The Cytology and Histochemistry of the Digestive Gland Cells ofHelix

1965 ◽  
Vol s3-106 (74) ◽  
pp. 173-192
Author(s):  
A. T. SUMNER
Keyword(s):  
Golgi Apparatus ◽  
Digestive Gland ◽  
Cell Types ◽  
Cell Protein ◽  
Zymogen Granules ◽  
High Concentration ◽  
Digestive Cells ◽  
Large Vacuole ◽  
Protein Granules ◽  
Calcium Cells

The digestive gland tubule epithelium of Helix aspersa is made up of 4 cell-types: thin cells, digestive cells, calcium cells, and excretory cells. Thin cells are narrow and undifferentiated. They divide by mitosis and are believed to develop into other celltypes. Digestive cells are highly vacuolated phagocytic and absorptive cells. Food materials are taken in by phagocytosis and are concentrated and digested in the vacuoles in the cell. When digestion is complete, the residual indigestible material in the vacuoles, and excretory material in the form of small granules of lipofuscin, are cast out of the cell surrounded by a portion of cytoplasm. Calcium cells are secretory, with a prominent Golgi apparatus and a high concentration of RNA in the cytoplasm. Most of the cell is occupied by spherules which contain calcium; apically there are protein granules which contain a high concentration of tryptophane. Both these types of inclusion are extruded from the cell. Protein granules may be zymogen granules, but the function of the calcium spherules is not known. Excretory cells are degenerate, and probably derived from calcium cells. They consist chiefly of a large vacuole, surrounded by a little cytoplasm. The vacuole contains one or more granules of lipofuscin. Similar granules can be found in the faeces, and thus they are excretory material.

scholarly journals Defensive ink pigment processing and secretion in Aplysia californica: concentration and storage of phycoerythrobilin in the ink gland.

1998 ◽  
Vol 201 (10) ◽  
pp. 1595-1613 ◽  
Author(s):  
J Prince ◽  
T G Nolen ◽  
L Coelho
Keyword(s):  
Endoplasmic Reticulum ◽  
Digestive Gland ◽  
Aplysia Californica ◽  
Cell Types ◽  
Coated Vesicles ◽  
Coated Vesicle ◽  
Cell Type ◽  
Digestive Cells ◽  
Red Algal ◽  
Green Seaweed

The marine snail Aplysia californica obtains its defensive ink exclusively from a diet of red seaweed. It stores the pigment (phycoerythrobilin, the red algal photosynthetic pigment, r-phycoerythrin, minus its protein) in muscular ink-release vesicles within the ink gland. Snails fed a diet of green seaweed or romaine lettuce do not secrete ink and their ink-release vesicles are largely devoid of ink. Successive activation of individual ink-release vesicles by ink motor neurons causes them to secrete approximately 55 % of their remaining ink (similar to the percentage of ink reserves released from the intact gland). The peripheral activation of vesicles appears to be cholinergic: 70 % of isolated vesicles were induced to squeeze ink from their valved end by solutions of acetylcholine at concentrations of 0.5 mmol l-1 or below. Ultrastructural analysis commonly found three cell types in the ink gland. The RER cells, the most numerous, were characterized by an extensive rough endoplasmic reticulum with greatly distended cisternae. This cell type is probably the site for synthesis of the high molecular mass protein of secreted ink. The granulate cells, less common than RER cells, had nuclear and cell areas significantly larger than those of RER cells. In addition, granulate cells of red-algal-fed snails had 4-14 vacuoles that contained electron-dense material with staining characteristics similar to that of ink in mature ink-release vesicles. The granulate cell's plasma membrane was regularly modified into grated areas, which both localized and expanded the surface area for coated vesicle formation and provided a sieve structure that prevented large particles in the hemolymph either from being taken up by, or from occluding, the coated vesicles. Electron-dense particles within coated vesicles were similar in size to those in granulate vacuoles but larger (on average by approximately 1 nm) than those that make up the ink. In green-seaweed-fed snails, granulate cells and their vacuoles were present but the vacuoles were empty. The third cell type, the vesicle cell, expands markedly, with its nucleus enlarging concurrent with cell growth until it is on average 50 times larger in cross-sectional area than the nuclei of either RER or granulate cells; the cytoplasm eventually becomes filled with ink, which obscures the mitochondria, vacuoles and nucleus. Continued cell expansion ceases with the appearance of an encircling layer of muscle and 1-3 layers of cells of unknown origin, thereby becoming the ink-release vesicle itself. The absorption spectra of the soluble contents of mature ink-release vesicles from snails fed red algae had peaks characteristic of the red algal pigment r-phycoerythrin or/and phycoerythrobilin. Immunogold localization of r-phycoerythrin showed no statistical difference in the amount of label within the ink-release vesicles, RER or granulate cell types. Furthermore, there was no localization of phycoerythrin immunoreactivity within the various cellular compartments of either the RER or granulate cells (nucleus, endoplasmic reticulum, mitochondria, vacuoles). Immunogold labeling in the ink gland ranged from 11 to 16 % of that for the digestive vacuoles of the rhodoplast digestive cells lining the tubules of the digestive gland. Our observations suggest (a) that the main form of the ink pigment in the gland is phycoerythrobilin or/and a non-antigenic form of phycoerythrin, and (b) that separation of the bilin from phycoerythrin (or its modification so that it is no longer antigenic) occurs before it reaches the ink gland, probably within the vacuoles of the rhodoplast digestive cells of the digestive gland. We propose the following model. The ink pigment, phycoerythrobilin, is cleaved from its protein in rhodoplast digestive vacuoles in the digestive gland. (ABSTRACT TRUNCATED)

