Comparison of Class II open bite correction by temporomandibular joint prostheses or bimaxillary orthognathic surgery.

INTRODUCTION: The aim of this study was to evaluate the outcome of skeletal Class II and anterior open bite patients who received simultaneous Le fort I osteotomies with temporomandibular joint (TMJ) prostheses or bimaxillary orthognathic surgery. MATERIALS AND METHODS: Patients with condylar resorption (CR) were treated by TMJ prostheses and orthognathic surgery and divided into two groups. Cephalometric radiographs were obtained before and after operation to find out the surgical alteration by comparing measures at different time points. RESULTS: 23 patients were included. Mean overbite of the patients was increased by 3.39 mm in TMJ prostheses group and 3.24 mm in orthognathic group. Occlusal plane angle was averagely rotated -6.06° and 1.31°; mandibular plane counterclockwise rotated 12.23° and 5.81°, respectively. The increase of ramus height in TMJ prostheses group were significantly greater than orthognathic surgery group (8.02 ± 1.96 mm vs. -0.09 ± 1.29 mm). The overall treatment effect was stable in both groups during the 1-year follow up. DISCUSSION: Two surgical plans seem to be reliable treatments of anterior open bite and mandibular retrognathism caused by temporomandibular disease. TMJ prostheses with simultaneous Le fort I osteotomies close open bite by lengthening the height of ramus and rotating maxillo-mandibular complex counterclockwise, while bimaxillary orthognathic surgery by rotating maxilla clockwise and mandible counterclockwise without rebuilding ramus.

Heterogeneous Characteristics of the CD90+ Progenitors in the Fibrocartilage of Different Joints.

OBJECTIVE: This study aimed to isolate and compare the mesenchymal stem cell characteristics of CD90+ cells from different fibrocartilage tissues in the temporomandibular joint (TMJ), the knee joint, and the intervertebral joint to further understand the similarities and differences of these 4 fibrocartilage tissues. METHODS: CD90+ cells were isolated from TMJ disc, condylar cartilage, meniscus, and intervertebral disc by using magnetic-activated cell sorting. Cellular assays including 4.5-ethynyl-2'-deoxyuridine labeling, multilineage differentiation, colony formation, and cell migration were conducted to compare their mesenchymal stem cell characteristics. Immunofluorescent staining was performed for observing the expression of actively proliferating CD90+ cells within the tissues. H&E staining and Safranine O staining were used to compare the histological features. RESULTS: The CD90+ cells derived from these 4 fibrocartilage tissues exhibited comparable cell proliferation abilities. However, the cells from the TMJ disc displayed limited multilineage differentiation potential, colony formation, and cell migration abilities in comparison with the cells from the other fibrocartilage tissues. In vivo, there was relatively more abundant expression of CD90+ cells in the TMJ disc during the early postnatal stage. The limited EDU+ cell numbers signified a low proliferation capacity of CD90+ cells in the TMJ disc. In addition, we observed a significant decrease in cell density and a restriction in the synthesis of extracellular proteoglycans in the TMJ disc. CONCLUSION: Our study highlights the spatial heterogeneity of CD90+ cells in the fibrocartilages of different joint tissues, which may contribute to the limited cartilage repair capacity in the TMJ disc.

Divergent chondro/osteogenic transduction laws of fibrocartilage stem cell drive temporomandibular joint osteoarthritis in growing mice.

The anterior disc displacement (ADD) leads to temporomandibular joint osteoarthritis (TMJOA) and mandibular growth retardation in adolescents. To investigate the potential functional role of fibrocartilage stem cells (FCSCs) during the process, a surgical ADD-TMJOA mouse model was established. From 1 week after model generation, ADD mice exhibited aggravated mandibular growth retardation with osteoarthritis (OA)-like joint cartilage degeneration, manifesting with impaired chondrogenic differentiation and loss of subchondral bone homeostasis. Lineage tracing using Gli1-CreER+; Tmfl/-mice and Sox9-CreER+;Tmfl/-mice showed that ADD interfered with the chondrogenic capacity of Gli1+ FCSCs as well as osteogenic differentiation of Sox9+ lineage, mainly in the middle zone of TMJ cartilage. Then, a surgically induced disc reposition (DR) mouse model was generated. The inhibited FCSCs capacity was significantly alleviated by DR treatment in ADD mice. And both the ADD mice and adolescent ADD patients had significantly relieved OA phenotype and improved condylar growth after DR treatment. In conclusion, ADD-TMJOA leads to impaired chondrogenic progenitor capacity and osteogenesis differentiation of FCSCs lineage, resulting in cartilage degeneration and loss of subchondral bone homeostasis, finally causing TMJ growth retardation. DR at an early stage could significantly alleviate cartilage degeneration and restore TMJ cartilage growth potential.

