Showing papers by "Yu Huang published in 2011"

Plasmon resonance enhanced multicolour photodetection by graphene

Abstract: Graphene has the potential for high-speed, wide-band photodetection, but only with very low external quantum efficiency and no spectral selectivity. Here we report a dramatic enhancement of the overall quantum efficiency and spectral selectivity that enables multicolour photodetection, by coupling graphene with plasmonic nanostructures. We show that metallic plasmonic nanostructures can be integrated with graphene photodetectors to greatly enhance the photocurrent and external quantum efficiency by up to 1,500%. Plasmonic nanostructures of variable resonance frequencies selectively amplify the photoresponse of graphene to light of different wavelengths, enabling highly specific detection of multicolours. Being atomically thin, graphene photodetectors effectively exploit the local plasmonic enhancement effect to achieve a significant enhancement factor not normally possible with traditional planar semiconductor materials.

Platinum nanocrystals selectively shaped using facet-specific peptide sequences

Abstract: The properties of a nanocrystal are heavily influenced by its shape. Shape control of a colloidal nanocrystal is believed to be a kinetic process, with high-energy facets growing faster then vanishing, leading to nanocrystals enclosed by low-energy facets. Identifying a surfactant that can specifically bind to a particular crystal facet is critical, but has proved challenging to date. Biomolecules have exquisite specific molecular recognition properties that can be explored for the precise engineering of nanostructured materials. Here, we report the use of facet-specific peptide sequences as regulating agents for the predictable synthesis of platinum nanocrystals with selectively exposed crystal surfaces and particular shapes. The formation of platinum nanocubes and nanotetrahedrons are demonstrated with Pt-{100} and Pt-{111} binding peptides, respectively. Our studies unambiguously demonstrate the abilities of facet-selective binding peptides in determining nanocrystal shape, representing a critical step forward in the use of biomolecules for programmable synthesis of nanostructures.

Endothelium-mediated control of vascular tone: COX-1 and COX-2 products

Abstract: Endothelium-dependent contractions contribute to endothelial dysfunction in various animal models of aging, diabetes and cardiovascular diseases. In the spontaneously hypertensive rat, the archetypal model for endothelium-dependent contractions, the production of the endothelium-derived contractile factors (EDCF) involves an increase in endothelial intracellular calcium concentration, the production of reactive oxygen species, the predominant activation of cyclooxygenase-1 (COX-1) and to a lesser extent that of COX-2, the diffusion of EDCF towards the smooth muscle cells and the subsequent stimulation of their thromboxane A2-endoperoxide TP receptors. Endothelium-dependent contractions are also observed in various models of hypertension, aging and diabetes. They generally also involve the generation of COX-1- and/or COX-2-derived products and the activation of smooth muscle TP receptors. Depending on the model, thromboxane A2, PGH2, PGF2α, PGE2 and paradoxically PGI2 can all act as EDCFs. In human, the production of COX-derived EDCF is a characteristic of the aging and diseased blood vessels, with essential hypertension causing an earlier onset and an acceleration of this endothelial dysfunction. As it has been observed in animal models, COX-1, COX-2 or both isoforms can contribute to these endothelial dysfunctions. Since in most cases, the activation of TP receptors is the common downstream effector, selective antagonists of this receptor should curtail endothelial dysfunction and be of therapeutic interest in the treatment of cardiovascular disorders. LINKED ARTICLES This article is part of a themed issue on Vascular Endothelium in Health and Disease. To view the other articles in this issue visit http://dx.doi.org/10.1111/bph.2011.164.issue-3

Method and system for video summarization

Abstract: A video summary method comprises dividing a video into a plurality of video shots, analyzing each frame in a video shot from the plurality of video shots, determining a saliency of each frame of the video shot, determining a key frame of the video shot based on the saliency of each frame of the video shot, extracting visual features from the key frame and performing shot clustering of the plurality of video shots to determine concept patterns based on the visual features. The method further comprises fusing different concept patterns using a saliency tuning method and generating a summary of the video based upon a global optimization method.