Experiments with P32 and I131 on Species of Helix, Arion, and Agriolimax

1952 ◽  
Vol s3-93 (22) ◽  
pp. 133-146
Author(s):  
VERA FRETTER
Keyword(s):  
Salivary Glands ◽  
Digestive Gland ◽  
Radioactive Iodine ◽  
Helix Pomatia ◽  
Relative Activity ◽  
The Body ◽  
Ionic Exchange ◽  
Digestive Cells ◽  
Metabolic Activities ◽  
Calcium Cells

If Helix aspersa, H. pomatia, Arion hortensis, and Agriolimax agrestis be fed on a diet which contains P32, autoradiographs show that the isotope is taken up by the digestive and lime cells of the digestive gland. From the formermost of it passes to the haemocoel, though some is retained for immediate metabolic activities; in the lime cells it is stored in calcium spherules. A very small amount of the tracer enters the body through the wall of the oesophagus, and more through the intestine, this site of diffusion being most pronounced directly after hibernation. The P33 in the haemocoel is dispersed to all tissues: all of them take up a little; in some it becomes concentrated. Concentrations appear in the nerve ring, the mucous and salivary glands, the odontophore and certain cells of the mantle. In the nervous system deposits are heavy around the fibres and slight in the cytoplasm of the cells; they indicate a compound, soluble in alcohol, which may be phospholipine, associated with medullated nerves. The phosphorus in mucous cells, most pronounced in the pedal and salivary glands, may be combined with the calcium which stabilizes mucus and prevents its rapid dispersal. The incorporation of isotope into the developing tooth of the radula indicates the relative activity of the basoblasts and cuspidoblasts: in early development of a tooth the basoblast secretes more actively, but as it becomes effete secretion by the cuspidoblast is accelerated. When the tooth is liberated from the latter there is no further addition to its substance. Phosphorus deposits in the mantle are in the calcium cells which secrete the shell. Here, as in the lime cells, and around certain blood-vessels, excess may be stored as calcium phosphate; reserves in the digestive gland are the largest. Amoebocytes concerned with the regeneration of the shell of Helix pomatia and H. aspersa carry the tracer element, and some of it is deposited in the shell. Also in the slug the tracer is transported by amoebocytes. Radioactive iodine in the lumen of the gut is taken up most readily by digestive cells; some enters the lime cells. Only in sparing quantities does this isotope pass from the gland to the rest of the body, and this entry is presumably associated with ionic exchange. It is not accumulated in any cell, except in the kidney whence it is excreted; it leaves the digestive cells to pass from the body with the faeces.

Processing of defensive pigment in Aplysia californica: acquisition, modification and mobilization of the red algal pigment, r-phycoerythrin by the digestive gland.

1998 ◽  
Vol 201 (3) ◽  
pp. 425-438 ◽  
Author(s):  
L Coelho ◽  
J Prince ◽  
T G Nolen
Keyword(s):  
Digestive Gland ◽  
Photosynthetic Pigment ◽  
Aplysia Californica ◽  
Cell Types ◽  
The Body ◽  
Digestive Cell ◽  
Digestive Cells ◽  
Red Seaweeds ◽  
Red Algal ◽  
Green Seaweed

