Cell-Surface Protein Profiling Identifies Distinctive Markers of Progenitor Cells in Human Skeletal Muscle

SummarySkeletal muscle contains two distinct stem/progenitor populations. One is the satellite cell, which acts as a muscle stem cell, and the other is the mesenchymal progenitor, which contributes to muscle pathogeneses such as fat infiltration and fibrosis. Detailed and accurate characterization of these progenitors in humans remains elusive. Here, we performed comprehensive cell-surface protein profiling of the two progenitor populations residing in human skeletal muscle and identified three previously unrecognized markers: CD82 and CD318 for satellite cells and CD201 for mesenchymal progenitors. These markers distinguish myogenic and mesenchymal progenitors, and enable efficient isolation of the two types of progenitors. Functional study revealed that CD82 ensures expansion and preservation of myogenic progenitors by suppressing excessive differentiation, and CD201 signaling favors adipogenesis of mesenchymal progenitors. Thus, cell-surface proteins identified here are not only useful markers but also functionally important molecules, and provide valuable insight into human muscle biology and diseases

Negatively Curved Nanographene with Heptagonal and [5]Helicene Units

Negatively curved nanographene (NG) 4, having two heptagons and a [5]helicene, was unexpectedly obtained by aryl rearrangement and stepwise cyclodehydrogenations. X-ray crystallography confirmed the saddle-shaped structures of intermediate 3 and NG 4. The favorability of rearrangement over helicene formation following radical cation or arenium cation mechanisms is supported by theoretical calculations. NG 4 demonstrates a reversible mechanochromic color change and solid-state emission, presumably benefiting from its loose crystal packing. After resolution by chiral high-performance liquid chromatography, the circular dichroism spectra of enantiomers 4-(P) and 4-(M) were measured and showed moderate Cotton effects at 350 nm [Formula: see text]

Catch and release with DNA by imidazolium-presenting iron oxide nanoparticles via anion exchange

We present the catch and release technique with DNA using imidazolium-presenting nanoparticles via anion exchange. The imidazolium-tethered superparamagnetic iron oxide (SPIO) was prepared and the binding behavior to DNA was investigated. Accordingly, when the imidazolium cation forms an ion pair with the hydrophilic anion such as chloride, DNA can be absorbed onto the modified SPIO. In contrast, by anion exchange to hydrophobic anion such as TFSA−, the binding affinity greatly decreased, resulting in the release of DNA. Moreover, the release efficiency can be improved by introducing a silica layer at the surface of SPIOs. Finally, the catch and release with DNA was accomplished under mild conditions