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Ocean temperature prediction has always occupied an important position in the research of ocean-related fields. The current studies are mostly based on the temperature of the sea surface, but the prediction of ocean internal temperature is more important in practical applications. At present, most of the research studies on the prediction of ocean internal temperature are based on time series, few of which consider the dual characteristics of time and space. Therefore, the accuracy is insufficient, especially for the prediction of thermocline and deep-sea locations. This letter proposes the stereo spatial and temporal 4-D convolution model (SST-4D-CNN) to predict the temperature in the ocean, which fully considers the dual characteristics of time series and oceanic spatial relationship to improve the prediction accuracy. The model includes 4-D convolution module, residual module and recalibration module to predict the horizontal and profile temperature changes from the sea surface to 2000-m underwater. In this letter, the prediction experiment is carried out using the real-time analysis data-temperature dataset from National Marine Data Center. The results show that the accuracy of this method in horizontal and profile prediction is above 98.02%, and most of them are more than 99%.

In this study, a new method comprising graphene oxide (GO) and amino group modifications of carbon felt (CF) electrode material surfaces was employed to improve the initial adhesion capacities of b...

Microbe-photocatalyst biohybrids, integrating the optimal attributes of whole-cell catalysts and nanometer photocatalysts, have emerged as a promising strategy for environment-associated applications. However, few such biohybrids have been tested for complex pollution systems. Herein, we constructed an outer membrane photosensitized Geobacter sulfurreducens (G. sulfurreducens)-CdS biohybrid, which enabled to generate stronger photocurrent in response to irradiation and meanwhile achieved an significant promotion for the redox transformation of Cr(VI) and tetracycline compared with that of bare G. sulfurreducens or CdS counterparts. Further analysis revealed that the outer membrane played a significant role in photoelectron transfer. Differential pulse voltammetry (DPV) tests demonstrated that CdS enhanced the catalytic activity of C-type cytochromes on the outer membrane under irradiation, resulting in the increase of electron-hole pairs separation efficiency. The possible degradation pathway of tetracycline was proposed based on determined intermediates, whose toxicities were well evaluated. Importantly, the toxicity of the final detected intermediates was apparently decreased. Overall, this work aims to explore the working mechanisms of the novel G. sulfurreducens-CdS biohybrid system and opens up a new avenue to purifying combined wastewater by microbe-photocatalyst biohybrids.

Zingiberis Rhizoma (ZR) and Zingiberis Rhizoma Carbonisata (ZRC), as two forms of ginger-based herbal drugs used in China for at least 2000 years, have been recorded in Chinese Pharmacopoeia and applied for specific indications in traditional Chinese medicine (TCM).The present study aimed to explore the underlying therapeutic and processing mechanism of the absorbed components of ZR and ZRC on deficiency-cold and hemorrhagic syndrome (DCHS) using network pharmacological technique combined with pharmacokinetics strategy.In this study, a rapid and sensitive approach was conceived to simultaneously determine the seven components (zingiberone, 6-gingerol, 8-gingerol, 6-shogaol, 6-paradol, diacetyl-6-gingerol and 10-gingerol) in rat serum by HPLC-DAD-MS. The network pharmacological technique was employed to evaluate the effect of the absorbed components of ZR and ZRC on DCHS. Also, the vitro experiments were carried out to validate the functions of the seven compounds on coagulation and other major haematological effects.The values of intra-assay and inter-assay precision were determined to be less than 7.44%, with an accuracy value ranging from 83.64% to 107.99%. Analysis of rat plasma revealed that the extraction recoveries and matrix effects of the seven analytes were85.76%. The method for validation following oral administration of ZR and ZRC to rats was proved to be a success in the pharmacokinetic study of the seven ingredients. Pharmacokinetics showed that ZR processing could enhance the absorption and utilization of 6-shogaol, 6-paradol and diacetyl-6-gingerol, meanwhile reduce the absorption of 6-gingerol, 8-gingerol, and 10-gingerol. Through the pathway enrichment analysis, it was found that the significant biological process of ZR and ZRC on DCHS was primarily associated with complement, coagulation cascades and platelet activation pathways. The vitro experiments indicated that zingiberone, 6-paradol and diacetyl-6-gingerol had a hemostatic effect by upregulating the expression of one or more targets such as TNF-α, FⅩa, FⅫ, FⅧ, ICAM-1, vWF and ITGB3. While 6-gingerol, 6-shogaol, 8-gingerol and 10-gingerol played a critical role in promoting blood circulation by increasing the expression of TM and/or PORC, and/or reducing the expression of ITGB3.In brief, network pharmacological technique in combination with pharmacokinetics strategy provided an applicable method for pharmacological mechanism study of ZR and ZRC, which, also, could be used as reference for quality control of the two drugs. In a broader sense, this combined strategy might even be valuable in uncovering the therapeutic and processing mechanism of Chinese herbs on a systematic level.

