Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: UNIPROT:Q86TM3 (cage)
 29,987 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

It is proposed that cells store calcium in the hydrogen belt of their membranes, on the cytoplasmic side, with the Ca2+ ion captive in cages formed by the phosphate and carbonyl oxygens of two acidic phospholipid molecules; for instance, phosphatidylinositol and phosphatidylserine. Evidence for the existence of such Ca-cages is adduced from the properties of the [Ca(phosphatidate)2] complex. Cytoplasmic Ca2+ concentration, approx. 10(-7) M, corresponds to the calcium cage dissociation constant. The high stability of the cages is the result of multiple hydrogen bonds between inositol and serine, or inositol and inositol. Phosphorylation of the inositol in position 4 and 5 opens the calcium cage by breaking the inter-headgroup hydrogen bonds and by introducing electrostatic and steric hindrance. This allows the escape of Ca2+ into the cytosol. The mono in equilibrium with di in equilibrium with triphosphoinositide shuttle serves as a regulator of Ca2+ concentration in the cytoplasm: phosphorylation of the lipids will raise, dephosphorylation lower the level of free Ca2+. The inositide shuttle may be linked to a stimulus-induced inositide cycle in which inositol triphosphate is generated, and to Ca(phosphatidate)2 cross-membrane transport.
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PMID:Hypothesis: control of intracellular calcium level. 394 95

The molecular species that determine the unique structure and functions of the microtubules in the mitotic spindle are not known. We describe the results of two new approaches to the molecular structure of the spindle. Both approaches rely on detergent-extracted preparations of synchronized populations of cells metabolically labeled with 35S-methionine or 32P-phosphate. In these preparations, the original cellular microtubules are preserved. The microtubule components can be released from the detergent-extracted preparations by selective depolymerization with calcium ions. Alternatively, the microtubules can be stabilized by taxol, freed of chromatin by digestion with DNAase and freed of the surrounding cage of intermediate filaments by further extraction at low ionic strength. Gel electrophoresis of each of these preparations of mitotic microtubules demonstrates that they contain microtubule-associated proteins that we have previously shown to be present in interphase microtubules. They also contain a protein of 150,000 daltons, which is the first mitosis-specific microtubule-associated protein identified in mammalian cells.
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PMID:Proteins specifically associated with the microtubules of the mammalian mitotic spindle. 612 Jul 67

1. Rats were fed various diets ranging from the normal chow, pure flour containing large amounts of phytic acid, Ca-enriched flour and mixtures of flour and normal food with various levels of calcium. 2. It was found that the animals eating the pure flour grew less and were smaller. 3. They suffered from hypocalcemia and had low plasma alkaline phosphatase and 25-HCC-vitamin D3 levels. 4. These animals had rib-cage deformities. 5. Additional calcium in the flour improved the animals' growth and calcification. 6. The mixed food did not greatly affect the animals and additional calcium did not improve growth or bone mineralisation. 7. The Bedouin eat large amounts of unleavened bread containing large amounts of phytates. 8. It is concluded that uptake of large amounts of phytates by the Bedouin eating unleavened bread is due to the flour and that the clinical manifestations are a direct result of the flour and not the lack of vitamin D due to covering the skin from sunlight.
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PMID:Growth and bone mineralisation as affected by dietary calcium, phytic acid and vitamin D. 612 64

Transport of receptors by the coated vesicle pathway entails assembly of clathrin triskelions into a lattice in conjunction with receptors in a membrane. The processes by which the receptors are concentrated, the lattice is assembled, transformed into a cage during vesiculation, and subsequently removed from pinched off vesicles are not understood in regard to mechanism, energetics or control. Tubulin and actin assembly are looked to for analogies applicable to clathrin. The present model supposes that clathrin assembly is energy linked and can be described by kinetic equations of the same general form as those for treadmilling in linear polymers. The coat lattice assembles in a steady state involving the degradation of a high energy form of the clathrin triskelions. Diffuse endocytosis receptors are assumed to be associated with individual triskelions and to be able to trigger clustering and coated pit formation by influencing the assembly kinetics of the bound triskelions. A generalization of the treadmilling scheme is proposed by which the kinetic parameters associated with clathrin polymerization can shift simultaneously for an entire lattice to favor alternatively net assembly or disassembly. This shift is effected by a coordinated conversion of the lattice bound receptors. The conversion of the receptors in turn depends on some global property of the membrane compartments (arguably pH, calcium concentration or transmembrane voltage) which is likely to change as a consequence of vesiculation. Thereby, lattice disassembly can be coordinated with the topological conversion from coated pit to coated vesicle.
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PMID:Model for transformations of the clathrin lattice in the coated vesicle pathway. 613 95

