Evaluating the pro-survival potential of apoptotic bodies derived from 2D- and 3D- cultured adipose stem cells in ischaemic flaps.

In the realm of large-area trauma flap transplantation, averting ischaemic necrosis emerges as a pivotal concern. Several key mechanisms, including the promotion of angiogenesis, the inhibition of oxidative stress, the suppression of cell death, and the mitigation of inflammation, are crucial for enhancing skin flap survival. Apoptotic bodies (ABs), arising from cell apoptosis, have recently emerged as significant contributors to these functions. This study engineered three-dimensional (3D)-ABs using tissue-like mouse adipose-derived stem cells (mADSCs) cultured in a 3D environment to compare their superior biological effects against 2D-ABs in bolstering skin flap survival. The findings reveal that 3D-ABs (85.74 ± 4.51) % outperform 2D-ABs (76.48 ± 5.04) % in enhancing the survival rate of ischaemic skin flaps (60.45 ± 8.95) % (all p < 0.05). Mechanistically, they stimulated angiogenesis, mitigated oxidative stress, suppressed apoptosis, and facilitated the transition of macrophages from M1 to M2 polarization (all p < 0.05). A comparative analysis of microRNA (miRNA) profiles in 3D- and 2D-ABs identified several specific miRNAs (miR-423-5p-up, miR30b-5p-down, etc.) with pertinent roles. In summary, ABs derived from mADSCs cultured in a 3D spheroid-like arrangement exhibit heightened biological activity compared to those from 2D-cultured mADSCs and are more effective in promoting ischaemic skin flap survival. These effects are attributed to their influence on specific miRNAs.

Apoptotic Bodies Derived from Fibroblast-Like Cells in Subcutaneous Connective Tissue Inhibit Ferroptosis in Ischaemic Flaps via the miR-339-5p/KEAP1/Nrf2 Axis.

Preventing and treating avascular necrosis at the distal end of the flaps are critical to surgery success, but current treatments are not ideal. A recent study shows that apoptotic bodies (ABs) generated near the site of apoptosis can be taken up and promote cell proliferation. The study reveals that ABs derived from fibroblast-like cells in the subcutaneous connective tissue (FSCT cells) of skin flaps promoted ischaemic flap survival. It is also found that ABs inhibited cell death and oxidative stress and promoted M1-to-M2 polarization in macrophages. Transcriptome sequencing and protein level testing demonstrated that ABs promoted ischaemic flap survival in endothelial cells and macrophages by inhibiting ferroptosis via the KEAP1-Nrf2 axis. Furthermore, microRNA (miR) sequencing data and in vitro and in vivo experiments demonstrated that ABs inhibited KEAP1 by delivering miR-339-5p to exert therapeutic effects. In conclusion, FSCT cell-derived ABs inhibited ferroptosis, promoted the macrophage M1-to-M2 transition via the miR-339-5p/KEAP1/Nrf2 axis and promoted ischaemic flap survival. These results provide a potential therapeutic strategy to promote ischaemic flap survival by administering ABs.

Puerarin enhances TFEB-mediated autophagy and attenuates ROS-induced pyroptosis after ischemic injury of random-pattern skin flaps.

BACKGROUND AND AIM: Necrosis of random-pattern flaps restricts their application in clinical practice. Puerarin has come into focus due to its promising therapeutic effects in ischemic diseases. Here, we employed Puerarin and investigated its role and potential mechanisms in flap survival. EXPERIMENTAL PROCEDURE: The effect of Puerarin on the viability of human umbilical vein endothelial cells (HUVECs) was assessed by CCK-8, EdU staining, migration, and scratch assays. Survival area measurement and laser Doppler blood flow (LDBF) were utilized to assess the viability of ischemic injury flaps. Levels of molecules related to oxidative stress, pyroptosis, autophagy, transcription factor EB (TFEB), and the AMPK-TRPML1-Calcineurin signaling pathway were detected using western blotting, immunofluorescence, dihydroethidium (DHE) staining, RT-qPCR and Elisa. KEY RESULTS: The findings demonstrated that Puerarin enhanced the survivability of ischemic flaps. Autophagy, oxidative stress, and pyroptosis were implicated in the ability of Puerarin in improving flap survival. Increased autophagic flux and augmented tolerance to oxidative stress contribute to Puerarin's suppression of pyroptosis. Additionally, Puerarin modulated the activity of TFEB through the AMPK-TRPML1-Calcineurin signaling pathway, thereby enhancing autophagic flux. CONCLUSIONS AND IMPLICATIONS: Puerarin promoted flap survival from ischemic injury through upregulation of TFEB-mediated autophagy and inhibition of oxidative stress. Our findings offered valuable support for the clinical application of Puerarin in the treatment of ischemic diseases, including random-pattern flaps.