Semiconducting minerals are ubiquitous in soil and their association with microbes often affects the environment. In this study, the impacts of zinc sulfide (ZnS, used as a model compound for semiconducting sphalerite) on As/Fe mobility of flooded tailing soils under dark and intermittent illumination conditions were elucidated for the first time. Microbial reductive dissolution of As(V) and Fe(III) was more pronounced under intermittent illumination than under dark conditions. In ZnS-amended soils, release of As(III) and Fe(II) was 1.3 and 1.7 times higher, respectively, under intermittent illumination than the highest concentrations released from soils amended with acetate alone under dark conditions (12741.1 ± 714.3 μg/L and 37.9 ± 2.3 mg/L, respectively). However, under dark conditions in ZnS-amended soil, the release of As(III) and Fe(II) was 0.8 and 0.7 times that of the highest concentrations released from soils amended with acetate under dark conditions, respectively. Treatment with ZnS potentially decreased the abundance of several metal-reducing bacteria (e.g., Bacillus, Geobacter, Clostridium, and Desulfitobacterium), which resulted in lower As/Fe reduction than for the acetate alone treatment under dark conditions. However, under intermittent illumination, the excited mineral photoholes were scavenged by humic/fulvic acids, and photoelectrons were synchronously separated and participated in the microbial electron chain. The fortification provided by the photoelectrons subsequently boosted As/Fe reduction, even though there was a lower abundance of metal-reducing bacteria. Hence, this study provides an in-depth understanding of the impacts of semiconducting minerals on the fates of metal pollutants, microbial diversity, and the bioavailability of dissolved organic matter in flooded soils.

Microbially mediated bioreduction of iron oxyhydroxide plays an important role in the biogeochemical cycle of iron. Geobacter sulfurreducens is a representative dissimilatory iron-reducing bacterium that assembles electrically conductive pili and cytochromes. The impact of supplementation with γ-Fe2O3 nanoparticles (NPs) (0.2 and 0.6 g) on the G. sulfurreducens-mediated reduction of ferrihydrite was investigated. In the overall performance of microbial ferrihydrite reduction mediated by γ-Fe2O3 NPs, stronger reduction was observed in the presence of direct contact with γ-Fe2O3 NPs than with indirect contact. Compared to the production of Fe(II) derived from biotic modification with ferrihydrite alone, increases greater than 1.6- and 1.4-fold in the production of Fe(II) were detected in the biotic modifications in which direct contact with 0.2 g and 0.6 g γ-Fe2O3 NPs, respectively, occurred. X-ray diffraction analysis indicated that magnetite was a unique representative iron mineral in ferrihydrite when active G. sulfurreducens cells were in direct contact with γ-Fe2O3 NPs. Because of the sorption of biogenic Fe(II) onto γ-Fe2O3 NPs instead of ferrihydrite, the addition of γ-Fe2O3 NPs could also contribute to increased duration of ferrihydrite reduction by preventing ferrihydrite surface passivation. Additionally, electron microscopy analysis confirmed that the direct addition of γ-Fe2O3 NPs stimulated the electrically conductive pili and cytochromes to stretch, facilitating long-range electron transfer between the cells and ferrihydrite. The obtained findings provide a more comprehensive understanding of the effects of iron oxide NPs on soil biogeochemistry.