In 50 consecutive patients with cancer-associated hypercalcemia, we measured nephrogenous cyclic AMP, tubular phosphorus threshold, fasting calcium excretion, plasma 1,25-dihydroxyvitamin D, and immunoreactive parathyroid hormone as determined by four region-specific antiserums. Nephrogenous cyclic AMP excretion was elevated in 41 patients and suppressed in nine (means, 5.85 vs. 0.51 nmol per 100 ml of glomerular filtrate). There was no overlap between these groups. When compared with 15 patients with primary hyperparathyroidism, the group with increased cyclic AMP excretion had similar reductions in tubular phosphorus threshold; higher fasting calcium excretion (means, 0.66 vs. 0.25 mg per 100 ml of glomerular filtrate, P < 0.01); marked reductions in 1,25-dihydroxyvitamin D (means, 20 vs. 83 pg per milliliter, P < 0.001); and lower levels of immunoreactive parathyroid hormone in all four assays. The data suggest that elevated excretion of nephrogenous cyclic AMP may be a useful marker of humorally mediated cancer-associated hypercalcemia, that this type of hypercalcemia is common, that the humoral factor responsible for this syndrome is not native 1-84 parathyroid hormone, and that the various subtypes of cancer-associated hypercalcemia are biochemically distinguishable from primary hyperparathyroidism.
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PMID:Biochemical evaluation of patients with cancer-associated hypercalcemia: evidence for humoral and nonhumoral groups. 625 85

Phosphatidic acid can act as Ca2+ cross-membrane ionophore without the necessity of previous autoxidation. The apparent PA-CA2+ dissociation constant is 3 X 10(-3), i.e., in the range of extracellular Ca2+ concentration. There is at least 100-fold preference for Ca2+ over Mg2+. Ca2+ transfer rates are proportional to the square of phosphatidic acid concentration in the bilayer. Removal of the fatty acid ester CO groups reduces the Ca2+ ferrying rate by more than 90 percent. It appears that the cation is held in a cage formed by phosphate and carbonyl oxygens of two PA molecules. In this coordination complex both Ca2+ and the phosphatidic acid headgroups are dehydrated, and the Ca(phosphatide)2 assembly becomes lipid-soluble and can traverse the bilayer.
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PMID:Ca(phosphatidate)2 can traverse liposomal bilayers. 648 61

Four strains of laying hens, including one brown egg strain, were force-rested in February at approximately 62 weeks of age. Hens from the same four strains, which were the same age, were also force-tested under similar conditions during August of the same year. In each of the two trials, a total of 2300 hens were housed at the rate of two per 25.4 x 45.7-cm cage. The resting procedure for both studies included feed withdrawal for 9 or 10 days followed by feeding a 8.6% protein diet for 25 days. Water was supplied at all times. After the 35-day resting period, the hens were assigned to four calcium and phosphorus combinations, which varied from the duplication of a first-year pullet phase feeding program to the feeding of a final phase type diet for the entire postrest production period. Nutrient level within each dietary system was adjusted periodically based on daily feed intake. Strain performance differences were observed in both seasons. Rate of return to production and postrest production rates were similar to the patterns observed within the respective strain's performance during the pullet year. This was noted in both studies. Relative strain production performance, however, when compared to the other strains, was not consistent between the two rest seasons. There was no difference in performance due to calcium and phosphorus treatment utilized in either postrest production season.(ABSTRACT TRUNCATED AT 250 WORDS)
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PMID:The performance of four strains of laying hens subjected to various postrest combinations of calcium and phosphorus after forced rest in winter or summer. 663 9