Immobilization of zinc and cadmium by biochar-based sulfidated nanoscale zero-valent iron in a co-contaminated soil: Performance, mechanism, and microbial response.

Mining and smelting of mineral resources causes excessive accumulation of potentially toxic metals (PTMs) in surrounding soils. Here, biochar-based sulfidated nanoscale zero-valent iron (SNZVI/BC) was designed via a one-step liquid phase reduction method to immobilize cadmium (Cd) and zinc (Zn) in a copolluted arable soil. A 60 d soil incubation experiment revealed that Cd and Zn immobilization efficiency by 6 % SNZVI/BC (25.2-26.2 %) was higher than those by individual SNZVI (13.9-18.0 %) or biochar (14.0-19.3 %) based on the changes in diethylene triamine pentaacetic acid (DTPA)-extractable PTM concentrations in soils, exhibiting a synergistic effect. Cd2+ or Zn2+ replaced isomorphously Fe2+ in amorphous ferrous sulfide, as revealed by XRD, XPS, and high-resolution TEM-EDS, forming metal sulfide precipitates and thus immobilizing PTMs. PTM immobilization was further enhanced by adsorption by biochar and oxidation products (Fe2O3 and Fe3O4) of SNZVI via precipitation and surface complexation. SNZVI/BC also increased the concentration of dissolved organic carbon and soil pH, thus stimulating the abundances of beneficial bacteria, i.e., Bacilli, Clostridia, and Desulfuromonadia. These functional bacteria further facilitated microbial Fe(III) reduction, production of ammonium and available potassium, and immobilization of PTMs in soils. The predicted function of the soil microbial community was improved after supplementation with SNZVI/BC. Overall, SNZVI/BC could be a promising functional material that not only immobilized PTMs but also enhanced available nutrients in cocontaminated soils.

A single-cell transcriptional atlas reveals resident progenitor cell niche functions in TMJ disc development and injury.

The biological characteristics of the temporomandibular joint disc involve complex cellular network in cell identity and extracellular matrix composition to modulate jaw function. The lack of a detailed characterization of the network severely limits the development of targeted therapies for temporomandibular joint-related diseases. Here we profiled single-cell transcriptomes of disc cells from mice at different postnatal stages, finding that the fibroblast population could be divided into chondrogenic and non-chondrogenic clusters. We also find that the resident mural cell population is the source of disc progenitors, characterized by ubiquitously active expression of the NOTCH3 and THY1 pathways. Lineage tracing reveals that Myh11+ mural cells coordinate angiogenesis during disc injury but lost their progenitor characteristics and ultimately become Sfrp2+ non-chondrogenic fibroblasts instead of Chad+ chondrogenic fibroblasts. Overall, we reveal multiple insights into the coordinated development of disc cells and are the first to describe the resident mural cell progenitor during disc injury.

Integration of biochar into Ag3PO4/α-Fe2O3 heterojunction for enhanced reactive oxygen species generation towards organic pollutants removal.

A biochar (BC) harbored Ag3PO4/α-Fe2O3 type-Ⅰ heterojunction (Ag-Fe-BC) was prepared by a hydrothermal-impregnation method to transfer active center of heterojunctions. The electrochemical and spectroscopic tests demonstrated that BC enhanced the catalytic performance of the heterojunction by enhancing photocurrent, reducing fluorescence intensity, and facilitating separation of electron-hole pairs. The photocatalytic activity showed the Ag-Fe-BC (5:1:3) could degrade Rhodamine B (20 mg/L) by up to 92.7%, which was 3.35 times higher than Ag3PO4/α-Fe2O3. Tetracycline and ciprofloxacin (20 mg/L) were degraded efficiently by 58.3% and 79.4% within 2 h, respectively. Electron paramagnetic resonance and scavenging experiments confirmed the major reactive oxygen species (ROS) consisted of singlet oxygen (1O2) and superoxide (·O2-). Excellent RhB adsorption and electrons capturing capacity of BC facilitated electron-hole pairs separation and ROS transferring to target organics followed by elevated degradation. Thus, a facile method was proposed to synthesize a highly efficient visible-light responsive photocatalyst for degradation of various organics in water.