The marine snail Aplysia californica obtains its purple defensive ink exclusively from the accessory photosynthetic pigment r-phycoerythrin, which is found in the red seaweeds of its diet. The rhodoplast digestive cell, one of three types of cell lining the tubules of the digestive gland, appears to be the site of catabolism of red algal chloroplasts (rhodoplasts) since thylakoid membranes, including phycobilisome-sized membrane-associated particles, were found within the large digestive vacuoles of this cell. Immunogold localization showed that there was a statistically significant occurrence of the red algal phycobilisome pigment r-phycoerythrin within these rhodoplast digestive vacuoles, but not in other compartments of this cell type (endoplasmic reticulum, mitochondria, nucleus) or in other tissues (abdominal ganglion). Immunogold analysis also suggested that the rhodoplast vacuole is the site for additional modification of r-phycoerythrin, which makes it non-antigenic: the chromophore is either cleaved from its biliprotein or the biliprotein is otherwise modified. The hemolymph had spectrographic absorption maxima typical of the protein-free chromophore (phycoerythrobilin) and/or r-phycoerythrin, but only when the animal had been feeding on red algae. Rhodoplast digestive cells and their vacuoles were not induced by the type of food in the diet: snails fed green seaweed and animals fed lettuce had characteristic rhodoplast cells but without the large membranous inclusions (rhodoplasts) or phycobilisome-like granules found in animals fed red seaweed. Two additional cell types lining the tubules of the digestive gland were characterized ultrastructurally: (1) a club-shaped digestive cell filled with electron-dense material, and (2) a triangular 'secretory' cell devoid of storage material and calcium carbonate. The following model is consistent with our observations: red algal rhodoplasts are freed from algal cells in the foregut and then engulfed by rhodoplast digestive cells in the tubules of the digestive diverticula, where they are digested in membrane-bound vacuoles; r-phycoerythrin is released from phycobilisomes on the rhodoplast thylakoids and chemically modified before leaving the digestive vacuole and accumulating in the hemolymph; the pigment then circulates throughout the body and is concentrated in specialized cells and vesicles of the ink gland, where it is stored until secreted in response to certain predators.

scholarly journals Role of the Digestive Gland in Ink Production in Four Species of Sea Hares: An Ultrastructural Comparison

2013 ◽  
Vol 2013 ◽  
pp. 1-5 ◽  
Author(s):  
Jeffrey S. Prince ◽  
Paul Micah Johnson
Keyword(s):  
Digestive Gland ◽  
Common Ancestor ◽  
Aplysia Californica ◽  
Digestive Cell ◽  
Digestive Cells ◽  
Sea Hare ◽  
Red Algal ◽  
The Common ◽  
Algal Chloroplast

The ultrastructure of the digestive gland of several sea hare species that produce different colored ink (Aplysia californicaproduces purple ink,A. julianawhite ink,A. parvulaboth white and purple ink, whileDolabrifera dolabriferaproduces no ink at all) was compared to determine the digestive gland’s role in the diet-derived ink production process. Rhodoplast digestive cells and their digestive vacuoles, the site of digestion of red algal chloroplast (i.e., rhodoplast) inA. californica, were present and had a similar ultrastructure in all four species. Rhodoplast digestive cell vacuoles either contained a whole rhodoplast or fragments of one or were empty. These results suggest that the inability to produce colored ink in some sea hare species is not due to either an absence of appropriate digestive machinery, that is, rhodoplast digestive cells, or an apparent failure of rhodoplast digestive cells to function. These results also propose that the digestive gland structure described herein occurred early in sea hare evolution, at least in the common ancestor to the generaAplysiaandDolabrifera. Our data, however, do not support the hypothesis that the loss of purple inking is a synapomorphy of the white-ink-producing subgenusAplysia.

Correlation between phosphorylation of a 34,000-molecular-weight protein, pp60src-associated kinase activity, and tumorigenicity in transformed and revertant vole cells

1984 ◽  
Vol 4 (1) ◽  
pp. 212-215
Author(s):  
J F Nawrocki ◽  
A F Lau ◽  
A J Faras
Keyword(s):  
Molecular Weight ◽  
Rous Sarcoma Virus ◽  
Kinase Activity ◽  
Cell Types ◽  
Cell Protein ◽  
Protein Kinase Activity ◽  
Rous Sarcoma ◽  
Tumorigenic Potential ◽  
Sarcoma Virus ◽  
Weight Protein

The phosphorylation of a 34,000-molecular-weight (34K) cell protein, purported to be a substrate of the avian retrovirus pp60src-associated protein kinase activity, was compared in three types of Rous sarcoma virus-infected vole cells: fully transformed cells, partial revertants which are morphologically normal in appearance but retain their tumorigenic potential, and full revertants which are similar to normal vole cells in all parameters including a lack of tumorigenicity. Although similar amounts of 34K protein are present in all three cell types, phosphorylation of the 34K protein was significantly reduced in the full revertant cell type. The reduced phosphorylation occurred at the tyrosine residue.

