571 research outputs found
Structural basis for cell surface patterning through NetrinG-NGL interactions
Brain wiring depends on cells making highly localized and selective connections through surface protein-protein interactions, including those between NetrinGs and NetrinG ligands (NGLs). The NetrinGs are members of the structurally uncharacterized netrin family. We present a comprehensive crystallographic analysis comprising NetrinG1-NGL1 and NetrinG2-NGL2 complexes, unliganded NetrinG2 and NGL3. Cognate NetrinG-NGL interactions depend on three specificity-conferring NetrinG loops, clasped tightly by matching NGL surfaces. We engineered these NGL surfaces to implant custom-made affinities for NetrinG1 and NetrinG2. In a cellular patterning assay, we demonstrate that NetrinG-binding selectivity can direct the sorting of a mixed population of NGLs into discrete cell surface subdomains. These results provide a molecular model for selectivity-based patterning in a neuronal recognition system, dysregulation of which is associated with severe neuropsychological disorders
Perspectives for a mixed two-qubit system with binomial quantum states
The problem of the relationship between entanglement and two-qubit systems in
which it is embedded is central to the quantum information theory. This paper
suggests that the concurrence hierarchy as an entanglement measure provides an
alternative view of how to think about this problem. We consider mixed states
of two qubits and obtain an exact solution of the time-dependent master
equation that describes the evolution of two two-level qubits (or atoms) within
a perfect cavity for the case of multiphoton transition. We consider the
situation for which the field may start from a binomial state. Employing this
solution, the significant features of the entanglement when a second qubit is
weakly coupled to the field and becomes entangled with the first qubit, is
investigated. We also describe the response of the atomic system as it varies
between the Rabi oscillations and the collapse-revival mode and investigate the
atomic inversion and the Q-function. We identify and numerically demonstrate
the region of parameters where significantly large entanglement can be
obtained. Most interestingly, it is shown that features of the entanglement is
influenced significantly when the multi-photon process is involved. Finally, we
obtain illustrative examples of some novel aspects of this system and show how
the off-resonant case can sensitize entanglement to the role of initial state
setting.Comment: 18 pages, 9 figure
Low-dose TNF augments fracture healing in normal and osteoporotic bone by up-regulating the innate immune response
The mechanism by which trauma initiates healing remains unclear. Precise understanding of these events may define interventions for accelerating healing that could be translated to the clinical arena. We previously reported that addition of low-dose recombinant human TNF (rhTNF) at the fracture site augmented fracture repair in a murine tibial fracture model. Here, we show that local rhTNF treatment is only effective when administered within 24h of injury, when neutrophils are the major inflammatory cell infiltrate. Systemic administration of anti-TNF impaired fracture healing. Addition of rhTNF enhanced neutrophil recruitment and promoted recruitment of monocytes through CCL2 production. Conversely, depletion of neutrophils or inhibition of the chemokine receptor CCR2 resulted in significantly impaired fracture healing. Fragility, or osteoporotic, fractures represent a major medical problem as they are associated with permanent disability and premature death. Using a murine model of fragility fractures, we found that local rhTNF treatment improved fracture healing during the early phase of repair. If translated clinically, this promotion of fracture healing would reduce the morbidity and mortality associated with delayed patient mobilization
Constraining clay hydration state and its role in active fault systems
To understand the role of hydrated clay minerals in active fault systems, a humidity chamber connected to an X‐ray diffractometer was used to determine the adsorption of water onto and/or into the crystal structure of smectite. This new type of analysis was carried out under specific temperature and humidity conditions, using powdered clay size fractions (< 2 µm) of rock samples from the San Andreas Fault (USA) and the Nankai Trough (Japan). Pressure cannot be controlled, but does not significantly affect clay swelling at shallow conditions. Air‐dried samples show a discrete smectite phase that swells after traditional ethylene glycolation to an interlayer distance of 1.5 and 1.7 nm. Using the humidity chamber, however, the samples show a shorter interlayer distance, between 1.09 and 1.54 nm. Based on our analysis, we show that (i) ethylene glycol overestimates the size of the interlayer space, and therefore water content, so is a crude maximum only; (ii) interlayer swelling occurs in smectite clay minerals at all temperatures between 25 and 95°C; and (iii) particle orientation increases with increasing humidity, indicating a higher mobility of smectite from interlayer hydration. Detailed characterization of the hydration state of smectite under original conditions is critical for understanding of clay‐fluid interaction, the mechanical behavior during fault displacements, and fluid budgets at depth. We propose that humidity chamber experiments should be the new standard procedure to constrain swelling characteristics of natural and synthetic clay minerals. Key Points Investigating smectite swelling behavior Humidity chamber connected to an X‐ray diffractometer Implications for weak fault behaviorPeer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/98123/1/ggge20077.pd
