L'Organisation Ultrastructurale Corticale de la Gregarine Lecudina pellucida; ses Rapports avec l'Alimentation et la Locomotion

SYNOPSIS. The structure of the cortical region (epicyte and ectoplasm) of the gregarine Lecudina pellucida , an intestinal parasite of the polychete worm Perinereis cultrifera was studied by electron microscopy.
The epicitary folds have 3 unit type membranes. Between the 1st and 2nd is a layer probably composed of fine longitudinal fibrils which has an arch-like or gutter-like structure at the crest of the folds. Inside these folds is cytoplasm without any noticeable differentiation or inclusion except for a granular (or finely fibrillar) layer under the limiting inner membrane and close to it.
The ectoplasmic zone of the entocyte is separated from the epicitary region by a lengthwise discontinuous cylindrical opaque layer, inwardly tangential to the folds. The ectoplasm lacks paraglycogen granules but has various organelles: apparently pinocytic vesicles against the wall between the folds, vesicles with myelinic membranes, opaque granules, a few mitochondria with blistered internal vesicles, and a few circular tubular fibers.
The superficial zone of the gregarine is supposed to contribute to nutrition, thru the extensive surface furnished by its folds and thru the pinocytic vesicles; but this alimentary intake is incomplete compared with that of the previously studied anterior region.
Insufficient mucus is discharged to account for locomotion. There are some circular ectoplasmic fibers, but locomotory myonemes are completely absent. However, there are deformations of the folds and corresponding waves that could account for locomotion by creeping or swimming. These movements of the folds might be due to the action of the contractile proteins and correspond with some of the layers seen in the wall.     

Sphinctocystis phyllodoces gen. n., sp. n. (Eugregarinida: Lecudinidae)--a new gregarine from Phyllodoce citrina (Polychaeta: Phyllodocidae)

A new species of aseptate gregarine, Sphinctocystis phyllodoces gen. n., sp. n., from the gut of a polychaete Phyllodoce citrina Malmgren, 1865 from White Sea is described. The electron and light microscopic data on trophozoits are presented. Taxonomy of the described species is discussed. Certain ultrastructural characters are included in generic and specific diagnoses. Order Eugregarinida Leger, 1900; suborder Aseptata Chakravarty, 1960; family Lecudinidae Kamm, 1922. GENUS: Sphinctocystis gen. n. TYPE SPECIES: Sphinctocystis phyllodoces sp. n. DIAGNOSIS: Characters of the family. Free trophozoits elongated, often with several annular constrictions. Anterior end asymmetric, without hooks, not separated from the body, with small apical papilla encircled by smooth area. Epicyte "classical", without additional axial formations at the tops of folds; epicytic folds high, monomorphic in cross sections, finger-shaped, with parallel sidewalls. In the gut of polychaetes. DIFFERENTIAL DIAGNOSIS: The new genus differs from Lecudina by having asymmetric anterior end, developed smooth area around the apical papilla, and monomorphic epicytic folds looking finger-shaped in cross sections. It also differs from Lankesteria by the absence of additional axial formations at the tops of the epicytic folds. It differs from both named genera by presence of annular constrictions on the trophozoit body. Sphinctocystis phyllodoces sp. n. DIAGNOSIS: Characters of the genus. Free trophozoits elongated, large, up to 617 x x 77 um. The average height of epicytic folds 976 nm, thickness 194 nm; there are 6-8 apical filaments and rippled dense structures per fold. Nucleus spherical (ellipsoid after fixation), 24-52 microm along longest axis, localised in anterior third of the body, carries several karyosomes of various size; 25-30 nm thick fibrils (possible fragments of nucleolonema) may be present in karyolymph. Other stages unknown. TYPE SERIES: Microscope preparation with 7 trophozoits, Karacci's haematoxylin stained, is kept in the Zoological museum of the Moscow State University (collection number: Z-1). TYPE HOST: Phyllodoce citrina Malmgren, 1865 (Polychaeta: Phyllodocidae). LOCALISATION: Mid-gut. TYPE LOCALITY: White Sea Biological Station of the Moscow State University, Yeremeyevsky Rapid, Velikaya Salma Strait, Kandalaksha Bay, White Sea.     

