Extensive jejunal injury is repaired by migration and transdifferentiation of ileal enterocytes in zebrafish.

A major cause of intestinal failure (IF) is intestinal epithelium necrosis and massive loss of enterocytes, especially in the jejunum, the major intestinal segment in charge of nutrient absorption. However, mechanisms underlying jejunal epithelial regeneration after extensive loss of enterocytes remain elusive. Here, we apply a genetic ablation system to induce extensive damage to jejunal enterocytes in zebrafish, mimicking the jejunal epithelium necrosis that causes IF. In response to injury, proliferation and filopodia/lamellipodia drive anterior migration of the ileal enterocytes into the injured jejunum. The migrated fabp6+ ileal enterocytes transdifferentiate into fabp2+ jejunal enterocytes to fulfill the regeneration, consisting of dedifferentiation to precursor status followed by redifferentiation. The dedifferentiation is activated by the IL1ß-NFκB axis, whose agonist promotes regeneration. Extensive jejunal epithelial damage is repaired by the migration and transdifferentiation of ileal enterocytes, revealing an intersegmental migration mechanism of intestinal regeneration and providing potential therapeutic targets for IF caused by jejunal epithelium necrosis.

Fluorinated Solid Electrolyte Interphase Derived From Fluorinated Polymer Electrolyte To Stabilize Li Metal.

Unstable interface between highly reductive Li metal and a conventional liquid electrolyte leads to uncontrollable Li dendrites and Li pulverization, thus limiting the practical applications of Li metal batteries with high energy density. Herein, a fluorinated quasi-solid polymer electrolyte is synthesized to stabilize Li metal via the C-F/LiF enriched solid electrolyte interphase (SEI) derived from the fluorinated polymer skeleton. Benefiting from the homogenized ion plating/stripping process guided by lithophilic C-F and rapid Li+ transportation assisted by LiF, Li dendrites and Li pulverization are suppressed. As a result, the Li||Li symmetrical cell with the fluorinated quasi-solid polymer electrolyte remains stable over 1400 h at a current density of 0.3 mA cm-2 . LiNi0.8 Co0.1 Mn0.1 O2 ||Li battery delivers a long-term cycling performance, where the capacity retains 87.77 % of its initial state after 300 cycles at 0.5 C in the voltage range from 2.8 to 4.4 V.

Ionic Conduction in Polymer-Based Solid Electrolytes.

Good safety, high interfacial compatibility, low cost, and facile processability make polymer-based solid electrolytes promising materials for next-generation batteries. Key issues related to polymer-based solid electrolytes, such as synthesis methods, ionic conductivity, and battery architecture, are investigated in past decades. However, mechanistic understanding of the ionic conduction is still lacking, which impedes the design and optimization of polymer-based solid electrolytes. In this review, the ionic conduction mechanisms and optimization strategies of polymer-based solid electrolytes, including solvent-free polymer electrolytes, composite polymer electrolytes, and quasi-solid/gel polymer electrolytes, are summarized and evaluated. Challenges and strategies for enhancing the ionic conductivity are elaborated, while the ion-pair dissociation, ion mobility, polymer relaxation, and interactions at polymer/filler interfaces are highlighted. This comprehensive review is especially pertinent for the targeted enhancement of the Li-ion conductivity of polymer-based solid electrolytes.

Intestinal precursors avoid being misinduced to liver cells by activating Cdx-Wnt inhibition cascade.

During coordinated development of two neighboring organs from the same germ layer, how precursors of one organ resist the inductive signals of the other to avoid being misinduced to wrong cell fate remains a general question in developmental biology. The liver and anterior intestinal precursors located in close proximity along the gut axis represent a typical example. Here we identify a zebrafish leberwurst (lbw) mutant with a unique hepatized intestine phenotype, exhibiting replacement of anterior intestinal cells by liver cells. lbw encodes the Cdx1b homeoprotein, which is specifically expressed in the intestine, and its precursor cells. Mechanistically, in the intestinal precursors, Cdx1b binds to genomic DNA at the regulatory region of secreted frizzled related protein 5 (sfrp5) to activate sfrp5 transcription. Sfrp5 blocks the mesoderm-derived, liver-inductive Wnt2bb signal, thus conferring intestinal precursor cells resistance to Wnt2bb. These results demonstrate that the intestinal precursors avoid being misinduced toward hepatic lineages through the activation of the Cdx1b-Sfrp5 cascade, implicating Cdx/Sfrp5 as a potential pharmacological target for the manipulation of intestinal-hepatic bifurcations, and shedding light on the general question of how precursor cells resist incorrect inductive signals during embryonic development.

Self-Healing Polymer Electrolyte for Dendrite-Free Li Metal Batteries with Ultra-High-Voltage Ni-Rich Layered Cathodes.

Practical applications of polymer electrolytes in lithium (Li) metal batteries with high-voltage Ni-rich cathodes have been hindered by the dendrite growth and poor oxidative stability of electrolytes. Herein, a self-healing polymer electrolyte is developed by in situ copolymerization of 2-(3-(6-methyl4-oxo-1,4-dihydropyrimidin-2-yl)ureido)ethyl methacrylate (UPyMA) and ethylene glycol methyl ether acrylate (EGMEA) monomers. With the electrolyte, the dendrite growth is inhibited by spontaneously repairing dendrite-induced defects, cracks, and voids at the Li/electrolyte interface; the suppressed dendrite growth and associated electro-chemo behaviors are visualized by the kinetic Mont-Carlo simulation. Benefitting from the high ionic conductivity, wide electrochemical window and good interfacial stability, the self-healing polymer electrolyte enables stable cycling of the LiNi0.8 Mn0.1 Co0.1 O2 (NMC811) cathode under 4.7 V, achieving a high specific capacity of ≈228.8 mAh g-1 and capacity retention of 80.4% over 500 cycles. The new electrolyte is very promising for developing highly safe and dendrite-free Li metal batteries with high energy density.

Highly flexible reduced graphene oxide@polypyrrole-polyethylene glycol foam for supercapacitors.

A flexible and free-standing 3D reduced graphene oxide@polypyrrole-polyethylene glycol (RGO@PPy-PEG) foam was developed for wearable supercapacitors. The device was fabricated sequentially, beginning with the electrodeposition of PPy in the presence of a PEG-borate on a sacrificial Ni foam template, followed by a subsequent GO wrapping and chemical reduction process. The 3D RGO@PPy-PEG foam electrode showed excellent electrochemical properties with a large specific capacitance of 415 F g-1 and excellent long-term stability (96% capacitance retention after 8000 charge-discharge cycles) in a three electrode configuration. An assembled (two-electrode configuration) symmetric supercapacitor using RGO@PPy-PEG electrodes exhibited a remarkable specific capacitance of 1019 mF cm-2 at 2 mV s-1 and 95% capacitance retention over 4000 cycles. The device exhibits extraordinary mechanical flexibility and showed negligable capacitance loss during or after 1000 bending cycles, highlighting its great potential in wearable energy devices.