scholarly journals FINE STRUCTURE OBSERVATIONS OF THE UPTAKE OF INTRAVENOUSLY INJECTED PEROXIDASE BY THE RAT CHOROID PLEXUS

1967 ◽  
Vol 15 (3) ◽  
pp. 160-165 ◽  
Author(s):  
NORWIN H. BECKER ◽  
ALEX B. NOVIKOFF ◽  
H. M. ZIMMERMAN

The uptake by the choroid plexus of adult rats of intravenously injected horseradish peroxidase has been investigated by electron microscopy. Within 4 min, the injected protein passes the capillary and is rapidly distributed through extracellular space and choroidal cells. Peroxidase enters the choroidal cells within coated vesicles which act as pinocytotic vesicles. At 15 min, peroxidase activity is present in numerous membrane-bound vesicles, multivesicular bodies, dense bodies and what appear to be segments of smooth endoplasmic reticulum. None of the peroxidase-containing organelles is seen to empty to the ventricular surface. Egress of the extracellular peroxidase into the cerebrospinal fluid is apparently blocked by apical zonulae occludentes between the choroidal cells.

1982 ◽  
Vol 60 (7) ◽  
pp. 1103-1114 ◽  
Author(s):  
S. Raghu Kumar

In the thraustochytrid Ulkenia amoeboidea (Bahnweg & Sparrow) Gaertner the contents of the mature vegetative thallus escape from the cell wall in the form of a limax cell. The limax cell is covered by a layer of scales and possesses a nucleus, a paranuclear body, Golgi bodies, mitochondria, bands of smooth endoplasmic reticulum, vacuoles, multivesicular bodies, and cisternae with filamentous contents. The posterior end is filled with smooth endoplasmic reticulum and fusiform vesicles. The anterior end is organelle free and filled with cytoplasm with free ribosomes. Subspherical dense bodies, bounded by a single membrane, are present. The limax cell rounds up prior to mitosis and the Golgi bodies increase in number. During mitosis, the nuclear membrane breaks down totally. Chromosomes are not well defined. Spindle microtubules arise from the centriole and enter the nucleus. After nuclear division, the nuclear envelope is reformed. Cytokinesis is by cleavage into two cells, accompanied by formation of microtubules along the cleavage furrows. The zoospore possesses a nucleus, a paranuclear body, mitochondria, vesicles with presumptive mastigonemes and kinetosome rootlet microtubules and they are covered by a layer of scales. An electron-dense granule and two peripheral thickenings are present within the lumen of the kinetosome.


Author(s):  
M. F. Lalli ◽  
V. Lacroix ◽  
L. Hermo ◽  
Y. Clermont ◽  
C. E. Smith

The testosterone-secreting Leydig cells contain an abundance of smooth endoplasmic reticulum, peroxisomes, mitochondria as well as a large, spheroidal, juxtanuclear Golgi apparatus composed of interconnected stacks of saccules (Figs. 1,2). Each Golgi stack appears to be composed of between 5 to 7 saccules or sacculo-tubular elements (Figs.1,2). These cells also possess pale and dense multivesicular bodies and dense membrane-bound bodies identified assecondary lysosomes, all of which have been shown to be involved in fluid phase and adsorptive endocytosis as well as in receptor mediated endocytosis. The purpose of the present study was to characterize the reactivity of Golgi saccules, multivesicular bodies and lysosomes of Leydig cells for different phosphatases.


1992 ◽  
Vol 40 (2) ◽  
pp. 153 ◽  
Author(s):  
MM Li ◽  
NA Watson ◽  
K Rohde

Spermatogenesis of Syndisyrinx punicea is described. Spermatogonia are little differentiated, with few organelles and inclusions: polyribosomes, ribosomes, small round mitochondria with few cristae and some endoplasmic reticulum. Primary spermatocytes are large and contain multivesicular bodies that are also found in the cytoplasm of spermatids in greater numbers. Spermatids contain Golgi complexes consisting of a series of concentric circles, and numerous membrane-bound, rod-shaped electron-dense bodies. A zone of differentiation develops with peripheral microtubules, followed by the appearance of a prominent intercentriolar body. Two axonemes grow out in opposite directions from centrioles adjacent and perpendicular to the intercentriolar body. The area of differentiation protrudes and elongates to form the sperm shaft into which the nucleus and mitochondria migrate. Typical rootlets were not observed, although rod-shaped structures situated on each side of the nucleus, seen in one section, may be rudimentary rootlets. Spermatocytes and spermatids are linked by different kinds of cytoplasmic bridges. Spermatogenesis of S. punicea is compared with that in other groups of turbellarians and Neodermata.


