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Biomedical subjects

M Vaughan

Publications and source records attributed to M Vaughan.

At least 199 records · Page 11Linked to original sources
PubMed1982

Subcellular localization and quantification of cholesterol in cultured human fibroblasts exposed to human low density lipoprotein.

Subcellular localization of nonesterified cholesterol has been determined in normal human fibroblasts from cultures incubated with human low density lipoprotein (LDL). Nonesterified and esterified cholesterol content of fibroblasts, grown initially in the absence of cholesterol, increased significantly after a 1-hour incubation with LDL. Digitonin was used to localize nonesterified cholesterol that was accumulated within multivesicular and lamellar lysosomal inclusions. This was observed only in fibroblasts from cultures incubated with LDL. Accumulation of LDL-derived nonesterified cholesterol within lysosomes is consistent with the suggestion of other investigators that LDL is metabolized within lysosomes.

Cell Membrane↗
PubMed1981

Calmodulin-activated cyclic nucleotide phosphodiesterase from brain. Relationship of subunit structure to activity assessed by radiation inactivation.

The apparent target sizes of the basal and calmodulin-dependent activities of calmodulin-activated phosphodiesterase from bovine brain were estimated using target theory analysis of data from radiation inactivation experiments. Whether crude or highly purified samples were irradiated, the following results were obtained. Low doses of radiation caused a 10 to 15% increase in basal activity, which, with further irradiation, decayed with an apparent target size of approximately 60,000 daltons. Calmodulin-dependent activity decayed with an apparent target size of approximately 105,000 daltons. The percentage stimulation of enzyme activity by calmodulin decreased markedly as a function of radiation dosage. These observations are consistent with results predicted by computer-assisted modeling based on the assumptions that: 1) the calmodulin-activated phosphodiesterase exists as a mixture of monomers which are fully active in the absence of calmodulin and dimers which are inactive in the absence of calmodulin; 2) in the presence of calmodulin, a dimer exhibits activity equal to that of two monomers; 3) on radiations destruction of a dimer, an active monomer is generated. This monomer-dimer hypothesis provides a plausible explanation for and definition of basal and calmodulin-dependent phosphodiesterase activity.

3',5'-Cyclic-GMP Phosphodiesterases↗
PubMed1981

ADP ribosylation of membrane proteins from human fibroblasts. Effect of prior exposure of cells to choleragen.

Major labeled bands of Mr = 42,000 and 47,000 were observed on sodium dodecyl sulfate polyacrylamide gel electrophoresis of human skin fibroblast membranes incubated with choleragen and [32P]NAD. Prior incubation of intact fibroblasts with choleragen blocked specifically the subsequent in vitro labeling of these two proteins. The effect of choleragen was dependent on time, temperature, and toxin concentration. Neither the choleragen A subunit nor the B subunit nor the A1 peptide could replace the holotoxin in cell incubations. Inhibition of subsequent in vitro labeling by prior exposure of cells to choleragen was correlated with increased cellular cAMP. Incubation of fibroblasts with prostaglandin E1 and isoproterenol, which activate adenylate cyclase by different mechanisms, did not block subsequent labeling with choleragen and [32P]NAD. The results suggest that proteins of Mr = 42,000 and 47,000 may be in vivo substrates for choleragen in human fibroblasts.

Adenosine Diphosphate Ribose↗
PubMed1981

Presence of autoantibody for phospholipase inhibitory protein, lipomodulin, in patients with rheumatic diseases.