The Fine Structure of Rhynchocystis pilosa (Sporozoa, Eugregarinida)

SYNOPSIS. The trophozoite of Rhynchocystis pilosa obtained from the seminal vesicles of the earthworm Lumbricus terrestris was studied by light and electron microscopy. The trophozoite's cortical organization is particularly interesting because of its unusual evaginations and associated fibrillar structures. The pellicle is formed by 2 concentric membranes elevated into 60–70 alternating primary and secondary ridges extending posteriad. Numerous long ‘hairs’ or cytopilia originate along the primary ridges and each contains a system of fibrils originating from an underlying longitudinal myoneme. Longitudinal rows of pores lie between adjacent pollicular ridges. Three systems of fibrils lie in the cortex of the trophozoite. A longitudinal myoneme consisting of 12–18 fibrils lies below each primary pellicular ridge. Circular myonemes lie below the pellicle in a parallel array along the length of the organism. Each myoneme consists of 4–8 fibrils structurally similar to those of the longitudinal myonemes. Pairs of fine filaments also lie in the inner pellicular membrane along the apex of each ridge. The trophozoite's anterior end is modified as an attachment organelle consisting of 30–35 delicate pellicular folds which originate at the base of an anterior papilla. The folds extend approximately 15 μ posteriad where they become continuous with the primary pellicular ridges. The nucleus lies in the cytoplasm near the posterior level of the attachment organelle and is surrounded by a double membrane perforated by numerous pores. The cytoplasm contains numerous small vesicles which may be found in dense aggregations. These aggregations often occur in proximity to Golgi complexes and certain membrane-bound bodies. Mitochondria are abundant in the cytoplasm as are large, ovoid paraglycogen bodies. Occasionally layers of granular membranes are arranged parallel to the surface of the paraglycogen bodies but also occur thruout the cytoplasm.     

Chronology of the ultrastructural modifications during the growth of Gregarina blaberae]

In an ultrastructural study the development of the sporozoite as well as the growth and development of the trophozoite of Gregarina blaberae were followed in the course of experimental infections of larvae of the cokroach Blaberus craniifer. The spectacular growth involved the transformation within 18 days of the sporozoite, measuring 15 X 1 micronm, to a cephaline--trophozoite affixed to the intestinal epithelium--of 250 micronm length and 65 micronm diameter. The sporozoite's ultrastructure is not different from that of sporozoites of other Sporozoa studies to date--the conoid and dense bodies are present. The pellicle consists of 3 membranes, but there are some interruptions in the internal membrane complex. The first dictyosomes are formed from the nuclear envelope. The migration of the nucleus and of the dense bodies, followed by the regression of all the structures characteristic of the sporozoites, and the establishment of a cortical zone that comes to cover the epimerite, take place within 48 h after infection and mark the transformation of the sporozoite into the trophozoite. Development of the cephaline involves the formation of the epicytic folds, which occurs at the base of the deutomerite, starting on the 3rd day of development. A regular system of longitudinal or epicytic folds is formed over the entire surface of the gregarine. On the 4th and 5th days of development, a vacuolar system and a chondriome become differentiated in the epimerite, while a fibrillar septum separates the protomerite from the deutomerite. The next stage, starting on the 6th day, is characterized by distribution of polysaccharide reserves between these 2 segments. The model studied allows us to determine the role of the epimerite in the parasite's nutrition, as well as the development of the chondriome and of the cortical membranes in the course of the vegetative growth phase of the cephaline gregarine.     

The fine structure of the cortical zone in the gregarine Bothriopsides histrio (Eugregarinida: Actinocephalidae)

Attached and non-attached trophozoites of the septate gregarine Bothriopsides histrio were found in the intestine of the freshwater beetle Acilius sulcatus. Circular folds in the border between proto- and deutomerites and longitudinal striation, running along the entire body of the parasite, were revealed in an optical microscope. Our studies have demonstrated that circular folds, forming a specific collar, are formed of ecto- and endocytes. The longitudinal striation is represented by overdeveloped folds developed by the epicyte and the ectocite. Numerous typical epicite folds were observed over the entire cell surface. Additionally, the symbiosis between gregarine cells and bacteria was revealed.     

