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Salinity stress severely limits rice productivity and grain quality worldwide. Although exogenous foliar application of titanium dioxide nanoparticles (nano-TiO2) has been reported to enhance crop stress tolerance, its regulatory roles in yield formation and grain quality in rice varieties with differing salt tolerance are not well understood. In the present study, two contrasting rice varieties, viz., Jingliangyou 3261 (JLY3261; salt-tolerant) and Yuxiangyouzhan (YXYZ; salt-sensitive), were applied with five nano-TiO2 foliar application treatments-viz., CK: water spray; Ti1: 15 mg L-1; Ti2: 30 mg L-1; Ti3: 45 mg L-1; and Ti4: 60 mg L-1-at the jointing and panicle initiation stages. Plants were irrigated with 0.3% saltwater to simulate salt stress. The results showed that Ti2 and Ti3 treatments led to 8.59% and 14.80% increases in grain yield in JLY3261 and YXYZ, respectively, compared with CK. Ti2 and Ti3 treatments significantly increased the leaf area index, net photosynthetic rate, and aboveground biomass of both varieties at the heading stage. Meanwhile, the activities of antioxidant enzymes such as superoxide dismutase and peroxidase, as well as nitrogen metabolism enzymes including nitrate reductase and glutamine synthetase, were improved with a substantial reduction in malondialdehyde contents. Application of nano-TiO2 upregulated the expression of ion transport-related genes such as OsSOSs, OsNHXs and OsHKTs, thus improving leaf K+ accumulation and reducing Na+ content to optimize the K+/Na+ ratio. In addition, Ti2 and Ti3 treatments improved the milled rice rate, head rice rate, and protein content, while they decreased the chalkiness degree of both rice cultivars. Principal component analysis showed that the aboveground biomass at the heading stage was a core evaluation index for both varieties. Overall, foliar application of 30-45 mg L-1 nano-TiO2 was found to be effective regarding growth and yield improvement in rice under saline conditions. This study provides a theoretical basis for agro-management strategies for rice cultivation in saline-alkaline soils.

The pathogenesis of atherosclerosis is defined by impaired lipid handling by macrophages which increases intracellular lipid accumulation. This dysregulation of macrophages triggers the accumulation of apoptotic cells and chronic inflammation which contributes to disease progression. We previously reported that mice with increased macrophage-specific angiotensin-converting enzyme, termed ACE10/10 mice, resist atherosclerosis in an adeno-associated virus-proprotein convertase subtilisin/kexin type 9 (AAV-PCSK9)-induced model. This is due to increased lipid metabolism by macrophages which contributes to plaque resolution. However, the importance of ACE in peripheral blood monocytes, which are the primary precursors of lesional-infiltrating macrophages, is still unknown in atherosclerosis. Here, we show that the ACE-mediated metabolic phenotype is already triggered in peripheral blood circulating monocytes and that this functional modification is directly transferred to differentiated macrophages in ACE10/10 mice. We found that Ly-6Clo monocytes were increased in atherosclerotic ACE10/10 mice. The monocytes isolated from atherosclerotic ACE10/10 mice showed enhanced lipid metabolism, elevated mitochondrial activity, and increased adenosine triphosphate (ATP) levels which implies that ACE overexpression is already altered in atherosclerosis. Furthermore, we observed increased oxygen consumption (VO2), respiratory exchange ratio (RER), and spontaneous physical activity in ACE10/10 mice compared to WT mice in atherosclerotic conditions, indicating enhanced systemic energy consumption. Thus, ACE overexpression in myeloid lineage cells modifies the metabolic function of peripheral blood circulating monocytes which differentiate to macrophages and protect against atherosclerotic lesion progression due to better lipid metabolism.

Hyperlipidemia is a major risk factor for erectile dysfunction (ED). Oxidative stress and phenotypic modulation of corpus cavernosum smooth muscle cells (CCSMCs) are the key pathological factors of ED. N-acetylcysteine (NAC) can inhibit oxidative stress; however, whether NAC can alleviate pathological variations in the corpus cavernosum and promote erectile function recovery in hyperlipidemic rats remains unclear. A hyperlipidemia model was established using 27 eight-week-old male Sprague-Dawley (SD) rats fed a high-fat and high-cholesterol diet (hyperlipidemic rats, HR). In addition, 9 male SD rats were fed a normal diet to serve as controls (NC). HR rats were divided into three groups: HR, HR+normal saline (NS), and HR+NAC (n = 9 for each group; NS or NAC intraperitoneal injections were administered daily for 16 weeks). Subsequently, the lipid profiles, erectile function, oxidative stress, phenotypic modulation markers of CCSMCs, and tissue histology were analyzed. The experimental results revealed that erectile function was significantly impaired in the HR and HR + NS groups, but enhanced in the HR + NAC group. Abnormal lipid levels, over-activated oxidative stress, and multi-organ lesions observed in the HR and HR + NS groups were improved in the HR + NAC group. Moreover, the HR group showed significant phenotypic modulation of CCSMCs, which was also inhibited by NAC treatment. This report focuses on the therapeutic effect of NAC in restoring erectile function using a hyperlipidemic rat model by preventing CCSMC phenotypic modulation and attenuating oxidative stress.