Author(s):  
J. C. Russ ◽  
E. McNatt

In order to study the retention of copper in cirrhotic liver, rats were made cirrhotic by carbon tetrachloride inhalation twice weekly for three months and fed 0.2% copper acetate ad libidum in drinking water for one month. The liver tissue was fixed in osmium, sectioned approximately 2000 Å thick, and stained with lead citrate. The section was examined in a scanning electron microscope (JEOLCO JSM-2) in the transmission electron mode.Figure 1 shows a typical area that includes a red blood cell in a sinusoid, a disse, and a portion of the cytoplasm of a hepatocyte which contains several mitochondria, peribiliary dense bodies, glycogen granules, and endoplasmic reticulum.


Author(s):  
S.M. Geyer ◽  
C.L. Mendenhall ◽  
J.T. Hung ◽  
E.L. Cardell ◽  
R.L. Drake ◽  
...  

Thirty-three mature male Holtzman rats were randomly placed in 3 treatment groups: Controls (C); Ethanolics (E); and Wine drinkers (W). The animals were fed synthetic diets (Lieber type) with ethanol or wine substituted isocalorically for carbohydrates in the diet of E and W groups, respectively. W received a volume of wine which provided the same gram quantity of alcohol consumed by E. The animals were sacrificed by decapitation after 6 weeks and the livers processed for quantitative triglycerides (T3), proteins, malic enzyme activity (MEA), light microscopy (LM) and electron microscopy (EM). Morphometric analysis of randomly selected LM and EM micrographs was performed to determine organellar changes in centrilobular (CV) and periportal (PV) regions of the liver. This analysis (Table 1) showed that hepatocytes from E were larger than those in C and W groups. Smooth endoplasmic reticulum decreased in E and increased in W compared to C values.


1981 ◽  
Vol 59 (5) ◽  
pp. 908-928 ◽  
Author(s):  
Martha J. Powell ◽  
Charles E. Bracker ◽  
David J. Sternshein

The cytological events involved in the transformation of vegetative hyphae of the zygomycete Gilbertella persicaria (Eddy) Hesseltine into chlamydospores were studied with light and electron microscopy. Thirty hours after sporangiospores were inoculated into YPG broth, swellings appeared along the aseptate hyphae. Later, septa, traversed by plasmodesmata, delimited each end of the hyphal swellings and compartmentalized these hyphal regions as they differentiated into chlamydospores. Nonswollen regions adjacent to chlamydospores remained as isthmuses. Two additional wall layers appeared within the vegetative wall of the developing chlamydospores. An alveolate, electron-dense wall formed first, and then an electron-transparent layer containing concentrically oriented fibers formed between this layer and the plasma membrane. Rather than a mere condensation of cytoplasm, development and maturation of the multinucleate chlamydospores involved extensive cytoplasmic changes such as an increase in reserve products, lipid and glycogen, an increase and then disappearance of vacuoles, and the breakdown of many mitochondria. Underlying the plasma membrane during chlamydospore wall formation were endoplasmic reticulum, multivesicular bodies, vesicles with fibrillar contents, vesicles with electron-transparent contents, and cisternal rings containing the Golgi apparatus marker enzyme, thiamine pyrophosphatase. Acid phosphatase activity was localized cytochemically in a cisterna which enclosed mitochondria and in vacuoles which contained membrane fragments. Tightly packed membrane whorls and single membrane bounded sacs with finely granular matrices surrounding vacuoles were unique during chlamydospore development. Microbodies were rare in the mature chlamydospore, but endoplasmic reticulum was closely associated with lipid globules. As chlamydospores developed, the cytoplasm in the isthmus became highly vacuolated, lipid globules were closely associated with vacuoles, mitochondria were broken down in vacuoles, unusual membrane configurations appeared, and eventually the membranes degenerated. Unlike chlamydospores, walls of the isthmus did not thicken, but irregularly shaped appositions containing numerous channels formed at intervals on the inside of these walls. The pattern of cytoplasmic transformations during chlamydospore development is similar to events leading to the formation of zygospores and sporangiospores.