High efficiency photocatalysts capable of disinfecting a broad-spectrum microorganisms are needed for the practical application of photodisinfection technology. Herein, we synthesized a highly efficient photodisinfection catalyst composed of Ti

Cellular internalization of nanomaterials to endow cells with more functionalities is highly desirable. Herein, a straightforward strategy for internalizing red-emission carbon dots (CDs) into Shewanella xiamenensis is proposed. This suggests that the internalized CDs not only afford enhanced conductivity of bacteria but also trigger the cellular physiological response to secrete abundant electron shuttles to aid the boosting of extracellular electron transfer (EET) efficiency. Additionally, once illuminated, internalized CDs can also serve as light absorbers to allow for photogenerated electrons to be transferred into cellular metabolism to further facilitate light-enhanced EET processes. Specifically, the findings advance the fundamental understanding of the interaction between internalized carbon-based semiconductor and cells in the dark and light, and provide a facile and effective strategy for enhancing EET efficiency.

Ni-doped TiO2 nanospheres decorated with silver plasmonic nanoparticles (Ni-TiO2/Ag) have been successfully synthesized via sol-gel method and photo-deposition approach. In contrast with pure TiO2 and Ni-TiO2, the Ni-TiO2/Ag composite photocatalysts exhibit markedly enhanced visible-light photocatalytic sterilization efficiencies towards Escherichia coli (E. coli). And more importantly, antifungal experiment reveals that the composite can also disinfect ca. 2.0 log10 cfu·mL−1 Fusarium graminearum (F. graminearum) macroconidia within 3 h. The highly efficient antimicrobial activities are ascribed to the introduction of Ni doping and Ag nanoparticles, which increases the visible light utilization and promotes the separation of electron-hole pairs. The photocatalytic disinfection mechanism is studied with scavengers trapping experiments and electron spin-resonance spectroscopy (ESR), which verifies the key role of •O2- and •OH during the microbial inactivation. Our study indicates that the Ni-TiO2/Ag nanocomposite has great potential for use in pathogenic microorganism remediation.

High efficiency photocatalysts capable of disinfecting a broad-spectrum microorganisms are needed for the practical application of photodisinfection technology. Herein, we synthesized a highly efficient photodisinfection catalyst composed of Ti3+ self-doped TiO2 decorated with carbon dots (CDs) and palladium nano-photocatalyst, designated as Pd/CDs/Ti3+-TiO2, via a facile hydrothermal-calcination approach. XPS and ESR analyses were performed to verify that the composite contained Ti3+, while TEM imaging and FTIR confirmed that the samples contained CDs. The as synthesized photocatalysts, particularly the 1% Pd/CDs/Ti3+-TiO2 sample, exhibited superior photocatalyzed antibacterial activity to pure TiO2 against E. coli (～6.5 orders of magnitude increase at 30 min). The 1% Pd/CDs/Ti3+-TiO2 photocatalyst also exhibited efficient photodisinfection of five pathogenic agricultural fungi. The dark cytotoxicity of the 1% Pd/CDs/Ti3+-TiO2 nanocomposites was evaluated on HepG2 and Chinese hamster lung (V79) cells via Cell Counting Kit-8 (CCK-8) and found to be minimal. Lastly, the recycling capacity for the photodisinfective activity of the nanocomposites was evaluated and found to be unchanged after five cycles. Four active species were identified as contributing to the photoinduced antimicrobial activity of the catalyst: h+, •O2−, •OH, and e−. Together, our results indicate that Pd/CDs/Ti3+-TiO2 nanocomposites have great potential in agricultural plant pathogen disinfection.

