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J Scott

Publications and source records attributed to J Scott.

At least 559 records · Page 31Linked to original sources

Isolation and nucleotide sequence of a cDNA encoding the precursor of mouse nerve growth factor.

Nerve growth factor (NGF) is a polypeptide that enhances survival, nerve fibre outgrowth and neurotransmitter biosynthesis in sympathetic and sensory neurones. Administration of antibodies against NGF to developing animals leads to atrophy of the sympathetic system. NGF is not normally detectable in innervated tissues but ablation of the innervating neurones leads to the production of measurable NGF in the target tissue. After transplantation of the denervated tissue, reinnervation occurs, then NGF decreases to undetectable levels. Thus NGF seems to act as a neurotrophic messenger and its level is regulated by innervating neurones. Because of the minute levels present it is very difficult to study NGF biosynthesis in innervated tissue. However, NGF can be isolated from male mouse submaxillary glands, where it exists in inexplicably high levels. Its amino acid sequence has been determined, and the synthesis of NGF and its larger precursors has been demonstrated in cultured submaxillary glands. We report here the nucleotide sequence of a submaxillary cDNA encoding the mouse NGF precursor (preproNGF). In contrast to previous suppositions the NGF moiety is situated near the carboxyterminus of the polyprotein precursor. It is flanked at the amino-terminus by 187 amino acids which may be cleaved at dibasic residues to generate three peptides; there are only two additional amino acids at the carboxy-terminus.

Amino Acid Sequence↗

Protection of epithelial function in human jejunum cultured with hydrocortisone.

Over 24-h culture with hydrocortisone (400 nM), activity of brush-border alkaline phosphatase, alpha-glucosidase, and leucyl-2-naphthylamidase and cytoplasmic-mitochondrial malate dehydrogenase increased (P less than 0.05) by 80-133% compared with controls. Uptake of 3-O-methyl-D-[14C]glucose after 24-h culture was increased (P less than 0.05) by 30% compared with cultures without hydrocortisone. Labeling of protein with L-[14C]tyrosine and glycoprotein with D-[3H]glucosamine increased (P less than 0.05) by 40 and 88%, respectively, with hydrocortisone. The effects of hydrocortisone were dose dependent at normal serum concentrations (100-600 nM) and not further stimulated by larger concentrations. Cytoplasmic lactate dehydrogenase and lysosomal hexosaminidase activity, specific radioactivity of soluble precursor pools for protein and glycoprotein labeling, incorporation of [3H]thymidine into DNA, and morphology were unaffected by hydrocortisone. Inhibitors of glucocorticoid receptor binding (progesterone), mRNA transcription (alpha-amanitin), and protein synthesis (cycloheximide) prevented the effects of hydrocortisone. We suggest that hydrocortisone maintains the digestive, absorptive, and cellular function of cultured human jejunum. These protective effects were associated with increased protein synthesis and glycosylation and dependent on a classical steroid-hormone mechanism.

3-O-Methylglucose↗

Ambulatory surgery.

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Ambulatory Surgical Procedures↗

A quantitative histological analysis of the effects of age and sex on human lingual epithelium.

After exclusion criteria had eliminated changes of pathological origin, tongues were obtained from 86 necropsies evenly divided by sex and age from 16-98 years. Epithelium was examined from two precisely defined sites on the lateral and dorsal lingual surfaces. Morphometric techniques were employed to determine various epithelial parameters. The epithelium was thicker in males but rates of ageing change between the sexes were similar. Generally, age changes were similar at each site: the mean epithelial thickness underwent a 30% reduction over the age range studied; the progenitor cell layer remained of constant thickness but its nuclear/cytoplasm ratio reduced significantly; significant reductions also occurred in the rete surface area of the lateral epithelium and in the papillary surface area of the dorsal epithelium. Although some of the parameters showed steeper rates of change in the younger half of the age range, the overall pattern of ageing in the lingual epithelium suggested a continuous trend towards atrophy and simplification of structure occurring evenly throughout the entire adult life span.

Adolescent↗

Generation of alloreactive cytotoxic T lymphocytes: evidence for a differentiation factor distinct from IL 2.