Ultrastructure of the cyst wall of sarcocysts of the roe deer (Capreolus capreolus L.) (author's transl)]

The ultrastructure of the cyst wall of two types of sarcocysts from roe deer is described. In the thin-walled cyst (wall thickness 0.18-00.26 micrometer), the primary cyst wall forms long, finger-shaped protrusions distant from one another and running in parallel with the surface of the cyst (Figs. 1a--d, FP). No fibrils are observable in the protrusions. The primary cyst wall between them forms numerous bubble-like invaginations (Fig. 1c, arrows). In the thick-walled cysts (wall thickness 4.9--7.49 micrometer), the primary cyst wall forms massive, palisade-like protrusions lying close one to another (Figs. 2a, c). There are numerous fibrillar and tubular structures in these protrusions (Fig. 2d), and the primary cyst wall occasionally forms shallow invaginations at the base of some protrusions (Fig. 2b). The unit membrane onthe surface of some protrusions is slightly undulated and covered with a layer of short and thick bars on the outside. The sarcocysts found in roe deer are compared with those from cattle and sheep.     

Cytochemical Nature and Fine Structure of the Gregarine Zeylanocystis burti Dissanaike, with Special Reference to Microfilaments, Microtubules and Movement

SYNOPSIS. The mature trophozoite of the acephaline gregarine Zeylanocystis burti Dissanaike, parasitic in the seminal vesicles of the Sri Lankan earthworm Pheretima peguana Rosa, was studied by cytochemical methods and by electron microscopy. Some observations were also made on gametocysts and oocysts. The trophozoite has a peculiar saucer shape, unlike other monocystid gregarines, and has marginal papillae with cytoplasmic hairs. Its fine structure conforms broadly to that of other gregarines, but differs with respect to its fibrillar organization and in some details of cytoplasmic organelle structure. The pellicle is composed of 2 parallel unit membranes elevated into a number of stumpy epicytary folds, more or less evenly distributed on both surfaces of the gregarine. Some of these are associated with adjacent accessory cells and may have a nutritive role. Bundles of fine microfilaments (5–6 nm) were detected both in the ectoplasm and deep in the endoplasm; these are possibly the main contractile elements (“myonemes”) involved in movement. Microtubules are larger (22–24 nm) and are found predominantly in papillae and cytoplasmic hairs, but extend also in small bundles beneath the pellicle—they appear to be more skeletal in nature. The significance of these findings is discussed in the light of recent work on the roles of microfilaments and microtubules in nonmuscle cells. Mitochondria are located superficially and have a complex organization. The endoplasmic reticulum is poorly developed, but ribosomes are abundant. Golgi lamellae-like membranes and vesicles akin to lysosomes were observed. Typical paraglycogen granules were found together with blobs of lipid and glycogen. The nucleus had a wrinkled envelope, a homogeneous matrix, and a spherical nucleolus. A variety of staining reactions and cytochemical tests were carried out. The distribution of lipids, polysaccharides, nucleic acids, calcium, and melanin were studied. Succinate dehydrogenase was detected in mitochondria, thiamine pyrophosphatase in Golgi bodies, and acid phosphatase in lysosomes. Golgi structures were found to be chemically very complex. Gametocysts and oocysts were associated with extraneous cells which probably contribute to the formation of their walls. The gametocyst wall is thin and consists of 2 membranes of the unit type. The oocyst wall is thicker and composed of 2 chemically different layers. Telolysosomes were seen in the disorganized residual cytoplasm within gametocysts.     

