Gene/Protein Disease Symptom Drug Enzyme Compound
Pivot Concepts:   Target Concepts:
Query: UMLS:C0038187 (starvation)
 24,951 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

1. Plasma fibronectin, a glycoprotein, is an opsonin of the reticuloendothelial system. 2. In ten healthy volunteers starved for 4.5 d, daily measurements showed a rapid reduction in plasma fibronectin, no alteration in either C3 or plasma transferrin and, at the end of the starvation period, an elevated serum albumin. 3. On refeeding, plasma fibronectin rapidly returned to its prestarvation level but plasma transferrin was significantly reduced and did not recover by the end of the study. 4. Changes in plasma fibronectin may be a sensitive index of nutritional status. The reduction of plasma fibronectin in short-term starvation may compromise host defence tolerance of injury and sepsis.
 ...
PMID:Changes in plasma fibronectin during acute nutritional deprivation in healthy human subjects. 366 79

The effect of Glc deprivation (starvation) on hexose transporter (GT) polypeptide(s) (pp) was studied in 3T3-C2 murine fibroblasts. Cells deprived of Glc exhibit 5-fold increases in hexose transport and Glc-displaceable cytochalasin B binding. Immunoblots of membranes reveal a Mr 55,000 GT pp in fed (4 g of Glc/liter) cells and Mr 55,000 and Mr 42,000 GT pp in starved cells. A 10-40-fold increase in total GT pp occurs upon Glc deprivation; part of this accumulation (2-5-fold) is in the Mr 55,000 GT pp, and the remaining increase is in the Mr 42,000 GT pp. During the first 12 h of Glc deprivation only the Mr 55,000 GT pp accumulates. At later times (24-72 h) the Mr 42,000 GT pp appears and constitutes a larger fraction of the total accumulation. Similarly, the Glc concentration dependence of these phenomena reveals that the Mr 55,000 GT pp accumulates at higher concentrations of Glc (less than or equal to g/liter) than the Mr 42,000 GT pp (less than or equal to 0.5 g/liter). Using alternative nutrients, sugar analogs, and inhibitors we observed that the accumulation of total GT pp is dependent upon both hexose phosphate metabolism and the interaction of substrate with the GT. The role(s) of oligosaccharide biosynthesis, protein synthesis, and the transport process itself in the Glc deprivation-induced accumulation of GT pp were examined. The appearance of the Mr 42,000 GT pp but not the Mr 55,000 GT pp was dependent upon protein synthesis. The Glc deprivation-induced accumulation of GT pp is reversible upon refeeding with Glc (4 g/liter, 12 h). This reversal was dependent upon protein synthesis. The electrophoretic mobility of the Mr 42,000 GT pp is similar to the GT pp observed after tunicamycin treatment. The Mr 55,000 but not the Mr 42,000 GT pp binds specifically to agarose-bound wheat germ agglutinin and is sensitive to endoglycosidase F digestion. Oligosaccharide-stripped GT pp and the Mr 42,000 GT pp have the same Mr. The results suggest that the accumulation of total GT pp induced by Glc deprivation is partially independent of the effect of Glc deprivation on glycoprotein biogenesis. The appearance of the Mr 42,000 GT pp with aglyco characteristics is the result of the latter. The accumulation of total GT pp, however, is the result of a specialized and sensitive adaptation of the cell to Glc deprivation. The GT pp synthesized during chronic Glc deprivation has an Mr of 42,000; fed cells synthesize the Mr 55,000 GT pp. Neither the level of in vitro translatable GT mRNA nor the rate of GT pp synthesis are increased by Glc deprivation.(ABSTRACT TRUNCATED AT 400 WORDS)
 ...
PMID:Glucose deprivation and hexose transporter polypeptides of murine fibroblasts. 370 Apr 14

A monoclonal antibody, mAb 47-19-2, was used to study the subunit topology of the rod-shaped alpha-actinin molecules of Dictyostelium discoideum and to screen for mutants defective in the production of alpha-actinin. Electron microscopy of rotary-shadowed alpha-actinin-antibody complexes showed binding of mAb 47-19-2 to both ends of the alpha-actinin rods and cleavage of the rods into its subunits, indicating that the two subunits of alpha-actinin extend in an anti-parallel mode through the whole length of the rod. The antibody binding sites were located in close proximity to the sites responsible for actin cross-linking, which is consistent with the blocking activity of the antibody. In a mutant, HG1130, no antibody label was detected in colony blots, and by immunoblotting of mutant proteins separated by SDS-PAGE, only trace amounts of alpha-actinin were found. The mutant showed normal binding of antibodies directed against the actin-binding proteins severin and capping protein. The mutation responsible for the alpha-actinin defect was recessive and located on linkage group I of the genetic map of D. discoideum. HG1130 cells grew on bacteria at a normal rate and also axenically like cells of the parent strain AX2. After starvation the mutant cells expressed the contact site A glycoprotein, a marker of the aggregation-competent stage, and reacted chemotactically to cyclic AMP. The aggregation patterns and fruiting bodies of the mutant appeared to be normal. Patching and capping on the surface of HG1130 cells was induced by antibodies against the contact site A glycoprotein.(ABSTRACT TRUNCATED AT 250 WORDS)
 ...
PMID:Selection of Dictyostelium mutants defective in cytoskeletal proteins: use of an antibody that binds to the ends of alpha-actinin rods. 395 80

