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Biomedical subjects

C Kerr

Publications and source records attributed to C Kerr.

At least 73 records · Page 4Linked to original sources

Immunohistochemical analysis of the cellular infiltrate in multiple sclerosis lesions.

Immunohistochemical staining of 16 brains post mortem from patients with progressive multiple sclerosis and of two biopsy specimens from patients with acute demyelinating disease was performed using a panel of monoclonal antibodies reactive with T cells and T-cell subsets, B cells, and Ia (HLA-DR) antigens. Lymphocytic perivascular cuffs were most prominent at the edge of active plaques and were occasionally seen in areas with no evidence of demyelination or macrophage infiltration. Perivascular cuffs consisted predominantly of T cells and Ia+ cells, with many T8+ cells and variable numbers of T4+ cells. T8/T4 ratios in cuffs varied between 1:1 and 50:1. In normal-appearing white matter, cuffs were sparse and were predominantly T8+. The distribution of T cells in the parenchyma resembled that seen in perivascular cuffs, namely, predominantly T8+ cells and variable numbers of T4+ cells. Many Ia+ cells were present in active lesions, and the majority of these cells appeared, by histological criteria, to be macrophages. Tissue macrophages were also stained lightly by the anti-T4 antibody. No brain had more T4+ than T8+ cells, determined using both T4 and Leu3a monoclonal antibodies. B1+ cells were rare. These results suggest that the cellular infiltrate in multiple sclerosis consists predominantly of T cells and macrophages and that there is an overrepresentation of T8+ cells compared with T4+ cells.

Antibodies, Monoclonal↗

Cellular proliferation in the vitreous: the use of vitreous explants as a model system.

An in vitro model of cellular proliferation in the vitreous has been developed using explants of bovine vitreous gel. Various cell types, including chick embryo pigmented retinal epithelium, choroidal fibroblasts, retinal glial cells, bovine retinal capillary endothelial cells, and peritoneal mouse macrophages, were cultured at 37 degrees C on vitreous gels for periods up to 8 days and compared for their effects on the structure of the gel. Choroidal fibroblasts caused a very marked reduction in the size of the gel and produced the strongest traction on the gel fibril structure; in contrast, peritoneal macrophages caused virtually no reduction in vitreous volume and little or no visible traction on the gel as detected by phase-contrast microscopy. The remaining cell types usually formed sheets on the surface of the gel; this was associated with an initial reduction in vitreous volume of approximately 50%, but little change thereafter. The cell mediated traction events on the structure of the vitreous gel were followed by time lapse video microscopy and by electron microscopy at various times after seeding of cells on the gels. The appearances corresponded closely with reported clinico-pathological studies of cellular proliferation in the vitreous. We believe that this in vitro model has several advantages over in vivo models of cellular proliferation in the vitreous, in that it permits analysis of individual cell behaviour and it is eminently suitable for pharmacologic manipulation.

Animals↗

"Carryback": effect of viscous liquid controls on the preceding sample analyzed with the SMA II continuous-flow analyzer.

We systematically studied the "carryback" effect of ethylene glycol-based controls on the preceding sample on an SMA II continuous-flow analyzer. Including Beckman Level 1 unassayed liquid control material as a sample lowered the 12 analyte values of the preceding sample by an average of 2.7%, Level 2 (the most viscous) by an average of 4.4%, and Level 3 by 3.2%. Water-reconstituted lyophilized control material caused no carryback effect, but lyophilized control reconstituted with 330 mL/L ethylene glycol decreased the preceding sample's results by 4.1% (average carryback). We believe that carryback is caused by the drag placed on the sample line by a viscous sample, which decreases the volume of the preceding sample that is delivered to the reagent or pre-dilution mixing coils. Our findings were confirmed on another SMA II. Limited study of a SMAC analyzer gave inconclusive results, but further evaluation of continuous-flow systems for carryback is warranted. Carryback substantially increases total analytical variability.

Autoanalysis↗

Modification of low density lipoprotein metabolism by growth factors in cultured vascular cells and human skin fibroblasts. Dependence upon duration of exposure.

The influences of specific growth factors upon binding, internalization and degradation of low density lipoproteins (LDL) were investigated in cultured vascular smooth muscle cells and skin fibroblasts. Platelet-derived growth factor (PDGF) and fibroblast growth factor (FGF) significantly stimulated the binding of LDL to high affinity receptors of smooth muscle cells and fibroblasts. The effects of enhanced binding were reflected in elevated rates in internalization and degradation of LDL. FGF and PDGF elicited a mitogenic response as measured by [3H]thymidine autoradiography, indicating that altered LDL metabolism was associated with entry into the cell cycle. When fibroblasts were exposed to mitogen for periods long enough to commit the cells to the growth cycle, after which growth factor was removed before addition of LDL however, enhanced LDL binding to cycling fibroblasts appeared to be dependent upon the length of the period of exposure to growth factors in the early part of the cell cycle. LDL binding was stimulated in the presence of PDGF or FGF but not after their removal within 8 h of entry into the cell cycle. Exposure to the growth factors for 16 h or longer resulted in stimulation of LDL metabolism whether or not mitogens were present at the cell surface. PDGF and FGF, therefore, appear to exert a direct influence upon LDL receptor expression in addition to that mediated via the cell cycle.

Animals↗

Incidence of homozygous beta-thalassaemia in New South Wales, 1961-1976.

A case-finding survey yielded 58 persons with transfusion-dependent homozygous beta-thalassaemia who lived either in New South Wales or in the Australian Capital Territory. Of those born between 1961 and 1976 in New South Wales, nearly 70% were of Greek or Greek-Cypriot origin and 18% of Italian origin. The New South Wales incidence rates for homozygous beta-thalassaemia were estimated as follows: one in 934 births, Greek origin; one in 264 births, Cypriot origin and one in 3441 births, Italian origin.

Adolescent↗

Antipodean 2,4,5-T.

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2,4,5-Trichlorophenoxyacetic Acid↗