NDPase Activity Research Articles

Ultrastructure of the cells forming amyloid fibers in Alzheimer disease and scrapie

Ultrastructural, three-dimensional reconstruction of cells surrounding the amyloid star in classical plaques in Alzheimer disease (AD) and histochemical studies of the cells associated with the deposits of amyloid fibers in scrapie were carried out. These studies showed that in both diseases, the fibers appear within the smooth endoplasmic reticulum (ER) and infoldings of cytoplasmic membranes of microglia/macrophages. Additional information about the site of formation of the amyloid fibers derives from histochemical studies of the localization of nucleoside diphosphatase (NDPase) activity. In normal microglia, this enzyme is associated with smooth ER and cell membranes. In the cells that form amyloid fibers, the NDPase activity is associated with the newly formed amyloid fibers within the distended cisternae of ER and the finger-like cytoplasmic projections. In the center of the amyloid star, the NDPase activity disappears. The presence of NDPase-positive amyloid fibers in the same location, where the enzyme is found in non-amyloid-forming cells, further supports our conclusion that the microglia/macrophages are the source of amyloid deposits. These studies also show that in spite of the differences in the proteins that produce the amyloid fibers in AD and scrapie, in both diseases, the microglia/macrophages play a key role in amyloid formation.

Microglial cells in the retina of Carassius auratus: effects of optic nerve crush.

To study the morphology and distribution of the retinal microglial cells of the goldfish retina in normal conditions and after optic nerve crush, we have used the nucleoside diphosphatase (NDPase) technique, applied to whole-mounts or sections, for light and electron microscopy. In normal retinas, two populations of NDPase-positive cells were identified: compact cells associated with the retinal vessels on the vitreal surface of the retina and microglial cells in various retinal layers. The microglial cells had a bipolar or multipolar morphology. Bipolar cells were observed in the nerve fibre layer, and multipolar cells were visualised in the ganglion cell layer (GCL), inner plexiform layer (IPL), and outer plexiform layer. The highest densities of multipolar cells were observed in the IPL layer, where they adopted a regular mosaic-like arrangement in which the occasional spaces were occupied by cells of the GCL. After optic nerve crush, we observed an increase in the number of compact cells associated with the vessels and changes in NDPase activity, morphology, and distribution of the retinal microglial cells. These cells showed an increase in NDPase activity in all retinal layers from day 1 to day 15 after axotomy, and retraction of their processes from day 1 to day 7. In addition, the densities of microglial cells increased in the GCL between 2 and 15 days after axotomy, and decreased in the IPL by day 4 after axotomy. These microglial changes resemble those observed in other regenerating and nonregenerating neuronal systems and may reflect a general response of microglia directed to help the regeneration process.

Mutagenesis of two conserved tryptophan residues of the E-type ATPases: inactivation and conversion of an ecto-apyrase to an ecto-NTPase.

A human brain E-type ATPase (HB6 ecto-apyrase) was subjected to site-directed mutagenesis to assess the functional significance of two highly conserved tryptophan residues (Trp 187 and Trp 459), the only two tryptophans conserved in nearly all E-type ATPases. Mutation of tryptophan 187 to alanine yielded a poorly expressed ecto-apyrase completely devoid of nucleotidase activity. Immunolocalization of the W187A mutant in mammalian COS cells showed a cellular distribution clearly different from that of the wild-type enzyme, with the majority of the immunoreactivity concentrated in the interior of the cell. Unlike the wild-type enzyme, this mutant did not bind the nucleotide analogue Cibacron Blue and was sensitive to proteolytic digestion by chymotrypsin. These results suggest alteration of the tertiary structure, causing the enzyme to be improperly folded and retained within the cell. In contrast, mutation of tryptophan 459 to alanine resulted in an ecto-apyrase with enhanced NTPase activity, but diminished NDPase activity. Immunolocalization of this active mutant ecto-apyrase revealed a cellular pattern similar to that of the wild-type enzyme, distributed along the cell periphery and in cell processes. Coupling this active W459A mutation to a previously described mutation (D219E) resulted in an enzyme which preferentially hydrolyzes nucleoside triphosphates over diphosphates. The D219E/W459A double mutant had an ATPase:ADPase ratio of 11:1 and a UTPase:UDPase ratio of 148:1. In addition, the double mutant is substantially less sensitive to inhibition by azide, a more potent inhibitor of ecto-apyrases than ecto-ATPases. Thus, mutation of only two amino acids of an E-type ATPase essentially converts an ecto-apyrase to an ecto-NTPase.