Plasma fibronectin, which is an alpha 2-glycoprotein of importance for the immunodefence, has been reported to decrease after starvation and in severely ill patients with cancer. To evaluate the usefulness of fibronectin as an indicator of nutritional repletion, 18 patients with gastrointestinal disorders were studied over a 2-wk period of total parenteral nutrition (TPN). According to nutritional assessment on admission the patients were divided into well nourished (n = 6) and malnourished (n = 12). For comparison nine patients with anorexia nervosa were also studied over a 3-wk period of TPN. Before and after TPN fibronectin, albumin, prealbumin, transferrin, and two acute-phase reactants, haptoglobin and orosomucoid were measured in plasma. The majority of the malnourished patients had an inflammatory reaction in contrast to only a few of the well-nourished and anorexia nervosa patients. Of the proteins measured, only fibronectin rose significantly in the malnourished patients (malnourished and anorexia nervosa), but not in the well nourished patients during TPN. Our results may indicate the usefulness of fibronectin as an indicator of short-term TPN in malnourished subjects, irrespective of the presence or absence of inflammatory response.
 ...
PMID:Influence of total parenteral nutrition on plasma fibronectin in malnourished subjects with or without inflammatory response. 620 90

We have studied the changes in glycoprotein patterns on the surface of Dictyostelium discoideum cells during development on a membrane filter and in suspension culture. Cell-surface carbohydrates were detected by a periodate-[3H]borohydride method. The appearance and the increase of some glycoproteins during the early developmental stage on a membrane filter were induced 6 h after the onset of starvation. In suspension culture the same proteins appeared about 2 h earlier and less copies per cell were made. Some glycoproteins present in growth-phase cells, especially with high molecular weights, partially disappear during development on a membrane filter. However, the latter changes were not observed in suspension culture. Pulses of cAMP, which generally accelerate cell development, induced only the appearance of one glycoprotein. We conclude that the changes in patterns of plasma membrane glycoproteins during early development are regulated by several factors; starvation, pulses of cAMP, cell-cell contact and transfer onto a membrane filter.
 ...
PMID:Developmentally regulated glycoprotein alterations in Dictyostelium discoideum. 627 78

The inhibitor of the cAMP phosphodiesterase of Dictyostelium discoideum is a cysteine-rich glycoprotein, which binds to the enzyme and inactivates it. When the inhibitor is removed, enzymatic activity is restored. Following translation in vitro of RNA from developing cells and immunoprecipitation with anti-inhibitor serum, newly synthesized inhibitor can be detected by sodium dodecylsulfate/polyacrylamide gel electrophoresis and fluorography. The inhibitor can be labeled using [35S]cysteine but not [35S]methionine, in agreement with the previously determined amino acid composition, and can be detected after cell-free translation only if it has been previously acetylated. Purified native inhibitor blocks immunoprecipitation of the inhibitor polypeptide synthesized in vitro. No inhibitor mRNA was detected in growing cells. Translatable mRNA was present 2 h after the beginning of starvation, reached a maximal level after 3 h, and decreased thereafter. Addition of 1 mM cAMP at the beginning of starvation delayed the appearance of translatable inhibitor mRNA. In the presence of 5 microM adenosine cyclic-3',5'-phosphorothioate, a slowly hydrolyzed cAMP analogue, no translatable mRNA could be detected. Following removal of the analogue, the mRNA appeared within one hour and inhibitor was secreted after another hour.
 ...
PMID:Detection and regulation of the mRNA for the inhibitor of extracellular cAMP phosphodiesterase of Dictyostelium discoideum. 630 86