Pyrolysis temperature and feedstock affected Cr(VI) removal capacity of sulfidated zerovalent iron: Importance of surface area and electrical conductivity.

Herein, feedstock (pinewood, rice straw, and dairy manure) and pyrolysis temperature (300, 500, and 700 °C) were selected as the influencing factors of properties of biochar (BC) to identify the contribution of biochar's matrix on Cr(VI) removal by BC-supported sulfidated zero-valent iron (S-ZVI/BC). Results showed that higher temperature was more conducible to improve the electrochemical properties and specific surface areas of composites. Raman spectra of S-ZVI supported by pinewood-derived BC (S-ZVI/PBC) showed the ID/IG ratio increased from 0.639 to 0.975 for the composites prepared at 300-700 °C, indicating the increased structural defects and resulting in the greatest Cr(VI) removal (35.81 mg g-1) and reduction (30.21 mg g-1) amounts of S-ZVI/PBC700. Besides, S-ZVI/PBC exhibited greater electrochemical reactivity and surface area than S-ZVI harbored by BC from dairy manure and rice straw. Additionally, Pearson correlation analysis revealed that Cr(VI) removal was significantly positively correlated to surface area (R2 = 0.90) and negatively correlated to Tafel corrosive potential (R2 = 0.88). Both desorption experiment and XPS spectra of spent sorbents showed that reduction predominated the detoxifying mechanism of Cr(VI) followed by adsorption (due to corrosively-generated iron oxides and BC) and precipitation (Cr2S3). This suggested that biochar with greater specific surface area and electrical conductivity is more favorable to immobilize S-ZVI with respect to Cr(VI) removal.

Carbon matrix of biochar from biomass modeling components facilitates electron transfer from zero-valent iron to Cr(VI).

Biochar-harbored zero-valent iron (ZVI/BC) has been extensively used to detoxify hexavalent chromium (Cr(VI)). However, the role played by biochar in promoting electron transfer of ZVI and Cr(VI) reduction was not fully uncovered. Herein, three biomass modeling components (cellulose, hemicellulose, and lignin) and their blends were utilized to synthesize ZVI/BC via co-pyrolysis with hematite. X-ray diffraction analysis showed that hematite was successfully reduced to ZVI in nitrogen ambience. Batch sorption experiment showed that mass ratio (hematite to lignocellulosic component) of 1:20 is most optimal for reduction of Cr(VI) by ZVI/BCs. ZVI supported by BC derived from cellulose, hemicellulose, and their binary mixture demonstrated better Cr(VI) removal capacity (23.8-38.3 mg g-1) owing to higher ordered and graphitic carbon structure as revealed by Raman spectrum. In addition, lower Tafel corrosion potentials and smaller electrochemical impedance arc radiuses were observed based on electrochemical analysis, suggesting their higher electrical conductivity and faster electron transfer, whereas the BCs derived from lignin and lignin-containing hybrids were not conducive to electron transfer of ZVI due to lower degree of graphitization, thus compromising Cr(VI) removal by ZVI/BC (7.7-17.7 mg g-1). As per X-ray photoelectron spectroscopy analysis, reduction, complexation, and co-precipitation were the main mechanisms for Cr(VI) removal. The present study provided a scientific evidence for screening plant-derived biomass feedstock with high contents of cellulose and hemicellulose and low lignin content to fabricate ZVI/BC to achieve high Cr(VI) removal.

Increased structural defects of graphene oxide compromised reductive capacity of ZVI towards hexavalent chromium.