Two nanostructured electrode materials are fabricated and used to construct cost-effective asymmetric supercapacitors (ASCs). Hierarchical nickel cobalt oxide nanoarrays (NCO-NA) consisting of nanosheets (NCO-NS) or nanowires (NCO-NW) are uniformly grown on Ni foam by a simple, effective, and generally applicable method, while biowaste-derived hierarchical porous carbon (Bio-HPC) with an interconnected microstructure is fabricated by pretreatment with potassium hydroxide and followed by direct pyrolysis. Considering the mass of NiCo2O4, the maximum specific capacitance of the hierarchical NCO-NS and NCO-NW electrodes are 2300 and 2333 F g–1, respectively, and the specific capacitance of the Bio-HPC electrode is 253.9 F g–1 at a scan rate of 5 mV s–1. NCO-NA, Bio-HPC, a piece of polypropylene membrane, and 30 wt % KOH solution are assembled into a high-performance, low-cost ASC with the capability of rapidly storing electrical energy. The NCO-NW//Bio-HPC ASC exhibits a higher energy density compared with N...

An integrated assembled recyclable catalytic material was fabricated by grafting Shewanella xiamenensis (S. xiamenensis) onto poly(vinyl alcohol)/graphene oxide films (denoted as S. xiamenensis–GO/...

Baculovirus entry into insect midgut cells is dependent on a multiprotein complex of per os infectivity factors (PIFs) on the envelopes of occlusion-derived virions (ODVs). The structure and assembly of the PIF complex are largely unknown. To reveal the complete members of the complex, a combination of blue native polyacrylamide gel electrophoresis, liquid chromatography-tandem mass spectrometry, and Western blotting was conducted on three different baculoviruses. The results showed that the PIF complex has a molecular mass of ~500 kDa and consists of nine PIFs, including a newly discovered member (PIF9). To decipher the assembly process, each pif gene was knocked out from the Autographa californica multicapsid nucleopolyhedrovirus (AcMNPV) genome individually by use of synthetic baculovirus technology, and the impact on PIF complex formation was investigated. Deletion of pif8 resulted in the formation of an ~400-kDa subcomplex. Deletion of pif0, -4, -6, -7, or -9 resulted in a subcomplex of ~230 kDa, but deletion of pif1, -2, or -3 abolished formation of any complex. Taken together, our data identified a core complex of ~230 kDa, consisting of PIF1, -2, and -3. This revised the previous knowledge that the core complex was about 170 kDa and contained PIF1 to -4. Analysis of the PIF complex in cellular fractions suggested that it is assembled in the cytoplasm before being transported to the nucleus and subsequently incorporated into the envelopes of ODVs. Only the full complex, not the subcomplex, is resistant to proteolytic attack, indicating the essentiality of correct complex assembly for oral infection. IMPORTANCE Entry of baculovirus into host insects is mediated by a per os infectivity factor (PIF) complex on the envelopes of occlusion-derived viruses (ODVs). Knowledge of the composition and structure of the PIF complex is fundamental to understanding its mode of action. By using multiple approaches, we determined the complete list of proteins (nine) in the PIF complex. In contrast to previous knowledge in the field, the core complex is revised to ~230 kDa and consists of PIF1 to -3 but not PIF4. Interestingly, our results suggest that the PIF complex is formed in the cytoplasm prior to its transport to the nucleus and subsequent incorporation into ODVs. Only the full complex is resistant to proteolytic degradation in the insect midgut, implying the critical role of the entire complex. These findings provide the baseline for future studies on the ODV entry mechanism mediated by the multiprotein complex.