Template-free fabrication and growth mechanism of uniform (BiO)2CO3 hierarchical hollow microspheres with outstanding photocatalytic activities under both UV and visible light irradiation

Abstract: The morphology-controlled fabrication of nano-/microstructured functional materials has opened up new possibilities to enhance their physical and chemical properties and remains a great challenge. This work represents a one-pot template-free fabrication and growth mechanism of novel rose-like uniform (BiO)2CO3 hierarchical hollow microspheres, which are self-assembled by single-crystal nanosheets. The observation of time-dependent evolution of crystal structure and morphology revealed that the growth mechanism of such a novel structure might involve a unique multistep pathway. First, an amorphous particle was formed during a nucleation and aggregation process. Then, the intermediate (BiO)4CO3(OH)2 of embryonic stacked buds with attached particles were produced due to Ostwald ripening. The driving force for the formation of such embryonic structure is the intrinsic dipole field introduced by the nanosheets as a result of selective adsorption of the citrate ions on some polar surfaces of the nanoparticles. Subsequently, all the particles were consumed and (BiO)4CO3(OH)2 crystals started to transform to (BiO)2CO3 phase by means of repeated reaction-dissolution-recrystallization process in a homocentric layer-by-layer growth style, where carbonate ions substituted OH− groups. Monodisperse buds were then generated and the size of the hollow in the center becomes smaller to reduce surface energy. Finally, all (BiO)4CO3(OH)2 transformed to (BiO)2CO3 phase and uniform monodisperse (BiO)2CO3 roses were produced through layers splitting driven by the OH− group deintercalating from the interlayer spaces of (BiO)4CO3(OH)2. More interestingly, the novel (BiO)2CO3 microspheres exhibited outstanding activities under both UV and visible light irradiation for indoor NO removal, far exceeding that of commercial P25, synthetic C-doped TiO2 and (BiO)2CO3 with particle morphology due to the special hierarchical morphology and band gap structure.

Rescue of mesangial cells from high glucose-induced over-proliferation and extracellular matrix secretion by hydrogen sulfide

Abstract: Background. Hydrogen sulfide (H2S) is considered as the third gasotransmitter after nitric oxide and carbon monoxide. This gas molecule participates in the regulation of renal function. Diabetic nephropathy (DN) is one of the major chronic complications of diabetes. The present study aimed to explore the changes in H2S metabolism in the early stage of DN and the effects of H2S on cultured rat renal glomerular mesangial cells (MCs). Methods. Cultured rat MCs and streptozotocin (STZ)induced diabetic rats were used in this study. Expression levels of cystathionine γ-lyase (CSE), transforming growth factor-β1 (TGF-β1) and collagen IV in rat renal cortex and in cultured MCs were determined by quantitative real-time PCR and western blot. Reactive oxygen species (ROS) released from rat MCs was assessed by fluorescent probe assays. MCs proliferation was analyzed by 5′-bromo-2′deoxyuridine incorporation assay. Results. H2S levels in the plasma and renal cortex and the levels of CSE messenger RNA (mRNA) and protein in renal cortex were significantly reduced, while the levels of TGF-β1 and collagen IV increased 3 weeks after STZ injection. Administration of NaHS, a H2S donor, reversed the increases in TGF-β1 and collagen IV in diabetic rats. By contrast, NaHS did not alter the TGF-β1 and collagen IV levels in non-diabetic rats. But NaHS lowered the CSE mRNA level in renal cortex. Exposure to high glucose promoted ROS generation and cell proliferation, up-regulated the expression of TGF-β1 and collagen IV but decreased the CSE expression in cultured MCs. Treatment of cultured MCs with NaHS reversed the effect of high glucose. NaHS did not change ROS generation, cell proliferation, TGF-β1 and collagen IVexpression in the cells cultured with normal glucose. Reduction of endogenous H2S generation by DLpropargylglycine,aCSEinhibitor,producedsimilarcellular effects as high glucose, including increases in cell proliferation, TGF-β1 and collagen IV expressions and ROS generation. Conclusion. Suppressed CSE-catalyzed endogenous H2S production in the kidney by hyperglycemia may play an important role in the pathogenesis of DN.

Apple Polyphenols Extend the Mean Lifespan of Drosophila melanogaster

Abstract: Apple polyphenols (AP) are an excellent source of dietary antioxidants. The present study investigated the effect of AP on the lifespan of fruit flies and their interaction with gene expressions of superoxide dismutase (SOD), catalase (CAT), methuselah (MTH), Rpn11, and cytochrome c oxidase (CcO) subunits III and VIb. Results showed the mean lifespan was significantly extended by 10% in fruit flies fed the AP diet. This was accompanied by up-regulation of genes SOD1, SOD2, and CAT and down-regulation of MTH in the aged fruit flies. Paraquat and H(2)O(2) challenge tests demonstrated that AP prolonged the survival time only for Oregon R wild type flies but not for SOD(n108) or Cat(n1) mutants, in which either SOD or CAT was knocked out. Chronic paraquat exposure could shorten the maximum lifespan from 68 to 31 days and reduce the climbing ability by 60%, whereas AP could partially reverse the paraquat-induced mortality and decline in climbing ability. AP could up-regulate Rpn11 at day 30, whereas it appeared to have no significant effect on gene expression of ubiquitinated protein, CcO subunits III and VIb. These AP-induced changes were unlikely associated with caloric restriction as the gustatory assay found no difference in average body weight and stomach redness index between the control and AP fruit flies. It was therefore concluded that the antiaging activity of AP was, at least in part, mediated by its interaction with genes SOD, CAT, MTH, and Rpn11.

