46 results match your criteria: "1 University Station C0800[Affiliation]"

Weakly Internalized Receptors Use Coated Vesicle Heterogeneity to Evade Competition during Endocytosis.

Biochemistry

July 2021

Department of Biomedical Engineering, The University of Texas at Austin, 1 University Station C0800, Austin, Texas 78712, United States.

The uptake of receptors by clathrin-mediated endocytosis underlies signaling, nutrient import, and recycling of transmembrane proteins and lipids. In the complex, crowded environment of the plasma membrane, receptors are internalized when they bind to components of the clathrin coat, such as the major adaptor protein, AP2. Receptors with higher affinity for AP2 are known to be more strongly internalized compared to receptors with lower affinity.

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Background: Polyploidy provides new genetic material that facilitates evolutionary novelty, species adaptation, and crop domestication. Polyploidy often leads to an increase in cell or organism size, which may affect transcript abundance or transcriptome size, but the relationship between polyploidy and transcriptome changes remains poorly understood. Plant cells often undergo endoreduplication, confounding the polyploid effect.

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The bases for bedtime hypertension chronotherapy (BHCT) as superior chronoprevention against cardiovascular disease (CVD) are: (1) correlation between blood pressure (BP) and various risks is greater for ambulatory BP monitoring (ABPM) than office BP measurements (OBPM); (2) asleep BP mean is a better predictor of CVD risk than ABPM awake and 24-hour means and OBPM; and (3) targeting of asleep BP by BHCT with one or more conventional medications versus usual on-awakening therapy better reduces major and total CVD events. BHCT offers the most cost-effective chronoprevention against adverse CVD outcomes in regular and vulnerable renal, diabetic, and resistant hypertensive patients.

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A miniature laser ablation probe relying on an optical fiber to deliver light requires a high coupling efficiency objective with sufficient magnification in order to provide adequate power and field for surgery. A diffraction-limited optical design is presented that utilizes high refractive index zinc sulfide to meet specifications while reducing the miniature objective down to two lenses. The design has a hypercentric conjugate plane on the fiber side and is telecentric on the tissue end.

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Differences in forward angular light scattering distributions between M1 and M2 macrophages.

J Biomed Opt

November 2015

University of Texas Health Science Center at San Antonio, Division of Cardiology, Department of Medicine, 7703 Floyd Curl Drive, San Antonio, Texas 78229, United StatesbSouth Texas Veterans Health Care System, Department of Veterans Affairs, 7400 Merton M.

The ability to distinguish macrophage subtypes noninvasively could have diagnostic potential in cancer, atherosclerosis, and diabetes, where polarized M1 and M2 macrophages play critical and often opposing roles. Current methods to distinguish macrophage subtypes rely on tissue biopsy. Optical imaging techniques based on light scattering are of interest as they can be translated into biopsy-free strategies.

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New optical imaging techniques that provide contrast to study both the anatomy and composition of atherosclerotic plaques can be utilized to better understand the formation, progression and clinical complications of human coronary artery disease. We present a dual-modality fiber-based optical imaging system for simultaneous microstructural and molecular analysis of atherosclerotic plaques that combines optical coherence tomography (OCT) and two-photon luminescence (TPL) imaging. Experimental results from ex vivo human coronary arteries show that OCT and TPL optical contrast in recorded OCT-TPL images is complimentary and in agreement with histological analysis.

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Background And Objectives: Atherosclerosis and plaque rupture leads to myocardial infarction and stroke. A novel hybrid optical coherence tomography (OCT) and two-photon luminescence (TPL) fiber-based imaging system was developed to characterize tissue constituents in the context of plaque morphology.

Study Design/materials And Methods: Ex vivo coronary arteries (34 regions of interest) from three human hearts with atherosclerotic plaques were examined by OCT-TPL imaging.

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Intravascular optical coherence tomography light scattering artifacts: merry-go-rounding, blooming, and ghost struts.