The Golgi apparatus of the ciliated protozoon Ichthyophthirius multifiliis: A cytochemical study

Summary The trophozoites of the ciliated protozoon Ichthyophthirius multifiliis , a fish parasite, possess many small dictyosomes. Each one is associated with a modified cisterna of the endoplasmic reticulum. AcPase, TPPase and NDPase activities were located at the trans face of these dictyosomes. In the cell cortex, thick-membrane cisternae with coated dilated rims are abundant and possess AcPase, TPPase and NDPase activities. Our results suggest that the thick membrane cisternae of ciliated protozoa may be a terminal compartment of the Golgi apparatus, equivalent to the trans-Golgi network. After osmium impregnation all dictyosomal cisternae are filled with electron-dense deposits that are also found in thick-membrane cisternae and in some alveolar sacs. The presence of TPPase and NDPase activities in the alveolar sacs may be related to glycosyltransferase activities, as proved in other cells. Our new results suggest that the previous detection of AcPase activity in the alveolar sacs was an artefact.

Nucleoside diphosphatase (NDPase) activity associated with human ?-protein amyloid fibers

Nucleoside diphosphatase (NDPase) activity was studied by electron microscope cytochemistry in surgical specimens obtained from aged human cerebral cortices. The presence of NDPase activity on the surface of the microglial cells (MCs) and especially within the endoplasmic reticulum (ER) cisternae that are filled with amyloid fibers and that are in continuity with the extracellular amyloid deposits in plaques suggests a possible role of this enzyme in final elaboration of amyloid protein. The close structural relationship between MCs and amyloid plaques, suggesting the participation of these cells in the synthesis or final elaboration of amyloid fibers, was observed. The comparison of these observations with previously reported data on the distribution of NDPase in MCs and amyloid fibers in scrapie-infected mouse brain suggests that presumably similar mechanisms are acting in both cases. These observations, as compared with the results of other cytochemical and biochemical studies, also suggest that co-localization of NDPase activity with newly formed amyloid fibers in plaques can be associated with glycosyltransferase activities engaged in the amyloid or amyloid precursor protein glycosylation.

Microglial cell responses in the rabbit retina following transection of the optic nerve

The response of retinal microglial cells, which accompanies retrograde degeneration of ganglion cell axons and perikarya (induced by transection of the optic nerve), was studied in whole-mounted rabbit retinae labeled enzyme-histochemically for nucleoside diphosphatase (NDPase), which is a microglial cell marker. A few days after transection, the number of microglial cells/mm2, as well as their staining intensity, began to increase in the inner plexiform layer. The mosaic-like distribution of the star-shaped microglial cells present in the inner plexiform layer of a normal rabbit retina was preserved during ganglion cell degeneration. As in the normal retina, processes of individual cells never overlapped with those of neighboring cells in the inner plexiform layer because individual cells in the "degenerating" retina acquired shorter processes, i.e., the cells occupied a smaller territory compared to the normal retina. In the nerve fiber layer the number and staining intensity of NDPase-labeled microglial cell processes (most of which are aligned in parallel with degenerating ganglion cell axons) transiently increased and returned to normal values by 5 months post-transection. Microglial cells that are not detectably NDPase labeled in the outer plexiform layer of a normal rabbit retina acquire intense staining a few days after the nerve is cut. The functional significance of the increased NDPase activity in the plasma membrane of microglial cells during degeneration remains to be determined.

Ultrastructural localization of phosphatase activity in the guinea pig pineal gland by the cerium technique.