The activity of phospholipase inhibitory protein, lipomodulin, partially purified from rabbit neutrophils, was markedly decreased after treatment with sera from patients with rheumatic diseases such as systemic lupus erythematosus, rheumatoid arthritis, and dermatomyositis. The decrease of the protein's inhibitory activity on phospholipase A2 paralleled the amount of [35S]methionine-labeled lipomodulin precipitated by the sera. Absorption of patients' sera with anti-human IgM (mu chain) or protein A-agarose, but not with anti-human IgG (gamma chain), decreased their ability to decrease the activity of lipomodulin on phospholipase A2 or to precipitate the radioactive lipomodulin. The IgM fraction of patients' sera could precipitate [35S]methionine-labeled lipomodulin (40,000 daltons) which comigrated with highly purified lipomodulin on gel electrophoresis with sodium dodecyl sulfate. All of these observations suggest that the sera of many patients with rheumatic diseases contain autoantibody against lipomodulin. A monoclonal antibody against lipomodulin was also obtained. Stimulating human fibroblasts with bradykinin in the presence of monoclonal antilipomodulin antibody markedly enhanced arachidonic acid release due to the activation of phospholipase(s) in the intact cells, and this stimulatory effect was blocked by adding purified lipomodulin. These findings suggest that lipomodulin regulates the activity of phospholipase(s) on the cell surface and that autoantibodies against lipomodulin may play a role in certain symptoms of rheumatic diseases, especially by the formation of prostaglandins and other metabolites of arachidonic acid.

Animals↗
PubMed1981

Changes in frequency and distress during prolonged repetition of obsessional thoughts.

Five obsessive-compulsive patients were treated for intrusive thoughts by three sessions of repetition of the thought. Within- and between-session changes in both frequency and subjective distress lent only partial support to the habituation and conditioned inhibition models which have been used to account for the effects of prolonged repetition. Alternative explanations should be sought.

Adult↗
PubMed1980

Effects of nucleoside triphosphates on choleragen-activated brain adenylate cyclase.

To investigate the effects of nucleoside triphosphates on the activation of adenylate cyclase by choleragen and on the stability and catalytic function of the choleragen-activated enzyme, we treated samples of particulate preparation from bovine brain successively in three separate incubations with extensive washing between each step. In incubation I, choleragen and NAD were pesent to activte the adenylate cyclase. In incubation II, conditions were varied to assess enzyme stability. Finally, adenylate cyclase activity was assayed with ATP or adenylyl imidodiphosphate [App-(NH)p] as the substrate. Even when assays contained an optimal concentration of GTP, nucleoside triphosphate (plus a regenerating system) was required in incubation I for maximal choleragen activation; in order of effectiveness, GTP > ITP > ATP greater than or equal to CTP = UTP. During incubation II (at 30 degrees C), activity of the choleragen-treated fractions was essentially completely stable when 100 microM GTP (plus a regenerating system) was present. ITP and ATP were less effective. Activation produced by guanylyl imidodiphosphate was more stable than that resulting from choleragen, GTP, and NAD. After activation of membranes with choleragen, NAD, and GTP, nucleoside triphosphate plus a regenerating system (but not NAD or additional choleragen) was essential for expression of maximal activity. In order of effectiveness, GTP > ITP > ATP greater than or equal to CTP = UTP. It appears that GTP, which was effective in micromolar concentrations, plays an important role not only in the activation of adenylate cyclase by choleragen but also in the stabilization and expression of the catalytic function of the activated enzyme.

Adenosine Triphosphate↗
PubMed1980

Circular dichroism spectra show that repeating dinucleotide DNAs may form helices in which every other base is looped out.

We have found that the CD spectrum of poly [d(C-T)] undergoes a marked change upon protonation, taking on the unmistakable features of the spectrum of poly[d(C) x d(C+)]. The acid poly[d9C-T)] structure appears to be one in which each of the T residues is individually looped out of a helix formed by stacked C x C+ base pairs. We also present data for poly[d(C-A)] and review data for the other four possible repeating DNA dinucleotide sequences. These data show that self-complexes in which up to 50% of the residues are extrahelical may be unexceptional.

Circular Dichroism↗
PubMed1980

ADP-ribosyltransferase activity of mono- and multi-(ADP-ribosylated) choleragen.