1989 ◽  
Vol 3 (10) ◽  
pp. 1559-1568 ◽  
Author(s):  
Lucy Y.-H. Tseng ◽  
Alexandra L. Brown ◽  
Yvonne W.-H. Yang ◽  
Joyce A. Romanus ◽  
Craig C. Orlowski ◽  
...  

1985 ◽  
Vol 75 (1) ◽  
pp. 411-421
Author(s):  
B. Van der Schueren ◽  
D. Gasser ◽  
P. Marynen ◽  
F. Van Leuven ◽  
G. David ◽  
...  

The receptor-mediated endocytosis of gold-labelled alpha 2-macroglobulin complexes with trypsin or methylamine (alpha 2M-T-Au or alpha 2M-MA-Au) was studied by electron microscopy in human skin fibroblasts. The gold label was found in coated structures and very small tubules as well as in tubulovesicular structures and in multivesicular bodies/lysosomes. Thick sections (200 nm), but especially serial thin sections, clearly showed the polymorphic character of the cellular structures involved in endocytosis. Numerous intercommunications were particularly obvious between the tubulovesicular structures, the larger vesicles and the multivesicular bodies (MVB). Continuities between MVBs and endoplasmic reticulum and interconnections between MVBs were also observed. The specificity of the staining reaction was confirmed by indirect labelling of intracellular alpha 2M by polyclonal and by monoclonal antibodies on ultracryosections. These findings are discussed in relation to observations made on epithelial cells with other ligands.


1977 ◽  
Vol 55 (4) ◽  
pp. 408-414 ◽  
Author(s):  
J. C. Jamieson

Ultrasonic extracts of rough and smooth endoplasmic reticulum fractions and Golgi fractions from rat liver were examined by immunoelectrophoresis using antiserum to α1-acid glycoprotein. Rough endoplasmic reticulum fractions contained only sialic acid free α1-acid glycoprotein, whereas smooth endoplasmic reticulum and Golgi fractions also contained sialic acid containing α1-acid glycoprotein. Determination of the sialic acid contents of immune precipitates isolated from the extracts suggested that the Golgi complex was the main site of addition of sialic acid to α1-acid glycoprotein. Immunological studies on puromycin extracts of polyribosomes showed that polypeptide chains of α1-acid glycoprotein and albumin were assembled mainly on membrane-bound polyribosomes. Evidence is presented from incorporation studies with labelled leucine and glucosamine that initial glycosylation of α1-acid glycoprotein occurs mainly or entirely after release of nascent polypeptide from the ribosomal site.


1965 ◽  
Vol 26 (1) ◽  
pp. 99-123 ◽  
Author(s):  
Milton W. Brightman

From 10 minutes to 3½ hours after the intraventricular injection into rats of 15 to 100 mg of ferritin, an appreciable fraction of the protein, visualized electron microscopically, traverses the ependymal epithelium by diffusing along the dense intercellular substance of the luminal open junction and thence, by circumventing discrete intercellular fusions which partition rather than seal the interspace. These partitions shunt additional protein into the cell, where ferritin is transported within pinocytotic vesicles to the lateral and basal plasma-lemma and, presumably, back into the interspace again. The basal interspace is irregularly distended by pools of moderately dense "filler" within which ferritin accumulates. The larger fraction of protein enters the ependyma by pinocytosis and is eventually segregated within membrane-enclosed organelles such as vacuoles, multivesicular bodies, and dense bodies, where the molecules may assume a crystalline packing. As a result of the accumulation of ferritin within these inclusions and within filler substance, only a small amount of protein remains to enter the underlying parenchyma. Presentation of ferritin to prefixed cells leads to a random dispersion of free cytoplasmic ferritin. This artifactual distribution in both prefixed and postfixed cells is concurrent with disruption of cell membranes.


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