Thiamine pyrophosphatase (TPPase), nucleoside diphosphatase (NDPase), and glucose-6-phosphatase (G-6-Pase) were localized by the cerium technique in guinea pig pinealocytes and compared with the corresponding lead technique. NDPase and TPPase were also compared at different pH values using the cerium technique. Vibratome sections of perfusion-fixed tissue were incubated with cerium chloride or lead nitrate. Substrates used were thiamine pyrophosphate (for TPPase), sodium inosine diphosphate (NDPase), and disodium glucose-6-phosphate (G-6-Pase). The 1-2 trans saccules of the Golgi apparatus showed TPPase and NDPase activity but none for G-6-Pase. The endoplasmic reticulum (ER) cisternae and perinuclear space had NDPase and G-6-Pase activity but not TPPase. The abluminal plasmalemma of endothelial cells and the plasmalemma of Schwann cells demonstrated TPPase and NDPase activity but the luminal plasmalemma of the endothelial cells and the plasmalemma of pinealocyte processes showed only NDPase activity. TPPase was active at all pH values tested, but NDPase was most active at pH values of 6.5 and 7.0. Lead phosphate precipitate was frequently seen in nuclei, perinuclear space, ER cisternae, and "synaptic" vesicles when lead was used as the capturing agent. These sites were usually not labeled when cerium was used.

The endomembrane system of cholinergic and non-cholinergic neurons in the medial septal nucleus and vertical limb of the diagonal band of Broca: a cytochemical and immunocytochemical study.

Coronal vibratome sections of the rostral part of the medial septum (MS) and vertical limb of the diagonal band of Broca (VDB) nuclei were studied by an immunocytochemical technique using a monoclonal antibody against choline acetyltransferase (ChAT) and a double histochemical method for detection of acid phosphatase (AcPase) and nucleoside diphosphatase (NDPase) activity. The electron microscopic morphology of ChAT-immunoreactive and non-immunoreactive neurons was compared with similar neurons showing both AcPase and NDPase activity. ChAT-labeled and non-labeled neurons were well differentiated by the organization of the endomembrane system and especially by the structure of the rough endoplasmic reticulum (RER) and associated lamellar bodies. These results support the theory that the peculiar ultrastructure of the lamellar bodies in each neuron is related to the pattern of organization of the endomembrane system and its function. The significance of the lamellar bodies is discussed, and the data of the present work, together with findings described by other investigators. These data suggest that these bodies are predominant in efferent projection neurons in the basal forebrain nuclei.

Histochemical studies of the differentiation of microglial cells in the cerebral hemispheres of chick embryos and chicks.

Using histochemical procedures to reveal the presence of nucleoside diphosphatase (NDPase), thiamine pyrophosphatase (TPPase) and acid phosphatase (AcPase), we investigated the appearance, distribution and ultrastructure of amoeboid and microglial cells in the cerebral hemispheres of chick embryos and young chicks, in order to elucidate the relationship between these two cell populations. On day 6 of incubation, a few round cells exhibiting NDPase, TPPase and AcPase activity were first detected in the thin mantle layer of the cerebral hemisphere. In the corpus striatum, these round cells increased rapidly in abundance until day 13 of incubation, after which their numbers gradually decreased, so that, on day 19 of incubation, they had entirely disappeared. Between day 10 and day 17 or 18 of incubation, round cells were located mainly in the zone of the mantle layer closest to the lumen. On day 10 of incubation, NDPase-, TPPase- and AcPase-positive cells that had a few short cytoplasmic processes (poorly ramified cells) were detected in the intermediate and basal zones of mantle layer. They increased in abundance until day 17 or 18 of incubation and thereafter rapidly decreased in number. Round and poorly ramified cells exhibited NDPase activity on their plasma membranes and in their cytoplasmic vacuoles, with TPPase and AcPase activity being localized within their vacuoles. On day 19 of incubation, NDPase- and TPPase-positive cells with long, well-ramified cytoplasmic processes (well-ramified cells) were observed in the corpus striatum, these being mainly localized in the basal zone. After hatching, these cells increased rapidly in abundance and were distributed throughout the corpus striatum.(ABSTRACT TRUNCATED AT 250 WORDS)

Cytochemical staining of the endoplasmic reticulum and glycogen in mouse anterior pituitary cells.