In this study, Z-scheme TiO2-x/AgI heterostructure photocatalysts were fabricated through a solvothermal route and an in situ precipitation method. Compared with pure TiO2-x and AgI, the obtained composite photocatalysts displayed significantly higher photocatalytic degradation efficiency of Rhodamine B (RhB) and tetracycline (TC). The analysis of antimicrobial properties demonstrated that the TiO2-x/AgI-20% composite could also effectively inactivate Escherichia coli (E. coli) and Fusarium graminearum (F. graminearum) macroconidia under visible light. Active species trapping experiments as well as electron spin resonance spectra (ESR) revealed the importance of •O2– and •OH during photocatalysis. Analysis of transient photocurrents and electrochemical impedance spectroscopy (EIS) confirmed that the charge transfer and separation efficiency was significantly improved through the Z-scheme system. It was expected that the novel TiO2-x/AgI composite would be a promising candidate photocatalyst for the environmental applications.

The control and characterization of microbial extracellular electron transfer (EET) reaction-mediated soil arsenic mobilization is still not well understood, which has limited the application of biotechnologies for the remediation of contaminated wastes. In this study, we developed an improved soil bioelectrochemical system (BES) that can decrease the dissolution of As-bearing Fe/Al oxides from anoxic submerged soil by more than 80 % under the application of a 0.9 V external voltage. Combining the results of chemical property and microbial characteristic analyses indicated that an applied voltage was accompanied by a dramatic increase in acetate oxidization and soil substrate bioavailability, facilitating electron transfer reactions for methanogenesis, whereas the applied voltage exhibited a negative effect on microbial EET activities for As/Fe reduction. Subsequently, an additional dual-chamber configuration was employed for comparison and to study the effect of bacteria-electrode interactions on arsenic mobilization; we found that the bioanode and biocathode had reverse effects on the release of As/Fe, suggesting a correlation between the disparate microbial communities and EET-mediated reaction mechanisms on the electrodes. Overall, this study is vital to expand the knowledge of the intimate links between arsenic speciation transformation and microbial electron transport system activity, improve our understanding of BES operation and move towards its application.

In this study, we synthesized a series of rhodium-modified and Ti3+ self-doped TiO2 (Rh/Ti3+-TiO2) nanocomposites via the one-pot method. We prepared samples of Rh/Ti3+-TiO2, which were analyzed using X-ray diffraction (XRD), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), Electron Spin Resonance (ESR), and Uv-vis-NIR analysis. We found that the ability of TiO2 to absorb near-infrared and visible light was significantly improved by the Rh/Ti3+-TiO2 nanocomposites, due to Ti3+ doping as well as modification of Rh. The disinfection properties of these materials were tested using Staphylococcus aureus under visible light and NIR light excitations. The synthesized photocatalyst was found to exhibit significantly enhanced photocatalytic inactivation of S. aureus under both visible and NIR light irradiation, as compared to pure TiO2. This was particularly true with respect to the 5% Rh/Ti3+-TiO2 sample. Our results suggest that the Rh/Ti3+-TiO2 composites could extend the range of optical response range of pure nano TiO2 materials to the Vis -NIR region.

In this study, Ti3+ self-doped TiO2 decorated with metallic copper photocatalyst (marked as Cu/Ti3+-TiO2) was successfully prepared by a novel method. The ESR (Electron Spin Resonance) analysis indicated that the synthesized sample contained Ti3+. The TEM (transmission electron microscopy) images showed that the TiO2 nanoparticles were modified with nano copper. The as-synthesized photocatalyst was found to exhibit markedly enhanced photocatalytic inactivation of E. coli under visible light irradiation compared with pure TiO2, especially in the case of the 10% Cu/Ti3+-TiO2 sample. The photodisinfection effect of the 10% Cu/Ti3+-TiO2 sample was further confirmed using five agricultural pathogenic fungal spores. The photocatalytic inactivation effect against F. graminearum and Botryosphaeria dothidea spores was certified by fluorescent staining of CFDA-AM (the acetoxymethyl ester of the esterase substrate 5-carboxyfluorescein diacetate)/PI (Propidium Iodide). In addition, fluorescent staining by H2DCFDA demonstrated that the intracellular ROS (reactive oxygen species) of the F. graminearum macroconidia was increased after treatment by the photocatalysis.

