Sino-Africa relations: Gradual changes in Chinese foreign strategy towards African countries

China is one of the world's foremost economic powers, affecting many countries' economies and political issues. China standing by the five principles of peaceful coexistence, is ready to cultivate friendly cooperation and ties with all countries that contribute to international peace, security, and mutual prosperity. Africa is an important factor for global stability and prosperity with the highest number of developing countries. Africa is still of considerable significance to the Chinese Government. Therefore, the Chinese government wishes to present China's African strategy and its action to implement them and its plans for cooperation in different areas to facilitate the steady development of China-Africa ties in the long period. However, China's foreign policies are changing and developing recently. This study utilized qualitative analysis to identify the collaboration and relations between African countries and China to know how Chinese foreign strategy changes Africa's strategic ramifications and repercussions. The findings showed that the partnership between China and Africa by win-win strategy, from moral emphasis throughout the colonial phase to tactical considerations and non-intervention to constructive involvement on the continent, are three strands of foreign strategy shifts

Agonist-induced membrane nanodomain clustering drives GLP-1 receptor responses in pancreatic beta cells

The glucagon-like peptide-1 receptor (GLP-1R), a key pharmacological target in type 2 diabetes (T2D) and obesity, undergoes rapid endocytosis after stimulation by endogenous and therapeutic agonists. We have previously highlighted the relevance of this process in fine-tuning GLP-1R responses in pancreatic beta cells to control insulin secretion. In the present study, we demonstrate an important role for the translocation of active GLP-1Rs into liquid-ordered plasma membrane nanodomains, which act as hotspots for optimal coordination of intracellular signaling and clathrin-mediated endocytosis. This process is dynamically regulated by agonist binding through palmitoylation of the GLP-1R at its carboxyl-terminal tail. Biased GLP-1R agonists and small molecule allosteric modulation both influence GLP-1R palmitoylation, clustering, nanodomain signaling, and internalization. Downstream effects on insulin secretion from pancreatic beta cells indicate that these processes are relevant to GLP-1R physiological actions and might be therapeutically targetable

Agonist-induced membrane nanodomain clustering drives GLP-1 receptor responses in pancreatic beta cells

The glucagon-like peptide-1 receptor (GLP-1R), a key pharmacological target in type 2 diabetes (T2D) and obesity, undergoes rapid endocytosis after stimulation by endogenous and therapeutic agonists. We have previously highlighted the relevance of this process in fine-tuning GLP-1R responses in pancreatic beta cells to control insulin secretion. In the present study, we demonstrate an important role for the translocation of active GLP-1Rs into liquid-ordered plasma membrane nanodomains, which act as hotspots for optimal coordination of intracellular signaling and clathrin-mediated endocytosis. This process is dynamically regulated by agonist binding through palmitoylation of the GLP-1R at its carboxyl-terminal tail. Biased GLP-1R agonists and small molecule allosteric modulation both influence GLP-1R palmitoylation, clustering, nanodomain signaling, and internalization. Downstream effects on insulin secretion from pancreatic beta cells indicate that these processes are relevant to GLP-1R physiological actions and might be therapeutically targetable

Moisture-Resilient Graphene-Dyed Wool Fabric for Strain Sensing

E-textile consisting of natural fabrics has become a promising material to construct wearable sensors due to its comfortability and breathability on the human body. However, the reported fabric-based e-textile materials, such as graphene-treated cotton, silk, and flax, generally suffer from the electrical and mechanical instability in long-term wearing. In particular, fabrics on the human body have to endure heat variation, moisture evaporation from metabolic activities, and even the immersion with body sweat. To face the above challenges, here we report a wool-knitted fabric sensor treated with graphene oxide (GO) dyeing followed by l-ascorbic acid (l-AA) reduction (rGO). This rGO-based strain sensor is highly stretchable, washable, and durable with rapid sensing response. It exhibits excellent linearity with more than 20% elongation and, most importantly, withstand moisture from 30 to 90% (or even immersed with water) and still maintains good electrical and mechanical properties. We further demonstrate that, by integrating this proposed material with the near-field communication (NFC) system, a batteryless, wireless wearable body movement sensor can be constructed. This material can find wide use in smart garment applications

Hyodeoxycholic acid ameliorates nonalcoholic fatty liver disease by inhibiting RAN-mediated PPARα nucleus-cytoplasm shuttling

Abstract Nonalcoholic fatty liver disease (NAFLD) is usually characterized with disrupted bile acid (BA) homeostasis. However, the exact role of certain BA in NAFLD is poorly understood. Here we show levels of serum hyodeoxycholic acid (HDCA) decrease in both NAFLD patients and mice, as well as in liver and intestinal contents of NAFLD mice compared to their healthy counterparts. Serum HDCA is also inversely correlated with NAFLD severity. Dietary HDCA supplementation ameliorates diet-induced NAFLD in male wild type mice by activating fatty acid oxidation in hepatic peroxisome proliferator-activated receptor α (PPARα)-dependent way because the anti-NAFLD effect of HDCA is abolished in hepatocyte-specific Pparα knockout mice. Mechanistically, HDCA facilitates nuclear localization of PPARα by directly interacting with RAN protein. This interaction disrupts the formation of RAN/CRM1/PPARα nucleus-cytoplasm shuttling heterotrimer. Our results demonstrate the therapeutic potential of HDCA for NAFLD and provide new insights of BAs on regulating fatty acid metabolism