Abstract. We investigate a class of quasi-linear nonlocal problems, including as a particular case semi-linear problems involving the fractional Laplacian and arising in the framework of continuum mechanics, phase transition phenomena, population dynamics and game theory. Under different growth assumptions on the reaction term, we obtain various existence as well as finite multiplicity results by means of variational and topological methods and, in particular, arguments from Morse theory.

Permafrost on the Qinghai–Tibet Plateau (QTP) has undergone degradation as a result of recent climate change. This may alter the thermo‐hydrological processes and unlock soil organic carbon, and thereby affect local hydrological, ecological, and climatic systems. The relationships between permafrost and climate change have received extensive attention, and in this paper we review climate change for permafrost regions of the QTP over the past 30 years. We summarize the current state and changes in permafrost distribution and thickness, ground temperature, and ground ice conditions. We focus on changes in permafrost thermal state and in active‐layer thickness (ALT). Possible future changes in ground temperature and ALT are also discussed. Finally, we discuss the changes in hydrological processes and to ecosystems caused by permafrost degradation. Air temperature and ground temperature in the permafrost regions of the QTP have increased from 1980 to 2018, and the active layer has been thickening at a rate of 19.5 cm per decade. The response of permafrost to climate change is not as fast as in some reports, and permafrost degradation is slower than projected by models that do not account for conditions deep in permafrost.

No abstract

Cell–cell interactions and communications play fundamental roles in life processes but remain largely uncharacterized. We developed an enzyme-mediated proximity cell labeling (EXCELL) strategy as a general method to detect and record cell–cell interactions under living conditions. EXCELL relies on an evolved Staphylococcus aureus transpeptidase sortase A variant (mgSrtA) capable of promiscuous labeling of various cell surface proteins containing a monoglycine residue at the N-terminus. Displaying mgSrtA on the surface of a cell of interest allows the labeling and detection of interacting cells in a proximity-dependent fashion.

No abstract

No abstract

Enzyme-linked immunosorbent assay (ELISA) is a popular laboratory technique for detection of disease-specific protein biomarkers with high specificity and sensitivity. However, ELISA requires labor-intensive and time-consuming procedures with skilled operators and spectroscopic instrumentation. Simplification of the procedures and miniaturization of the devices are crucial for ELISA-based point-of-care (POC) testing in resource-limited settings. Here, we present a fully integrated, instrument-free, low-cost and portable POC platform which integrates the process of ELISA and the distance readout into a single microfluidic chip. Based on manipulation using a permanent magnet, the process is initiated by moving magnetic beads with capture antibody through different aqueous phases containing ELISA reagents to form bead/antibody/antigen/antibody sandwich structure, and finally converts the molecular recognition signal into a highly sensitive distance readout for visual quantitative bioanalysis. Without additional equipment and complicated operations, our integrated ELISA-Chip with distance readout allows ultrasensitive quantitation of disease biomarkers within 2h. The ELISA-Chip method also showed high specificity, good precision and great accuracy. Furthermore, the ELISA-Chip system is highly applicable as a sandwich-based platform for the detection of a variety of protein biomarkers. With the advantages of visual analysis, easy operation, high sensitivity, and low cost, the integrated sample-in-answer-out ELISA-Chip with distance readout shows great potential for quantitative POCT in resource-limited settings.

Magnolol, the major active compound found in Magnolia officinalis has a wide range of clinical applications due to its anti-inflammation and anti-oxidation effects. This study investigated the effects of magnolol on the growth of human gallbladder carcinoma (GBC) cell lines. The results indicated that magnolol could significantly inhibit the growth of GBC cell lines in a dose- and time-dependent manner. Magnolol also blocked cell cycle progression at G0/G1 phase and induced mitochondrial-related apoptosis by upregulating p53 and p21 protein levels and by downregulating cyclin D1, CDC25A, and Cdk2 protein levels. When cells were pretreated with a p53 inhibitor (pifithrin-a), followed by magnolol treatment, pifithrin-a blocked magnolol-induced apoptosis and G0/G1 arrest. In vivo, magnolol suppressed tumor growth and activated the same mechanisms as were activated in vitro. In conclusion, our study is the first to report that magnolol has an inhibitory effect on the growth of GBC cells and that this compound may have potential as a novel therapeutic agent for the treatment of GBC.