Fine Structure of the Cyst Wall of Laurentiella acuminata (Hypotrichida: Oxytrichidae)

1983 ◽  
Vol 102 (1) ◽  
pp. 55 ◽  
Author(s):  
Juan C. Gutierrez ◽  
A. Torres ◽  
J. Perez-Silva
Keyword(s):  
Fine Structure ◽  
Cyst Wall

The Fine Structure of the Cyst Wall of the Metacercaria of Fasciola hepatica

1964 ◽  
Vol s3-105 (72) ◽  
pp. 385-389
Author(s):  
K. E. DIXON ◽  
E. H. MERCER
Keyword(s):  
Fine Structure ◽  
Electron Microscope ◽  
Cyst Wall ◽  
Fasciola Hepatica ◽  
Fibrous Layer ◽  
Protein Layer ◽  
Compact Layer

Observations with the electron microscope have shown that 4 major layers can be distinguished in the cyst wall: (a) an outer tanned-protein layer, consisting of a meshwork of irregular bodies made up of cigar-shaped particles; (b) a predominantly mucopolysaccharide, finely-fibrous layer, closely adherent to the tanned layer; (c) an inner, mainly mucopolysaccharide layer, which can be resolved into two layers differing in fine texture; (d) a dense, compact layer, composed of numerous protein sheets stabilized by disulphide linkages. This layer is formed from tightly wound scrolls, developed in intracellular vacuoles, which are unrolled at the surface of the animal after secretion.

On the histology, histochemistry and ultrastructure of the cysticercoid of Raillietina cesticillus (Molin, 1858) Fuhrmann, 1920 (Cestoda, Cyclophyllidea)

Parasitology ◽  
1971 ◽  
Vol 62 (2) ◽  
pp. 233-245 ◽  
Author(s):  
P. J. Baron
Keyword(s):  
Fine Structure ◽  
Cyst Wall ◽  
Financial Support ◽  
North East ◽  
The North ◽  
College Of Technology ◽  
Histochemical Tests ◽  
Electron Microscopes ◽  
The University

The structure of the cysticercoid of Raillietina cesticillus has been studied with the aid of light and electron microscopes. While the ultrastructure of the superficial parts of the scolex closely resembles that of other cestodes, the fine structure of the cyst wall differs from both these. The arrangement and functions of the tissues in the cyst wall are discussed and interpreted with reference to the tissues of the scolex of the cysticercoid of R. cesticillus and to the tissues of other cestodes. R. cesticillus cysticercoids, subjected to various histochemical tests, were shown to contain proteins and carbohydrate materials.The author wishes to thank the Principal and Governors of West Ham College of Technology, a constituent college of the North-east London Polytechnic, for their general and financial support of this work. Thanks are also due to the Directors and Governors of the several institutions whose electron microscopes the author used. The work described here forms part of a thesis approved by the University of London for the degree of Ph.D.

The Fine Structure of the Cyst Wall of the Ciliated ProtozoonDidinium nasutum1

1971 ◽  
Vol 18 (4) ◽  
pp. 604-614 ◽  
Author(s):  
PORTIA A. HOLT ◽  
GEORGE B. CHAPMAN
Keyword(s):  
Fine Structure ◽  
Cyst Wall

The histochemistry of the cystogenous gland cells and cyst wall of Parorchis acanthus Nicoll, and some details of the morphology and fine structure of the cercaria

Parasitology ◽  
1967 ◽  
Vol 57 (1) ◽  
pp. 87-110 ◽  
Author(s):  
Gwendolen Rees
Keyword(s):  
Fine Structure ◽  
Cyst Wall ◽  
Cell Structure ◽  
Middle Layer ◽  
Outer Wall ◽  
Acid Mucopolysaccharide ◽  
Gland Cells ◽  
The Central Nervous System ◽  
Parorchis Acanthus ◽  
Ventral Wall