Localized Medium Concentration Electrolyte with Fast Kinetics for Lithium Metal Batteries.

Localized high-concentration electrolyte is widely acknowledged as a cutting-edge electrolyte for the lithium metal anode. However, the high fluorine content, either from high-concentration salts or from highly fluorinated diluents, results in significantly higher production costs and an increased environmental burden. Here, we have developed a novel electrolyte termed "Localized Medium-Concentration Electrolyte" (LMCE) to effectively address these issues. This LMCE is designed and produced by diluting a medium concentration (0.5 M-1.5 M) electrolyte which is incompatible with lithium metal anode before diluting. It has ultralow concentration (0.1 M) and demonstrates remarkable compatibility with lithium metal anode. Surprisingly, our LMCE, despite having an ultralow concentration (0.1 M), exhibits excellent kinetics in Li/Cu, Li/Li, LiFePO4 /Li, and NCM811/Li batteries. Additionally, LMCE effectively inhibits the corrosion of the Al current collector caused by LiTFSI salt under high voltage (>4 V) conditions. This groundbreaking LMCE design transforms the seemingly "incompatible" into the "compatible", opening up new avenues for exploring various electrolyte formulations, including all liquid electrolyte-based batteries.

High Mass Loading of Edge-Exposed Cu3P Nanocrystal in 3D Freestanding Matrix Regulating Lithiophilic Sites for High-Performance Lithium Metal Anode.

Lithium (Li) dendrites and volume expansion during repeated Li plating and stripping processes are the major obstacles to the development of advanced Li metal batteries. Li nucleation and dendrite growth can be controlled and inhibited spatially by using 3-dimensional (3D) hosts together with efficient lithiophilic materials. To realize next-generation Li-metal batteries, it is critical to effectively regulate the surface structure of the lithiophilic crystals. Herein, exposed-edged Cu3P faceted nanoparticles anchored along the interlaced carbon nanofibers (ECP@CNF) are developed as a highly efficient 3D Li host. Through the 3D interlaced rigid carbon skeleton, volume expansion can be accommodated. The (300)-dominant edged crystal facets of Cu3P with abundant exposed P3- sites not only exhibit strong micro-structural Li affinity but also have relatively high charge transference to nucleate uniformly and effectively, resulting in reduced polarization. Consequently, under a high current density of 10 mA cm-2 with a high discharge of depth (60%), ECP@CNF/Li symmetric cells demonstrate outstanding cycling stability for 500 h with a small voltage hysteresis of 32.8 mV. Notably, the ECP@CNF/Li∥LiFePO4 full cell exhibits a more stable cycling performance for 650 cycles under a high rate of 1 C, with capacity retention up to 92% (N/P = 10, 4.7 mg cm-2 LiFePO4). Even under a limit Li (3.4 mA h) with an N/P ratio of 2 (8.9 mg cm-2 LiFePO4), ECP@CNF/Li∥LiFePO4 full cell can also demonstrate excellent reversibility and stable cycling performance with higher utilization of Li. This work provides an insight view into constructing high-performance Li-metal batteries under more strict conditions.

Constructing Co3S4 Nanosheets Coating N-Doped Carbon Nanofibers as Freestanding Sulfur Host for High-Performance Lithium-Sulfur Batteries.

Lithium-sulfur batteries (LSBs) have shown great potential as a rival for next generation batteries, for its relatively high theoretical capacity and eco-friendly properties. Nevertheless, blocked by the shuttle effect of lithium polysulfides (LPSs, Li2S4-Li2S8) and insulation of sulfur, LSBs show rapid capacity loss and cannot achieve the practical application. Herein, a composite of carbon nanofibers coated by Co3S4 nanosheets (denoted as CNF@Co3S4) is successfully synthesized as freestanding sulfur host to optimize the interaction with sulfur species. The combination of the two materials can lead extraordinary cycling and rate performance by alleviating the shuttle of LPSs effectively. N-doped carbon nanofibers serve as long-range conductive networks and Co3S4 nanosheets can accelerate the conversion of LPSs through its electrocatalytic and chemical adsorption ability. Benefiting from the unique structure, the transporting rate of Li+ can be enhanced. Distribution of Li+ is uniform for enough exposed negative active sites. As a result, the cell with CNF@Co3S4 as sulfur host is able to stabilize at 710 mA h g-1 at 1 C after 200 cycles with average coulombic efficiency of 97.8% in a sulfur loading of 1.7 mg cm-2 and deliver 4.1 mA h cm-2 at 0.1 C even in 6.8 mg cm-2 for 100 cycles.

