Novel Solvent–Latex Mixing: Thermal Insulation Performance of Silica Aerogel/Natural Rubber Composite

In this work, the novel natural rubber latex (NRL) mixing was approached. The mixing process was carried out by using n-hexane as the dispersed phase of silica aerogel which acted as thermal insulation filler prior to NRL mixing. The silica aerogel/NR composites were prepared with different silica aerogel contents of 20, 40, 60, 80, and 100 parts per hundred rubber (phr). The morphology of the 40 phr composite showed the NR macropore formation with silica aerogel intercalated layers. The optimal content of silica aerogels and n-hexane were the key to obtaining the NR macropore. The thermal insulation performance of silica aerogel/NR composites was investigated because of their porous structures. The thermal conductivity of the composites were lower than that of the neat NR sheet and decreased from 0.081 to 0.055 W m−1·K−1 with increasing silica aerogel content. The lower densities of the composites than that of the NR sheet were revealed noticeably. In addition, the silica aerogel/NR composites exhibited a higher heat retardant ability than that of the NR sheet, and the comparable glass transition temperatures (Tg) of the composites and the neat NR indicated the maintained flexibility at ambient temperature or higher, which can benefit various temperature applications. The overall results demonstrated that the silica aerogel/NR composites from the novel NRL mixing preparation could be a promising technique to develop the porous materials and be utilised as thermal insulation products and building constructions.

Preparation of a Nickel Layer with Bell-Mouthed Macropores via the Dual-Template Method

A relatively static and unique bubble template is successfully realized on a microporous substrate by controlling the surface tensions of the electrodeposit solution, and a nickel layer containing macropores is prepared using this bubble template. When the surface tension of the solution is 50.2 mN/m, the desired bubble template can be formed, there are fewer bubbles attached to other areas on the substrate, and a good nickel layer is obtained. In the analysis of the macropore formation process, it is found that the size of the bell-mouthed macropores can be tailored by changing the solution stirring speed or the current density to adjust the growth rate of the bubble template. The size change of a macropore is measured by the profile angle of the longitudinal macropore, section. As the solution stirring speed increases from 160 to 480 r/min, the angle range of the bell-mouthed macropores cross-sectional profile is increased from 21.0° to 44.3°. In addition, the angle range of the bell-mouthed macropore cross-sectional profile is increased from 39.3° to 46.3° with the current density increasing from 1 to 2.5 A/dm2. Different from the dynamic hydrogen bubble template, the bubble template implemented in this paper stays attached on the deposition and grows slowly, which is novel and interesting, and the nickel layer containing macropores prepared using this bubble template is applied in completely different fields.

P2X7 Receptors and TMEM16 Channels Are Functionally Coupled with Implications for Macropore Formation and Current Facilitation

P2X7 receptors (P2X7) are cationic channels involved in many diseases. Following their activation by extracellular ATP, distinct signaling pathways are triggered, which lead to various physiological responses such as the secretion of pro-inflammatory cytokines or the modulation of cell death. P2X7 also exhibit unique behaviors, such as “macropore” formation, which corresponds to enhanced large molecule cell membrane permeability and current facilitation, which is caused by prolonged activation. These two phenomena have often been confounded but, thus far, no clear mechanisms have been resolved. Here, by combining different approaches including whole-cell and single-channel recordings, pharmacological and biochemical assays, CRISPR/Cas9 technology and cell imaging, we provide evidence that current facilitation and macropore formation involve functional complexes comprised of P2X7 and TMEM16, a family of Ca2+-activated ion channel/scramblases. We found that current facilitation results in an increase of functional complex-embedded P2X7 open probability, a result that is recapitulated by plasma membrane cholesterol depletion. We further show that macropore formation entails two distinct large molecule permeation components, one of which requires functional complexes featuring TMEM16F subtype, the other likely being direct permeation through the P2X7 pore itself. Such functional complexes can be considered to represent a regulatory hub that may orchestrate distinct P2X7 functionalities.

P2X7 Receptors and TMEM16 Channels Form a Hub with Implications for Macropore Formation and Current Facilitation

P2X7 receptors (P2X7) are cationic channels involved in many diseases. They exhibit unique behaviors, such as “macropore” formation, which corresponds to enhanced large molecule cell membrane permeability, and current facilitation, which is caused by prolonged activation. These two phenomena have often been confounded, but thus far no clear mechanisms have been resolved. Here we provide evidence that current facilitation and macropore formation involve functional complexes comprised of P2X7 and TMEM16, a family of Ca2+-activated ion channel/scramblases. We found that current facilitation results in an increase of complex-embedded P2X7 open channel probability, a result mimicked by plasma membrane cholesterol depletion. We further show that macropore formation entails two distinct large molecule permeation components, one of which requires protein complexes featuring TMEM16F subtype, the other likely being direct permeation through the P2X7 pore itself. Such protein complexes can be considered to represent a regulatory hub intimately involved in distinct P2X7 functionalities.

Fatty Acid Binding Protein 5 Mediates Cell Death by Psychosine Exposure through Mitochondrial Macropores Formation in Oligodendrocytes

Oligodendrocytes, the myelinating cells in the central nervous system (CNS), are critical for producing myelin throughout the CNS. The loss of oligodendrocytes is associated with multiple neurodegenerative disorders mediated by psychosine. However, the involvement of psychosine in the critical biochemical pathogenetic mechanism of the loss of oligodendrocytes and myelin in krabbe disease (KD) remains unclear. Here, we addressed how oligodendrocytes are induced by psychosine treatment in both KG-1C human oligodendroglial cells and mouse oligodendrocyte precursor cells. We found that fatty acid binding protein 5 (FABP5) expressed in oligodendrocytes accelerates mitochondria-induced glial death by inducing mitochondrial macropore formation through voltage-dependent anion channels (VDAC-1) and BAX. These two proteins mediate mitochondrial outer membrane permeabilization, thereby leading to the release of mitochondrial DNA and cytochrome C into the cytosol, and the activation of apoptotic caspases. Furthermore, we confirmed that the inhibition of FABP5 functions by shRNA and FABP5-specific ligands blocking mitochondrial macropore formation, thereby rescuing psychosine-induced oligodendrocyte death. Taken together, we identified FABP5 as a critical factor in mitochondrial injury associated with psychosine-induced apoptosis in oligodendrocytes.

Pore Morphology of Heavily Doped P-Type Porous Silicon

Tuning the pore diameter of porous silicon (PS) is essential for some applications such as biosensing, where the pore size can filter the entrance of some analytes or increase its sensitivity. However, macropore (>50 nm) formation on p-type silicon is still poorly known due to the strong dependence on resistivity. Electrochemically etching heavily doped p-type silicon usually forms micropores (<5 nm), but it has been found that bigger sizes can be achieved by adding an organic solvent to the electrolyte. In this work, we present the results of using dimethylformamide (DMF), dimethylsulfoxide (DMSO), potassium hydroxide (KOH) and sodium hydroxide (NaOH) for macropore formation in p-type silicon with a resistivity between 0.001 and 0.02 Ω∙cm, achieving pore sizes from 5 to 100 nm.