Effect of Growth Rate on Resistance ofCandida albicans Biofilms to Antifungal Agents

1998 ◽  
Vol 42 (8) ◽  
pp. 1900-1905 ◽  
Author(s):  
George S. Baillie ◽  
L. Julia Douglas
Keyword(s):  
Growth Rate ◽  
Amphotericin B ◽  
Growth Rates ◽  
Antifungal Agents ◽  
Cell Types ◽  
Planktonic Cells ◽  
High Concentration ◽  
Glucose Limitation ◽  
Daughter Cells ◽  
Cell Counts

ABSTRACT A perfused biofilm fermentor, which allows growth-rate control of adherent microbial populations, was used to assess whether the susceptibility of Candida albicans biofilms to antifungal agents is dependent on growth rate. Biofilms were generated under conditions of glucose limitation and were perfused with drugs at a high concentration (20 times the MIC). Amphotericin B produced a greater reduction in the number of daughter cells in biofilm eluates than ketoconazole, fluconazole, or flucytosine. Similar decreases in daughter cell counts were observed when biofilms growing at three different rates were perfused with amphotericin B. In a separate series of experiments, intact biofilms, resuspended biofilm cells, and newly formed daughter cells were removed from the fermentor and were exposed to a lower concentration of amphotericin B for 1 h. The susceptibility profiles over a range of growth rates were then compared with those obtained for planktonic cells grown at the same rates under glucose limitation in a chemostat. Intact biofilms were resistant to amphotericin B at all growth rates tested, whereas planktonic cells were resistant only at low growth rates (≤0.13 h−1). Cells resuspended from biofilms were less resistant than intact biofilm populations but more resistant than daughter cells; the susceptibilities of both these cell types were largely independent of growth rate. Our findings indicate that the amphotericin B resistance of C. albicans biofilms is not simply due to a low growth rate but depends on some other feature of the biofilm mode of growth.

scholarly journals Morphological characteristics of respiratory and digestive organs of Roman snail (Helix pomatia L., 1758)

2020 ◽  
Vol 22 (97) ◽  
pp. 7-12
Author(s):  
M. P. Horvat ◽  
R. S. Dankovych
Keyword(s):  
Helix Pomatia ◽  
Morphological Characteristics ◽  
Internal Surface ◽  
The Body ◽  
Digestive Cells ◽  
Green Color ◽  
Excretory Function ◽  
Intracellular Digestion ◽  
Snail Helix Pomatia ◽  
Calcium Cells

The aim of this work was to study the structure of lung and hepatopancreas of Roman snail (Helix of pomatia of L., 1758). The study found that the lung occupies the lower turn of shell and presented by a saccate cavity, in the wall of that there are a kidney and heart with a pericardium, and also a rectum and ureter pass. An external surface of lungs covered by a shell and covered by an epidermis. An internal surface is covered by a flat ciliated epithelium and forms numerous folds in which pulmonary vessels and lacunae are accommodated. The branches of pulmonary vein have a thick muscular wall, that consists of circular and longitudinal muscular layers. An internal surface of lungs covered by the layer of mucus. Inhalation and exhalation are carried out due to reduction and relaxation of muscles of dorsal wall of the body that is named a “diaphragm”. Gas exchange occurs through the hemolymphatic capillaries of the lung wall. Respiratory motions take place not rhythmically, but through the different intervals of time depending on a requirement in oxygen. The frequency of pneumostome closing and opening is typically one time in a minute. At subzero humidity of atmospheric air of pneumostome closed by a mantle, and also one (or a few) epiphragms. The hepatopancreas (“liver” or liver gland) is in the upper rotation of the sink and formed by two parts: right and left, from which two liver ducts enter into the stomach respectively. The liver gland consists of many acinuss, surrounded by connecting tissue, that contains small number of muscular fibres. Calcium cells have a pyramidal form and usually do not reach the lumen of the acinus. Cytoplasm of calcium cells contains inclusions: grains of phosphoricacid lime and drops of fat. The digestive cells of the hepatopencreas are more elongated, often clavicular. Сytoplasm of digestive cells is loose and vacuolated and contain inclusions of yellow-green color. Enzyme cells on histopreparations are difficult to distinguish from digestive ones. They contain transparent vacuoles with a large round inclusion of yellow-green color, which consists of a cluster of several grains of different sizes. Hepatopancreas performs the following functions: secretory (enzyme cells), absorption and intracellular digestion (digestive cells), preservation of nutrients and calcium (calcium cells), and also excretory function.

scholarly journals The fine structure produced in cells by primary fixatives 2. Potassium dichromate