Controllable Underwater Oil‐Adhesion‐Interface Films Assembled from Nonspherical Particles

Abstract: A controllable underwater oil-adhesion-interface is presented based on colloidal crystals assembled from nonspherical latex particles. The underwater oil-adhesive force of the as-prepared film can be effectively controlled from high to low adhesion by varying the latex structures from spherical or cauliflower-like to single cavity, which effectively adjusts the solid/liquid contact mode/wetting state of oil droplets on the films. This facile fabrication of functional films with special underwater oil-adhesion properties based on a flexible design of a latex structure will offer significant insight for the design and creation of novel underwater antifouling materials.

Top-gated chemical vapor deposition grown graphene transistors with current saturation.

Abstract: Graphene transistors are of considerable interest for radio frequency (rf) applications. In general, transistors with large transconductance and drain current saturation are desirable for rf performance, which is however nontrivial to achieve in graphene transistors. Here we report high-performance top-gated graphene transistors based on chemical vapor deposition (CVD) grown graphene with large transconductance and drain current saturation. The graphene transistors were fabricated with evaporated high dielectric constant material (HfO(2)) as the top-gate dielectrics. Length scaling studies of the transistors with channel length from 5.6 μm to 100 nm show that complete current saturation can be achieved in 5.6 μm devices and the saturation characteristics degrade as the channel length shrinks down to the 100-300 nm regime. The drain current saturation was primarily attributed to drain bias induced shift of the Dirac points. With the selective deposition of HfO(2) gate dielectrics, we have further demonstrated a simple scheme to realize a 300 nm channel length graphene transistors with self-aligned source-drain electrodes to achieve the highest transconductance of 250 μS/μm reported in CVD graphene to date.

Composition Tuning the Upconversion Emission in NaYF4:Yb/ Tm Hexaplate Nanocrystals

Abstract: Single crystal hexagonal NaYF4:Yb/Tm nanocrystals have been synthesized with uniform size, morphology and controlled chemical composition. Spectroscopic studies show that these nanocrystals exhibit strong energy upconversion emission when excited with a 980 nm diode laser, with two primary emission peaks centered around 452 nm and 476 nm. Importantly, the overall and relative emission intensity at these wavelengths can be readily tuned by controlling the concentration of the trivalent rare earth element dopants at the beginning of the synthesis which has been confirmed by EDX for the first time. Through systematic studies, the optimum rare earth ion doping concentration can be determined for the strongest emission intensity at the selected peak(s). Confocal microscopy studies show that the upconversion emission from individual NCs can be readily visualized. These studies demonstrate a rational approach for fine tuning the upconversion properties in rare-earth doped nanostructures and can broadly impact areas ranging from energy harvesting, energy conversion to biomedical imaging and therapeutics.

Inhibition of Renin-Angiotensin System Reverses Endothelial Dysfunction and Oxidative Stress in Estrogen Deficient Rats

Abstract: Background Estrogen deficiency increases the cardiovascular risks in postmenopausal women. Inhibition of the renin-angiotensin system (RAS) and associated oxidative stress confers a cardiovascular protection, but the role of RAS in estrogen deficiency-related vascular dysfunction is unclear. The present study investigates whether the up-regulation of RAS and associated oxidative stress contributes to the development of endothelial dysfunction during estrogen deficiency in ovariectomized (OVX) rats.

Synthesis of platinum single-twinned right bipyramid and {111}-bipyramid through targeted control over both nucleation and growth using specific peptides.

Abstract: Shape-controlled synthesis requires rigorous kinetic control over both nucleation and growth. For platinum (Pt), to date it is still challenging to generate twinned seeds in nucleation in a controllable fashion. Here, we report that a specific Pt binding peptide BP7A is able to mediate and stabilize single-twinned seeds formation at the nucleation stage under mild conditions. Importantly, it targets the control over nucleation directly. Combining with control over growth, we further demonstrate the rational design and synthesis of single-twinned structures, right bipyramid and {111}-bipyramid, by incorporating targeted facet stabilization over {100} facet and {111} facet, respectively. To the best of our knowledge, this is the first report on the successful synthesis of single-twinned bipyramids for Pt nanocrystals (NCs) with high yields. The work here demonstrates the power of biomolecules in recognizing and mediating inorganic nanomaterials synthesis, guiding the formation of material structures that ar...