Caged Sex-Sal (DeKalb Warren) replacement pullets were fed diets containing .30%, .35%, or .41% available phosphorus from 0 to 20 weeks of age; in a second study pullets were fed the above levels plus a level of .25% available phosphorus from 2 to 20 weeks of age. Some of the pullets were fed diets restricted by 11 to 16% from 8 weeks of age. Reducing the dietary phosphorus did no harm weight gain, feed intake, feed conversion efficiency, bone ash or total calcium and inorganic phosphorus levels in plasma. There was a very small but significant reduction in weight gain and feed intake when .30% or .35% available phosphorus was fed from 0 to 4 weeks of age, but this difference disappeared at the later ages. With the nonstimulatory lighting schedule used, plasma phosphorus decreased markedly in the latter phase of the studies at all levels of dietary phosphorus and thus represented a nondietary age effect. These results show that dietary available phosphorus for cage, brown egg type pullets on full or restricted feeding programs can be decreased to a level as low as .25% from 2 to 20 weeks, and .30% from hatching to 20 weeks without adverse effect.
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PMID:Dietary phosphorus levels during growth of brown egg type replacement pullets. 737 28

Two siblings with hypophosphatasia, one of whom was autopsied, were reported. The first case which was a product of a 26-year-old mother complicated by hydroamnios represented poor mineralization of the entire bones on X-ray examination and died shortly after birth. The second case weighing 1850 g delivered from the same mother had a rhizomelic micromelia and poor visualization of the skull, long bones and vertebral bones on X-ray at postmortem. The autopsy on the second case showed small thoracic cage with rachitic rosaries of ribs, membranous skull and poorly ossified vertebral and long bones. Microscopically, there was a marked disturbance of both enchondral and membranous ossifications similar to the histology of rachitis. A biochemical examination showed low alkaline phosphatase, high calcium and normal PTH in the serum. Further examination of their family revealed relatively low level of alkaline phosphatase of the parents and one of their brothers which suggsted they were carriers of hypophosphastasia. Previous reports on hypophosphatasia were reviewed and differential diagnosis of hypophosphatasia from the other congenital dwarfisms was discussed.
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PMID:Two siblings with hypophosphatasia. 741 41

Three experiments were conducted to compare limestone to fly fly ash from a coal-fired generator station as a calcium source for broilers. In Experiment 1, 5 male and 5 female broiler chicks were placed in each of 32 cages. Sixteen cages of birds were fed a ration with limestone supplying 30% of the total calcium and 16 cages were fed a ration with 30% of the total calcium supplied by fly ash. The total calcium and phosphorus levels of the rations were 1.0% and .5% respectively. In this experiment no significant difference (P < .05) was found for 8-week body weight between diets where the added calcium was from limestone or fly ash. In Experiment 2 a group of 40 male and 40 female cage reared broilers and 40 male and 40 female floor reared broilers were fed a basal diet of limestone providing 33% of the total calcium. Three diets with increasing fly ash levels were fed to three cage groups of 40 male and 40 female broilers providing 33, 46, and 45% of the total calcium of .9, 1.1, and 1.8%, respectively. Broilers fed the highest fly ash level weighed significantly less (P < .05) at 8 weeks than the caged controls but did not differ from the other treatments. Bone breaking strength as measured by the Allo Kramer Shear Press was similar between the basal and low level fly ash group and increased with higher fly fly ash levels. Humerus and radius bone strength were greatest in floor broilers when compared with cage broilers. Tibia ash content of the floor-reared broilers and higher fly ash level of caged broilers were similar and greater than that of the basal cage group. Humerus and radius ash content were higher for the higher calcium groups. In Experiment 3 four groups of 40 male broilers in cages were fed limestone diets with graded levels of limestone for the calcium source. Another four groups of 40 caged male broilers were fed fly ash diets with equivalent graded levels of fly ash for the calcium source. Both limestone and fly ash diets provided .17, .34, .51, and .68% calcium of a total calcium content of .28, .45, .62 and .79%, respectively. The four limestone groups exhibited a definite linear improvement in both 3-week body weight and bone weight (tibia and femur combined) as the dietary calcium level was upgraded. The two low fly ash groups were similar in body and bone weight to their counterpart limestone groups, but further increases in the fly ash component did not improve body or bone weight. Bone ash values for both limestone and fly ash groups showed a similar improvement with each calcium increase, except the high value for the second level of fly ash.
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PMID:The use of fly ash in diets of cage and floor broilers. 743 65


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