Scanning Electron Microscopy of Gregarines (Protozoa, Sporozoa) and Its Contribution to the Theory of Gregarine Movement

SYNOPSIS. Scanning electron microscopy was used to reveal detailed surface structure of 4 septate ( Gregarina cuneata, G. steini, G. rhyparobiae, Pileocephalus blaberae ) and one aseptate species ( Nematocystis elmassiani ) of eugregarines. The epicyte of all these gregarines is differentiated into a system of regular longitudinal folds. In the septate species these folds undulate so that these organisms glide along. The undulatory pattern is absent from Nematocystis , which does not glide. The theories and the mechanism of gregarine gliding are discussed.     

Chronologie des Modifications Ultrastructurales au Cours de la Croissance de Gregarina blaberae*

SYNOPSIS. In an ultrastructural study the development of the sporozoite as well as the growth and development of the trophozoite of Gregarina blaberae were followed in the course of experimental infections of larvae of the cockroach Blaberus craniifer. The spectacular growth involved the transformation within 18 days of the sporozoite, measuring 15 × 1 μm, to a cephaline—trophozoite affixed to the intestinal epithelium—of 250 μm length and 65 μm diameter. The sporozoite's ultrastructure is not different from that of sporozoites of other Sporozoa studied to date—the conoid and dense bodies are present. The pellicle consists of 3 membranes, but there are some interruptions in the internal membrane complex. The first dictyosomes are formed from the nuclear envelope. The migration of the nucleus and of the dense bodies, followed by the regression of all the structures characteristic of the sporozoites, and the establishment of a cortical zone that comes to cover the epimerite, take place within 48 hr after infection and mark the transformation of the sporozoite into the trophozoite. Development of the cephaline involves the formation of the epicytic folds, which occurs at the base of the deutomerite, starting on the 3rd day of development. A regular system of longitudinal or epicytic folds is formed over the entire surface of the gregarine. On the 4th and 5th days of development, a vacuolar system and a chondriome become differentiated in the epimerite, while a fibrillar septum separates the protomerite from the deutomerite. The next stage, starting on the 6th day, is characterized by distribution of polysaccharide reserves between these 2 segments. The model studied allows us to determine the role of the epimerite in the parasite's nutrition, as well as the development of the chondriome and of the cortical membranes in the course of the vegetative growth phase of the cephaline gregarine.     

Ameloblastic secretion and calcification of the enamel layer in shark teeth

Tooth primordia at early stages of mineralization in the sharks Negaprion brevirostris and Triaenodon obesus were examined electron microscopically for evidence of ameloblastic secretion and its relation to calcification of the enamel (enameloid) layer. Ameloblasts are polarized with most of the mitochondria and all of the Golgi dictyosomes localized in the infranuclear end of the cell toward the squamous outer cells of the enamel organ. Endoplasmic reticular membranes and ribosomes are also abundant in this region. Ameloblastic vesicles bud from the Golgi membranes and evidently move through perinuclear and supranuclear zones to accumulate at the apical end of the cell. The vesicles secrete their contents through the apical cell membrane in merocrine fashion and appear to contribute precursor material both for the basal lamina and the enameline matrix. The enamel layer consists of four zones: a juxta-laminar zone containing newly polymerized mineralizing fibrils (tubules); a pre-enamel zone of assembly of matrix constituents; palisadal zones of mineralizing fibrils (tubules); and interpalisadal zones containing granular amorphous matrix, fine unit fibrils, and giant cross-banded fibers with a periodicity of 17.9 nm. It seems probable that amorphous, non-mineralizing fibrillar and mineralizing fibrillar constituents of the matrix are all products of ameloblastic secretion. Odontoblastic processes are tightly embedded in the matrix of the palisadal zones and do not appear to be secretory at the stages investigated. The shark tooth enamel layer is considered homologous with that of other vertebrates with respect to origin of its mineralizing fibrils from the innerental epithelium. The term enameloid is appropriate to connote the histological distinction that the enamel layer contains odontoblastic processes but should not signify that shark tooth enamel is a modified type of dentine. How amelogenins and/or enamelins secreted by amelo- blasts in the shark and other vertebrates are related to nucleation and growth of enamel crystallites is still not known.     