Fabrication of functional colloidal photonic crystals based on well-designed latex particles

Abstract: Colloidal photonic crystals (PCs) have attracted a wide research interest due to their special light manipulation properties, demonstrating wide applications in optical sensing materials and various optical devices. In this paper, we review recent research progress related to the fabrication of functional colloidal PCs with tough mechanical properties, controllable wettability and anisotropic structures based on well-designed latex particles. For example, tough colloidal PCs are assembled from latex particles with hard-core and soft-shell structures, or based on a crosslinked structure among latex particles; the wettability of colloidal PCs is controlled by modifying the assembly temperature, pH, electronic potential, etc, using latex particles with well-designed surface chemical composition; the anisotropic colloidal PCs are fabricated based on the particles' anisotropic chemical composition or their response to external fields. Otherwise, large-scale fabrication of colloidal PCs by coating or printing has also been demonstrated based on the use of the latex particles with additional assembly force. This fabrication of functional colloidal PCs will greatly extend their applications in various fields.

APPL1 Counteracts Obesity-Induced Vascular Insulin Resistance and Endothelial Dysfunction by Modulating the Endothelial Production of Nitric Oxide and Endothelin-1 in Mice

Abstract: OBJECTIVE Insulin stimulates both nitric oxide (NO)-dependent vasodilation and endothelin-1 (ET-1)–dependent vasoconstriction. However, the cellular mechanisms that control the dual vascular effects of insulin remain unclear. This study aimed to investigate the roles of the multidomain adaptor protein APPL1 in modulating vascular actions of insulin in mice and in endothelial cells. RESEARCH DESIGN AND METHODS Both APPL1 knockout mice and APPL1 transgenic mice were generated to evaluate APPL1’s physiological roles in regulating vascular reactivity and insulin signaling in endothelial cells. RESULTS Insulin potently induced NO-dependent relaxations in mesenteric arteries of 8-week-old mice, whereas this effect of insulin was progressively impaired with ageing or upon development of obesity induced by high-fat diet. Transgenic expression of APPL1 prevented age- and obesity-induced impairment in insulin-induced vasodilation and reversed obesity-induced augmentation in insulin-evoked ET-1–dependent vasoconstriction. By contrast, genetic disruption of APPL1 shifted the effects of insulin from vasodilation to vasoconstriction. At the molecular level, insulin-elicited activation of protein kinase B (Akt) and endothelial NO synthase and production of NO were enhanced in APPL1 transgenic mice but were abrogated in APPL1 knockout mice. Conversely, insulin-induced extracellular signal–related kinase (ERK)1/2 phosphorylation and ET-1 expression was augmented in APPL1 knockout mice but was diminished in APPL1 transgenic mice. In endothelial cells, APPL1 potentiated insulin-stimulated Akt activation by competing with the Akt inhibitor Tribbles 3 (TRB3) and suppressed ERK1/2 signaling by altering the phosphorylation status of its upstream kinase Raf-1. CONCLUSIONS APPL1 plays a key role in coordinating the vasodilator and vasoconstrictor effects of insulin by modulating Akt-dependent NO production and ERK1/2-mediated ET-1 secretion in the endothelium.

Endothelial nitric oxide synthase enhancer reduces oxidative stress and restores endothelial function in db/db mice.

Abstract: Aims Endothelial dysfunction is caused by reduced nitric oxide (NO) bioavailability and/or over-produced reactive oxygen species (ROS). The present study investigated a vascular benefit of AVE3085, an endothelial nitric oxide synthase (eNOS) enhancer, in preserving endothelial function in diabetic mice and the mechanisms involved. Methods and results Male db/db and db/m+ mice were orally administered AVE3085 for 7 days (10 mg kg−1 day−1). Vascular reactivity of arteries was studied via myography under both isometric and isobaric conditions. ROS levels in aortas were determined using dihydroethidium fluorescence dye and electron paramagnetic resonance spin trapping. Chronic treatment with AVE3085 reduced blood pressure, enhanced endothelium-dependent relaxations (EDR) to acetylcholine in aortas, mesenteric, and renal arteries, lowered oxidative stress, and augmented the attenuated flow-dependent dilatation in mesenteric resistance arteries from db/db mice. Incubation of aortas from C57BL/6J mice in high glucose (30 mmol L−1) culture medium for 48 h impaired EDR and elevated ROS generation, and these effects were reversed by co-treatment with AVE3085 (1 µmol L−1). Benefits of AVE3085 were abolished by the transcription inhibitor actinomycin D, the NOS inhibitor N G-nitro-l-arginine methyl ester, and in eNOS−/− mice. NO production in primary endothelial cells from mouse aortas was detected with a NO-sensitive fluorescence dye. Protein expression was assayed by western blotting. Treatment with AVE3085 enhanced NO production in endothelial cells and eNOS expression in aortas. Conclusion AVE3085 ameliorates endothelial dysfunction in db/db mice through increased NO bioavailability, which reduces oxidative stress in the vascular wall. Targeting eNOS and NO production may be a promising approach to combat diabetic vasculopathy.

