Identification of Host Trafficking Genes Required for HIV-1 Virological Synapse Formation in Dendritic Cells.

Dendritic cells (DCs) are one of the earliest targets of HIV-1 infection acting as a "Trojan horse," concealing the virus from the innate immune system and delivering it to T cells via virological synapses (VS). To explicate how the virus is trafficked through the cell to the VS and evades degradation, a high-throughput small interfering RNA screen targeting membrane trafficking proteins was performed in monocyte-derived DCs. We identified several proteins including BIN-1 and RAB7L1 that share common roles in transport from endosomal compartments.

Epithelial chemokine CXCL14 synergizes with CXCL12 allosteric modulation of CXCR4.

The chemokine receptor, CXC chemokine receptor 4 (CXCR4), is selective for CXC chemokine ligand 12 (CXCL12), is broadly expressed in blood and tissue cells, and is essential during embryogenesis and hematopoiesis. CXCL14 is a homeostatic chemokine with unknown receptor selectivity and preferential expression in peripheral tissues. Here, we demonstrate that CXCL14 synergized with CXCL12 in the induction of chemokine responses in primary human lymphoid cells and cell lines that express CXCR4.

Strain energy density used as the biomechanical signal for osteophyte growth in the cervical spine - biomed 2009.

Cervical spondylosis is a degenerative disease of the cervical spine that affects over 50% of the population older than 50 years. Spondylosis is a progressive disease where the intervertebral disc degenerates and bony growths called osteophytes form. Osteophyte growth has been identified by numerous investigators as an example of Wolff's law of bone remodeling acting on the abnormal strain energy density (SED) caused by the degenerating spine.

Wyckoff positions and the expression of polarization singularities in photonic crystals.

We reveal the fundamental relation between linear photonic crystal symmetries and the local polarization states of its Bloch modes, in particular the location and nature of polarization singularities as established by rigorous group theoretic analysis, encompassing the full system symmetry. This is illustrated with the fundamental transverse electric mode of a two-dimensional hexagonal photonic crystal, in the vanishing contrast limit and at the K point. For general Wyckoff positions within the fundamental domain, the transformation of a local polarization state is determined by the nature of the symmetry operations that map to members of its crystallographic orbit.

Validation of a finite element model of the young normal lower cervical spine.

A Finite Element Model (FEM) of the young adult human cervical spine has been developed as a first step in studying the process of spondylotic degeneration. The model was developed using normal geometry and material properties for the lower cervical spine. The model used a three-zone composite disc annulus to reflect the different material properties of the anterior, posterior, and lateral regions of the annulus.

Symmetry constraints and the existence of Bloch mode vortices in linear photonic crystals.

Modal phase singularities are identified in linear photonic crystals and the vortex state is explored in detail. Using group theory and phasor geometry, in the vanishing contrast limit, the modal symmetry requirements for the existence of phase singularities are determined. The vortex states are the partner functions of the symmetry groups, and hence one has a qualitative map of these modes in reciprocal space.

Experimental flexion/extension data corridors for validation of finite element models of the young, normal cervical spine.

Finite element (FE) modeling is an important tool for studying the cervical spine in normal, injured and diseased conditions. To understand the role of mechanical changes on the spine as it goes from a normal to a diseased or injured state, experimental studies are needed to establish the external response of young, normal cervical spinal segments compared to injured or degenerated cervical spinal segments under physiologic loading. It is important to differentiate injured or degenerated specimens from young, normal specimens to provide accurate experimental results necessary for the validation of FE models.

Finite element model of human cervical spinal column.

The purpose of this study was to develop a detailed anatomically accurate finite element model (FEM) of the whole cervical column (C2-T1) using sagittal and coronal computed tomography (CT) scan images and cryomicrotome anatomical sections. The bony vertebrae were defined using CT scan images. The geometrical details of intervertebral discs, uncovertebral joints and ligaments were obtained from cryomicrotome sections.

A combined cytogenetic and molecular approach to diagnosis in a case of desmoplastic small round cell tumor with a complex translocation (11;22;21).

Desmoplastic small round cell tumor (DSRCT) has recently been described as a discrete tumor entity. It is distinguished from other small round cell tumors by its prominent desmoplastic quality, its preponderance in adolescent males, its almost exclusive intraabdominal location, a multi-immunophenotypic profile, and its aggressive nature. Diagnosis on histology alone is not always unequivocal.

Detection of colorectal cancer cells in peripheral blood by reverse-transcriptase polymerase chain reaction for cytokeratin 20.

