448 research outputs found
Towards fully integrated CMOS RF receivers
The evolution of the mobile telephony is demanding new multi-function terminals (cellular and cordless phones, GPS, pagers) compatible with a variety of standard (GSM, DCS, DECT, CDMA). At the same time the reduction of cost, size and power dissipation is mandatory. All this requires an higher integration level for the RF part, that is presently using a big number of components. This explains the big research effort put in silicon RF circuits particularly in CMOS technology. In this paper the state of the art of CMOS RF circuits is outlined. In particular some results regarding critical building blocks obtained by the STMicroelectronics and Pavia University research team are given. Future evelopments and the progress needed to successfully implement them are also pointed out
Electromagnetic Transition in Waveguide with Application to Lasers
The electromagnetic transition of two-level atomic systems in a waveguide is
calculated. Compared with the result in free space, the spontaneous emission
rate decrease because the phase space is smaller, and meanwhile, some resonance
appears in some cases. Moreover, the influence of non-uniform electromagnetic
field in a waveguide on absorption and stimulated emission is considered.
Applying the results to lasers, a method to enhance the laser power is
proposed.Comment: 4 pages, 2 figure
Lovastatin-induced cholesterol depletion affects both apical sorting and endocytosis of aquaporin-2 in renal cells.
A novel human aquaporin-4 splice variant exhibits a dominant-negative activity: a new mechanism to regulate water permeability.
Two major isoforms of aquaporin-4 (AQP4) have been described in human tissue. Here we report the identification and functional analysis of an alternatively spliced transcript of human AQP4, AQP4-Δ4, that lacks exon 4. In transfected cells AQP4-Δ4 is mainly retained in the endoplasmic reticulum and shows no water transport properties. When AQP4-Δ4 is transfected into cells stably expressing functional AQP4, the surface expression of the full-length protein is reduced. Furthermore, the water transport activity of the cotransfectants is diminished in comparison to transfectants expressing only AQP4. The observed down-regulation of both the expression and water channel activity of AQP4 is likely to originate from a dominant-negative effect caused by heterodimerization between AQP4 and AQP4-Δ4, which was detected in coimmunoprecipitation studies. In skeletal muscles, AQP4-Δ4 mRNA expression inversely correlates with the level of AQP4 protein and is physiologically associated with different types of skeletal muscles. The expression of AQP4-Δ4 may represent a new regulatory mechanism through which the cell-surface expression and therefore the activity of AQP4 can be physiologically modulated
A novel formulation of glucose‐sparing peritoneal dialysis solutions with l‐carnitine improves biocompatibility on human mesothelial cells
The main reason why peritoneal dialysis (PD) still has limited use in the management of patients with end‐stage renal disease (ESRD) lies in the fact that the currently used glucose‐based PD solutions are not completely biocompatible and determine, over time, the degeneration of the peritoneal membrane (PM) and consequent loss of ultrafiltration (UF). Here we evaluated the biocompatibility of a novel formulation of dialytic solutions, in which a substantial amount of glucose is replaced by two osmometabolic agents, xylitol and L‐carnitine. The effect of this novel formulation on cell viability, the integrity of the mesothelial barrier and secretion of pro‐inflammatory cytokines was evaluated on human mesothelial cells grown on cell culture inserts and exposed to the PD solution only at the apical side, mimicking the condition of a PD dwell. The results were compared to those obtained after exposure to a panel of dialytic solutions commonly used in clinical practice. We report here compelling evidence that this novel formulation shows better performance in terms of higher cell viability, better preservation of the integrity of the mesothelial layer and reduced release of pro‐inflammatory cytokines. This new formulation could represent a step forward towards obtaining PD solutions with high biocompatibility
NKCC2 activity is inhibited by the Bartter's syndrome type 5 gain-of-function CaR-A843E mutant in renal cells.
The gain-of-function A843E mutation of the calcium sensing receptor (CaR) causes Bartter syndrome type 5. Patients carrying this CaR variant show a remarkably reduced renal NaCl reabsorption in the thick ascending limb (TAL) of Henle's loop resulting in renal loss of NaCl in the absence of mutations in renal Na(+) and Cl(-) ion transporters. The molecular mechanisms underlying this clinical phenotype are incompletely understood. We investigated, in human embryonic kidney 293 (HEK 293) cells and porcine kidney epithelial (LLC-PK1) cells, the functional cross-talk of CaR-A843E with the Na(+):K(+):2Cl(-) co-transporter, NKCC2, which provides NaCl reabsorption in the TAL.
