Domains of neuronal heparan sulphate proteoglycans involved in neurite growth on laminin

Summary A single neuronal cell assay of neurite growth was utilized to determine types and domains of neuronal proteoglycans involved in neurite growth on laminin. Perturbations of biosynthesis and processing, enzymatic digestion with specific lyases, and competition with glycosaminoglycan side chains produced complementary data consistent with a molecular model implicating glycosaminoglycan (GAG) residues of heparan sulphate proteoglycans (HSPGs) in neurite growth. The observations suggest that HSPGs promote neurite growth on laminin by bridging between binding domains for HSPGs on laminin and on the neuronal cell surface, and that the bridge is tethered at both ends by noncovalent interactions between the binding domains and GAG side chains. Sulphation of the GAGs of HSPGs appears to be critical to the tethering and/or neurite growth-promoting activity of neuronal HSPGs.     

Environmental versus social factors as determinants of growth in nestlings of a communally breeding bird

Summary Nestlings of the communally breeding Greycrowned Babbler (Pomatostomus temporalis) were studied to discover if supplemental feeding by auxiliary birds at nests enhanced their growth. Growth of wing, bill, tarsus and weight was measured. Growth curves were fitted by computer using a commercial program (MLAB). Our data provided little support for possible sibling competition. A significant component of the variance in asymptote and growth constant for some variables could be attributed to differences among nests. Environmental variables such as temperature and rainfall were much more strongly associated with nestling growth than were the numbers of auxiliary birds feeding broods.     

Gene-Enzyme Relationships in Neurospora Invertase

A spontaneous, single-gene mutation responsible for a total lack of invertase activity in Neurospora crassa is described. The mutation is believed to lie in the structural gene for invertase, since an immunologically cross-reacting protein is made by the mutant strain. In addition, there was no evidence for a defect in regulation of invertase activity or synthesis by the following criteria. (i) The invertaseless condition was recessive in heterokaryons; (ii) no invertase inhibitor was found in mutant extracts by mixing experiments; and (iii) none of the several sugars able to induce activity in wild-type strains was able to induce activity in the mutant strain. It was also discovered that most of the wild-type enzyme (55 to 75%) cannot be washed free from the rapidly sedimenting cell debris. This finding provided additional support for the hypothesis that Neurospora invertase is located within or about the cell wall.     

Direct contact is required between serum albumin and hamster spermatozoa for capacitation in vitro

A dialysis unit was used to test whether direct physical contact between serum albumin and hamster spermatozoa is required for capacitation and/or the acrosome reaction. Sperm and bovine serum albumin (BSA) were incubated cither together (direct incubation) or separated by a dialysis membrane (indirect incubation). Sperm viability was supported with “sperm motility factors” (hypotaurine and epinephrine) and polyvinylalcohol (PVA). Spermatozoa became capacitated and underwent acrosome reactions when directly incubated in medium containing BSA (TALP-PVA), but did not undergo acrosome reactions when indirectly incubated with BSA (medium TLP-PVA). When sperm were first incubated for 4 hr indirectly with BSA, followed by 4 hr direct incubation with BSA, capacitation did not occur during indirect incubation. These findings indicate that an “intimate association” is necessary between serum albumin and spermatozoa to support capacitation under in vitro incubation conditions. The data are consistent with the concept of direct transfer of compounds from sperm to albumin and/or vice versa during sperm capacitation.     

Retinotopy and orientation columns in the monkey: A new model

A model is presented in which orientation columns arise directly out of retinotopy. According to the model, iso-orientation lines are arrayed radially around nodal centers which correspond to cytochrome oxidase patches. The nodal centers form a square matrix superimposed upon the map of ocular dominance stripes. In the supragranular layers horizontal iso-orientation lines run down the centers of ocular dominance stripes, with vertical iso-orientation lines crossing perpendicularly. Diagonal orientations (45 degrees and 135 degrees) are represented as alternating iso-orientation zones at the centers of the interstices in the matrix (internodal centers). Preferred orientations in the infragranular layers are reversed with respect to the supragranular layers. The model is consistent with new data concerning ocularity and preferred orientation in systematic penetrations through striate cortex, and helps to explain some previously puzzling features of the relationship between ocular dominance columns, orientation columns and retinotopy.     

Microprobe analysis of Na,K, Cl,P, S,Ca, Mg and H2O in frozen-hydrated sections of anterior caeca of the locust, Schistocerca gregaria

Electron probe X-ray microanalysis of frozen-hydrated sections was carried out for sodium, potassium, chlorine, calcium, magnesium, sulphur, phosphorus and water concentrations in the lumen and epithelial cells of freshly-fed adult female desert locusts, and in blood of fed and starved locusts.Sodium and chloride were found to be at a much lower level in the lumen and cells than potassium, and at a much higher level in the blood. The luminal folds were plugged with a dense organic matrix, presumed to be polyanionic glycosaminoglycans, which appeared to restrict access of charged moieties of the absorptive sites. The data were consistent with a model of caecal fluid absorption in which a passive flux of potassium from lumen to blood, possibly assisted by an active absorption of chloride, drives fluid into the blood. Unlike the case of the vertebrate intestine, active absorption of sodium from the lumen would not contribute significantly to the fluid transport in vivo.