Neuroanatomy of the central nervous system of the wandering spider,Cupiennius salei (Arachnida,Araneida)

Summary In Cupiennius salei (Ctenidae), as in other spiders, the central nervous system is divided into the supraoesophageal ganglion or brain and the suboesophageal ganglia (Fig. 1). The two masses are interconnected by oesophageal connectives. The brain gives off four pairs of optic and one pair of cheliceral nerves. From the suboesophageal ganglia arise a pair of pedipalpal, four pairs of leg, and several pairs of opisthosomal nerves (Fig. 2). 1. Cell types. In the brain a total of 50900 cells were counted, in the suboesophageal ganglia 49000. They are all monopolar cells, found in the ganglion periphery and may be classified into four types: (a) Small globuli cells (nuclear diameter 6–7 m) forming a pair of compact masses in the protocerebrum (Fig. 10b); (b) Small and numerous cells (cell diameter 12–20 m) with processes forming the bulk of the neuropil in the brain and suboesophageal ganglia; (c) Neurosecretory cells (cell diameter ca. 45 m) in the brain and suboesophageal ganglia; (d) Large motor and interneurons (cell daimeter 40–112 m), mostly in the suboesophageal ganglia (Figs. 10a and c). 2. Suboesophageal mass. The cell bodies form a sheet of one to several cell layers on the ventral side of each ganglion and are arranged in groups. Three such groups were identified as motor neurons, four as interneurons. At the dorsal, dorso-lateral, and mid-central parts of the ganglion there are no cell somata. The fibre bundles arising from them form identifiable transverse commissural pathways (Fig. 9b). They form the fibrous mass in the central part of the suboesophageal mass.Neuropil is well-formed in association with the sensory terminations of all major nerves (Fig. 9a). As these proceed centrally they break up into five major sensory tracts forming five layers one above the other. There are six pairs of additional major longitudinal tracts arranged at different levels dorsoventrally (Fig. 8). They ascend into the brain through the oesophageal connectives and terminate mostly in the mushroom bodies and partly in the central body. 3. Protocerebrum. Fine processes of the globuli cells form the most important neuropil mass in the fibrous core, called the mushroom bodies. These consist of well developed glomeruli, hafts, and bridge which are interconnected with the optic masses of the lateral eyes and most fibre tracts from the brain and suboesophageal mass (Fig. 7). The median eye nerves form a small optic lamella and optic ganglia, connected to the central body through an optic tract. Each posterior median and posterior lateral eye nerve ends in large optic lamellae (Fig. 13a). These are connected through chiasmata to a large optic mass where fibres from globuli cells form conspicuous glomeruli. There are 10–12 large fibres (diameter 9 m) of unknown origin on each side, terminating in the optic lambella of the posterior lateral eye.The central body, another neuropil mass (Fig. 13b) in the protocerebrum, is well developed in Cupiennius and located transversely in its postero-dorsal region (Fig. 10d). It consists of two layers and is interconnected with optic masses of the median and lateral eyes through optic tracts. Fibre tracts from the brain and suboesophageal mass join the central body.     

Nitrate assimilation in Crotalaria juncea (Linn.) pollen suspension culture

In vivo and in vitro activities of nitrate reductase were assayedin Crotalaria juncea pollen suspension cultures. This enzymewas found to be substrate-inducible and enhanced activity wasobserved when it was extracted with cysteine buffer or incubatedwith NADH (0.6 mM) at 25?C or when the germinated pollen grainswere treated with red light for 10 min. Enzymes of ammonia assimilation,glutamate dehydrogenase and glutamate synthetase, and also thepentose phosphate-shunt enzyme, glucose-6-phosphate dehydrogenase,which catalyzes the step that provides reducing power to thesystem, are described. (Received October 20, 1977; )     

Crystallization and preliminary X-ray investigation of a sarcoplasmic calcium-binding protein from amphioxus

Crystals of a sarcoplasmic Ca(2+)-binding protein from the protochordate amphioxus have been grown from solutions of ammonium sulfate. The crystals are orthorhombic, space group C222(1), with unit cell axes a = 59.6(1) A, b = 81.3(1) A and c = 82.4(1) A. There is one molecule in the asymmetric unit. The crystals diffract beyond 2.5 A and show less than 20% decline in diffraction intensities after a three day exposure to X-rays from a laboratory rotating anode source.     

Purification, crystallization and preliminary crystallographic analysis of porcine aldose reductase

Large crystals of porcine aldose reductase have been grown from polyethylene glycol solutions. The crystals are triclinic, space-group P1, with a = 81.3 A, b = 85.9 A, c = 56.6 A, alpha = 102.3 degrees, beta = 103.3 degrees and gamma = 79.0 degrees. The crystals grow within ten days to dimensions of 0.6 mm x 0.4 mm x 0.2 mm and diffract to at least 2.5 A. There are four molecules in the unit cell related by a set of three mutually perpendicular non-crystallographic 2-fold axes.     

Evidence for autophosphorylation of hyaluronate binding protein and its enhanced phosphorylation in rat histiocytoma.

