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E.R. Hall

Publications and source records attributed to E.R. Hall.

3 recordsLinked to original sources

Quantifying Population Dynamics Based on Community Structure Fingerprints Extracted from Biosolids Samples.

This paper presents a standardized metric for quantifying the rate change in community structure of complex mixed microbial cultures such as those maintained in biological wastewater treatment systems. Quantifying the stability of microbial community structures is a first step toward more aggressive monitoring and control of biological systems for greater reliability in contaminant removal. Statistical analysis of compositions that uniquely specify the balance of populations of species in a mixed culture sample can be used to specify a biosolids community state as a unique position in an orthogonal coordinate system. Changes in biosolids state are observable as a trajectory within this coordinate space, and the rate of passage along this trajectory relates to the population dynamics. The geometric interpretation and the statistical analysis methods necessary for the proposed calculation methodology are introduced by way of simulated case studies with a simple model system. With the example of this model system, concepts of changing microbial community shape and size are contrasted. The rate change in community structure is defined geometrically in terms of a rate change in relative proportions of the characteristic community shape at constant biomass. A change in biomass is defined as the rate change in the quantity of biosolids at constant shape. The method robustness with respect to random measurement error was also demonstrated using the model system. The potential applications of the approach are presented with experimental data of microbial fatty acid compositions extracted from samples during the operation of bench-scale bioreactors degrading contaminants found in pulp mill wastewater. Scaling the level of population dynamics with a metric that is independent of chemotypic content presents a standard for direct comparisons of community responses between distinct cultures and experiments.

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Characterization of a Human Stromal Cell Line Supporting Hematopoietic Progenitor Cell Proliferation: Effect of HIV Expression.

Our objective was to determine the role that bone marrow-derived stromal cells have on human hematopoiesis in HIV infection. In particular, we dissected the heterogeneous bone marrow microenvironment to study the effect HIV expression might have on the cell population capable of producing the cytokines which will support human CD34+ cell differentiation. A stromal cell line, Lof(11-10), was established from human bone marrow by transfecting a plasmid containing the SV40 large T-antigen and isolating foci exhibiting a transformed phenotype. The Lof(11-10) cell line was characterized to determine its susceptibility to HIV infection, to identify its cytokine production profile, and to test the ability of conditioned media from this line to support CD34+ cell differentiation in the presence and absence of HIV expression. Nine cytokines were detected by RT-PCR and ELISA analysis. Conditioned media obtained from the Lof(11-10) cell line was able to support CD34+ celle differentiation. However, because the Lof(11-10) cells are not infectible by HIV, molecular clones of HIV were introduced into these cells by transfection. There was no qualitative difference in the levels of cytokine production between HIV-expressing and control Lof(11-10) cells. Furthermore, conditioned media derived from HIV-expressing and control Lof(11-10) cells added to bone marrow-derived CD34+ progenitor cells yielded similar colony formation in methylcellulose assays. Our data suggest that HIV infection of the cytokine-producing cells within the bone marrow microenvironment, as represented by the Lof(11-10) cell line, results in both normal cytokine production and hematopoiesis in spite of HIV expression. This report adds to the evidence against stromal cells being a significant target of HIV and establishes a system for comparison with more relevant models. Copyright 1995 S. Karger AG, Basel

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Providing a Microenvironment for the Development of Human CD34+ Hematopoietic Cells in SCID Mice.

In order to develop a convenient small-animal model that can support the differentiation of human bone-marrow-derived CD34+ cells, we transplanted SCID mice with an immortalized human stromal cell line, Lof(11-10). The Lof(11-10) cell line has been characterized to produce human cytokines capable of supporting primitive human hematopoietic cell proliferation in vitro. Intraperitoneal injection of Lof(11-10) cells into irradiated SCID mice by itself resulted in a dose-dependent survival of the mice from lethal irradiation. The radioprotective survival was reflected by an increase in the growth and number of mouse bone-marrow-derived committed hematopoietic progenitors. The Lof(11-10) cells localized to the spleen, but not to the bone marrow of these animals and resulted in detectable levels of circulating human IL-6 in their plasma. Secondary intravenous injections of either human or simian CD34+ cells into the Lof(11-10)-transplanted SCID mice resulted in engraftment of injected cells within the bone marrow of these mice. The utility of this small-animal model that allows the growth and differentiation of human CD34+ cells and its potential use in clinical gene therapy protocols are discussed. Copyright 1997 S. Karger AG, Basel

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