Neogenin expression may be inversely correlated to the tumorigenicity of human breast cancer
BACKGROUND: Neogenin is expressed in cap cells that have been suggested to be mammary stem or precursor cells. Neogenin is known to play an important role in mammary morphogenesis; however its relationship to tumorigenesis remains to be elucidated. METHODS: To compare the expression levels of neogenin in cells with different tumorigenicity, the expression levels in M13SV1, M13SV1R2 and M13SV1R2N1 cells, which are immortalized derivatives of type I human breast epithelial cells, were evaluated. Then we measured the expression level of neogenin in paired normal and cancer tissues from eight breast cancer patients. Tissue array analysis was performed for 54 human breast tissue samples with different histology, and the results were divided into four categories (none, weak, moderate, strong) by a single well-trained blinded pathologist and statistically analyzed. RESULTS: The nontumorigenic M13SV1 cells and normal tissues showed stronger expression of neogenin than the M13SV1R2N1 cells and the paired cancer tissues. In the tissue array, all (8/8) of the normal breast tissues showed strong neogenin expression, while 93.5% (43/46) of breast cancer tissues had either no expression or only moderate levels of neogenin expression. There was a significant difference, in the expression level of neogenin, in comparisons between normal and infiltrating ductal carcinoma (p < 0.001). CONCLUSION: Neogenin may play a role in mammary carcinogenesis as well as morphogenesis, and the expression may be inversely correlated with mammary carcinogenicity. The value of neogenin as a potential prognostic factor needs further evaluation
Randomized controlled trial using bosentan to enhance the impact of exercise training in subjects with type 2 diabetes mellitus
In type 2 diabetes patients, endothelin (ET) receptor blockade may enhance blood flow responses to exercise training. The combination of exercise training and ET receptor blockade may represent a more potent stimulus than training alone to improve vascular function, physical fitness and glucose homeostasis. We assessed the effect of an 8 week exercise training programme combined with either ET blockade or placebo on vasculature, fitness and glucose homeostasis in people with type 2 diabetes. In a double-blind randomized controlled trial, brachial endothelium-dependent and -independent dilatation (using flow-mediated dilatation and glyceryl trinitrate, respectively), glucose homeostasis (using Homeostasis Model Assessment for Insulin Resistance (HOMA-IR)) and physical fitness (maximal cycling test) were assessed in 18 men with type 2 diabetes (60 ± 6 years old). Subjects underwent an 8 week exercise training programme, with half of the subjects receiving ET receptor blockade (bosentan) and the other half a placebo, followed by reassessment of the tests above. Exercise training improved physical fitness to a similar extent in both groups, but we did not detect changes in vascular function in either group. This study suggests that there is no adaptation in brachial and femoral artery endothelial function after 8 weeks of training in type 2 diabetes patients. Endothelin receptor blockade combined with exercise training does not additionally alter conduit artery endothelial function or physical fitness in type 2 diabetes
Axon growth and guidance genes identify nascent, immature, and mature olfactory sensory neurons
Neurogenesis of projection neurons requires that axons be initiated, extended, and connected. Differences in the expression of axon growth and guidance genes must drive these events, but comprehensively characterizing these differences in a single neuronal type has not been accomplished. Guided by a catalog of gene expression in olfactory sensory neurons (OSNs), in situ hybridization and immunohistochemistry revealed that Cxcr4 and Dbn1 , two axon initiation genes, marked the developmental transition from basal progenitor cells to immature OSNs in the olfactory epithelium. The CXCR4 immunoreactivity of these nascent OSNs overlapped partially with markers of proliferation of basal progenitor cells and partially with immunoreactivity for GAP43, the canonical marker of immature OSNs. Intracellular guidance cue signaling transcripts Ablim1, Crmp1, Dypsl2, Dpysl3, Dpysl5, Gap43, Marcskl1, and Stmn1–4 were specific to, or much more abundant in, the immature OSN layer. Receptors that mediate axonal inhibition or repulsion tended to be expressed in both immature and mature OSNs ( Plxna1, Plxna4, Nrp2, Efna5 ) or specifically in mature OSNs ( Plxna3, Unc5b, Efna3, Epha5, Epha7 ), although some were specific to immature OSNs ( Plxnb1, Plxnb2, Plxdc2, Nrp1 ). Cell adhesion molecules were expressed either by both immature and mature OSNs ( Dscam, Ncam1, Ncam2, Nrxn1 ) or solely by immature OSNs ( Chl1, Nfasc1, Dscaml1 ). Given the loss of intracellular signaling protein expression, the continued expression of guidance cue receptors in mature OSNs is consistent with a change in the role of these receptors, perhaps to sending signals back to the cell body and nucleus. © 2010 Wiley‐Liss, Inc.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/106698/1/22497_ftp.pd
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