J Biomed Opt

December 2014

The University of Texas Health Science Center at San Antonio, Division of Cardiology, Department of Medicine, 7703 Floyd Curl Drive, San Antonio, Texas 78229, United StatesbSouth Texas Veterans Health Care System, The Department of Veterans Affairs, San A.

We sought to elucidate the mechanisms underlying two common intravascular optical coherence tomography (IV-OCT) artifacts that occur when imaging metallic stents: “merry-go-rounding” (MGR), which is an increase in strut arc length (SAL), and “blooming,” which is an increase in the strut reflection thickness (blooming thickness). Due to uncontrollable variables that occur in vivo, we performed an in vitro assessment of MGR and blooming in stented vessel phantoms. Using Xience V and Driver stents, we examined the effects of catheter offset, intimal strut coverage, and residual blood on SAL and blooming thickness in IV-OCT images.

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Bedtime hypertension chronotherapy: concepts and patient outcomes.

Curr Pharm Des

September 2015

Department of Biomedical Engineering, Cockrell School of Engineering, The University of Texas at Austin, 1 University Station C0800, Austin, Texas 78712-0238.

Recent findings indicate cardiovascular disease (CVD) risk is best predicted by asleep systolic blood pressure (SBP), and lowering it by scheduling ≥1 conventional long-acting hypertension medications, alone or in combination, at bedtime significantly lessens vascular-associated risks. Some 20 years ago, four controlled-onset extended-release drug-delivery systems incorporating a calcium channel or β-blocker, with the treatment goal specifically being attenuation of morning rather than asleep BP, were conceived as one type of bedtime hypertension chronotherapy. However, the CONVINCE outcomes trial failed to substantiate the merit of targeting morning and daytime BP to decrease CVD risk.

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Diurnal and twenty-four hour patterning of human diseases: cardiac, vascular, and respiratory diseases, conditions, and syndromes.

Sleep Med Rev

June 2015

Department of Laboratory Medicine & Pathology, University of Minnesota, HealthPartners Institute for Education and Research and the Department of Pathology, Regions Hospital, St. Paul, MN, USA.

Various medical conditions, disorders, and syndromes exhibit predictable-in-time diurnal and 24 h patterning in the signs, symptoms, and grave nonfatal and fatal events, e.g., respiratory ones of viral and allergic rhinorrhea, reversible (asthma) and non-reversible (bronchitis and emphysema) chronic obstructive pulmonary disease, cystic fibrosis, high altitude pulmonary edema, and decompression sickness; cardiac ones of atrial premature beats and tachycardia, paroxysmal atrial fibrillation, 3rd degree atrial-ventricular block, paroxysmal supraventricular tachycardia, ventricular premature beats, ventricular tachyarrhythmia, symptomatic and non-symptomatic angina pectoris, Prinzmetal vasospastic variant angina, acute (non-fatal and fatal) incidents of myocardial infarction, sudden cardiac arrest, in-bed sudden death syndrome of type-1 diabetes, acute cardiogenic pulmonary edema, and heart failure; vascular and circulatory system ones of hypertension, acute orthostatic postprandial, micturition, and defecation hypotension/syncope, intermittent claudication, venous insufficiency, standing occupation leg edema, arterial and venous branch occlusion of the eye, menopausal hot flash, sickle cell syndrome, abdominal, aortic, and thoracic dissections, pulmonary thromboembolism, and deep venous thrombosis, and cerebrovascular transient ischemic attack and hemorrhagic and ischemic stroke.

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We propose a method to utilize colloidal quantum dots (QDs) as a swept light source for hyperspectral microscopy. The use of QD allows for uniform multicolor emission which covers visible-NIR wavelengths. We used 8 colors of CdSe/ZnS and CdTe/ZnS colloidal quantum dots with the peak emission wavelengths from 520 nm to 800 nm.

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Electric field stimulation through a substrate influences Schwann cell and extracellular matrix structure.