This report documents for the first time the in vitro autophosphorylation of purified 68 kDa hyaluronate binding protein in presence of [32P] ATP. The rate of phosphorylation is proportional to the concentration of protein and to the time of incubation up to 5 min. By both phosphoamino acid and western blot analysis with antiphosphotyrosine antibodies, we have confirmed that the phosphorylation occurs at tyrosine residues. Immunoprecipitation with anti HA binding protein antibody shows a 5 fold increase in the phosphorylation in macrophage histiocytoma compared to normal macrophage. Supplementing hyaluronate with hyaluronate binding protein in the medium is further shown to enhance total protein phosphorylation in rat histiocytoma.     

Evidence for secretion of high molecular weight mucins by canine tracheal epithelial cells in primary culture: Effects of select secretagogues on mucin secretion

Summary The purpose of this investigation was to provide evidence for the secretion of high molecular weight mucins, CTM-A and CTM-B, in primary culture of canine tracheal epithelial (CTE) cells. The cells were isolated from tracheas of mongrel dogs by pronase treatment. Primary cultures of the epithelial cells were established using ICN cellagen inserts in Dulbecco’s modified Eagle’s/F12 medium supplemented with growth factors and could be maintained for up to 23 days. The evidence for the mucin secretion in culture medium and their localization in the cells was established by a) positive immunocytochemical staining using specific antibodies developed against purified native as well as deglycosylated CTM-A and CTM-B; b) incorporation of labeled amino acids, followed by electrophoresis and autoradiography detection of glycoconjugates purified from the culture medium; c) comparison of the amino acid compositions of mucin purified from canine tracheal pouch secretions and that purified from the culture medium; and d) Western blot analyses using specific polyclonal antibodies directed against deglycosylated CTM-A and CTM-B. Immunoaffinity purified secreted labeled glycoconjugates were resistant to hyaluronidase treatment. The effects of cyclic AMP (1 × 10⁻⁵ M), dibutyryl cyclic AMP (1 × 10⁻⁵ M), 8-bromocyclic AMP (1 × 10⁻⁵ M), and prostaglandin E₁ (1 × 10⁻⁶ M) on mucin secretion by CTE cells were also investigated. Secretion of mucins by CTE cells in culture was considerably more enhanced by 8-bromocyclic AMP than that observed for other secretagogues used in this study.     

Hereditary high-adenosine triphosphate syndrome: Study of a new variant

A new variant of hereditary hemolytic anemia in a family due to high adenosine triphosphate (ATP) is reported. The increase in ATP levels varied from 83 to 105% in the family members. Low 2,3-diphosphoglycerate levels and low 2,3-diphosphoglyceromutase activity were observed in three family members, with normal glucose-6-phosphate dehydrogenase and pyruvate kinase activity.     

Effect of long term starvation on the biochemical composition of the muscles and hepatopancreas in the crab Menippe rumphii (Fabricius) (Crustacea: Brachyura)

During the process of long term starvation both muscles and hepatopancreas are affected in their biochemical composition at different rates. During early days of starvation an increase in the muscular and hepatopancreatic glycogen is observed. At the same time a simultaneous decrease in the muscular lipid content is also observed. At a slightly later period a decrease in the hepatopancreatic lipid content is also noticed. This amount of decrease is slow in the early days of starvation and rapid in later days. Decrease in the muscular and hepatopancreatic protein content is observed when there is not an adequate quantity of hepatopancreatic lipid to be consumed.     

Diclofenac-induced stimulation of SMCT1 (SLC5A8) in a heterologous expression system: A RPE specific phenomenon

SMCT1 is a Na⁺-coupled monocarboxylate transporter expressed in a variety of tissues including kidney, thyroid, small intestine, colon, brain, and retina. We found recently that several non-steroidal anti-inflammatory drugs (NSAIDs) inhibit the activity of SMCT1. Here we evaluated the effect of diclofenac, also a NSAID, on SMCT1. SMCT1 cDNA was expressed heterologously in the human retinal pigment epithelial cell lines HRPE and ARPE-19, the human mammary epithelial cell line MCF7, and in Xenopus laevis oocytes. Transport was monitored by substrate uptake and substrate-induced currents. Na⁺-dependent uptake/current was considered as SMCT1 activity. The effect of diclofenac was evaluated for specificity, dose-response, and influence on transport kinetics. To study the specificity of the diclofenac effect, we evaluated the influence of this NSAID on the activity of several other cloned transporters in mammalian cells under identical conditions. In contrast to several NSAIDs that inhibited SMCT1, diclofenac stimulated SMCT1 when expressed in HRPE and ARPE-19 cells. The stimulation was marked, ranging from 2- to 5-fold depending on the concentration of diclofenac. The stimulation was associated with an increase in the maximal velocity of the transport system as well as with an increase in substrate affinity. The observed effect on SMCT1 was selective because the activity of several other cloned transporters, when expressed in HRPE cells and studied under identical conditions, was not affected by diclofenac. Interestingly, the stimulatory effect on SMCT1 observed in HRPE and ARPE-19 cells was not evident in MCF7 cells nor in the X. laevis expression system, indicating that SMCT1 was not the direct target for diclofenac. The RPE-specific effect suggests that the target of diclofenac that mediates the stimulatory effect is expressed in RPE cells but not in MCF7 cells or in X. laevis oocytes. Since SMCT1 is a concentrative transporter for metabolically important compounds such as pyruvate, lactate, β-hydroxybutyrate, and nicotinate, the stimulation of its activity by diclofenac in RPE cells has biological and clinical significance.