Baculovirus entry into insect midgut cells is dependent on a multiprotein complex of per os infectivity factors (PIFs) on the envelopes of occlusion-derived virions (ODVs). The structure and assembly of the PIF complex are largely unknown. To reveal the complete members of the complex, a combination of blue native polyacrylamide gel electrophoresis, liquid chromatography-tandem mass spectrometry, and Western blotting was conducted on three different baculoviruses. The results showed that the PIF complex has a molecular mass of ∼500 kDa and consists of nine PIFs, including a newly discovered member (PIF9). To decipher the assembly process, each pif gene was knocked out from the Autographa californica multicapsid nucleopolyhedrovirus (AcMNPV) genome individually by use of synthetic baculovirus technology, and the impact on PIF complex formation was investigated. Deletion of pif8 resulted in the formation of an ∼400-kDa subcomplex. Deletion of pif0, -4, -6, -7, or -9 resulted in a subcomplex of ∼230 kDa, but deletion of pif1, -2, or -3 abolished formation of any complex. Taken together, our data identified a core complex of ∼230 kDa, consisting of PIF1, -2, and -3. This revised the previous knowledge that the core complex was about 170 kDa and contained PIF1 to -4. Analysis of the PIF complex in cellular fractions suggested that it is assembled in the cytoplasm before being transported to the nucleus and subsequently incorporated into the envelopes of ODVs. Only the full complex, not the subcomplex, is resistant to proteolytic attack, indicating the essentiality of correct complex assembly for oral infection. IMPORTANCE Entry of baculovirus into host insects is mediated by a per os infectivity factor (PIF) complex on the envelopes of occlusion-derived viruses (ODVs). Knowledge of the composition and structure of the PIF complex is fundamental to understanding its mode of action. By using multiple approaches, we determined the complete list of proteins (nine) in the PIF complex. In contrast to previous knowledge in the field, the core complex is revised to ∼230 kDa and consists of PIF1 to -3 but not PIF4. Interestingly, our results suggest that the PIF complex is formed in the cytoplasm prior to its transport to the nucleus and subsequent incorporation into ODVs. Only the full complex is resistant to proteolytic degradation in the insect midgut, implying the critical role of the entire complex. These findings provide the baseline for future studies on the ODV entry mechanism mediated by the multiprotein complex.

Microbially mediated bioreduction of iron oxyhydroxide plays an important role in the biogeochemical cycle of iron. Geobacter sulfurreducens is a representative dissimilatory iron-reducing bacterium that assembles electrically conductive pili and cytochromes. The impact of supplementation with γ-Fe

Fibroblast growth factor receptor-1 (FGFR1) over-expression was broadly found in squamous cancer, where it induced cellular proliferation, differentiation, and metastasis by activating various signaling pathway. However, the role of FGFR1 gene expression in predicting prognosis of Esophageal Squamous Cell Carcinoma (ESCC) and its regulatory function in the progression of ESCC are not well understood. Therefore, we performed an analysis of FGFR1 mRNA expression by quantitative RT-PCR in tumor tissue of 145 patients with ESCC. The relationships between FGFR1 gene expression and clinicopathological parameters, also the prognosis were further examined. Results suggested that higher FGFR1 gene expression predicted worse overall survival (HR = 1.502, 95%[CI] = 1.005-2.246, P = 0.045). Disease-free survival tends to be shorter in patients with higher FGFR1 expression but without statistical significance (HR = 1.398, 95%[CI] = 0.942-2.074, P = 0.096). FGFR1 was up regulated in multiple ESCC cell lines. Subsequent in vitro experiments demonstrated that anti-FGFR1 treatment by PD173074 inhibited TE-1 and EC9706 cell viability along with the attenuation of MEK-ERK signaling pathway. In vivo, PD173074 administration also had shown potent ESCC growth arresting effect. Overall, our study suggested that FGFR1 gene expression could be an independent prognosis predictive factor in patients with ESCC. Anti-FGFR1 inhibited ESCC growth and could be a potential strategy in ESCC targeted therapy.

