Internalization of apoptotic cells during efferocytosis requires Mertk-mediated calcium influx.

Phagocytosis of apoptotic cells, called efferocytosis, requires calcium inside and outside of phagocytes. Due to its necessity, calcium flux is sophisticatedly modulated, and the level of intracellular calcium in phagocytes is ultimately elevated during efferocytosis. However, the role of elevated intracellular calcium in efferocytosis remains elusive. Here, we report that Mertk-mediated intracellular calcium elevation is necessary for internalization of apoptotic cells during efferocytosis. Drastic depletion of intracellular calcium abrogated the internalization step of efferocytosis by delaying phagocytic cup extension and closure. Especially, the defect of phagocytic cup closure for internalization of apoptotic cells was caused by impaired F-actin disassembly and the attenuated interaction of Calmodulin with myosin light chain kinase (MLCK), leading to diminished myosin light chain (MLC) phosphorylation. Genetic and pharmacological impairment of the Calmodulin-MLCK-MLC axis or Mertk-mediated calcium influx also resulted in inefficient efferocytosis due to a defect in internalization of the targets. Taken together, our observations imply that intracellular calcium elevation through Mertk-mediated calcium influx facilitates efferocytosis by inducing myosin II-mediated contraction and F-actin disassembly required for internalization of apoptotic cells.

Nanoporous Silver Telluride for Active Hydrogen Evolution.

Silver-based nanomaterials have been versatile building blocks of various photoassisted energy applications; however, they have demonstrated poor electrochemical catalytic performance and stability, in particular, in acidic environments. Here we report a stable and high-performance electrochemical catalyst of silver telluride (AgTe) for the hydrogen evolution reaction (HER), which was synthesized with a nanoporous structure by an electrochemical synthesis method. X-ray spectroscopy techniques on the nanometer scale and high-resolution transmission electron microscopy revealed an orthorhombic structure of nanoporous AgTe with precise lattice constants. First-principles calculations show that the AgTe surface possesses highly active catalytic sites for the HER with an optimized Gibbs free energy change of hydrogen adsorption (-0.005 eV). Our nanoporous AgTe demonstrates exceptional stability and performance for the HER, an overpotential of 27 mV, and a Tafel slope of 33 mV/dec. As a stable catalyst for hydrogen production, AgTe is comparable to platinum-based catalysts and provides a breakthrough for high-performance electrochemical catalysts.

Mitrofanovite, Layered Platinum Telluride, for Active Hydrogen Evolution.

Two-dimensional (2D) layered catalysts have been considered as a class of ideal catalysts for hydrogen evolution reaction (HER) because of their abundant active sites with almost zero Gibbs energy change for hydrogen adsorption. Despite the promising performance, the design of stable and economic electrochemical catalyst based on 2D materials remains to be resolved for industrial-scale hydrogen production. Here, we report layered platinum tellurides, mitrofanovite Pt3Te4, which serves as an efficient and stable catalyst for HER with an overpotential of 39.6 mV and a Tafel slope of 32.7 mV/dec together with a high current density exceeding 7000 mA/cm2. Pt3Te4 was synthesized as nanocrystals on a metallic molybdenum ditelluride (MoTe2) template by a rapid electrochemical method. X-ray diffraction and high-resolution transmission microscopy revealed that the Pt3Te4 nanocrystals have a unique layered structure with repeated monolayer units of PtTe and PtTe2. Theoretical calculations exhibit that Pt3Te4 with numerous edges shows near-zero Gibbs free-energy change of hydrogen adsorption, which shows the excellent HER performance as well as the extremely large exchange current density for massive hydrogen production.