A Study of the Structure and Gliding Movement of Gregarina garnhami

SYNOPSIS The structure and gliding movement of Gregarina garnhami Canning, a eugregarine found in the midgut of the desert locust, Schistocerca gregaria , have been studied by light microscopy and transmission and scanning electron microscopy (EM). Ultrastructural studies revealed that the cytoplasm of G. garnhami is separated from the epicyte folds by a basal lamina. The pellicle consists of 3 membrane layers. At the tips of the epicyte folds there are 2 sets of longitudinally oriented filaments. An ectoplasmic network is present in the ectoplasm and the endoplasm contains numerous paraglycogen granules. The effect of cytochalasin B on G. garnhami was studied. Examination of scanning EM preparations of gliding and stationary gregarines yielded inconclusive results. In some instances the epicyte folds were thrown into waves; in others the folds were straight, regardless of treatment before fixation. Gregarina garnhami glides through its environment without any apparent deformation in shape. As it moves, a mucus trail is left behind it. Phase-contrast observations were made of centrifuged gregarines in which the endoplasm was displaced. Centrifuged gregarines continued to glide. Displacement of the endoplasm allows visualization of the epicyte folds in gliding animals. No lateral waves were seen in the epicyte folds of gliding centrifuged animals.     

Actin and myosin in Gregarina polymorpha

Actin and two class XIV unconventional myosins have been cloned from Gregarina polymorpha, a large protozoan parasite inhabiting the gut of the mealworm Tenebrio molitor. These proteins were most similar to their homologues expressed in the coccidian and haemosporidian Apicomplexa such as Toxoplasma and Plasmodium despite the significant morphological differences among these parasites. Both actin and G. polymorpha myosin A (GpMyoA), a 92.6-kDa protein characterized by a canonical myosin head domain and short, highly basic tail, localized to both the longitudinally-disposed surface membrane folds (epicytic folds) of the parasite as well as to the subjacent rib-like myonemes that gird the parasite cortex. G. polymorpha myosin B (GpMyoB), a 96.3-kDa myosin, localized exclusively to the epicytic folds of the parasite. Both myosins were tightly associated with the cortical cytoskeleton and were solubilized only with a combination of high salt and detergent. Both GpMyoA and GpMyoB could bind to actin in an ATP-sensitive fashion. The distribution of actin and the unconventional myosins in G. polymorpha was consistent with their proposed participation in both the rapid (1-10 microm/sec) gliding motility exhibited by the gregarines as well as the myoneme-mediated bending motions that have been observed in these parasites.     

Fine structure of trophozoites of the gregarine Leidyana ephestiae (Apicomplexa: Eugregarinida) parasitic in Ephestia kuehniella larvae (Lepidoptera)

The ultrastructure of the eugregarine Leidyana ephestiae, parasitic in the larval gut of the flour moth, Ephestia kuehniella, is described. Guts of experimentally infected larvae of E. kuehniella were fixed and sectioned for electron microscope studies of young and mature trophozoites. Young unsegmented trophozoites were small, oval to ovoid, and possessed a simple, globular epimerite. The plasma membrane covering the epimerite region was continuous with the plasma membrane of the protodeutomerite and was in close contact with that of the host cell. Three cortical membranes covered the protodeutomerite region. Folding of the protodeutomeritic epicyte occurred after about 2 days of development of the gregarine. After 3–4 days the body of the trophozoite became differentiated into three segments. A septum was visible between protomerite and deutomerite, but there was nothing similar to this structure between epimerite and protomerite. Fully developed trophozoites showed a large ovoid epimerite containing many mitochondria and vesicles. The epimerite was situated on a short neck filled with fibrils. The cytoplasm of protomerite and deutomerite was rich in amylopectin granules and electron-dense bodies.     

