BackgroundThe neuromuscular junction (NMJ) is a cholinergic synapse that rapidly conveys signals from motoneurons to muscle cells and exhibits a high degree of subcellular specialization characteristic of chemical synapses. NMJ formation requires agrin and its coreceptors LRP4 and MuSK. Increasing evidence indicates that Wnt signaling regulates NMJ formation in Drosophila, C. elegans and zebrafish.ResultsIn the study we systematically studied the effect of all 19 different Wnts in mammals on acetylcholine receptor (AChR) cluster formation. We identified five Wnts (Wnt9a, Wnt9b, Wnt10b, Wnt11, and Wnt16) that are able to stimulate AChR clustering, of which Wnt9a and Wnt11 are expressed abundantly in developing muscles. Using Wnt9a and Wnt11 as example, we demonstrated that Wnt induction of AChR clusters was dose-dependent and non-additive to that of agrin, suggesting that Wnts may act via similar pathways to induce AChR clusters. We provide evidence that Wnt9a and Wnt11 bind directly to the extracellular domain of MuSK, to induce MuSK dimerization and subsequent tyrosine phosphorylation of the kinase. In addition, Wnt-induced AChR clustering requires LRP4.ConclusionsThese results identify Wnts as new players in AChR cluster formation, which act in a manner that requires both MuSK and LRP4, revealing a novel function of LRP4.
Constructing heterojunctions is an efficient approach for enhancing charge separation to optimize photoreactivity. Although the aligned built‐in electric fields across the heterointerface are generally considered as the main driving force for charge separation, diffusion‐controlled charge separation also happens, which is poorly investigated in photocatalytic heterojunctions. Here, a perylene‐3,4,9,10‐tetracarboxylic diimide (PDI)–bismuth oxyiodide (BiOI) heterojunction is elaborately fabricated by in situ successive ion layer adsorption and reaction (SILAR) methods. Utilizing Kelvin probe force microscopy (KPFM), the local separation of photogenerated charge carriers across the heterointerface is directly mapped, which obeys a Z‐scheme mechanism. Experimental results and theoretical simulations reveal that the differences of electron densities between PDI and BiOI enable a diffusion‐controlled charge separation process, which overwhelm that of built‐in electric fields across heterointerfaces. Benefiting from the effective charge separation driven by a diffusion‐controlled driving force, this PDI/BiOI heterojunction exhibits superior photocatalytic activities even under infrared (IR)‐light irradiation. These findings highlight the importance of diffusion‐controlled charge separation, and also offer useful roadmaps for the design of high‐performance heterojunction photocatalysts for down‐to‐earth applications.
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