J Neural Eng

August 2013

Department of Biomedical Engineering, The University of Texas at Austin, 107 W. Dean Keeton, 1 University Station C0800, Austin, TX 78712, USA.

Objective: Electric field (EF) stimulation has been used to cue cell growth for tissue engineering applications. In this study, we explore the electrical parameters and extracellular mechanisms that elicit changes in cell behavior when stimulated through the substrate.

Approach: Rat Schwann cell morphology was compared when exposed to EF through the media or a conductive indium tin oxide substrate.

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Two-photon luminescence properties of gold nanorods.

Biomed Opt Express

April 2013

Department of Biomedical Engineering, University of Texas at Austin, 1 University Station C0800, Austin, Texas 78712, USA.

Gold nanorods can be internalized by macrophages (an important early cellular marker in atherosclerosis and cancer) and used as an imaging contrast agent for macrophage targeting. Objective of this study is to compare two-photon luminescence (TPL) properties of four aspect ratios of gold nanorods with surface plasmon resonance at 700, 756, 844 and 1060 nm respectively. TPL from single nanorods and Rhodamine 6G particles was measured using a laser-scanning TPL microscope.

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Ligand-mediated self-assembly of hybrid plasmonic and superparamagnetic nanostructures.

Langmuir

February 2013

The Department of Biomedical Engineering, The University of Texas at Austin, 1 University Station C0800, Austin, Texas 78712, USA.

Hybrid nanostructures with unique optical and magnetic properties have attracted considerable interest as effective mediators for medical imaging and therapy. An aqueous-based, self-assembly approach to synthesizing hybrid plasmonic-superparamagnetic nanostructures is presented. The building blocks of the hybrid nanostructure include plasmonic gold nanorods (AuNRs) and superparamagnetic iron oxide nanoparticles (SPIONs).

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Background And Objectives: The macrophage is an important early cellular marker related to risk of future rupture of atherosclerotic plaques. Two-channel two-photon luminescence (TPL) microscopy combined with optical coherence tomography (OCT) was used to detect, and further characterize the distribution of aorta-based macrophages using plasmonic gold nanorose as an imaging contrast agent.

Study Design/materials And Methods: Nanorose uptake by macrophages was identified by TPL microscopy in macrophage cell culture.

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Silver nanoplate contrast agents for in vivo molecular photoacoustic imaging.

ACS Nano

January 2012

Biomedical Engineering Department, The University of Texas at Austin, 1 University Station C0800, Austin, Texas 78712, USA.

Silver nanoplates are introduced as a new photoacoustic contrast agent that can be easily functionalized for molecular photoacoustic imaging in vivo. Methods are described for synthesis, functionalization, and stabilization of silver nanoplates using biocompatible ("green") reagents. Directional antibody conjugation to the nanoplate surface is presented along with proof of molecular sensitivity in vitro with pancreatic cancer cells.

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Environment-dependent generation of photoacoustic waves from plasmonic nanoparticles.

Small

January 2012

Department of Biomedical Engineering, University of Texas at Austin, 1 University Station C0800, Austin, TX 78712, USA.

Nanoparticle-augmented photoacoustics is an emerging technique for molecular imaging. This study investigates the fundamental process of the photoacoustic signal generation by plasmonic nanoparticles suspended in a weakly absorbing fluid. The photoacoustic signal of gold nanospheres with varying silica shell thicknesses is shown to be dominated by the heat transfer between the nanoparticles and the surrounding environment.

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Clinical benefits of integrating cardiac and vascular models.

Expert Opin Med Diagn

November 2011

University of Texas at Austin , Department of Biomedical Engineering , BME Building, Room 4.414, 107 W. Dean Keeton Street, 1 University Station C0800, Austin, TX 78712 , USA +1 512 232 2892 ; +1 512 471 0616 ;

Introduction: Recent advances in computational methods and medical imaging techniques have enabled non-invasive exploration of cardiovascular pathologies, from cardiac level to complex arterial networks. The potential of cardiac and vascular modeling in guiding and monitoring therapies could be further extended through the integration of the two systems.

