rac-(S)-2-(1H-Imidazol-1-yl)-3-methyl­butan-1-ol

In the crystal structure of the title compound, C8H14N2O, inter­molecular O—H⋯N hydrogen bonds link mol­ecules related by translation along the a axis into chains. Weak inter­molecular C—H⋯O hydrogen bonds and C—H⋯π inter­actions enhance the crystal packing stability

New ionic dinuclear Ir(III) Schiff base complexes with aggregation-induced phosphorescent emission (AIPE)

Two new ionic dinuclear Ir(III) Schiff base complexes which are straightforward to synthesise have luminescence quantum yields as high as 37% in neat films. These are the first examples of dinuclear ionic Ir(III) complexes that display aggregation-induced phosphorescent emission (AIPE)

Multiplexed Monitoring of Neurochemicals via Electrografting- Enabled Site-Selective Functionalization of Aptamers on Field-Effect Transistors

Neurochemical corelease has received much attention in understanding brain activity and cognition. Despite many attempts, the multiplexed monitoring of coreleased neurochemicals with spatiotemporal precision and minimal crosstalk using existing methods remains challenging. Here, we report a soft neural probe for multiplexed neurochemical monitoring via the electrografting-assisted site-selective functionalization of aptamers on graphene field-effect transistors (G-FETs). The neural probes possess excellent flexibility, ultralight mass (28 mg), and a nearly cellular-scale dimension of 50 μm × 50 μm for each G-FET. As a demonstration, we show that G-FETs with electrochemically grafted molecular linkers (−COOH or −NH2) and specific aptamers can be used to monitor serotonin and dopamine with high sensitivity (limit of detection: 10 pM) and selectivity (dopamine sensor \u3e22-fold over norepinephrine; serotonin sensor \u3e17-fold over dopamine). In addition, we demonstrate the feasibility of the simultaneous monitoring of dopamine and serotonin in a single neural probe with minimal crosstalk and interferences in phosphate-buffered saline, artificial cerebrospinal fluid, and harvested mouse brain tissues. The stability studies show that multiplexed neural probes maintain the capability for simultaneously monitoring dopamine and serotonin with minimal crosstalk after incubating in rat cerebrospinal fluid for 96 h, although a reduced sensor response at high concentrations is observed. Ex vivo studies in harvested mice brains suggest potential applications in monitoring the evoked release of dopamine and serotonin. The developed multiplexed detection methodology can also be adapted for monitoring other neurochemicals, such as metabolites and neuropeptides, by simply replacing the aptamers functionalized on the G-FETs

Allelopathic interactions of linoleic acid and nitric oxide increase the competitive ability of Microcystis aeruginosa

The frequency and intensity of cyanobacterial blooms are increasing worldwide with major societal and economic costs. Interactions between toxic cyanobacteria and eukaryotic algal competitors can affect toxic bloom formation, but the exact mechanisms of interspecies interactions remain unknown. Using metabolomic and proteomic profiling of co-cultures of the toxic cyanobacterium Microcystis aeruginosa with a green alga as well as of microorganisms collected in a Microcystis spp. bloom in Lake Taihu (China), we disentangle novel interspecies allelopathic interactions. We describe an interspecies molecular network in which M. aeruginosa inhibits growth of Chlorella vulgaris, a model green algal competitor, via the release of linoleic acid. In addition, we demonstrate how M. aeruginosa takes advantage of the cell signaling compound nitric oxide produced by C. vulgaris, which stimulates a positive feedback mechanism of linoleic acid release by M. aeruginosa and its toxicity. Our high-throughput system-biology approach highlights the importance of previously unrecognized allelopathic interactions between a broadly distributed toxic cyanobacterial bloom former and one of its algal competitors

Identification of miRs-143 and -145 that Is Associated with Bone Metastasis of Prostate Cancer and Involved in the Regulation of EMT

The principal problem arising from prostate cancer (PCa) is its propensity to metastasize to bone. MicroRNAs (miRNAs) play a crucial role in many tumor metastases. The importance of miRNAs in bone metastasis of PCa has not been elucidated to date. We investigated whether the expression of certain miRNAs was associated with bone metastasis of PCa. We examined the miRNA expression profiles of 6 primary and 7 bone metastatic PCa samples by miRNA microarray analysis. The expression of 5 miRNAs significantly decreased in bone metastasis compared with primary PCa, including miRs-508-5p, -145, -143, -33a and -100. We further examined other samples of 16 primary PCa and 13 bone metastases using real-time PCR analysis. The expressions of miRs-143 and -145 were verified to down-regulate significantly in metastasis samples. By investigating relationship of the levels of miRs-143 and -145 with clinicopathological features of PCa patients, we found down-regulations of miRs-143 and -145 were negatively correlated to bone metastasis, the Gleason score and level of free PSA in primary PCa. Over-expression miR-143 and -145 by retrovirus transfection reduced the ability of migration and invasion in vitro, and tumor development and bone invasion in vivo of PC-3 cells, a human PCa cell line originated from a bone metastatic PCa specimen. Their upregulation also increased E-cadherin expression and reduced fibronectin expression of PC-3 cells which revealed a less invasive morphologic phenotype. These findings indicate that miRs-143 and -145 are associated with bone metastasis of PCa and suggest that they may play important roles in the bone metastasis and be involved in the regulation of EMT Both of them may also be clinically used as novel biomarkers in discriminating different stages of human PCa and predicting bone metastasis