Within minutes of glucose starvation confluent monolayers of rat hepatoma cells synthesize glycoproteins, including alpha 1-acid glycoprotein, which appear on two-dimensional gels as size heterogeneous spot series. The longer the period of glucose starvation the more the production of the glycoproteins is shifted toward smaller molecular weight forms. To compare these forms with the corresponding glycoproteins synthesized either in a cell-free system or by nonstarved cells, a mapping of the N-glycan was done by endo-beta-N-acetylglucosaminidase digestion within a polyacrylamide gel. Glycoproteins from glucose-starved cells contain a reduced number of N-glycans which belong to both the endo H-sensitive and resistant type. The decrease of N-glycosylation may be correlated with the accumulation of truncated lipid-bound oligosaccharides, for the gel chromatography of the oligosaccharides released from the lipid and protein fractions of glucose-starved cells revealed a drastic reduction in their size. Most of the lipid-linked oligosaccharides synthesized during glucose starvation are resistant to endo H digestion. Under conditions of limiting glycosylation we were able to show by glycopeptide analysis, that in the case of alpha 1-acid glycoprotein, N-glycans are added randomly to the 6 possible N-glycosylation sites. Furthermore, non- or partially N-glycosylated proteins do not acquire additional oligosaccharide units after restoration of glucose although the proteins can undergo secondary modification and, in the case of the secretory proteins, can be exported.
 ...
PMID:Glucose starvation leads in rat hepatoma cells to partially N-glycosylated glycoproteins including alpha 1-acid glycoproteins. Identification by endoglycolytic digestions in polyacrylamide gels. 640 21

alpha-Mannosidase from Dictyostelium discoideum is a heterogenous glycoprotein which is derived from a precursor as a result of proteolytic processing. Its oligosaccharides are phosphorylated and sulfated. We investigated the sulfation of the enzyme by means of pulse-chase labeling and specific immunoprecipitation followed by endoglycosidase H treatment and sodium dodecyl sulfate-polyacrylamide gel electrophoresis. The earliest detectable form of the precursor was shown to be glycosylated and sensitive to endoglycosidase H. With time some of its oligosaccharides were sulfated and became partially resistant to endoglycosidase H. In the same time period, the precursor was proteolytically cleaved, yielding four species with different molecular masses (46-58 X 10(3) daltons). When first generated each of these was sensitive to endoglycosidase H but with time the 54,000- and 58,000-dalton forms developed degrees of endoglycosidase H resistance. The fully mature cleaved forms all contained sulfate. Sulfate from pulse-labeled precursor could only be detected in two of the forms implying that sulfation of the others occurs either after precursor cleavage or before cleavage but subsequent to the pulse period. When secretion of precursor was triggered by starvation only the endoglycosidase H-resistant forms were secreted.
 ...
PMID:Maturation of alpha-mannosidase in Dictyostelium discoideum. Acquisition of endoglycosidase H resistance and sulfate. 643 94

We previously reported that growth of influenza virus in the presence of cytochalasin B (CB), a drug that disrupts microfilaments and blocks hexose transport, yields particles with glycoproteins that are heterogeneous and unlabeled by [3H]glucosamine. When the virus was grown in glucose-free medium, we observed reduced virus titers similar to those produced by CB. In contrast, treatment of cells with cytochalasin D (CD) and dihydrocytochalasin B (H2CB), drugs which are known to inhibit microfilament function without affecting hexose transport, did not cause a reduction in virus titers or a change in the electrophoretic mobility of viral glycoproteins. Partial inhibition of glycosylation of viral glycoproteins resulting from either CB-induced inhibition of hexose transport or from glucose starvation resulted in the formation of aggregates of virions on cell surfaces. These aggregates can be dissociated by exogenous neuraminidase. Under these conditions the virions contained a functional hemagglutinin glycoprotein (HA) but an inactive neuraminidase glycoprotein (NA) which was not able to cleave sialic acid, the HA receptor, from viral glycoproteins, or from cellular glycoproteins and glycolipids. Neuraminidase treatment of membrane fractions of CB-treated cells did not cause a shift in the electrophoretic mobility of HA or in the gel elution profile of HA glycopeptides obtained after extensive pronase digestion from HA synthesized in glucose-free medium. These findings suggest that sialic acid is not present on labeled glycoproteins in either of these preparations. We obtained evidence that the sialic acid to which HA binds when NA is inactive is on glycoproteins and glycolipids of cellular origin. Our results support the idea that even when NA is functional, sialylated cellular components impede influenza virus release.
 ...
PMID:Effects of hexose starvation and the role of sialic acid in influenza virus release. 683 15

Upon inorganic phosphate starvation the cell wall glycoprotein acid phosphatase of yeast Saccharomyces cerevisiae is derepressed. Purified acid phosphatase isolated from early log phase cells differs in reactivity and stability from acid phosphatase from late log phase cells indicating that the two enzymes are structurally different. This demonstrates that the yeast cell has not only the capacity to regulate the amount of acid phosphatase but also the ability to vary (modulate) the structure of the secreted enzyme. Modulation of acid phosphatase may be a mechanism which is involved in morphogenetic and behavioral differentiation of the yeast cell.
 ...
PMID:Modulation of a cell surface glycoprotein in yeast: acid phosphatase. 703 61


<< Previous 1 2 3 4 5 6 7 8 Next >>