Prmt5 is a regulator of muscle stem cell expansion in adult mice.

Skeletal muscle stem cells (MuSC), also called satellite cells, are indispensable for maintenance and regeneration of adult skeletal muscles. Yet, a comprehensive picture of the regulatory events controlling the fate of MuSC is missing. Here, we determine the proteome of MuSC to design a loss-of-function screen, and identify 120 genes important for MuSC function including the arginine methyltransferase Prmt5. MuSC-specific inactivation of Prmt5 in adult mice prevents expansion of MuSC, abolishes long-term MuSC maintenance and abrogates skeletal muscle regeneration. Interestingly, Prmt5 is dispensable for proliferation and differentiation of Pax7(+) myogenic progenitor cells during mouse embryonic development, indicating significant differences between embryonic and adult myogenesis. Mechanistic studies reveal that Prmt5 controls proliferation of adult MuSC by direct epigenetic silencing of the cell cycle inhibitor p21. We reason that Prmt5 generates a poised state that keeps MuSC in a standby mode, thus allowing rapid MuSC amplification under disease conditions

Design and Implementation of a Full-Duplex Pipelined MAC Protocol for Multihop Wireless Networks

In multihop wireless networks, data packets are forwarded from a source node to a destination node through intermediate relay nodes. With half-duplex relay nodes, the end-to-end delay performance of a multihop network degrades as the number of hops increases, because the relay nodes cannot receive and transmit at the same time. Full-duplex relay nodes can reduce their per-hop delay by starting to forward a packet before the whole packet is received. In this paper, we propose a pipelined medium access control (PiMAC) protocol, which enables the relay nodes on a multihop path to simultaneously transmit and receive packets for full-duplex forwarding. For pipelined transmission over a multihop path, it is important to suppress both the self-interference of each relay node with the full-duplex capability and the intra-flow interference from the next relay nodes on the same path. In the PiMAC protocol, each relay node can suppress both the self- and intra-flow interference for full-duplex relaying on the multihop path by estimating the channel coefficients and delays of the interference during a multihop channel acquisition phase. To evaluate the performance of the PiMAC protocol, we carried out extensive simulations and software-defined radio-based experiments

Graphite-anchored lithium vanadium oxide as anode of lithium ion battery

Graphite-anchored lithium vanadium oxide (Li1.1V0.9O2) has been synthesized via a “one-pot” in situ method. The effects of the synthesis conditions, such as the ratio of reaction components and calcination temperature, on the electrochemical performance are systematically investigated by means of scanning electron microscopy (SEM), X-ray diffraction (XRD), electrochemical impedance spectroscopy (EIS), galvanostatic discharge/charge tests and differential scanning calorimetry (DSC). Compared with the simple mixture of graphite and lithium vanadium oxide, the graphite-anchored lithium vanadium oxide delivers an enhanced reversible capacity, rate capability and cyclic stability. It also shows better thermal stability.Web of Scienc

Complex 3D microfluidic architectures formed by mechanically guided compressive buckling.

Microfluidic technologies have wide-ranging applications in chemical analysis systems, drug delivery platforms, and artificial vascular networks. This latter area is particularly relevant to 3D cell cultures, engineered tissues, and artificial organs, where volumetric capabilities in fluid distribution are essential. Existing schemes for fabricating 3D microfluidic structures are constrained in realizing desired layout designs, producing physiologically relevant microvascular structures, and/or integrating active electronic/optoelectronic/microelectromechanical components for sensing and actuation. This paper presents a guided assembly approach that bypasses these limitations to yield complex 3D microvascular structures from 2D precursors that exploit the full sophistication of 2D fabrication methods. The capabilities extend to feature sizes <5 μm, in extended arrays and with various embedded sensors and actuators, across wide ranges of overall dimensions, in a parallel, high-throughput process. Examples include 3D microvascular networks with sophisticated layouts, deterministically designed and constructed to expand the geometries and operating features of artificial vascular networks

Three-dimensional, multifunctional neural interfaces for cortical spheroids and engineered assembloids.

Three-dimensional (3D), submillimeter-scale constructs of neural cells, known as cortical spheroids, are of rapidly growing importance in biological research because these systems reproduce complex features of the brain in vitro. Despite their great potential for studies of neurodevelopment and neurological disease modeling, 3D living objects cannot be studied easily using conventional approaches to neuromodulation, sensing, and manipulation. Here, we introduce classes of microfabricated 3D frameworks as compliant, multifunctional neural interfaces to spheroids and to assembloids. Electrical, optical, chemical, and thermal interfaces to cortical spheroids demonstrate some of the capabilities. Complex architectures and high-resolution features highlight the design versatility. Detailed studies of the spreading of coordinated bursting events across the surface of an isolated cortical spheroid and of the cascade of processes associated with formation and regrowth of bridging tissues across a pair of such spheroids represent two of the many opportunities in basic neuroscience research enabled by these platforms