The endoplasmic reticulum (ER) and glycogen in secretory cells of anterior pituitary glands from control and fasted mice were investigated ultrastructurally using cytochemical staining techniques. Potential enzyme cytochemical markers for the ER included glucose-6-phosphatase (G6Pase) and nucleoside diphosphatase (NDPase) activities. Presumptive glycogen particles were identified in tissue postfixed in 1% osmium tetroxide-1.5% potassium ferrocyanide or in ultrathin sections poststained with periodic acid-thiocarbohydrazide-silver proteinate. The ER appeared to be related structurally and cytochemically to the nuclear envelope and cis Golgi saccules. Similar relationships between the ER and the trans Golgi saccules or GERL were not observed. In anterior pituitary glands from control mice, G6Pase activity was prominent within the lumen of the ER, nuclear envelope, and cis Golgi saccules of all cells; reaction product was absent in the trans Golgi saccules and in GERL. G6Pase activity was sparse to non-existent in anterior pituitary cells from fasted mice. The cytochemical reaction utilizing the Gomori lead capture method indicated that G6Pase in anterior pituitary cells may function as a phosphohydrolase for converting glucose-6-phosphate to glucose. Cytochemical localization of NDPase activity was not evident in the ER; reaction product was localized consistently in one or two trans Golgi saccules and occasionally in GERL and nascent secretory granules. Presumptive glycogen particles in each of the different secretory cell types from control mice appeared as 20-30 nm wide, electron-dense particles scattered as single entities throughout the cytoplasm. Anterior pituitary glands from fasted mice exhibited conspicuous and numerous clumps of glycogen particles in addition to scattered particles in all cell types except corticotrophs, which appeared to be devoid of glycogen. Glycogen particles were absent in anterior pituitary cells incubated in a medium containing diastase. Our results suggest that in anterior pituitary cells of the mouse: 1) the phosphohydrolytic activity of G6Pase is a reliable cytochemical marker for the ER; 2) the ER is associated morphologically and cytochemically with the cis face but not with the trans face of the Golgi apparatus or with GERL; 3) some glucose-6-phosphate, a possible substrate for G6Pase in vivo, may be derived indirectly from glycogen stores; and 4) modulations in G6Pase activity and glycogen storage during fasting may reflect an alteration in energy metabolism.

Sur l'expression ultrastructurale de la differenciation des cellules vegetales.

The author has studied, at an ultrastructural level, the effects of differentiation in a number of cell types: female gametophyte cells in Gingko biloba, leaf gland cells in Hygrophila difformis, root tip, digestive gland cells in Drosera, stipular secretory trichomes in Psychotria bacteriophila, and vegetative cells in pollen grains from Angiosperms.Differentiation can be reversible (root tip statocytes and digestive gland cells in Drosera) or irreversible. It can manifest itself as a specialisation of some type of organelle, as an overall cellular organisation (statocytes) or as some special function (vegetative cell in pollen grains).The form taken by a given type of specialisation depends on cell type. Thus in mucilage-forming cells, differentiation can be reversible (Drosera cells) or irreversible (mucilage-forming root tip cells and trichomes in Psychotria). The dictyosomes produce large vesicles (root tip and digestive gland cell) or smaller entities (trichomes in Psychotria). But in all cases, the dictyosomes play the most important role in secretion and in all types of mucilage-forming cells these organelles show pronounce NDP-ase activity on their forming faces.

Morphological studies on neuroglia. VI. Postnatal development of microglial cells.