1965 ◽  
Vol s3-106 (73) ◽  
pp. 15-21
Author(s):  
JOHN R. BAKER
Keyword(s):  
Electron Microscopy ◽  
Plasma Membrane ◽  
Fine Structure ◽  
Golgi Apparatus ◽  
Nuclear Membrane ◽  
Osmium Tetroxide ◽  
Potassium Dichromate ◽  
Potassium Dichromate Solution ◽  
Zymogen Granules ◽  
Mouse Pancreas

The exocrine cells of the mouse pancreas were fixed in potassium dichromate solution, embedded in araldite or other suitable medium, and examined by electron microscopy. Almost every part of these cells is seriously distorted or destroyed by this fixative. The ergastoplasm is generally unrecognizable, the mitochondria and zymogen granules are seldom visible, and no sign of the plasma membrane, microvilli, or Golgi apparatus is seen. The contents of the nucleus are profoundly rearranged. It is seen to contain a large, dark, irregularly shaped, finely granular object; the evidence suggests that this consists of coagulated histone. The sole constituent of the cell that is well fixed is the inner nuclear membrane. The destructive properties of potassium dichromate are much mitigated when it is mixed in suitable proportions with osmium tetroxide or formaldehyde.

scholarly journals Bergamot Polyphenol Fraction Exerts Effects on Bone Biology by Activating ERK 1/2 and Wnt/β-Catenin Pathway and Regulating Bone Biomarkers in Bone Cell Cultures

Nutrients ◽  
2018 ◽  
Vol 10 (9) ◽  
pp. 1305 ◽  
Author(s):  
Arturo Pujia ◽  
Cristina Russo ◽  
Samantha Maurotti ◽  
Roberta Pujia ◽  
Vincenzo Mollace ◽  
...  
Keyword(s):  
Bone Cells ◽  
Citrus Fruit ◽  
Cell Types ◽  
Bone Cell ◽  
In Vivo Studies ◽  
Bone Biology ◽  
High Concentration ◽  
Mineral Density ◽  
Differentiation Markers

Epidemiological studies show that fruit consumption may modulate bone mineral density. However, data regarding the effect of the Citrus bergamia Risso (Bergamot orange), a citrus fruit containing a high concentration of flavonoids, on bone health are still lacking. In this study, we investigated the effects of Bergamot polyphenols on the Wnt/β-catenin pathway in two distinct bone cell types (Saos-2 and MG63). Findings showed that exposure to 0.01 and 0.1 mg/mL doses upregulate β-catenin expression (p = 0.001), osteoblast differentiation markers (e.g., RUNX2 and COL1A), and downregulate RANKL (p = 0.028), as compared to the control. Our results highlight, for the first time, that Bergamot polyphenols act on bone cells through the β-catenin pathway. In vivo studies are necessary to fully understand Bergamot’s role against bone resorption.

Bioprinting

2021 ◽  
Author(s):  
Kenneth Douglas
Keyword(s):  
Stem Cells ◽  
Neuromuscular Junctions ◽  
Cell Types ◽  
Passive Movement ◽  
Plain Language ◽  
High Concentration ◽  
Proliferation And Differentiation ◽  
The Common ◽  
Biological Environment ◽  
Lung And Kidney

Abstract: This book describes how bioprinting emerged from 3D printing and details the accomplishments and challenges in bioprinting tissues of cartilage, skin, bone, muscle, neuromuscular junctions, liver, heart, lung, and kidney. It explains how scientists are attempting to provide these bioprinted tissues with a blood supply and the ability to carry nerve signals so that the tissues might be used for transplantation into persons with diseased or damaged organs. The book presents all the common terms in the bioprinting field and clarifies their meaning using plain language. Readers will learn about bioink—a bioprinting material containing living cells and supportive biomaterials. In addition, readers will become at ease with concepts such as fugitive inks (sacrificial inks used to make channels for blood flow), extracellular matrices (the biological environment surrounding cells), decellularization (the process of isolating cells from their native environment), hydrogels (water-based substances that can substitute for the extracellular matrix), rheology (the flow properties of a bioink), and bioreactors (containers to provide the environment cells need to thrive and multiply). Further vocabulary that will become familiar includes diffusion (passive movement of oxygen and nutrients from regions of high concentration to regions of low concentration), stem cells (cells with the potential to develop into different bodily cell types), progenitor cells (early descendants of stem cells), gene expression (the process by which proteins develop from instructions in our DNA), and growth factors (substances—often proteins—that stimulate cell growth, proliferation, and differentiation). The book contains an extensive glossary for quick reference.

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