Double Morphology of Co9S8 Coated by N, S Co-doped Carbon as Efficient Anode Materials for Sodium-Ion Batteries.

Co9S8 is a potential anode material for its high sodium storage performance, easy accessibility, and thermostability. However, the volume expansion is a great hindrance to its development. Herein, a composite containing Co9S8 nanofibers and hollow Co9S8 nanospheres with N, S co-doped carbon layer (Co9S8@NSC) is successfully synthesized through a facile solvothermal process and a high-temperature carbonization. Ascribed to the carbon coating and the large specific surface area, severe volume stress can be effectively alleviated. In particular, with N and S heteroatoms introduced into the carbon layer, which is conducive to the Na+ adsorption and diffusion on the carbon surface, Co9S8@NSC can perform more capacitive sodium storage mechanism. As a result, the electrode can exhibit a favorable reversible capacity of 226 mA h g-1 at 5 A g-1 and a favorable capacity retention of 83.1% at 1 A g-1 after 800 cycles. The unique design provides an innovative thought for enhancing the sodium storage performance.

The fabrication of a 3D current collector with bitter melon-like TiO2-NCNFs for highly stable lithium-sulfur batteries.

The conductive 3D freestanding N-doped carbon nanofibers (NCNFs) current collector was embedded with homogeneously polar TiO2 nanoparticles. This current collector used for the sulfur cathode exhibits strong chemical adsorption for hindering the shuttle effect of polysulfides, and demonstrates a high specific capacity of 865 mA h g-1 at 0.2C and excellent cycle performance (200 cycles with capacity retention of 91%).

Flexible Freestanding Carbon Nanofiber-Embedded TiO2 Nanoparticles as Anode Material for Sodium-Ion Batteries.

Sodium-ion batteries (SIBs), owning to the low cost, abundant resources, and similar physicochemical properties with lithium-ion batteries (LIBs), have earned much attention for large-scale energy storage systems. In this article, we successfully synthesize flexible freestanding carbon nanofiber-embedded TiO2 nanoparticles (CNF-TiO2) and then apply it directly as anode in SIBs without binder or current collector. Taking the advantage of flexible CNF and high structural stability, this anode exhibits high reversible capacity of 614 mAh·g-1 (0.27 mAh·cm-2) after almost 400 cycles and excellent capacity retention ability of ~100.

Synthesis and Investigation of CuGeO3 Nanowires as Anode Materials for Advanced Sodium-Ion Batteries.

Germanium is considered as a potential anode material for sodium-ion batteries due to its fascinating theoretical specific capacity. However, its poor cyclability resulted from the sluggish kinetics and large volume change during repeated charge/discharge poses major threats for its further development. One solution is using its ternary compound as an alternative to improve the cycling stability. Here, high-purity CuGeO3 nanowires were prepared via a facile hydrothermal method, and their sodium storage performances were firstly explored. The as-obtained CuGeO3 delivered an initial charge capacity of 306.7 mAh g-1 along with favorable cycling performance, displaying great promise as a potential anode material for sodium ion batteries.

Flower-like Cu2SnS3 Nanostructure Materials with High Crystallinity for Sodium Storage.

In this study, ternary Cu2SnS3 (CTS) nanostructure materials with high crystallinity were successfully prepared via a facile solvothermal method, which was followed by high-temperature treatment. The morphology of the as-synthesized samples is uniform flower-like spheres, with these spheres consisting of hierarchical nanosheets and possessing network features. Sodium storage measurements demonstrate that the annealed CTS electrodes have high initial reversible capacity (447.7 mAh·g−1 at a current density of 100 mA·g−1), good capacity retention (200.6 mAh·g−1 after 50 cycles at a current density of 100 mA·g−1) and considerable rate capability because of their high crystallinity and unique morphology. Such good performances indicate that the high crystallinity CTS is a promising anode material for sodium ion batteries.