The postnatal development of microglial cells was investigated in the neonatal rat brain by use of light- and electron microscopy, including enzyme-histochemical techniques. Microglial cells were selectively stained by demonstration of their nucleoside diphosphatase (NDPase) activity and classified into three types: 1) In the early postnatal period "primitive microglial cells" showing scantily ramified processes were found in the cerebral cortex, the hippocampal formation, and the hypothalamus. During the course of the first postnatal week the processes of this cell type developed gradually and the cells were transformed into typical ramified microglial cells, called "resting microglial cells". 2) "Amoeboid microglial cells "showing typical features of macrophages were characteristic of the cerebral white matter. 3) "Round microglial cells" possessing a round soma and few pseudopodia but no characteristic processes occurred in large numbers in the subventricular zone of the lateral ventricle and as single elements in the vicinity of blood vessels. Histochemically, thiamine pyrophosphatase (TPPase) was demonstrated only in the fully developed, ramified microglial cells ("resting microglial cells"), which could be readily observed in the central nervous tissue from the age of 14 day. "Round and amoeboid microglial cells" did not show TPPase activity and disappeared after 14 days of postnatal life. By use of electron microscopy, in neonatal rats NDPase activity was apparent in the plasma membrane of the three types of microglial cells ("primitive, round, and amoeboid" types). They showed basically similar submicroscopic characteristics, i.e., well-developed Golgi apparatus, long strands of rough-surfaced endoplasmic reticulum, single dense bodies and vacuoles, and numerous ribosomes. "Amoeboid microglial cells" were characterized by their well-developed cytoplasmic vacuoles and phagocytic inclusion bodies. The present study strongly suggests a mesodermal origin for these microglial elements.

Morphological studies on neuroglia. V. Microglial cells in the cerebral cortex of the rat, with special reference to their possible involvement in synaptic function.

Electron-microscopic survey of selectively stained microglial cells in the cerebral cortex of the rat reveals that the processes of this cell type often encircle axo-dendritic synapses. Enzyme-histochemical methods for thiamine pyrophosphatase (TPPase) or nucleoside diphosphatase (NDPase) were used for the selective marking of the microglial cells; TPPase and NDPase activities were observed in the plasma membrane of microglial cells. The synapses encircled by microglial processes displayed presynaptic structures containing round clear vesicles (50 nm in diameter) and a prominent thickening of the postsynaptic membrane. In vitro, the above-mentioned enzymatic activities were completely suppressed by neuroactive agents such as catecholamines and phenothiazine derivatives. Examination using enzyme-histochemical techniques suggests that a single enzyme may be responsible for both microglial cells in the normal central nervous tissue is discussed.

Schistosoma mansoni: Cytochemistry and morphology of the gastrodermal Golgi apparatus

The gastrodermal Golgi apparatus of adult Schistosoma mansoni displays two distinct morphologies. In one type, there is an identifiable cis (forming) face where vesicles from the endoplasmic reticulum fuse to form the cisternae. A morphological change occurs in the cisternae as the trans (emitting) face is approached with the cisternae becoming progressively flattened. The cisternae at the emitting face produce a membrane-bound secretory granule with moderately electron-dense contents and a vacuolar structure that may be analogous to a condensing vacuole as reported in several vertebrate secretory cells. In a second type, vesicles possessing a thicker membrane than those of the transfer vesicles are observed at the emitting face. They are not observed when the secretory granules are present. Several cytochemical markers were used to aid in studying the polarity of the Golgi apparatus. Enzymes studied were thiamine pyrophosphatase (TPPase) (EC 3.6.1.1), nucleoside diphosphatase (NDPase) (EC 3.6.1.6) using uridine diphosphate as a substrate, and nicotinamide adenine dinucleotide phosphatase (NADPase) (EC 3.1.3.2). Reaction products from all enzyme markers were observed in the cisternae and, to some extent, in the transfer vesicles. At times, NADPase and TPPase reaction products were observed in all cisternae and in the transfer vesicles of the Golgi. When this distribution was evident, the latter vesicles were observed in clusters occasionally fusing with lipid-like globules dispersed throughout the gastrodermis. Heterogeneity in cisternae was observed when NDPase, TPPase, and osmium reduction techniques were used. NDPase activity was limited to the middle cisternae while reduced osmium was observed in the outer two cisternae and in some transfer vesicles. TPPase reaction product was also observed in the secretory granules and in the condensing vacuoles. It is hypothesized that a functional bipolarity may be demonstrated by the Golgi. Under certain stress conditions, the forming face of the Golgi may package lysosomal enzymes while the emitting region of the Golgi appears to be responsible for the packaging of the secretory granules. The fusion of transfer vesicles and, at times, secretory granules with lipid-like globules is postulated to represent a mechanism by which enzymes may be transported to the lumen of the cecum.

