Regions of the T cell receptor alpha and beta chains that are responsible for interactions with CD3.

The T cell antigen receptor consists of the Ti alpha/beta heterodimer which recognizes antigen, and the associated CD3 chains, thought to be involved in signal transduction. To understand the nature of the interaction between Ti and CD3, chimeric molecules which included the COOH-terminal segments of Ti alpha or beta linked to the extracellular segment of CD8, were transfected into a mutant T cell deficient in Ti beta chain expression and cell surface CD3. Both chimeric chains were required to express the chimeric Ti and to restore CD3 surface expression. CD8/Ti and CD3 cointernalized and coimmunoprecipitated. Stimulation of the chimeric receptor induced transmembrane signaling events and cell activation. These results demonstrate that the Ti alpha and beta COOH termini containing the transmembrane domains are sufficient for structural and functional coupling of Ti to CD3

Discrimination in Metropolitan Housing Markets Phase II: Asians and Pacific Islanders

This report documents the results of a an 11-city paired testing study by the Department of Housing and Urban Development of housing discrimination against Asian- Americans and Pacific Islanders. The study shows that one out of every five Asians and Pacific Islanders attempting to buy or rent a home are discriminated against, a rate similar to that of African Americans and Hispanics.

Documenting Antarctic Alteration of Eucrites

When meteorites were discovered in Antarctica, it was anticipated that terrestrial alteration would be at a minimum because of their deepfreeze storage where chemical reaction rates would be low. However, early compositional and petrologic studies established the presence of terrestrial alteration phases (e.g., [1, 2]). These were especially prevalent in chondrites because metal and troilite are most susceptible to terrestrial alteration [3]. Howardites, eucrites and diogenites (HEDs) are less prone to alteration because they have low abundances of metal and troilite. Nevertheless, investigations of HED meteorites document a wide array of mineralogical, compositional and isotopic effects of terrestrial alteration (e.g., [4-8]). Studies of the mineralogical effects of alteration [4] were done with old scanning electron microscope (SEM) technology which could only image small regions at a time. The micro-context of alteration phases was revealed, but larger-scale context was difficult to establish. Here we demonstrate the utility of wholethin-section X-ray mapping of eucrites by modern SEMs to document large-scale distributions of alteration materials which serve to evaluate sample freshness, highlight regions for detail study, and facilitate testing a hypothesis for alteration of eucrites [8

The Extraordinary Infrared Spectrum of NGC 1222 (Mkn 603)

The infrared spectra of starburst galaxies are dominated by the low-excitation lines of [NeII] and [SIII], and the stellar populations deduced from these spectra appear to lack stars larger than about 35 Msun. The only exceptions to this result until now were low metallicity dwarf galaxies. We report our analysis of the mid-infrared spectra obtained with IRS on Spitzer of the starburst galaxy NGC 1222 (Mkn 603). NGC 1222 is a large spheroidal galaxy with a starburst nucleus that is a compact radio and infrared source, and its infrared emission is dominated by the [NeIII] line. This is the first starburst of solar or near-solar metallicity, known to us, which is dominated by the high-excitation lines and which is a likely host of high mass stars. We model the emission with several different assumptions as to the spatial distibution of the high- and low-excitation lines and find that the upper mass cutoff in this galaxy is 40-100 Msun.Comment: accepted, Astronomical Journal. 29 pp, 4 figures. In replacement version an acknowledgment to NRAO is adde

Human infectivity trait in <i>Trypanosoma brucei</i>: stability, heritability and relationship to sra expression

Some Trypanosoma brucei lines infect humans whereas others do not because the parasites are lysed by human serum. We have developed a robust, quantitative in vitro assay based on differential uptake of fluorescent dyes by live and dead trypanosomes to quantify the extent and kinetics of killing by human serum. This method has been used to discriminate between 3 classes of human serum resistance; sensitive, resistant and intermediate. TREU 927/4, the parasite used for the T. brucei genome project, is intermediate. The phenotype is expressed in both bloodstream and metacyclic forms, is stably expressed during chromic infections and on cyclical transmission through tsetse flies. Trypanosomes of intermediate phenotype are distinguished from sensitive populations of cells by the slower rate of lysis and by the potential to become fully resistant to killing by human serum as a result of selection or long-term serial passaging in mice, and to pass on full resistance phenotype to its progeny in a genetic cross. The sra gene has been shown previously to determine human serum resistance in T. brucei but screening for the presence and expression of this gene indicated that it is not responsible for the human serum resistance phenotype in the trypanosome lines that we have examined, indicating that an alternative mechanism for HSR exists in these stocks. Examination of the inheritance of the phenotype in F1 hybrids for both bloodstream and metacyclic stages from 2 genetic crosses demonstrated that the phenotype is co-inherited in both life-cycle stages in a manner consistent with being a Mendelian trait, determined by only one or a few genes

Identification of the niche and phenotype of the first human hematopoietic stem cells

SummaryIn various vertebrate species, the dorsal aorta (Ao) is the site of specification of adult hematopoietic stem cells (HSCs). It has been observed that the upregulation of essential hematopoietic transcription factors and the formation of specific intra-aortic hematopoietic cell clusters occur predominantly in the ventral domain of the Ao (AoV). In the mouse, the first HSCs emerge in the AoV. Here, we demonstrate that in the human embryo the first definitive HSCs also emerge asymmetrically and are localized to the AoV, which thus identifies a functional niche for developing human HSCs. Using magnetic cell separation and xenotransplantations, we show that the first human HSCs are CD34+VE-cadherin+CD45+C-KIT+THY-1+Endoglin+RUNX1+CD38−/loCD45RA−. This population harbors practically all committed hematopoietic progenitors and is underrepresented in the dorsal domain of the Ao (AoD) and urogenital ridges (UGRs). The present study provides a foundation for analysis of molecular mechanisms underpinning embryonic specification of human HSCs

TRACKING PERFORMANCE OF A SWEPT-WING FIGHTER WITH A DIRECTORTYPE RADAR FIRE-CONTROL SYSTEM AND SCOPE PRESENTATION

Tracking performance of f-86d aircraft with radar fire-control syste

Non-equilibrium raft-like membrane domains under continuous recycling

We present a model for the kinetics of spontaneous membrane domain (raft) assembly that includes the effect of membrane recycling ubiquitous in living cells. We show that the domains have a broad power-law distribution with an average radius that scales with the 1/4 power of the domain lifetime when the line tension at the domain edges is large. For biologically reasonable recycling and diffusion rates the average domain radius is in the tens of nm range, consistent with observations. This represents one possible link between signaling (involving rafts) and traffic (recycling) in cells. Finally, we present evidence that suggests that the average raft size may be the same for all scale-free recycling schemes.Comment: 8 pages, 5 figure