Graphene oxide (GO) was treated with irradiation beams to understand the defective degree of carbon structure of GO in relation to electron transfer property of impregnated zerovalent iron (ZVI). The GO-supported ZVI (ZVI/GO) was synthesized and then characterized by an X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), Fourier transform infrared spectroscopy (FTIR) and Raman spectroscopy. The results showed that the oxygen-bearing functional groups, oxygen content and structural disorder were increased as a function of irradiation beam intensity. ZVI was dominant in the composites, but proportion of iron oxide increased with greater oxygen content. Batch sorption revealed that Cr(VI) removal decreased from 20.11 g kg-1 to 2.30 g kg-1 as solution pH rose from 3 to 9. Cr(VI) removal capacity was 26.39 g kg-1, 23.12 g kg-1 and 12.35 g kg-1 for ZVI/GO0, ZVI/GO12.3 and ZVI/GO36.9, respectively. The reduction capacity of sorbents followed similar trends as Cr(VI) sorption as per desorption experiment, which accounted for a major Cr(VI) detoxification mechanism by ZVI/GO composites. The electrochemical tests demonstrated that unfavorable electron transfer rate of ZVI/GO composites was aggravated by greater structural disorder of GO. Thus, higher dose of irradiations could create more disorder in graphitic carbon and promote oxidation of ZVI, which hindered Cr(VI) reduction.

The contribution of lignocellulosic constituents to Cr(VI) reduction capacity of biochar-supported zerovalent iron.

Biochars (BCs) derived from individual and blending lignocellulosic constituents were prepared to harbor zerovalent iron (ZVI/BC) in an effort to discriminate significance of each constituent or combination in ZVI/BC for Cr(VI) removal. BCs and ZVI/BC were characterized by TGA/GSC, XRD, Raman and BET analyses. Cellulose (BCC) and hemicellulose (BCH)-derived BCs has greater C content, H/C ratio, surface area and mass loss than BCs derived from lignin or lignin-containing biopolymer blends (BCLX). As per sorption and XPS analysis, ZVI/BC demonstrated greater Cr(VI) removal capacity than respective BCs, in which reduction accounted for over 77% Cr(VI) detoxification. Cr(VI) reduction by ZVI harbored by BCC and BCH was 19.72-16.54 g kg-1, compared to 5.97-4.26 g kg-1 for BCLX. ZVI/BC prepared by three-biopolymer blends with (12.63 g kg-1) or without (12.32 g kg-1) mineral approximated pinewood-BC (BCP) (13.02 g kg-1) for Cr(VI) reduction, suggesting minerals are not important constituent. Tafel analysis showed BCC and BCH, with lower ID/IG ratio owing to greater graphitization, were more conducible to transfer electron of ZVI in Cr(VI) reduction than BCLX. Thus, cellulose, hemicellulose and lignin can offer a good prediction of property of natural biomass, in which BCC and BCH favor electron transfer of ZVI but BCL is not electroactive.

Preparation of highly-conductive pyrogenic carbon-supported zero-valent iron for enhanced Cr(â ¥) reduction.

In this work, electron transfer (ET) moiety of PC was ascertained in chromate (Cr(Ⅵ)) reduction by zero-valent iron supported by pyrogenic carbon (PC) (ZVI/PC) prepared by pyrolysis of hematite (α-Fe2O3)-treated pinewood. X-ray diffraction analysis suggested successive phase transformation of α-Fe2O3→magnetite (Fe3O4)→wustite (FeO)→ZVI (Feo). Raman spectra and Brunauer-Emmett-Teller analysis revealed that ZVI/PC is characterized with more ordered graphitic carbon and greater surface area than pristine PC. Maximal Cr(Ⅵ) removal capacity (pH = 3) as predicted by Langmuir isotherm model were 5.78, 36.12 and 8.39 g kg-1 for PC, ZVI/PC and ZVI, respectively. ZVI/PC maintained significantly greater Cr(Ⅵ) removal capacity than ZVI and PC at pH 3-9, but Cr(Ⅵ) removal dropped rapidly to 6.78 g kg-1 at pH 4 and above. X-ray photoelectron spectroscopy and successive desorption of Cr-laden ZVI/PC and ZVI showed trivalent Cr was the dominant species, suggesting reduction was an important mechanism for Cr(Ⅵ) detoxification. Electrochemical analysis demonstrated that ZVI/PC exhibited greater Tafel corrosion rate and ET quantity, with lower electrical resistance. Besides, Cr(Ⅵ) reduction showed reversal trend with electrical resistance of ZVI/PC. To conclude, ET capacity was closely associated with electrical conductivity of ZVI/PC due to intensified conductive graphitic carbon structure of PC at higher pyrogenic temperatures.