In this study, PdO loaded WO3 composite was synthesized by precipitation method, followed by calcination. The as-synthesized composite was characterized and the photocatalytic disinfection of Escherichia coli was tested under visible light-irradiation. The characterization results showed that the PdO nanoparticles decorated on the surface of the WO3. The antibacterial test demonstrated that the as-synthesized material with 100:1 mole ratio of W:Pd and calcined at 200°C have the highest efficiency. After visible light irradiation of a short time, about 25 min, almost all of the tested E. coli cells were inactivated. Antimicrobial mechanism, revealed by scavengers of reactive oxygen species, demonstrated that the antibacterial activity was primarily due to the oxidation of photo-generated hole. And the oxidation-reduction reaction of superoxide radical and hydroxyl free radicals were assisted for the photo-disinfection of bacteria. Furthermore, the biosafety of the PdO/WO3 composite was evaluated by analysing the viability of Chinese hamster lung (V79) cells using Cell Counting Kit-8 (CCK-8).

Radiation-induced lung injury (RILI) presents a common and major obstacle in the radiotherapy of thoracic cancers. The aim of this study was to examine whether RILI could be alleviated by mesenchymal stem cells (MSCs) expressing soluble transforming growth factor-β (TGF-β) type II receptor via an adenovirus (Ad-sTβR). Here, we systemically administered male MSCs into female mice challenged with thoracic irradiation. The data showed that either MSCs or Ad-sTβR transduced MSCs (Ad-sTβR-MSCs) specifically migrated into radiation-injured lung. Ad-sTβR-MSCs obviously alleviated lung injury, as reflected by survival and histopathology data, as well as the assays of malondialdehyde (MDA), hydroxyproline, plasma cytokines, and the expression of connective tissue growth factor (CTGF) and α-smooth muscle actin (α-SMA). Furthermore, MSCs and Ad-sTβR-MSCs could adopt the characteristics of alveolar type II (ATII) cells. However, the MSCs levels in the lungs were relatively low to account for the noted therapeutic effects, suggesting the presence of other mechanisms. In vivo, MSCs-conditioned medium (MSCs CM) significantly attenuated RILI. In vitro, MSCs CM protected ATII cells against radiation-induced apoptosis and DNA damage, and modulated the inflammatory response, indicating the beneficial effects of MSCs are largely due to its paracrine activity. Our results provide a novel insight for RILI therapy that currently lack efficient treatments.

The purpose of this study is to explore why type 2 diabetes mellitus (T2DM) patients are susceptible to pulmonary tuberculosis through detection of serum Toll-like receptor 4 (TLR4), an important immune-related receptor, especially in terms of content and TLR4gene polymorphism. Patients with T2DM complicated by pulmonary tuberculosis (T2DMTB) were selected as the case group and T2DM patients without tuberculosis were selected as the control group. Forty patients in each group were randomly selected and their serum TLR4levels were detected and compared. Determination of six sites of TLR4gene polymorphism was carried out in 238 T2DMTB patients and 310 patients with T2DM, and results showed that the serum TLR4content of the T2DMTB group was significantly lower than that of the T2DM group (p<0.05). The six sites of TLR4gene polymorphism did not show significant associations with T2DMTB risk. No statistically significant differences in genotype distributions were observed between T2DMTB patients and patients with T2DM when studied using the recessive and dominant genetic models. How two diseases with contradictory nutritional statuses can occur in the same person is difficult to explain from environmental factors perspective alone. Future research should study the causes of T2DMTB from the perspective of genetics.