The fine structure of the leucocytes of the holothurian, Cucumaria miniata

1977 ◽  
Vol 55 (9) ◽  
pp. 1530-1544 ◽  
Author(s):  
A. R. Fontaine ◽  
Philip Lambert

The fine structure of amoebocytes, lymphocytes, and morula cells is described and related to their functions. Three morphological phases (bladder, transitional, and filiform) of the amoebocyte are distinguished. Their surface protrusions and activities are based on microtubule and microfilament systems and the transitional-filiform phases are functionally involved in coelomocyte aggregation. The bladder phase is phagocytic; bladder formation and activities are also microfilament based. Morula cells contain spherules composed of acid mucopolysaccharide and protein. Dilated rough endoplasmic reticulum (ER) cisternae apparently synthesize spherule material which is added by accretion. Lymphocytes have little cytoplasm and relatively few organelles, except for abundant rough ER and free ribosomes. Lymphocytes are probably stem cells for amoebocytes and morulas. These cells are compared with the leucocytes of other echinoderms.

Author(s):  
E. M. Eddy

Primordial germ cells are readily recognizable in embryos of the rat due to their large size, generally rounded shape and prominent nuclei with uniformly dispersed heterochromatin. They often have blunted pseudopodal processes at one end and small ruffles or trailing processes at the other, characteristics expected from their known ameboid activity- and migratory abilities. Also, the cytoplasm is rich in polyribosomes and contains a modest amount of rough endoplasmic reticulum and the mitochondria are frequently larger and less dense than those of adjacent somatic cells.In addition to these general characteristics, there are features unique to germ cells which allow them to be identified with certainty. These are: 1) small vesicles containing an irregular, dense core and 2) discrete accumulations of fibrous material known as nuage. Both of these features are present in other species and at other times in the life history of germ cells. The dense-cored vesicles have been noted in fetal and early postnatal mouse oogonia and oocytes, and in hamster and rabbit oocytes.


In the mud-dwelling amphipod, Corophium volutator the foregut is lined with cuticle and consists of an oesophagus and a stomach, with the latter divided into cardiac, pyloric and funnel regions. The midgut comprises an intestine that is enlarged considerably by three pairs of diverticula: the small anterior dorsal and posterior caeca and the massive ventral caeca. Anteriorly, the intestine encompasses the funnel region and the ventral caeca open into the floor of the stomach at the posterior end of the pyloric region. The hindgut is essentially a simple tube connnecting the intestine with the anus. Particles of food pass along the oesophagus and enter the stomach through a valve. Rows of setae, or folds of cuticle, divide the stomach longitudinally into food, circulation and filtration channels. Ingested particles with a diameter greater than 2 pm are confined to the food channel and supplied with fluids and enzymes from the circulation channels. The digestive enzymes are produced primarily by the ventral caeca and are supplied to the circulation channels through a valve at the entrance of each ventral caecum. Any fine particles and soluble materials extracted from the food channel in the cardiac region are transported into the filtration channels through the first filter of a two part system. Digestible material continues to be extracted in the pyloric region where the volume of the lumen of the food channel is reduced by the intrusion of the vertex of the ventral pyloric ridge. The basis of this ridge supports the second filter which produces a filtrate with particles less than 0.06 pm in diameter. Material retained on the filter membrane is returned to the food channel by brush-like setae facing the membrane. The final filtrate is transported to the ventral caeca. A valve at the entrance to each ventral caecum prevents contamination of the filtrate by material in the food channel. All indigestible food is passed sequentially along the funnel, intestine and, finally, the hindgut from which it is voided as a faecal pellet. Most digestion and absorption occur in the ventral caeca where the epithelium is differentiated into the R /F and B cells. The R /F cells have a much thicker and denser microvillous border than the B cells. Each R /F cell also has numerous mitochondria located mainly ventral to the nucleus in the mid-region. Rough and smooth endoplasmic reticula are sited primarily in the apical and basal regions of the cell, respectively. Furthermore, most of the rough endoplasmic reticulum is confined to cells in the distal region of the caecum which probably forms the main site for the production of digestive enzymes. The proximal region of the caecum contains numerous lipid droplets and is probably involved in the absorption, transport and storage of the products of digestion. Each B cell has a single large, fluid-filled vacuole, distal to which are mitochondria and numerous smaller vacuoles of varying size forming an ‘apical complex’. The nucleus is located proximal to the vacuole together with free ribosomes and rough endoplasmic reticulum. Material from the lumen of the caecum is taken by pinocy tosis into the ‘apical complex’. The large vacuole develops at the expense of the ‘apical complex’ and the microvillous border. The vacuole is eventually liberated into the lumen of the caecum and the cell disintegrates. These discharges may supply enzymes to other regions of the gut, or they could be waste products derived from intracellular digestion. The anterior dorsal caeca and most of the intestine contain cells with a normal complement of organelles. These cells probably make a minor contribution to the processes of digestion and absorption. However, the cells of the posterior caeca and those at the posterior end of the intestine have an extensive development of smooth endoplasmic reticulum. In some cells the mitochondria have a dense matrix and there are only a few free ribosomes and cisternae of rough endoplasmic reticulum. The fine structure of the epithelium in the posterior caeca is typical of tissue that transports fluids and ions. The hindgut has a microvillous border which abuts its cuticular lining. In addition, some cells have numerous mitochondria which are often associated with infolds of the basal cell membrane. The fine structure of this tissue is similar to the ‘ion pumps’ described in the gut of insects which serve to maintain the normal ionic concentration of the blood. The posterior region of the hindgut has no structural specializations.