水稻胚乳细胞质膜内陷的超微结构和磷酸酶的细胞化学定位

对生长分化期水稻胚乳细胞的质膜内陷进行了超微结构和磷酸酶的细胞化学研究。结果表明 ,胚乳细胞内的小泡、内质网常与胞间连丝相连 ;质膜形态多变 ,功能活跃 ,由局部起伏的波纹状发展成明显内陷 ,深浅不一 ,多呈袋状 ,袋中包含着大小不一的泡状物 ;有些内陷脱离质膜成为胞质中的囊泡 ,表现出活跃的内吞现象。除细胞间隙中含有圆球状的内含物外 ,在质膜内陷和囊泡中常含有大量的内含物。H ATP酶定位结果显示 ,质膜及其邻近的泡状物周围有酶的分布 ;而酸性磷酸酶定位在液泡、胞间隙和其中的泡状内含物周围 ;在质膜及其内陷形成的囊泡中有G6P酶的分布。这些结果表明胞间隙和质膜内陷在物质的运输中可能起着重要作用     

Localization of calcium and phosphorus in early predentin-matrix components by electron spectroscopic imaging (ESI)-analysis in rat molars

Summary The subcellular distribution of the inorganic elements calcium (Ca) and phosphorus (P) was studied in the first-formed dentin matrix during initial mineralization in neonatal rat molars. This most peripheral matrix region is comprised of a proteoglycan-rich ground substance, interwoven by a collagenous network, matrix vesicles, aperiodic fibrils derived from the dental basal lamina, and apical odontoblastic cell processes. All matrix components may possibly serve as templets for mineral deposition during initial calcification of first-formed mantle dentin and predentin. By means of the very sensitive ESI-analysis we studied the subcellular localization of Ca and P and their possible association with distinct organic extracellular matrix components and odontoblasts. Ca-signals were found in the ground substance, at striated collagen fibrils and plasma membranes of odontoblasts in the cuspal early matrix region, but occurred only sparsely in the ground substance of the more distal matrix region where odontoblast processes attach to aperiodic fibrils of the dental basal lamina. Ca was generally absent in matrix vesicles. In contrast, P-signals were found in matrix vesicles, at aperiodic fibrils and at the plasma membranes of odontoblasts. Ca and P co-localized at striated collagen fibrils (type I or II). These results suggest that striated collagen fibrils might serve as primary deposition sites for calcium phosphate during early biological calcification of organic extracellular macromolecules.     

3-dimensional characterization of the synoviocytes of the human synovial intima]

The intimal synovial surface in normal conditions, using a scanning electron microscope, has been studied. The three synovial membrane types are clearly recognizable: fibrous (Fig. 8), adipose (Figs. 9 and 10) and areolar (Figs. 1 and 2); but only in the areolar type, the characterization of the main two cellular types: synoviocytes B and A, is possible. Synoviocyte B represents the constitutive element which characterizes the synovial intima; it has a cellular body of irregular shape and long cytoplasmic processes directed towards the joint cavity (Figs. 3, 4 and 5). The cellular body and the cytoplasmic processes are covered by small blebs (Fig. 6). and similar vesicles, probably of the same cellular origin, are scattered throughout the extracellular matrix. These cells are likely responsible for the specific structure of the interstitial tissue adapted to the exchanges and to the regulation of the composition of the synovial fluid (Okada et. al. 1981; Linck and Porte, 1978, 1981). Synoviocyte A is a small minority; it has many long and irregular membrane infoldings which define a complicated system of intracellular canaliculi of various depth (Fig. 7). The ultrastructural characteristics of their surface and the peculiarity of their organelle apparatus, described by other AA. (Fell et. al., 1976), demonstrate that these elements carry out a macrophagic function. The clear majority of the synoviocytes B in the intimal surface suggests that in normal conditions, the synthesizing processes prevail over the phagocytosis ones.     

