Educação matemática pela arte
Gusmão, Lucimar Donizete
2013-08-28
Search results
10 records were found.
Development of crystalline inclusions (“ergosterol crystals”) in “snowflake”, a morphological mutant of Neurospora crassa has been examined. The inclusions which arise in membranebound organelles appear as electron dense deposits, increase in size, and occupy nearly all the space within the organelle at maturity. The presence of catalase activity in the organelle was not detected using cytochemical procedures employing diaminobenzidine.
A morphological mutant of Neurospora crassa, snowflake, is shown to contain filaments which are about 70 A in diameter, and up to several microns long, and which usually bunch in groups of a few to several hundred. They may be found longitudinally or transversely arranged with respect to the long axis of the cell and, in many cases, they run up to the plasma membrane, but not through it. The filaments often are arranged in crystalline arrays but may also be found as separate filaments. Sometimes the filaments are closely appressed to nuclei and may be found inside them. It is likely that the filaments are not the result of the dissociation of microtubules and are most likely microfilaments like those found in other organisms. Their relationship to the origin of certain morphological mutants in Neurospora is discussed.
The effect of cryopreservation on the ability of primary human cancer cells to form colonies in a two-layer agar system was examined. Although considerable variation occurred, concentrations of 5 or 10% dimethylsulfoxide employed with slow freezing rates allowed survival of colonies in the range 20-40% or greater of nonfrozen controls. The methods used in this study do not require elaborate freezing equipment, and can be used for the cryopreservation of a wide variety of types of cancers.
Growth of various strains of Neurospora crassa in the continued presence of cytochalasins A and B results in the following pattern. At low concentration the drugs cause an increase in branching which, depending on the strain, may also reveal an increase in dry weight. Increasing the concentration results in abnormal hyphae (swollen, irregular) and eventually in inhibition of growth. Most strains are inhibited at 10–20 Μg/ml cytochalasin A. Ultrastructure of hyphae grown in the presence of cytochalasin A reveals the presence of abnormal wall deposits. These deposits are not observed in cultures grown with cytochalasin B which generally causes a lower growth response also.
During aging, protein synthesis undergoes decremental changes in many organs and tissues. In the pancreas, as well as in other exocrine glands, the rate of protein synthesis declines with age. However, it is unknown whether this decline is related to intrinsic aging changes which affect the secretory cell function. In this study, we compared the ability of pancreatic acinar cells to synthesize amylase and its messenger RNA (mRNA) in response to insulin treatment of young and old rats rendered diabetic with streptozotocin (STZ). In STZ-induced diabetic rats, amylase protein and its mRNA levels were reduced drastically in the pancreas of young and old groups. Injections of these diabetic rats with insulin increased pancreatic amylase mRNA contents significantly in both young and old rats. Insulin also increased proportions of amylase pro...
Post-thaw suspension of red cells cryopreserved with hydroxyethyl starch (HES) gives rise to an increase in the quantity of supernatant hemoglobin and a reduction in cell recovery. This occurs regardless of the suspension media used but may be delayed by some solutions. Extended suspension with most solutions results in loss of intracellular contents from a number of cells. The resulting ghosts account for 12-14% of the total cell population. In the presence of 14% HES, deposits on the surface of damaged cells indicate that cellular contents are adherent to the cell membrane and therefore do not contribute to the free hemoglobin in the external solution. The result is a misleading high cell recovery value and suggests that this test does not accurately describe true cell damage in the presence of HES. Since the saline stability of susp...
Full units of red blood cells frozen with 14% hydroxyethyl starch (HES) yield cell recoveries near 97% and saline stabilities greater than 80%. Potassium leaves the cells during the freeze-thaw cycle and increases the extracellular concentration of this ion to near 35 meq/l. Unwashed cells (those with plasma present) and saline washed cells yield similar results. Storage of the thawed red cells at 4 [deg]C for up to 48 hr causes little change in the cells.Examination by electron microscopy of samples from thawed units reveals some red cells with portions of their membrane missing. We believe this represents damage from the freeze-thaw cycle and also that all free supernatant hemoglobin does not arise from completely lysed cells.
Prefreeze washing of red cells with saline and other wash solutions before freezing with 10% hydroxyethyl starch does not yield an improved product after thawing. The saline stabilities and cell recoveries are reduced and the level of supernatant hemoglobin increased. These data further support the use of 14% as the most acceptable concentration of hydroxyethyl starch for cryopreservation of red cells.
