore the relationship between miR-137 and PTN. RESULTS: The results showed that 0.1 ng/mL IL-1ß treatment during chondrogenic induction greatly impaired the chondrogenic differentiation of DPSCs. Supplementation with PTN and PTN overexpression inhibited chondrogenic differentiation of DPSCs, while PTN depletion promoted chondrogenic differentiation. MiR-137 negatively regulated the expression of PTN by binding to the 3'UTR of its mRNA. Moreover, miR-137 promoted chondrogenic differentiation of DPSCs in normal and inflammatory microenvironments. CONCLUSION: Our results suggest that PTN may play an inhibitory role in the chondrogenic differentiation of DPSCs in normal and inflammatory microenvironments, which is regulated by miR-137.

MicroRNAs in Small Extracellular Vesicles from Amniotic Fluid and Maternal Plasma Associated with Fetal Palate Development in Mice.

Cleft palate (CP) is a common congenital birth defect. Cellular and morphological processes change dynamically during palatogenesis, and any disturbance in this process could result in CP. However, the molecular mechanisms steering this fundamental phase remain unclear. One study suggesting a role for miRNAs in palate development via maternal small extracellular vesicles (SEVs) drew our attention to their potential involvement in palatogenesis. In this study, we used an in vitro model to determine how SEVs derived from amniotic fluid (ASVs) and maternal plasma (MSVs) influence the biological behaviors of mouse embryonic palatal mesenchyme (MEPM) cells and medial edge epithelial (MEE) cells; we also compared time-dependent differential expression (DE) miRNAs in ASVs and MSVs with the DE mRNAs in palate tissue from E13.5 to E15.5 to study the dynamic co-regulation of miRNAs and mRNAs during palatogenesis in vivo. Our results demonstrate that some pivotal biological activities, such as MEPM proliferation, migration, osteogenesis, and MEE apoptosis, might be directed, in part, by stage-specific MSVs and ASVs. We further identified interconnected networks and key miRNAs such as miR-744-5p, miR-323-5p, and miR-3102-5p, offering a roadmap for mechanistic investigations and the identification of early CP biomarkers.

Predicting membrane fouling in a high solid AnMBR treating OFMSW leachate through a genetic algorithm and the optimization of a BP neural network model.

Anaerobic membrane bioreactors are a promising technology in the treatment of high-strength wastewater; however, unpredictable membrane fouling largely limits their scale-up application. This study, therefore, adopted a backpropagation neural network model to predict the membrane filtration performance in a submerged system, which treats leachate from the organic fraction of municipal solid waste. Duration time, water yield flow, influent COD, pH, bulk sludge concentration, and the ratio of ΔTMP to filtration time were selected as input variables to simulate membrane permeability. The membrane pressure slightly increased by 1.1 kPa within 62 days of operation. The results showed that the AnMBR membrane filtration performance was acceptable when treating OFMSW leachate under a flux of 6 L/(m2·h). The model results indicated that the sludge concentration largely determined the membrane fouling with a contribution of 33.8%. Given the local minimization problem in the BP neural network process, a genetic algorithm was introduced to optimize the simulation process, and the relative error of the results was reduced from 5.57% to 3.57%. Conclusively, the artificial neural network could be a useful tool for the prediction of an AnMBR that is so far under development.

Zinc-doped bioactive glass-functionalized polyetheretherketone to enhance the biological response in bone regeneration.

Polyether ether ketone (PEEK) is gaining recognition as a highly promising polymer for orthopedic implants, attributed to its exceptional biocompatibility, ease of processing, and radiation resistance. However, its long-term in vivo application faces challenges, primarily due to suboptimal osseointegration from postimplantation inflammation and immune reactions. Consequently, biofunctionalization of PEEK implant surfaces emerges as a strategic approach to enhance osseointegration and increase the overall success rates of these implants. In our research, we engineered a multifaceted PEEK implant through the in situ integration of chitosan-coated zinc-doped bioactive glass nanoparticles (Zn-BGNs). This novel fabrication imbues the implant with immunomodulatory capabilities while bolstering its osseointegration potential. The biofunctionalized PEEK composite elicited several advantageous responses; it facilitated M2 macrophage polarization, curtailed the production of inflammatory mediators, and augmented the osteogenic differentiation of bone marrow mesenchymal stem cells. The experimental findings underscore the vital and intricate role of biofunctionalized PEEK implants in preserving normal bone immunity and metabolism. This study posits that utilizing chitosan-BGNs represents a direct and effective method for creating multifunctional implants. These implants are designed to facilitate biomineralization and immunomodulation, making them especially apt for orthopedic applications.

The materials flow and membrane filtration performance in treating the organic fraction of municipal solid waste leachate by a high solid type of submerged anaerobic membrane bioreactor.

The anaerobic digestion of leachate from organic fraction of municipal solid waste (OFMSW) is a long-standing challenge. A submerged anaerobic membrane bioreactor (AnMBR) embedding three flat sheet membrane was therefore continuously operated for 63 days to investigate the materials flow and membrane performance. The results obtained show that approximately 90% COD was removed and 86% was converted into methane under an OLR of 5.6 kgCOD/m3·d corresponding to a HRT of 10 days. Under the high solid condition (34.5-61.1 g/L total solids in AnMBR) and flux of 5 and 6 LMH, the membranes was operated practically at constant trans-membrane pressure (TMP). When the membrane was operated at a high flux of 7 LMH the TMP rapid increase occurred in 22 h resulting in a non-recoverable permeability. A sustainable flux was thus identified. This study demonstrated the feasibility of AnMBR treating OFMSW leachate under high solid condition with high flux.

Synthesis of Structurally Defined Cationic Polythiophenes for DNA Binding and Gene Delivery.

Water-soluble conjugated polymers (WCPs) have prospective applications in the field of bioimaging, disease diagnosis, and therapy. However, the use of WCPs with controllability and regioregularity for bioapplications have scarcely been reported. In this work, we synthesized polythiophenes containing ester side chains (P3ET) via Kumada catalyst-transfer polycondensation (KCTP) and confirmed a quasi-"living" chain-growth mechanism. In addition, we obtained cationic regioregular polythiophenes (cPTs) by aminolysis of P3ET with varied chain lengths, and studied DNA binding capability and gene delivery performance. Benefiting from photocontrolled generation of intracellular reactive oxygen species (ROS), the cationic polythiophenes successfully delivered DNA into tumor cells without additional polymer species.

Development of a versatile cell force transducer using moiré mechanism.

Cells alter their shape and morphology and interact with their surrounding environment. Mechanical forces developed by cells to their surrounding environments are fundamental to many physiological processes, such as cell growth, division, migration, and apoptosis. In this paper, a novel optical moiré based biomechanol force sensor was developed for cell traction force mapping. We utilized coherent laser beams to illuminate periodic polymeric substrates where isolated cells were cultured. We demonstrated one-dimensional and two-dimensional traction force mapping via optical moiré for both cardiac myocytes and vascular smooth muscle cells. The magnification effect of the moiré fringe pattern permits a real time monitoring of the mechanical interaction between isolated cells and their underlying periodic polymeric structures.