Localized articular cartilage defects

Current operative and non-operative treatments for articular cartilage (AC) defect repair still fail to meet clinical expectations. These treatment options and challenges will be reviewed from a clinical perspective. Various polymeric and naturally occurring materials serving as scaffolds have shown promising neocartilage formation, but few studies are able to draw good clinical correlations. While tissue and organ engineering have generated public demand and expectations that engineered tissues will soon be available, there are still several critical hurdles that need to be overcome. There is a general preference for (1) avoiding the harvesting of normal tissues, (2) a single minimally invasive operative procedure for material insertion, and (3) a durable material that reproduces normal hyaline cartilage and will provide a good lifetime warranty. To avoid harvesting normal tissues, alternative cell sourcing is considered. On the materials front, there is a demand for molecular diversity and synthetic flexibility. For minimally invasive surgery, injectable materials have been actively researched. While initial studies are promising, there still remain a few challenges to overcome before injectable scaffolds will become clinically relevant. Key considerations are reviewed in this article. Advances in nanotechnology have enabled us to employ bottom-up approaches to scaffold design, fabrication, and characterization to better mimic the biological dimensions of matter. One approach involves self-assembly of small DNA-like molecules into larger superaggregates with nanoscale dimensions. One such self-assembling organic system is the rosette nanotubes. The design and properties are highlighted as they are related to solving orthopedic problems.     

Localized and delocalized perfluorosemibullvalenes

On the basis of the experimental Gibbs free-energy barrier of the degenerate Cope arrangement in semibullvalene, B3P86 shows the best agreement, while B3LYP and MP2 underestimate and CCSD(T) overestimates the barrier. The substituent effect proposal by Hoffmann has been verified. In contrast to semibullvalenes with either localized energy-minimum structures or delocalized transition-state structures, perfluorosemibullvalene has both localized and delocalized energy-minimum structures that are very close in energy. Localized and delocalized perfluorosemibullvalenes Electronic supplementary material Supplementary material is available for this article at and is accessible for authorized users.     

Localized cutaneous nocardiosis in Japan

A turbidometric method was used to measure Candida albicans yeast cell growth and to quantitate the postantifungal effect (PAFE) after exposure to various concentrations of flucytosine and amphotericin B, alone and in combination, for 2 hr at 30°C. The drug concentrations used in the PAFE assays were determined by initial MIC and FIC (fractional inhibitory concentration) evaluations. The PAFE was calculated by the difference in time (hr) required for growth of the control and test cultures to reach the 0.5 absorbance level following removal of the drug by dilution. A synergistic PAFE was evidenced with combinations of the two drugs at concentrations below their individual MICs. Combinations of flucytosine (0.012 to 0.049 g ml^–1) and amphotericin B (0.195 to 0.39 g ml^–1) produced PAFEs ranging from 6.3 to 21.8 hr. These PAFEs persisted from 0.3 to 14.7 hr longer than those achieved when each of the two agents was assayed separately.     

Localized RNAs and their functions

The eukaryotic cell is partitioned by membranes into spatially and functionally discrete subcellular organelles. In addition, the cytoplasm itself is partitioned into discrete subregions that carry out specific functions. Such compartmentation can be achieved by localizing proteins and RNAs to different subcellular regions. This review will focus on localized RNAs, with a particular emphasis on RNA localization mechanisms and on the possible biological functions of localization of these RNAs. In recent years, an increasing number of localized RNAs have been identified in a variety of cell types among many animal species. Emphasis here will be on localized RNAs in the most intensively studied systems – Drosophila and Xenopus eggs and early embryos.     

Localized membrane-wall adhesions inPelvetia zygotes

Summary Membrane-wall adhesions in zygotes of the brown algaPelvetia were visualized following plasmolysis. Strands of cytoplasm remained firmly attached to the cell wall at discrete adhesion sites during plasmolysis. Adhesion sites were uniformly distributed in ungerminated zygotes, but were concentrated in the apical 5 m of the elongating rhizoid in germinated zygotes. Few adhesions were detected along the flanks of the rhizoid or in the thallus region of germinated zygotes. The structure, physiology and function of apical adhesions in the rhizoid were characterized. F-actin was found at adhesion sites in plasmolyzed zygotes labeled with rhodamine phalloidin, and disruption of cortical F-actin reduced the number of adhesions. Manipulation of cytosolic H⁺ and Ca²⁺ activities also disrupted adhesions. On the extracellular surface, the number of adhesions was reduced by inhibition of cellulose synthesis, protease cleavage of wall proteins, and changes in extracellular H⁺ and Ca²⁺ activities. Chronic treatment with the synthetic peptide RGDS, which prevents cell adhesion in fibroblasts, also reduced adhesion number. The number of adhesions per cell did not correlate with growth rate, but was inversely correlated with the ability to establish new rhizoid growth sites. The results indicate that membrane wall adhesions containing F-actin on the cytoplasmic face are localized in the growing rhizoid apex. The adhesions may be structurally related to focal adhesions in animal cells.Abbreviations ASB actin-stabilizing buffer - ASW artificial seawater - DCB 2,6-dichlorobenzonitrile - EGTA ethyleneglycol bis-(amino-ethyl ether) N,N,N,N-tetraacetic acid - Mes 2-(N-morpholino) ethanesulfonic acid - Pipes piperazone-N,N-bis-(2-ethanesulfonic acid) - Tris tris(hydroxymethyl)amino-methane     

Localized memories in idiotypic networks

The present paper investigates conditions under which immunological memory can be maintained by stimulatory idiotypic network interactions. The paper was motivated by the work of (De Boer & Hogeweg, 1989b, Bull. math. Biol. 51, 381-408.) which claimed that idiotypic memory is not possible because of percolation within the network. Here we reinvestigate the issue of percolation using both the previous model and a simpler one (Weisbuch, 1990, J. theor. Biol. 143, 507-522.) that allows analytic analysis. We focus on network topologies in which each Ab1 is connected to several Ab2s, which in turn are connected to several Ab3s. It is demonstrated that, for a considerable range of parameters, both models account for the existence of localized memory-states in which only the Ab1 and the Ab2 clones are activated and the clones of the Ab3 level remain virgin. The existence of localized memory-states seems to contradict the previous percolation result. This discrepancy will be shown to depend on the system dynamics. By simulation we explore the parameter regimes for which one finds percolation and those for which localized memory-states exists. We show that the conditions required for attaining the localized memory-state are considerably more stringent than those required for its existence and local stability. We conclude that both localized memory and percolation are possible in stimulatory idiotypic networks.