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Ma, Ke

Publications and source records attributed to Ma, Ke.

45 records · Page 3

Yb-doped fiber laser mode-locked with Au nanocages/SiO{sub 2} saturable absorber

Au nanocages/SiO{sub 2} (Au-NCs/SiO{sub 2}) are prepared through a seed-mediated growth method, and the performance is investigated in an all-fiber passively mode-locked ytterbium-doped fiber laser, for the first time. Its saturating intensity and modulation depth are measured to be about 0.461 MW/cm{sup 2} and 5.3%, respectively. With the Au-NCs/SiO{sub 2} saturable absorbers (SA) film, the pulse with the pulse duration of 1.116 ns and repetition rate of 32.02 MHz was generated at 1063.14 nm, under the pump power of 342 mW. And the corresponding average output power of 4.82 mW was obtained. These results indicate that Au-NCs/SiO{sub 2} has excellent saturable absorption properties with the potential for important applications in the field of ultra-short pulse lasers.

36 MATERIALS SCIENCE↗

DNA for Assembly and Charge Transport Photocatalytic Reduction of CO 2

Abstract This report demonstrates the use of DNA to spatially organize photoactive nanocrystals into well‐defined Z‐scheme architectures to facilitate CO 2 reduction to usable fuels upon solar irradiation through electron transfer. Coupling donor (Titanium Oxide, TiO 2 ) and acceptor (Cadmium Sulfide, CdS) nanocrystals with DNA yield a 5.25‐fold improvement in CO 2 reduction over simply mixing the photocatalysts in solution. In addition, it is demonstrated that electron transfer occurs over distances far greater than those achieved with polyethylene glycol spacer. Efficient Z‐scheme photocatalytic reduction of CO 2 is observed for DNA lengths of 10–80 bases, which separate the donor and acceptor nanocrystals by 3–24 nm. More significantly, an interparticle distance of 9–10 nm yields the highest conversion of CO 2 , which is found for nanocrystals spaced using either linear 30mer double strand DNA (dsDNA) or a 40mer DNA composed of both linear and hairpin DNA. When the amount of 30mer DNA linking the photocatalysts is lowered, a corresponding decrease in CO 2 reduction yields is seen, showcasing the role of DNA in mediating electron transfer. These results demonstrate the highly unique attributes of DNA as both a templating agent for precise nanoscale assembly and for enabling charge transport. This work uncovers new research directions for nanoelectronics, electrochemistry, and photocatalysis.

Ma, Ke↗

Angiotensin II type 1 receptor-associated protein regulates carotid intimal hyperplasia through controlling apoptosis of vascular smooth muscle cells

Highlights: • ATRAP as a negative regulator of AT1 receptor plays an inhibitory role in VSMCs proliferation both in vitro and in vivo. • ATRAP triggers the marked apoptosis of VSMCs in balloon-injuried carotid arteries and depresses neointimal formation. • ATRAP induces VSMCs apoptosis through the influence of the PI3K/Akt signaling pathway. Intimal hyperplasia is the main cause of restenosis after carotid artery injury, and the underlying mechanism involves the proliferation and migration of vascular smooth muscle cells (VSMCs). Angiotensin II Type 1 Receptor-Associated Protein (ATRAP) has been reported to withstand intimal hyperplasia by inhibiting VSMCs proliferation and migration; however, whether the beneficial effect of ATRAP associates with VSMCs apoptosis remains unclarified. We demonstrated that the adenoviral-mediated overexpression of ATRAP induced VSMC apoptosis, alleviating the balloon injury-induced neointima formation in rats. Under the condition of Angiotensin-II stimulation, ATRAP overexpression induced the apoptosis of rat VSMCs by depressing the PI3K-Akt signaling; whereas up-regulation of Akt by PTEN inhibitor abolished the apoptotic death. Thus, ATRAP regulates carotid intimal hyperplasia through controlling the PI3K-Akt signal-mediated VSMCs apoptosis.

60 APPLIED LIFE SCIENCES↗

Semiconductor-Based, Solar-Driven Photochemical Cells for Fuel Generation from Carbon Dioxide in Aqueous Solutions

There has been active interest to identify new methods to reduce CO 2 into usable fuel sources. In this work, we demonstrate two types of photo-electrochemical cells (PECs) that photoreduce CO 2 directly to formate in aqueous solutions both in the presence and absence of external bias or additional electron sources. The photocathodes were either a CuFeO 2 /CuO electrode or a bilayer of CdTe on NiO, whereas the photoanode was a bilayer of NiO x on CdS. The PECs were characterized by using both electrochemistry and spectroscopy, and the products formed from CO 2 reduction were characterized and quantified by using 1 H NMR spectroscopy and ESI-MS. In addition, an organohydride catalyst was tested in conjunction with the PECs, which not only showed a significant gain of 85 times in CO 2 reduction (27 μm formate without the catalyst, 2.3 mm formate with it) compared to the NiO/CdTe photocathode system but could also generate methanol under an external bias (10 μm).

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Brain and muscle Arnt-like 1 promotes skeletal muscle regeneration through satellite cell expansion

Circadian clock is an evolutionarily conserved timing mechanism governing diverse biological processes and the skeletal muscle possesses intrinsic functional clocks. Interestingly, although the essential clock transcription activator, Brain and muscle Arnt-like 1 (Bmal1), participates in maintenance of muscle mass, little is known regarding its role in muscle growth and repair. In this report, we investigate the in vivo function of Bmal1 in skeletal muscle regeneration using two muscle injury models. Bmal1 is highly up-regulated by cardiotoxin injury, and its genetic ablation significantly impairs regeneration with markedly suppressed new myofiber formation and attenuated myogenic induction. A similarly defective regenerative response is observed in Bmal1-null mice as compared to wild-type controls upon freeze injury. Lack of satellite cell expansion accounts for the regeneration defect, as Bmal1{sup −/−} mice display significantly lower satellite cell number with nearly abolished induction of the satellite cell marker, Pax7. Furthermore, satellite cell-derived primary myoblasts devoid of Bmal1 display reduced growth and proliferation ex vivo. Collectively, our results demonstrate, for the first time, that Bmal1 is an integral component of the pro-myogenic response that is required for muscle repair. This mechanism may underlie its role in preserving adult muscle mass and could be targeted therapeutically to prevent muscle-wasting diseases. - Highlights: • Bmal1 is highly inducible by muscle injury and myogenic stimuli. • Genetic ablation of Bmal1 significantly impairs muscle regeneration. • Bmal1 promotes satellite cell expansion during muscle regeneration. • Bmal1-deficient primary myoblasts display attenuated growth and proliferation.

60 APPLIED LIFE SCIENCES↗