Formation and rearrangement of spermatodesms in males of some Orthoptera Tettigoniidae

In the male genital tract of Tettigoniidae, the spermatodesms are composed of a limited number of spermatozoa whose nuclei and acrosomes are covered by a mucous cap. The formation of the cap begins in the testicular cyst during the lengthening of the apical prolongations of the spermatids and the spermatids’ simultaneous division into small bundles or spermatodesms. The cap material is formed from a loosely arranged material in the lumen of the cyst, probably produced by the secretory activity of the delimiting cells. Another characteristic aspect of the Tettigoniidae is the rearrangement of the cap inside the spermiduct that seems to start when material from the lumen of the organ enters from the basal part of the cap. Except for the fibrils of the peripheral lamina, the fibrils of the cap undergo a marked degradation process. The final organization of the spermatodesm cap is reached inside the seminal vesicles; it consists of the fibrillar peripheral lamina delimiting an interior made up of loosely arranged fibrils immersed in a finely granular matrix.     

Annular alpha-synuclein protofibrils are produced when spherical protofibrils are incubated in solution or bound to brain-derived membranes

The Parkinson's disease substantia nigra is characterized by the loss of dopaminergic neurons and the presence of cytoplasmic fibrillar Lewy bodies in surviving neurons. The major fibrillar protein of Lewy bodies is alpha-synuclein. Two point mutations in the alpha-synuclein gene are associated with autosomal-dominant Parkinson's disease (FPD). Studies of the in vitro fibrillization behavior of the mutant proteins suggest that fibril precursors, or alpha-synuclein protofibrils, rather than the fibrils, may be pathogenic. Atomic force microscopy (AFM) revealed two distinct forms of protofibrillar alpha-synuclein: rapidly formed spherical protofibrils and annular protofibrils, which were produced on prolonged incubation of spheres. The spherical protofibrils bound to brain-derived membrane fractions much more tightly than did monomeric or fibrillar alpha-synuclein, and membrane-associated annular protofibrils were observed. The structural features of alpha-synuclein annular protofibrils are reminiscent of bacterial pore-forming toxins and are consistent with their porelike activity in vitro. Thus, abnormal membrane permeabilization may be a pathogenic mechanism in PD.     

小麦幼苗拒Na+部位的拒Na+机理

采用日立Z 80 0 0原子吸收分光光度计测Na 、K 含量 ,采用不连续蔗糖梯度离心分离质膜和液泡膜微囊。递增盐度和盐冲击处理下 ,耐盐品种德抗 96 1的SK ,Na(吸收 ) 值和SK ,Na(运输 ) 值均明显大于盐敏感品种鲁麦 15 ;德抗 96 1根部和鲁麦 15根茎结合部Na 含量均呈递增趋势 ,表现出累积效应 ;德抗 96 1根细胞质膜微囊和液泡膜微囊H ATP酶活性均明显大于鲁麦15 ,鲁麦 15根茎结合部液泡膜微囊H ATP酶活性大于德抗 96 1,在同一品种的植株里 ,盐冲击的根和根茎结合部细胞质膜微囊和液泡膜微囊H ATP酶活性均小于递增盐度的酶活性。小麦拒Na 部位细胞质膜和液泡膜H ATP酶活性与其耐盐性强弱成正相关     

Myosin-Like Protein (MR 175,000) In Gregarina Blaberae

ABSTRACT. A myosin-like protein (M_r 175,000) was detected in the parasitic protozoan Gregarina blaberae , by both immunofluorescence and immunoblotting of one- and two-dimensional electrophoresis gels using anti-myosin antibodies. This protein was present in the trophozoite ghost but not in the cytoplasmic extract, nor in extract from the sexual stage, suggesting a protein-stage-dependent expression. the protein tightly bound to the cortical membranes was insoluble at low ionic strength, or in detergent solutions, but could be extracted from Gregarina ghosts by 6 M urea in high ionic strength solution (0.5 M NaCI) and in the presence of reducing agents (20 mM DTT). the protein was localized by indirect immunofluorescence in the cortex of the epimerite, in the fibrillar disc (the socalled septum) separating the proto- and the deutomerite segments, in the contractile ring or sphincter at the top of the protomerite, and as longitudinal lines underlying the G. blaberae epicyte folds. the presence of both actin-like and myosin-like proteins would be consistent with a role in gliding and other cell motility processes of this parasite.