Multi-user adaptive orthogonal frequency-division multiplexing system for indoor wireless optical communications

An adaptive orthogonal frequency-division multiplexing (OFDM) system is proposed for multi-user communications over indoor wireless optical channels. The designed system uses multi-user least-squares detection techniques applied to space-division multiple access and OFDM schemes, in conjunction with angle-diversity reception. The system, which does not present an excessive increase in complexity with respect to the previous schemes, can support high bit rates for multiple users, beyond 100 Mbits/s. It also mitigates the channel fluctuations induced when either the space distribution or the number of emitters and receivers varies. The performance of the new proposed scheme is compared with that of a non-adaptive multi-user system and an adaptive single-user system, both described in the previous works, when they face similar environmental situations. The obtained results show a significant enhancement with respect to both the previous multi-user system and the adaptive single-user one, since the new scheme allows adaptively managing the system throughput on a multi-user environment     

Design of an analytic constrained predictive controller using neural networks

This paper shows how the solution of the standard predictive control problem can be recast as a continuous function of the state, the reference signal, the noise and the disturbances, and hence can be approximated arbitrarily closely by a feed-forward neural network. The existence of such a continuous mapping eliminates the need for linear independency of the active constraints, and therefore the resulting analytic constrained predictive controller will combine constraint handling with speed while being applicable to fast and complex control systems with many constraints. The effectiveness of the proposed controller design methodology is shown for a simulation example of an elevator model and for a real-time laboratory inverted pendulum system.     

Microstructural and electrical properties of PbTIO3 screen-printed thick films

In this article we will study the structural and electrical properties of PbTiO₃ (PTO) screen-printed thick films. These properties can change with synthetic routes employed for synthesis of PTO. The ceramic powder has been synthesized by mechanical alloying and solid state route. This material crystallizes in the tetragonal system, with space group P4mm and unit cell dimensions a = b = 3.904, c = 4.152 Å, and Z = 1. From our results, it was observed that PTO obtained by mechanical alloying provides smaller crystallite size. The Rietveld refinement showed that the samples synthesized by mechanical alloying and solid state route crystallize in the tetragonal system but with different cell parameters. The Raman shifts of these films agree with modes from literature. However, some displacements happen, because the morphology and structural characteristics of the thick films are different, compared to single crystal and thin film. The photomicrographs of the PTO thick films showed that the choice of synthetic routes obtained samples with different microstructures.     

Evaluation of proteinase-activated receptor-1 (PAR1) agonists and antagonists using a cultured cell receptor desensitization assay: activation of PAR2 by PAR1-targeted ligands

We developed a calcium signaling-based assay, using cultured human embryonic kidney cells (HEK), that evaluates simultaneously, the activation/desensitization or blockade of the proteinase-activated receptors, PAR1 and PAR2. Using this assay, we analyzed the actions of a number of previously described putative PAR1-targeted peptide agonists and antagonists. We found that most of the previously described PAR1-targeted agents can also activate/desensitize PAR2, and most of these peptides can also activate a calcium signaling pathway in a target cell that possesses PAR2 along with PAR1. Furthermore, we used this assay to develop a PAR1 receptor-activating probe [Ala-parafluoroPhe-Arg-Cha-Cit-Tyr-NH2 (Cit-NH2)], which displays a high degree of specificity for PAR1 over PAR2, and we used the assay to quantitate the ability of trypsin to disarm the activation of PAR1 by thrombin. The abilities of the PAR1-targeted agents to desensitize or block PAR1 in the HEK cell assay were compared with their activities in a human platelet aggregation assay. Our data illustrate the usefulness of the HEK cell assay for evaluating the PAR1/PAR2 selectivity of PAR-activating agonists. The PAR1-selective agonist that we developed using the assay should prove useful for studying the effects of selectively activating PAR1 in vivo.     

Lymphotoxin alpha/beta and tumor necrosis factor are required for stromal cell expression of homing chemokines in B and T cell areas of the spleen

Mice deficient in the cytokines tumor necrosis factor (TNF) or lymphotoxin (LT) alpha/beta lack polarized B cell follicles in the spleen. Deficiency in CXC chemokine receptor 5 (CXCR5), a receptor for B lymphocyte chemoattractant (BLC), also causes loss of splenic follicles. Here we report that BLC expression by follicular stromal cells is defective in TNF-, TNF receptor 1 (TNFR1)-, LTalpha- and LTbeta-deficient mice. Treatment of adult mice with antagonists of LTalpha1beta2 also leads to decreased BLC expression. These findings indicate that LTalpha1beta2 and TNF have a role upstream of BLC/CXCR5 in the process of follicle formation. In addition to disrupted follicles, LT-deficient animals have disorganized T zones. Expression of the T cell attractant, secondary lymphoid tissue chemokine (SLC), by T zone stromal cells is found to be markedly depressed in LTalpha-, and LTbeta-deficient mice. Expression of the SLC-related chemokine, Epstein Barr virus-induced molecule 1 ligand chemokine (ELC), is also reduced. Exploring the basis for the reduced SLC expression led to identification of further disruptions in T zone stromal cells. Together these findings indicate that LTalpha1beta2 and TNF are required for the development and function of B and T zone stromal cells that make chemokines necessary for lymphocyte compartmentalization in the spleen.