Joint analysis of three genome-wide association studies of esophageal squamous cell carcinoma in Chinese populations

We conducted a joint (pooled) analysis of three genome-wide association studies (GWAS) 1-3 of esophageal squamous cell carcinoma (ESCC) in ethnic Chinese (5,337 ESCC cases and 5,787 controls) with 9,654 ESCC cases and 10,058 controls for follow-up. In a logistic regression model adjusted for age, sex, study, and two eigenvectors, two new loci achieved genome-wide significance, marked by rs7447927 at 5q31.2 (per-allele odds ratio (OR) = 0.85, 95% CI 0.82-0.88; P=7.72x10−20) and rs1642764 at 17p13.1 (per-allele OR= 0.88, 95% CI 0.85-0.91; P=3.10x10−13). rs7447927 is a synonymous single nucleotide polymorphism (SNP) in TMEM173 and rs1642764 is an intronic SNP in ATP1B2, near TP53. Furthermore, a locus in the HLA class II region at 6p21.32 (rs35597309) achieved genome-wide significance in the two populations at highest risk for ESSC (OR=1.33, 95% CI 1.22-1.46; P=1.99x10−10). Our joint analysis identified new ESCC susceptibility loci overall as well as a new locus unique to the ESCC high risk Taihang Mountain region

Light Competition Contributes to the Death of Masson Pines of Coniferous-Broadleaf Mixed Forests in Subtropical China

In the process of subtropical forest succession, it has long been recognized that population decline of Masson pines in coniferous-broadleaf mixed forest is caused by shading from broadleaf trees. However, little is known about the mechanism underlying the interaction between them. Here, we first chose two sets of Masson pine plots approximately aged 60 years in subtropical mountainous areas in eastern China (i.e., pure coniferous forest vs. coniferous-broadleaf mixed forest). Then, we measured and compared tree height, diameter at breast height, first branch height (FBH), live crown ratio (LCR) of Masson pines between the two sets of plots, and also determined the difference in growth performance of Masson pines relative to their neighboring broadleaf trees in the mixed forest stand. Compared with plots in pine forests, Masson pines in mixed plots had lower tree height and crown breadth, higher FBH, lower LCR, and leaf area. Furthermore, the difference of mean FBH between reference trees (Masson pines) and their neighboring trees (i.e., broadleaf trees) in mixed forest plots was greater than that in pine forest plots, and the ratio of LCR between Masson pines and their neighbors (0.46) in mixed forest was significantly smaller than in pine forest (1.05), indicating that those broadleaf trees around Masson pines probably affected their growth. The mean distance between Masson pines and neighboring trees (1.59 m) in mixed forest plots was significantly shorter than in pine forest plots (2.77 m) (p < 0.01), suggesting that strong competition may occur between reference trees and their neighbors. There was a significant difference in the ratio of crown volume between reference tree Masson pine and its neighboring trees in mixed forests (p < 0.01), indicating that the ratio of biomass synthesis to consumption of pines was much lower than their nearby broadleaf trees in mixed forest. Our results have demonstrated for the first time that Masson pines’ population decline is affected by shade-tolerant broadleaf late-successional species, which can be primarily attributed to the distinctive light transmittance of dominant species nearby (pure pine vs. mixed forest). This study provides a new perspective for future studies on the mechanism of forest succession

Light Competition Contributes to the Death of Masson Pines of Coniferous-Broadleaf Mixed Forests in Subtropical China

In the process of subtropical forest succession, it has long been recognized that population decline of Masson pines in coniferous-broadleaf mixed forest is caused by shading from broadleaf trees. However, little is known about the mechanism underlying the interaction between them. Here, we first chose two sets of Masson pine plots approximately aged 60 years in subtropical mountainous areas in eastern China (i.e., pure coniferous forest vs. coniferous-broadleaf mixed forest). Then, we measured and compared tree height, diameter at breast height, first branch height (FBH), live crown ratio (LCR) of Masson pines between the two sets of plots, and also determined the difference in growth performance of Masson pines relative to their neighboring broadleaf trees in the mixed forest stand. Compared with plots in pine forests, Masson pines in mixed plots had lower tree height and crown breadth, higher FBH, lower LCR, and leaf area. Furthermore, the difference of mean FBH between reference trees (Masson pines) and their neighboring trees (i.e., broadleaf trees) in mixed forest plots was greater than that in pine forest plots, and the ratio of LCR between Masson pines and their neighbors (0.46) in mixed forest was significantly smaller than in pine forest (1.05), indicating that those broadleaf trees around Masson pines probably affected their growth. The mean distance between Masson pines and neighboring trees (1.59 m) in mixed forest plots was significantly shorter than in pine forest plots (2.77 m) (p p < 0.01), indicating that the ratio of biomass synthesis to consumption of pines was much lower than their nearby broadleaf trees in mixed forest. Our results have demonstrated for the first time that Masson pines’ population decline is affected by shade-tolerant broadleaf late-successional species, which can be primarily attributed to the distinctive light transmittance of dominant species nearby (pure pine vs. mixed forest). This study provides a new perspective for future studies on the mechanism of forest succession