Dietary calcium decreases plasma cholesterol by down‐regulation of intestinal Niemann–Pick C1 like 1 and microsomal triacylglycerol transport protein and up‐regulation of CYP7A1 and ABCG 5/8 in hamsters

Abstract: Scope: It has been shown that calcium supplementation favorably modifies plasma lipoprotein profile in postmenopausal women. The present study investigated the interaction of dietary calcium with genes of transporters, receptors and enzymes involved in cholesterol metabolism. Methods and results: Forty-eight ovariectomized hamsters were fed one of the four diets containing 0, 2, 6 and 8 g calcium per kg. Plasma total cholesterol (TC), triacylglycerols (TG), and non-high density lipoprotein cholesterol were dose-dependently decreased, whereas high-density lipoprotein cholesterol (HDL-C) was dose-dependently increased with the increasing dietary calcium levels. Dietary calcium had no effect on protein mass of hepatic sterol regulatory element binding protein-2 (SREBP), liver X receptor-alpha (LXR), 3-hydroxy-3-methylglutaryl-CoA reductase (HMGR), LDL receptor (LDLR) and cholesterol-7α-hydroxylase (CYP7A1). However, dietary calcium up-regulated the mRNA levels of hepatic CYP7A1 and intestinal ATP binding cassette transporters (ABCG5/8) whereas it down-regulated the intestinal Niemann-Pick C1 like 1 (NPC1L1) and microsomal triacylglycerol transport protein (MTP). In addition, dietary calcium increased the activity of intestinal acyl coenzyme A: cholesterol acyltransferase 2, while it decreased plasma cholesteryl ester transport protein (CETP). Conclusion: Beneficial modification of lipoprotein profile by dietary calcium was mediated by sequestering bile acid absorption and enhancing excretion of fecal cholesterol, via up-regulation of mRNA CYP7A1 and intestinal ABCG 5/8 with down-regulation of mRNA NPC1L1 and MTP.

Telmisartan inhibits vasoconstriction via PPARγ-dependent expression and activation of endothelial nitric oxide synthase

Abstract: Aims Telmisartan activates peroxisome proliferator-activated receptor-γ (PPARγ) in addition to serving as an angiotensin II type 1 receptor (AT1R) blocker. The PPARγ activity of telmisartan on resistance arteries has remained largely unknown. The present study investigated the hypothesis that telmisartan inhibited vascular tension in mouse mesenteric resistance arteries, which was attributed to an increased nitric oxide (NO) production through the PPARγ-dependent augmentation of expression and activity of endothelial nitric oxide synthase (eNOS). Methods and results Second-order mesenteric arteries were isolated from male C57BL/6J, eNOS knockout and PPARγ knockout mice and changes in vascular tension were determined by isometric force measurement with a myograph. Expression and activation of relevant proteins were analysed by Western blotting. Real-time NO production was measured by confocal microscopy using the dye DAF. Telmisartan inhibited 9,11-dideoxy-11α,9α-epoxymethanoprostaglandin F2α (U46619)- or endothelin-1-induced contractions. An NOS inhibitor, N G-nitro-l-arginine methyl ester (l-NAME), or an inhibitor of soluble guanylate cyclase, 1H-[1,2,4]-oxadizolo[4,3-a]quinoxalin-1-one (ODQ), prevented telmisartan-induced inhibition of U46619 contractions. A PPARγ antagonist, GW9662, abolished telmisartan-induced inhibition. Likewise, the PPARγ antagonist rosiglitazone attenuated U46619-induced contractions. The effects of telmisartan and rosiglitazone were prevented by actinomycin-D, a transcription inhibitor. In contrast, losartan, olmesartan, and irbesartan did not inhibit contractions. The inhibition was absent in mesenteric arteries from eNOS knockout or PPARγ knockout mice. Telmisartan augmented eNOS expression, phosphorylation, and NO production, which were reversed by the co-treatment with GW9662. Conclusions The present results suggest that telmisartan-induced inhibition of vasoconstriction in resistance arteries is mediated through a PPARγ-dependent increase in eNOS expression and activity that is unrelated to AT1R blockade.