1979 ◽  
Vol 13 (2) ◽  
pp. 75-80 ◽  
Author(s):  
David J. Lewis ◽  
David E. Prentice

Summary The fine structure of rhesus monkey renomedullary interstitial cells was studied by electron microscopy. These stellate cells contained variable numbers of lipid droplets, moderate numbers of mitochondria, moderate amounts of rough endoplasmic reticulum, and prominent Golgi zones. In rare instances, apparent release of lipid droplets into the interstitium was observed. The most prominent feature of the interstitial cells was large nuclear pseudoinclusions which were observed in a high proportion of the animals examined.


1966 ◽  
Vol 31 (1) ◽  
pp. 79-93 ◽  
Author(s):  
Lalit M. Srivastava

The fine structure of ash cambium was studied after glutaraldehyde-osmium tetroxide fixation. The fusiform and ray initials are essentially alike, and both have the basic complement of organelles and membranes typical of parenchyma cells. The varied behavior of the two types of initials and the role of cambium in oriented production of the xylem and phloem are still unexplained phenomena. Actively growing cambial cells are highly vacuolate. They are rich in endoplasmic reticulum of the rough cisternal form, ribosomes, dictyosomes, and coated vesicles. Microtubules are present in the peripheral cytoplasm. The plasmalemma appears to be continuous with the endoplasmic reticulum and produces coated vesicles as well as micropinocytotic vesicles with smooth surfaces. The plastids have varying amounts of an intralamellar inclusion which may be a lipoprotein. The quiescent cambium is deficient in rough ER and coated vesicles and has certain structures which may be condensed proteins.


Author(s):  
Janice E. Kuster

The fine structure of photopic eucone eyes of Cicindela tranquebarica adults was examined using cryofracture SEM, TEM, and freeze-etch techniques. A “subcorneal layer” can be distinguished between the corneal lens and crystalline cone. In surface view (Fig. 1) this layer consists of concave polygons (po). It has parabolic lamellae (lm) of endocuticle consisting of microfibrils (mf) having a chitin core with protein deposits along their lengths (Fig. 2). Two primary pigment cells (lp) are devoid of pigment granules, but are rich in rough endoplasmic reticulum (rer) and surround a crystalline thread (ct) (Fig. 3). Extensions of the crystalline thread form inter-retinular fibers (f) containing microtubules between retinula cells 1/2, 3/4, 5/6, and 7/1 (Figs. 4, 5).Distal to each retinula cell nucleus are two basal bodies (bb), one perpendicular to the other (Fig. 4). The proximal body extends two fibrillar feet which fuse to form a horizontally banded ciliary rootlet which extends the retinula length peripheral to the rhabdom.


1967 ◽  
Vol 2 (1) ◽  
pp. 137-144
Author(s):  
H. C. MACGREGOR ◽  
J. B. MACKIE

The salivary glands of 3rd or 4th instar larvae of Simulium niditifrons are about 5 mm long and up to 400 µ wide. They have a capacious lumen which is normally filled with secretion. The apical (luminal) plasmalemma of the gland cells is thrown into numerous microvilli. The basal plasmalemma is usually straight but is infolded in places. The infoldings may be complex near to cell junctions. There is a thick, uniform basement membrane. Contact surfaces of adjacent cells often interdigitate. A septate junction extends inwards from the lumen for one-quarter the depth of the cells. Rough endoplasmic reticulum is distributed evenly throughout the cytoplasm. Many Golgi complexes with dark membrane-bounded granules are scattered throughout the cytoplasm. Solitary granules, often more than I µ in diameter, lie in the apical cytoplasm, especially near the apical border of the cell. These granules resemble the larger Golgi granules and the contents of the lumen. Solitary granules consisting of 2 components have been seen in various stages of passage through the cell membrane. The 2 components are present in roughly constant proportions and can be identified in the larger Golgi granules and in the secretion in the lumen. The nucleus is spherical. The nuclear envelope is smooth in the larger cells of a gland but may be folded in the smaller cells. There are 80-100 pores/µ2 of nuclear envelope. Each pore appears to have a small granule at its centre. Microtubules, about 180 Å thick, are numerous in the apical cytoplasm, particularly near the luminal border. Tubules which lie deep in the cytoplasm are flanked by a clear area 100-200 Å wide. The fine structure of a salivary gland cell of Simulium appears to indicate that the major components of the salivary secretion are synthesized in association with the ribosomes on the rough endoplasmic reticulum, concentrated in the Golgi regions, formed into secretion granules, and passed out of the cell into the lumen of the gland by reverse phagocytosis.