The staging of colorectal cancer currently depends on pathological examination of the surgical specimen and regional lymph nodes, accompanied by imaging tests such as computed tomography (CT) scanning. However, alternative molecular methods to detect circulating tumour cells in blood or bone marrow may provide additional information about the extent of disease and prognosis. We have previously reported the development of a reverse-transcriptase polymerase chain reaction (RT-PCR) for cytokeratin 20 (CK 20) mRNA to detect circulating epithelial tumour cells.

EWS-FLI1 fusion transcripts identified in patients with typical neuroblastoma.

The t(11.22)(q24.q12) results in expression of a chimeric RNA product, EWS-FLI1.

Modular data acquisition system updated using LabWindows/CVI Graphical User Interface.

The Biomechanics Laboratory of the Neuroscience Department of the Medical College of Wisconsin is currently engaged in research involving trauma biomechanics. For some experiments, 24 channels of analog data must be sampled at 10,000 Hertz. The Modular Data Acquisition System (MDAS) is able to acquire up to 60 channels of analog data at sampling intervals as low as 6 microseconds.

Intra-arterial pressure wave parameters modeled using electrical analogs.

An Electrical Model was developed to help identify parameters obtained from dynamic pressure data on the in vitro rat aortic artery. The data was obtained using a Multifunction Pressure Generator (MPG) and recording MPG Input Pressure (Pi) and Intraarterial Pressure (Po). Transfer functions of the form Po/Pi = (A1S+Ao)/(B2S2 + B1S+Bo) were obtained and it is necessary to link A1, Ao, B2, B1 and Bo to the Biological Parameters of Inertance (M), Vascular Resistance (R) and Compliance (C).

Arterial elastic modulus for fixed and varied wall volume.

It is commonly assumed that a blood vessel maintains a constant wall volume over a wide range of intraluminal pressures. We have found that vessel wall volume decreases under increasing load. To determine the effect of decreasing wall volume on values of Elastic modulus (Em), two computer models were used.

Dynamic intra-vascular pressure harmonic analysis.

The postulate that dynamic intra vascular pressure is a function of positional wall properties has been difficult to verify due to non-linear viscoelastic influences in arteries. It was tested, in rabbit carotid artery in vitro segments using dynamic and static input. A Multifunction Pressure Generator (MPG, Millar Inc.

The tubular maximum for calcium reabsorption: a normal range in children.

Objective: We aimed to establish a normal range for the tubular maximum rate of reabsorption of calcium corrected for glomerular filtration rate.

Design: A prospective survey was used.

Patients: One hundred and ten normal children aged 2-14 years were studied.

Progressive renal toxicity due to ifosfamide.

A prospective and follow up study of renal tubular and glomerular function in 11 children receiving ifosfamide treatment was conducted. Each child received between four and 14 courses of ifosfamide, given as a continuous infusion of 3 g/m2 over 24 hours for two or three days. Evidence of renal toxicity was seen in all patients.

Thalidomide treatment for chronic graft-versus-host disease.

The treatment of chronic graft-versus-host disease (GVHD) may present a difficult therapeutic problem. We used thalidomide to treat six patients with severe chronic GVHD who failed to respond to standard immunosuppressive agents. Four of the six patients showed a clear response to thalidomide, with the fifth patient showing a partial response.

Indices of intact serum parathyroid hormone and renal excretion of calcium, phosphate, and magnesium.

Up to date reference ranges were established for fasting renal excretion of calcium, phosphorus, and magnesium on 101 healthy children aged 2-15 years. A normal range for intact parathyroid hormone was also measured. The indices of calcium and magnesium excretion showed no correlation with age or sex so that a common range for all children could be established.

Pharmacokinetics of prednisolone in children with nephrosis.

The pharmacokinetics of prednisolone given intravenously were studied in 11 children with relapsed steroid responsive nephrotic syndrome, and four control subjects. The clearance of both total and unbound drug was decreased in these children and the unbound fraction of the drug in plasma was significantly correlated with the degree of hypoalbuminaemia. We conclude that changes in the clearance of prednisolone and altered protein binding might account for some of the variability in both therapeutic responses and the incidence of toxicity in patients treated with standard dosage regimens.

Pharmacokinetics of prednisolone in children with acute lymphoblastic leukaemia.

The pharmacokinetics of soluble oral prednisolone were studied during induction therapy in six children with acute lymphoblastic leukaemia. There was a three- to four-fold variation in the pharmacokinetics of total and free prednisolone. For total prednisolone, the mean elimination half-life was relatively short (1.

The separation of unbound prednisolone in plasma by centrifugal ultrafiltration.

To study variable plasma protein binding of prednisolone in children with nephrotic syndrome we have devised a simple rapid method for measuring unbound prednisolone. The plasma was initially ultrafiltered at 37 degrees C fixed angle head at 1500 g for 30 min then the filtrate was analysed by high pressure liquid chromatography. The effects of variable ultrafiltration conditions were studied.