Alzheimer's disease (AD) is a complex and progressive neurodegenerative disease with impaired synapse, imbalanced mineral metabolism, protein mis-folding and aggregation. Bis(ethylmaltolato)oxidovanadium(IV) (BEOV), an organic bioactive vanadium compound with low toxicity and high bioavailability, has been studied as therapeutic agent against tuberculosis and diabetes. However, its neuroprotective effects have rarely been reported. Therefore, in this study, the potential application of BEOV in intervening AD cognitive dysfunction and neuropathology was evaluated. Both low- and high-dose of BEOV (0.2mmol/L and 1.0mmol/L) supplementation for 2months improved the spatial learning and memory deficits of the triple-transgenic AD (3 × Tg AD) mice and mitigated the loss of synaptic proteins and synaptic dysfunction. By inhibiting the expression of amyloid-β precursor protein and β-secretase, and the phosphorylation of tau protein at Ser262, Ser396, Ser404, and Ser202/Thr205 residues, BEOV reduced the amyloid-β deposition and neurofibrillary tangle formation in AD mouse brains and primarily cultured neurons. Further analysis of the brain ionome revealed that BEOV supplementation could significantly affect the concentrations of a variety of metals, most of which, including several AD risk metals, showed reduced levels, particularly with a high-dose intake. Additionally, the elemental correlation network identified both conserved and specific elemental correlations, implying a highly complex and dynamic crosstalk between vanadium and other elements during long-term BEOV supplementation. Overall, our results suggest that BEOV is effective in AD intervention via both ameliorating the disease related pathology and regulating metal homeostasis.

More and more importance has been attached to multi‐view clustering due to its outstanding performance against single‐view clustering. Existing studies are on the basis of the assumption that every sample exists in all views. However, in reality, this is often not the case and the real data are always with incomplete views, which lead to the failure of the conventional methods. To address the issue, the authors present a novel method, referred to as incomplete multi‐view spectral clustering with proximity relation estimation (IMSC_PRE), which exploits the proximity relations of samples in different views to complete their affinity graphs. Different from existing methods, IMSC_PRE fully excavates the manifold structures of all views to estimate the proximity relations of missing samples in each view, which presents a brand‐new strategy to exploit the proximity information lying in the whole samples with good interpretation. Experimental results on four datasets demonstrate the advantages of the proposed method in comparison with the state‐of‐the‐art methods.

BackgroundHaemonchus contortus, a blood-feeding parasite, is constantly surrounded by large quantities of heme released from the catabolism of host red blood cells. To cope with the toxicity of free heme, H. contortus needs to uptake and detoxify the heme, a process believed to be paramount for parasite survival.MethodsA heme-responsive gene Hc-hrg-2 was identified which is the homologue of Ce-hrg-2. The transcriptional levels in all developmental stages and heme-responsive ability of Hc-hrg-2 were analyzed by qRT-PCR. Immunofluorescence analysis and cell transfections were performed to analyze the expression pattern of Hc-HGR-2. Statistical analyses were performed with GraghPad Prism 6.0 using Student’s t-test.ResultsTo investigate the heme homeostasis of H. contortus, we first identified a heme-responsive gene Hc-hrg-2, a homolog of Ce-hrg-2 that is involved in heme transport in the hypodermis of Caenorhabditis elegans. Using qRT-PCR, we showed that Hc-hrg-2 mRNA was expressed throughout all life-cycle stages of H. contortus with the highest level in the third-stage larvae (L3s). Notably, transcription of Hc-hrg-2 in the exsheathed L3s was significantly upregulated in the presence of high concentration of heme. We found that Hc-HRG-2 protein was mainly located in the hypodermal tissues of adult H. contortus in vivo and the endoplasmic reticulum in the transfected mammalian cells. Our in vitro assay demonstrated that Hc-HRG-2 is a heme-binding protein with glutathione S-transferase activity and heme had a significant effect on its enzymatic activity when a model substrate 1-chloro-2, 4-dinitrobenzene (CDNB) was used.ConclusionsHc-hrg-2 is a heme-responsive gene and engaged in heme homeostasis regulation in hypodermal tissues during the free-living stages of H. contortus.

The seventy samples of Polygoni Multiflori Radix were collected from three producing areas: Bozhou, Anhui province, Jingmen, Hubei province and Xichang, Sichuan province. Three stable isotope ratios and contents of 44 elements in the Polygoni Multiflori Radix samples were determined by EA-IR-MS and HR-ICP-MS. Three data mining methods，including partial least square discriminant analysis (PLS-DA), fisher linear discriminant analysis (FLDA) and decision tree CHAID were employed to establish a model for geographical origin discrimination．The study results showed that the stable isotope ratios expressed significant difference followed with the different producing areas, and will be used to discern the samples from different producing areas, effectively. Combined with the data of elemental analysis, the accuracy rates of model can be further improved. All the three methods showed the accuracy rates of external sample were over 90% using training dataset. These results confirmed that stable isotope ratios and multi-elemental analysis combined with chemometric method was effectiv in geographical tracing of Polygoni Multiflori Radix．The analysis method has great potential and prospect in geographical origin discriminant of Chinese medicinal materials, and provids a new study method to identify origin information of Chinese medicinal materials.

ABSTRACTIn this paper, we report the development of a label-free biosensor, based on surface plasmon resonance, for real-time monitoring of captured human CD4+T-cells, and their dynamic cytokine production upon specific antigen stimulation. Microarrays of CD4+T-cells, and interferon gamma (IFN-γ) specific antibody (Ab) spots were printed side by side onto the poly(OEGMA-co-HEMA) matrix. The placement of CD4+ T-cells near the anti IFN-γ Ab-coated spots ensured a high local concentration of secreted IFN-γ for detection. We have demonstrated that this approach enables the detection of tuberculosis (TB) infection in clinical samples, with an overall sensitivity of 85.5% and an overall specificity of 97.7%.