In this report we provide evidence that the generation of cytotoxic T lymphocytes (CTL) involves a differentiation signal in addition to a proliferative signal, and that the differentiation signal is mediated by a factor distinct from interleukin 2 (IL 2). Generation of CTL from nylon wool-nonadherent splenocytes stimulated by heat-treated thymocytes did not correlate with the addition of IL 2-containing supernatants to this factor-dependent bioassay. IL 2 from two different sources and prepared by different methods (purified IL 2 from the LBRM33 cell line and partially purified IL 2 from the EL4 cell line) was not sufficient to generate a cytotoxic response in the bioassay. The inability of IL 2 to generate a cytotoxic response was not due to the use of heat-treated stimulator cells because similar results were obtained with UV-treated cells. As we previously reported, supernatant fluids containing a differentiation/activation factor did generate CTL from nylon wool-nonadherent splenocytes. Supernatant fluid from co-cultures of activated T cells and M phi as well as from cultures of activated M phi contained this CTL helper factor; however, only the former supernatant contained IL 2 activity. These results suggest a factor distinct from IL 2 is providing a differentiation/activation signal that is necessary for CTL development. Although IL 2 was not effective at generating CTL from nylon wool-nonadherent splenocytes, it was capable in some, but not all, experiments of generating a cytotoxic response from unseparated splenocytes. The ability of IL 2 to induce a cytotoxic response from unseparated splenocytes appeared to correlate with the presence of a weak background response seen when unseparated cells were used as responder cells.

Animals↗

Individualizing theophylline therapy: the impact of clinical pharmacokinetics on patient outcomes.

We have studied 19 male patients whose theophylline therapy was individualized by a clinical pharmacokinetics service and 34 male patients with empirically derived dosages. All patients were admitted to the medical intensive care unit. Patients in the pharmacokinetics group had fewer adverse reactions (15.7 vs. 50%), shorter intensive care unit stay (6.6 +/- 5.5 vs. 12.4 +/- 16.3 days), shorter hospital stay (15.4 +/- 10 vs. 22.3 +/- 14.1 days), and a shorter period of time to be placed on oral therapy (5.2 +/- 3.1 vs. 8.6 +/- 7.2 days) than the group with empirically derived regimens. The pharmacokinetic method used to individualize theophylline therapy offered an accurate and efficient method of achieving therapeutic concentrations. We conclude that the use of clinical pharmacokinetics to individualize theophylline therapy offers substantial benefits over empirical assessments.

Aged↗

Prednisolone enhances aminopeptidase turnover in adult rat small intestine.

In adult male rats, fed prednisolone (0.75 mg/kg/day) for 7 days, brush border aminopeptidase activity was increased (P less than 0.001) by 106% compared to pair-fed controls. [14C]Tyrosine was injected intraperitoneally 16 h and [3H]tyrosine 6 h before death. The 3H/14C ratio was 1.79 +/- 0.21 (S.D.) in purified microvillus membranes from treated rats compared to 1.30 +/- 0.16 (P less than 0.01) in controls. Polyacrylamide gel electrophoresis of brush border membranes under denaturing conditions showed that the increased double-isotope ratio in membranes from treated rats was mainly in the high molecular weight protein subunits (greater than 80 kDa). Detergent-solubilized aminopeptidase was purified after in vivo labeling by protein A-Sepharose-antiaminopeptidase affinity chromatography. The 3H/14C ratio in aminopeptidase was 2.42 +/- 0.15 (P less than 0.05) in treated rats compared to 1.63 +/- 0.13 in controls. Over the experimental period steady-state isotope reutilization and protein labeling was demonstrated and there was no isotope metabolism. Total microvillus membrane lipid content was unaffected by prednisolone. We conclude that prednisolone increases brush border aminopeptidase activity by increasing enzyme turnover. Other high molecular weight brush border proteins were similarly affected.

Aminopeptidases↗

Myocardial injury: quantitation by cell sorting initiated with antimyosin fluorescent spheres.

Spheres coated with antibodies specific for myosin were used to detect myocardial cell membrane disruption by scanning electron microscopy. Injury in a population of cultured myocytes as then followed and measured by fluorescence-activated cell sorting. This approach provides a unique method for quantitating the evolution of myocardial injury and potentially for assessing the efficacy of interventions aimed at myocardial protection.

Animals↗

Why noncompliance?

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Decision Making↗