Choleragen (cholera toxin) catalyzed the NAD-dependent auto-ADP-ribosyltation of its A1 peptide. The number of ADP-ribose moieties incorporated into ech A1 peptide was dependent on incubation conditions and time as well as toxin concentration. There was no evidence for the formation of poly(ADP-ribosylated) toxin. The formation of mono- and multi-(ADP-ribosylated) A1 peptides was prevented by the addition of arginine, an alternative ADP-ribose acceptor. Triton X-100 polyacrylamide gel electrophoresis separated the A1 peptide of choleragen from the B complex and multi-(ADP-ribosylated) A1 peptides from unmodified A1. The A1 peptides ADP-ribosylated in the presence of [32P]NAD contained approximately 1, 2, or 3 ADP-ribose molecules/23,500-dalton units; under the conditions used for electrophoresis, the mobilities of the A1 peptides were enhanced by incorporation of ADP-ribose. The mono- and multi-(ADP-ribosylated) A1 peptides catalyzed the NAD-dependent ADP-ribosylation of arginine methyl ester. The turnover numbers of the mono- and multi-(ADP-ribosylated) A1 peptides were consistently 30 to 50% higher than that of the A1 peptide from native toxin.

Adenosine Diphosphate Ribose↗
PubMed1980

Effects of GTP on choleragen-catalyzed ADP ribosylation of membrane and soluble proteins.

Choleragen-dependent ADP ribosylation of soluble proteins from bovine thymus, using [32P]NAD as substrate, was increased 3- to 4-fold by GTP. The effect was specific for nucleoside triphosphate, with GTP approximately equal to ITP greater than CTP greater than ATP greater than UTP. Half-maximal enhancement was observed with 0.5 mM GTP. The magnitude of the GTP effect decreased with increasing NAD concentration; GTP had no effect on hydrolysis of NAD at low NAD concentrations. Digestion of ADP-ribosylated proteins with snake venom phosphodiesterase yielded primarily 5'-AMP. Sodium dodecyl sulfate-polyacrylamide gel electrophoresis of soluble proteins from thymus after incubation with choleragen and [32P]NAD separated numerous ADP-ribosylated proteins; radioactivity in all bands was increased by nucleoside triphosphate. Choleragen catalyzed the ADP ribosylation of several purified proteins; depending on the protein, GTP either increased, decreased, or had no effect on the extent of ADP ribosylation. Choleragen-dependent ADP ribosylation of a wide variety of proteins is consistent with the possibility that intoxication results in covalent modification of more than one cellular protein and perhaps alters the activity of other enzymes in addition to adenylate cyclase.

Adenosine Diphosphate Ribose↗
PubMed1980

Prostaglandins increase GTP hydrolysis by membranes from human mononuclear cells.

Both adenylate cyclase and GTPase activities in human mononuclear cell membranes were increased by prostaglandins. Adenylate cyclase activity, however, was enhanced by much lower concentrations of PGE1 (prostaglandin E1) than were required to increase GTPase. PGE2, PGA1, PGB1, and PGF1 alpha also stimulated GTPase activity. These same prostaglandins, with the notable exception of PGF1 alpha, increased adenylate cyclase activity (PGE2 greater than PGA1 greater than or equal to PGB1). Isoproterenol, 100 microM, doubled adenylate cyclase without altering GTPase activity. Choleragen activated adenylate cyclase in mononuclear cell membranes but had no effect on GTPase activity whether or not PGE1 was present. Mononuclear cells were separated into adherent and nonadherent populations by two different methods to examine the possibility that the prostaglandin-stimulated GTPase was confined to a specific type of mononuclear cell. Adenylate cyclase in membranes from both adherent and nonadherent cells was activated by PGE1, but neither PGE1 nor choleragen altered GTPase activity in these preparations. It appears that, although several prostaglandins can increase GTPase activity in mononuclear cell membranes, the increase in GTPase activity is not consistently associated with activation of adenylate cyclase by prostaglandins.

Animals↗