Enzyme histochemistry of ventricular choroid plexus (Part V). Localization of nucleoside diphosphatase and 5'--nucleotidase activities

Localization of nucleoside diphosphatase (NDPase) and 5'-nucleotidase (5'-Nase) activity in rat choroid plexus epithelial cells was studied electron microscopically. NDPase activity was observed only in the cytoplasm on the Golgi cisternae of the epithelial cells, and was positive on the pericyte and endothelial cells. 5'-Nase activity was found on the lysosomes and along the basal plasmalemma or basal infoldings of the epithelial cells. The reaction products were also found on the pericytes. The role of these enzymes in the choroid plexus was briefly discussed.

Properties of nucleosides diphosphatases in purified membrane fractions from maize coleoptiles. I. Study of latency

Evidence is given for the presence of nucleoside diphosphatase (NDPase) activities in two membrane fractions from maize coleoptiles, one enriched in endoplasmic reticulum (ER) and the other in plasma membranes (PM). The NDPase activity associated with the ER-rich fraction appears only after treatment of membranes with detergent. Enzyme inactivation experiments using trypsin were performed on intact and Triton X-100-treated vesicles. They suggest that in the endoplasmic reticulum-rich fraction, most of enzymatic sites have a lumenal location and that in plasma membrane vesicles, only 40–50% of enzymatic sites are not freely accessible to nucleosides diphosphate.

Histochemical characteristics of diphosphate nucleoside consumption in, cat and rat nervous system

Consumption of diphosphate nucleosides is investigated by histochemical methods in rat and cat nervous system. Results show NDP-ase is effectively in histological sections from animals previously perfused with glutaraldehyde or formaldehyde. Histochemical reaction is increased in presence of Ca++, Mg++, Mn++ or imidazole and inhibited by L-DOPA and Noradrenaline in incubation medium. A comparative study of TPP-ase and NDP-ase activities to dilucidate the identity of both enzymes is described.

Cytochemical localization of nucleoside diphosphatase and thiamine pyrophosphatase activities in the rabbit corneal endothelium

Localization of NDPase and TPPase activities in the rabbit corneal endothelium was investigated by cytochemical methods. After incubation at both pH 7.0 and 8.0, the NDPase activity was detected in cisternae of ER, nuclear envelope, and Golgi saccules, while the TPPase activity was demonstrated only in Golgi saccules. The reaction products of both enzymes were decreased when incubated at pH 8.0. The NDPase activity was inhibited by uranyl nitrate but not by sodium fluoride, while the TPPase was inhibited by fluoride but not by uranium.

Localization of nucleoside diphosphatase in the onion root tip.

Nucleoside diphosphatase activity occurs in the Golgi apparatus, on the plasmalemma, between the plasmalemma and the definitive cell wall, and in the endoplasmic reticulum of the onion root tip. The presence and/or relative concentrations of reaction product at each of these cellular sites occur in distinctive developmental patterns within the root. Cells with high NDPase activity at any combination of these sites also produce large amounts of a polysaccharide-rich product. A vacuolar activity also occurs in the pericycle and cortex in a developmentally distinctive pattern, but its location has not been correlated to polysaccharide secretory activity.

Localization of phosphatase activities in the rat anterior pituitary gland.

All five known secretory cell types of the rat anterior pituitary gland display nucleoside diphosphatase (NDPase) activity throughout the endoplasmic reticulum (ER), including the nuclear envelope but not the specialized region of ER at the inner aspect of the Golgi apparatus known as GERL. The functions of the ER diphosphatase are currently unknown. However, speculations concerning its association with glucuronyl transferase may focus on the metabolic roles of the ER in pituitary cells other than those directly related to secretory protein transport. The gonadotrophs have been studied for thiamine pyrophosphatase and acid phosphatase activities as well as NDPase activity. The results suggest that the secretory granules of gonadotrophs arise from GERL and not from the inner element of the Golgi apparatus. The innermost Golgi element of this cell type shows NDPase and thiamine pyrophosphatase activities and appears to be composed, in part at least, of anastomosing tubules. Nucleoside phosphatase activity is also present at the surfaces of all five secretory cell types and between the cells and adjacent blood capillaries.