Areas Covered: This review includes advances in methods for cardiac electromechanics and vascular flow simulations.

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Light scattering in the normally white sclera prevents diagnostic imaging or delivery of a focused laser beam to a target in the underlying choroid layer. In this study, we examine optical clearing of the sclera and changes in blood flow resulting from the application of glycerol to the sclera of rabbits. Recovery dynamics are monitored after the application of saline.

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Fibrillar films obtained from sodium soap fibers and polyelectrolyte multilayers.

J Biomed Mater Res A

August 2011

Department of Biomedical Engineering, The University of Texas at Austin, 1 University Station C0800, Austin, Texas 78712, USA.

An objective of tissue engineering is to create synthetic polymer scaffolds with a fibrillar microstructure similar to the extracellular matrix. Here, we present a novel method for creating polymer fibers using the layer-by-layer method and sacrificial templates composed of sodium soap fibers. Soap fibers were prepared from neutralized fatty acids using a sodium chloride crystal dissolution method.

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Probe pressure effects on human skin diffuse reflectance and fluorescence spectroscopy measurements.

J Biomed Opt

May 2011

The University of Texas at Austin, Department of Biomedical Engineering, 1 University Station C0800, Austin, Texas 78712, USA.

Diffuse reflectance and fluorescence spectroscopy are popular research techniques for noninvasive disease diagnostics. Most systems include an optical fiber probe that transmits and collects optical spectra in contact with the suspected lesion. The purpose of this study is to investigate probe pressure effects on human skin spectroscopic measurements.

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Prospects of molecular photoacoustic imaging at 1064 nm wavelength.

Opt Lett

August 2010

Biomedical Engineering Department, The University of Texas at Austin, 1 University Station C0800, Austin, Texas 78712, USA.

An analysis of the photoacoustic (PA) signal from murine tissue in vivo revealed several benefits of contrast-enhanced PA imaging at a wavelength of 1064nm. Of all the wavelengths tested in a range from 710 to 1064nm, the background PA signal from tissue in vivo was lowest and more homogeneous at 1064nm. For blood-laden tissue, the background PA signal was up to 70% less at 1064nm.

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Simultaneous imaging of oxygen tension and blood flow in animals using a digital micromirror device.

Opt Express

April 2010

Department of Biomedical Engineering, University of Texas at Austin, 1 University Station C0800, Austin, Texas 78712, USA.

In this study we present a novel imaging method that combines high resolution cerebral blood flow imaging with a highly flexible map of absolute pO(2). In vivo measurements of pO(2) in animals using phosphorescence quenching is a well established method, and is preferable over electrical probes which are inherently invasive and are limited to single point measurements. However, spatially resolved pO(2) measurements using phosphorescence lifetime quenching typically require expensive cameras to obtain images of pO(2) and often suffer from poor signal to noise.

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Elucidation of the mechanisms by which external chemical cues regulate polarized cellular behaviors requires tools that can rapidly recast chemical landscapes with subcellular resolution. Here, we describe an approach for creating steep microscopic gradients of cellular effectors at any desired position in culture that can be reoriented rapidly to evaluate dynamic responses. In this approach, micrometre pores are ablated in a membrane that supports cell adherence, allowing dosing reagent from an underlying reservoir to enter the cell-culture flow chamber as sharp streams that are directed at subcellular targets by using a system of paired sources and drains to specify flow direction.

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Silver nanosystems for photoacoustic imaging and image-guided therapy.

J Biomed Opt

September 2010

The University of Texas at Austin, Biomedical Engineering Department, 1 University Station C0800, Austin, Texas 78712, USA.

Due to their optical absorption properties, metallic nanoparticles are excellent photoacoustic imaging contrast agents. A silver nanosystem is presented here as a potential contrast agent for photoacoustic imaging and image-guided therapy. Currently, the nanosystem consists of a porous silver layer deposited on the surface of spherical silica cores ranging in diameter from 180 to 520 nm.

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