1974 ◽  
Vol 61 (3) ◽  
pp. 613-632 ◽  
Author(s):  
Frank Slaby ◽  
Carolyn Brown

The equilibrium density distribution, protein composition, and secretory character of mouse mammary epithelial rough microsomes have been determined during differentiation. The density range exhibited by the rough microsomes broadens during mammary development; rough microsomes within the 1.25–1.29 g/ml density range appear soon after conception and then within the 1.30–1.34 range after the onset of lactation. The appearance of these denser microsomes represents the progressive increase of the average ribosome content of the rough endoplasmic reticulum (ER) during gestation and lactation. Fractionation of rough microsomal proteins by sodium dodecyl sulfate-polyacrylamide gel electrophoresis reveals that two proteins, having molecular weights of 57,000 and 76,000, occur to a significant extent only during lactation and are then most prominent in the very dense rough microsomes of the 1.30–1.34 range. Nascent polypeptide chains discharged (by incubation with puromycin) from 17-days lactation rough microsomes in either the 1.21–1.29 or 1.30–1.34 density range are distributed equally between the intra- and extravesicular compartments. Whereas 36% of the chains are discharged intravesicularly from 1-day lactation rough microsomes in the 1.30–1.34 range, only 25% are so discharged from those in the 1.21–1.29 range. The results indicate (a) that there is no correlation between the relative levels in lactation rough microsomes of the two microsomal proteins which become prominent during lactation and the extent of secretory activity and (b) that for a short period after parturition the rough ER elements bearing high surface densities of ribosomes have a greater proportion of ribosomes synthesizing milk proteins than the rough ER elements with moderate ribosome densities.


Author(s):  
Odell T. Minick ◽  
Hidejiro Yokoo ◽  
Fawzia Batti

Biliary epithelial cells have previously been shown to be a site of alcoholic hyalin (AH) deposition. To learn more of the nature and pathogenesis of this inclusion, the fine structure of proliferating biliary ductules was studied in 20 patients with alcoholic liver disease. The changes were compared with those observed in hepatocytes containing alcoholic hyalin.The ductular cells often displayed dilated cisternae of rough endoplasmic reticulum, prominent Golgi complexes, and an increase in lysosomes. Mitochondria were larger, more numerous and contained more cristae than those usually seen in ductules (Fig. 1). Double nuclei were common. Dense, compact cells, probably degenerative in nature, were often noted.


2005 ◽  
Vol 16 (4) ◽  
Author(s):  
Ashraf Montasser ◽  
Amr Amin

The integument of Argas persicus was investigated using light, scanning and transmission electron microscopy. The study revealed that two layers, viz. an outer epicuticle and an inner procuticle, form the cuticle. The epicuticle includes wax, cuticulin and protein epicuticular layers. The wax layer carries numerous crater-like deposits, oval or circular discs and numerous infoldings. The procuticle contains an exo-, endo- and a subcuticle.Underlining the cuticle, flattened epidermal cells are connected via desmosomes and contain rough endoplasmic reticulum, free ribosomes and mitochondria. Scattered dermal glands are located beneath the cuticle and are continuous with the outside through dermal ducts and surface pores.


1999 ◽  
Vol 19 (5) ◽  
pp. 491-498
Author(s):  
Sandrine Duvet ◽  
Jean Dubuisson ◽  
Myriam Ermonval ◽  
René Cacan ◽  
André Verbert

Recent studies have shown that newly synthesized proteins and glycoproteins are submitted to a quality control mechanism in the rough endoplasmic reticulum (ER). In this report we present two models: One model will illustrate a transient retention in rough ER leading to a further degradation of glycoproteins in the cytosol, (soluble alkaline phosphatase expressed in Man-P-Dol deficient CHO cells lines). The second model will illustrate a strict retention of glycoproteins in rough ER without degradation nor recycling through the Golgi (E1, E2 glycoproteins of Hepatitis C virus in stably transfected UHCV-11.4 cells and in infected Hep G2 cells). In both cases, oligomannoside structures are markers of these phenomena, either as free soluble released oligomannosides in the case of degradation, or as N-linked oligomannosides for strict retention in rough ER.


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