RESULTS:
The expression of the CaR mutant did not alter the apical localisation of NKCC2 in LLC-PK1 cells. However, the steady-state NKCC2 phosphorylation and activity were decreased in cells transfected with CaR-A843E compared with the control wild-type CaR (CaR WT)-transfected cells. Of note, low-Cl(-)-dependent NKCC2 activation was also strongly inhibited upon the expression of CaR-A843E mutant. The use of either P450 ω-hydroxylase (CYP4)- or phospholipase A2 (PLA2)-blockers suggests that this effect is likely mediated by arachidonic acid (AA) metabolites.
CONCLUSIONS:
The data suggested that the activated CaR affects intracellular pathways modulating NKCC2 activity rather than NKCC2 intracellular trafficking in renal cells, and throw further light on the pathological role played by active CaR mutants in Bartter syndrome type 5
Intercellular crosstalk mediated by tunneling nanotubes between central nervous system cells. What we need to advance
Long-range intercellular communication between Central Nervous System (CNS) cells is an essential process for preserving CNS homeostasis. Paracrine signaling, extracellular vesicles, neurotransmitters and synapses are well-known mechanisms involved. A new form of intercellular crosstalk mechanism based on Tunneling Nanotubes (TNTs), suggests a new way to understand how neural cells interact with each other in controlling CNS functions. TNTs are long intercellular bridges that allow the intercellular transfer of cargoes and signals from one cell to another contributing to the control of tissue functionality. CNS cells communicate with each other via TNTs, through which ions, organelles and other signals are exchanged. Unfortunately, almost all these results were obtained through 2D in-vitro models, and fundamental mechanisms underlying TNTs-formation still remain elusive. Consequently, many questions remain open, and TNTs role in CNS remains largely unknown. In this review, we briefly discuss the state of the art regarding TNTs identification and function. We highlight the gaps in the knowledge of TNTs and discuss what is needed to accelerate TNTs-research in CNS-physiology. To this end, it is necessary to: 1) Develop an ad-hoc TNTs-imaging and software-assisted processing tool to improve TNTs-identification and quantification, 2) Identify specific molecular pathways involved into TNTs-formation, 3) Use in-vitro 3D-CNS and animal models to investigate TNTs-role in a more physiological context pushing the limit of live-microscopy techniques. Although there are still many steps to be taken, we believe that the study of TNTs is a new and fascinating frontier that could significantly contribute to deciphering CNS physiology
An insight into polarization states of solid-state organic lasers
The polarization states of lasers are crucial issues both for practical
applications and fundamental research. In general, they depend in a combined
manner on the properties of the gain material and on the structure of the
electromagnetic modes. In this paper, we address this issue in the case of
solid-state organic lasers, a technology which enables to vary independently
gain and mode properties. Different kinds of resonators are investigated:
in-plane micro-resonators with Fabry-Perot, square, pentagon, stadium, disk,
and kite shapes, and external vertical resonators. The degree of polarization P
is measured in each case. It is shown that although TE modes prevail generally
(P>0), kite-shaped micro-laser generates negative values for P, i.e. a flip of
the dominant polarization which becomes mostly TM polarized. We at last
investigated two degrees of freedom that are available to tailor the
polarization of organic lasers, in addition to the pump polarization and the
resonator geometry: upon using resonant energy transfer (RET) or upon pumping
the laser dye to an higher excited state. We then demonstrate that
significantly lower P factors can be obtained.Comment: 12 pages, 12 figure
Characterization of Two Novel Missense Mutations in the AQP2 Gene Causing Nephrogenic Diabetes Insipidus
Here, we report the aquaporin 2 (AQP2) mutational analysis of a patient with nephrogenic diabetes insipidus heterozygote due to two novel missense mutations. Direct sequencing of DNA in the male patient revealed that he was compound heterozygote for two mutations in the AQP2 gene: a thymine-to-adenine transversion at position 450 (c.450T>A) in exon 2 and a guanine-to-thymine at nucleotide position 643 (c.643G>T) in exon 4. The double heterozygous 450T>A and 643G>T transversion causes the amino acid substitution D150E and G215C. Direct sequencing of exons 2 and 4 of the AQP2 gene from each of the parents revealed that the c.450T>A mutation was inherited from the father while the c.643G>T mutation was inherited from the mother. Analysis of AQP2 excretion demonstrated that no AQP2 was detectable in the urine of the proband, whereas normal AQP2 levels were measured in both parents. When expressed in renal cells, both proteins were retarded in the endoplasmic reticulum and no redistribution was observed after forskolin stimulation. Of note, homology modeling revealed that the two mutations involve two highly conserved residues providing important clues about the role of the wt residues in AQP2 stability and function
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