The cyst wall of Parorchis acanthus Nicoll, consists of an outer wall of three layers and an inner wall of two layers. The outer wall is hemispherical, complete, attached to the substratum and extends as a flange around the margin. The composition of its three layers differ dorsally and ventrally. Dorsally the layers are: (1) acid mucopolysaccharide and neutral mucopolysaccharide, (2) protein and lipoprotein, (3) acid mucopolysaccharide, neutral mucopolysaccharide and glyco-protein. Ventrally the layers are: (1) acid mucopolysaccharide, protein and lipoprotein, (2) acid mucopolysaccharide. The middle layer in both is secreted by the ventral granular cystogenous glands and the outer and inner layers, dorsally and ventrally, by the dorsal and ventral agranular cystogenous glands respectively.The inner cyst wall is oval in surface view. It consists of two layers, both of neutral mucopolysaccharide, the outer giving a more pronounced reaction. Both are secreted by the dorsal granular cystogenous glands. The ventral wall is strengthened by a secretion from the plug-forming gland cells and consists of neutral mucopolysaccharide. All the layers of the cyst wall show the same histochemical reactions as the glands which secrete them.Studies on the fine structure of the cercaria have revealed mammalian-type synapses in the neuropile of the central nervous system, rind cells around the ganglia, an elaborate arrangement of muscles in the wall of the oral sucker, the flame cell structure and the structure of the granules contributing to the formation of the cyst wall.

Fine Structure of Platelet Interaction with a New Microcrystalline Collagen Preparation

1974 ◽  
Vol 32 ◽  
pp. 58-59
Author(s):  
W. H. Zucker ◽  
R. G. Mason
Keyword(s):  
Fine Structure ◽  
Platelet Aggregation ◽  
Hydrochloric Acid ◽  
Whole Blood ◽  
Platelet Adhesion ◽  
Hemostatic Agent ◽  
Native Collagen ◽  
Fibrillar Morphology ◽  
Clinical Interest ◽  
New Form

Platelet adhesion initiates platelet aggregation and is an important component of the hemostatic process. Since the development of a new form of collagen as a topical hemostatic agent is of both basic and clinical interest, an ultrastructural and hematologic study of the interaction of platelets with the microcrystalline collagen preparation was undertaken.In this study, whole blood anticoagulated with EDTA was used in order to inhibit aggregation and permit study of platelet adhesion to collagen as an isolated event. The microcrystalline collagen was prepared from bovine dermal corium; milling was with sharp blades. The preparation consists of partial hydrochloric acid amine collagen salts and retains much of the fibrillar morphology of native collagen.

Pituitary Follicular Cells: Their Origin, Possible Function and Fate

1974 ◽  
Vol 32 ◽  
pp. 34-35
Author(s):  
E. Horvath ◽  
K. Kovacs ◽  
G. Penz ◽  
C. Ezrin
Keyword(s):  
Fine Structure ◽  
Secretory Granules ◽  
Follicular Cells ◽  
Human Pituitary ◽  
Rat Pituitary ◽  
Pituitary Glands ◽  
Junctional Complexes

Follicular structures, in the rat pituitary, composed of cells joined by junctional complexes and possessing few organelles and few, if any, secretory granules, were first described by Farquhar in 1957. Cells of the same description have since been observed in several species including man. The importance of these cells, however, remains obscure. While studying human pituitary glands, we have observed wide variations in the fine structure of follicular cells which may lead to a better understanding of their morphogenesis and significance.

Ultrastructure and Staining of Developing Elastic Tissue

1971 ◽  
Vol 29 ◽  
pp. 244-245
Author(s):  
E. N. Albert
Keyword(s):  
Fine Structure ◽  
Phosphotungstic Acid ◽  
Staining Method ◽  
Rat Aorta ◽  
Uranyl Acetate ◽  
The Other ◽  
Elastic Fibers ◽  
Elastic Tissue ◽  
Lead Citrate ◽  
New Born

Silver tetraphenylporphine sulfonate (Ag-TPPS) was synthesized in this laboratory and used as an electron dense stain for elastic tissue (Fig 1). The procedures for the synthesis of tetraphenylporphine sulfonate and the staining method for mature elastic tissue have been described previously.The fine structure of developing elastic tissue was observed in fetal and new born rat aorta using tetraphenylporphine sulfonate, phosphotungstic acid, uranyl acetate and lead citrate. The newly forming elastica consisted of two morphologically distinct components. These were a central amorphous and a peripheral fibrous. The ratio of the central amorphous and the peripheral fibrillar portion changed in favor of the former with increasing age.It was also observed that the staining properties of the two components were entirely different. The peripheral fibrous component stained with uranyl acetate and/or lead citrate while the central amorphous portion demonstrated no affinity for these stains. On the other hand, the central amorphous portion of developing elastic fibers stained vigorously with silver tetraphenylporphine sulfonate, while the fibrillar part did not (compare figs 2, 3, 4). Based upon the above observations it is proposed that developing elastica consists of two components that are morphologically and chemically different.

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