A fish gill system for quantifying the ultrastructural effects of environmental stressors: methylmercury, Kepone®, and heat shock

1995 ◽  
Vol 52 (6) ◽  
pp. 1165-1182 ◽  
Author(s):  
Jon Mallatt ◽  
Steven J. Lampa ◽  
J. Franklin Bailey ◽  
Marc A. Evans ◽  
Steve Brumbaugh

In previous histopathological studies, fish gills have been used to study nonspecific responses of tissue to injury; however, such studies have revealed little about the specific effects of different toxicants on cells. Here, we used transmission electron microscopy plus a morphometric technique (stereology) to determine how several types of gill cells are specifically altered by three stressors: methylmercury, heat shock, and the insecticide Kepone® (chlordecone). Larval sea lampreys, Petromyzon marinus, were exposed to various concentrations of waterborne stressor (ranging from the incipient lethal concentrations to a 24-h LC50) for different periods (half a day or 3 weeks). Methylmercury increased the volumes of gill epithelial cells and their nuclei and mitochondria, presumably by inducing ambient water to leak into these structures. Heat shock, by contrast, decreased the volumes of most cells and their organelles, presumably by causing cells to shed pieces of cytoplasm. Kepone had almost no effect, but the few changes that were recorded (increased mitochondrial volume in one cell type) are consistent with known actions of Kepone® (alteration of mitochondrial respiration). The results prove that a fish gill can be used to probe the specific actions of different toxicants and pollutants.

2009 ◽  
Vol 11 (12) ◽  
pp. 1750-1767 ◽  
Author(s):  
Anna Fahlgren ◽  
Linda Westermark ◽  
Karen Akopyan ◽  
Maria Fällman

Genome ◽  
1997 ◽  
Vol 40 (3) ◽  
pp. 379-385
Author(s):  
Klaus Werner Wolf

Kinetochore structure was examined in a total of 6 species from 5 different families of the Coleoptera using transmission electron microscopy of ultrathin serial sections. Metaphase spermatogonia and primary and secondary spermatocytes were studied in Tenebrio molitor (Tenebrionidae) to determine whether kinetochore structure varies depending on the cell type. In all three cell types, the kinetochore microtubules (MTs) were in direct contact with the chromosomal surface, and kinetochore plates were not detectable. In the other species, only metaphase I spermatocytes were examined. As in T. molitor, distinct kinetochore plates were also absent in Adelocera murina (Elateridae), Agapanthia villosoviridescens (Cerambycidae), and Coccinella septempunctata (Coccinellidae). However, bivalents in male meiosis of two representatives of the Chrysomelidae, Agelastica alni and Chrysolina graminis, showed roughly spherical kinetochores at their poleward surfaces. Microtubules were in contact with this material. Thus, although the present survey covers only a small number of species, it is clear that at least two kinetochore types occur in the Coleoptera. The cytological findings are discussed in the context of chromosome number and genome size variability in the Coleopteran families studied. It is suggested that properties of the kinetochores could play a role in karyotype evolution in the Coleoptera.Key words: bivalent, microtubule, meiosis, metaphase, spermatocyte.


2020 ◽  
Author(s):  
Caitlin A. Murphy ◽  
Matthew I. Banks

ABSTRACTBackgroundWhile their behavioral effects are well-characterized, the mechanisms by which anaesthetics induce loss of consciousness are largely unknown. Anaesthetics may disrupt integration and propagation of information in corticothalamic networks. Recent studies have shown that isoflurane diminishes synaptic responses of thalamocortical (TC) and corticocortical (CC) afferents in a pathway-specific manner. However, whether the synaptic effects of isoflurane observed in extracellular recordings persist at the cellular level has yet to be explored.MethodsHere, we activate TC and CC layer 1 inputs in non-primary mouse neocortex in ex vivo brain slices and explore the degree to which isoflurane modulates synaptic responses in pyramidal cells and in two inhibitory cell populations, somatostatin-positive (SOM+) and parvalbumin-positive (PV+) interneurons.ResultsWe show that the effects of isoflurane on synaptic responses and intrinsic properties of these cells varies among cell type and by cortical layer. Layer 1 inputs to L4 pyramidal cells were suppressed by isoflurane at both TC and CC synapses, while those to L2/3 pyramidal cells and PV+ interneurons were not. TC inputs to SOM+ cells were rarely observed at all, while CC inputs to SOM+ interneurons were robustly suppressed by isoflurane.ConclusionsThese results suggest a mechanism by which isoflurane disrupts integration and propagation of thalamocortical and intracortical signals.


2018 ◽  
Vol 223 (8) ◽  
pp. 3689-3709 ◽  
Author(s):  
Marta Zagrebelsky ◽  
N. Gödecke ◽  
A. Remus ◽  
Martin Korte

PEDIATRICS ◽  
1978 ◽  
Vol 62 (5) ◽  
pp. 795-800
Author(s):  
Thomas R. Walters ◽  
Jun Minowada ◽  
Teruhiko Tsubota ◽  
Katsuko Kataoka ◽  
Tin Han

A child with chronic myelocytic leukemia (CML), Philadelphia chromosome positive, developed a non-T cell, non-B cell, acute lymmphocytic leukemia (ALL) during her blast cell crisis. The diagnosis was suggested by light microscopy and supported by histochemical stains and transmission electron microscopy. Immunologic studies showed the presence of a non-T, non-B leukemic blast population—indistinguishable from the most common form of ALL (null cell type). Markedly elevated terminal deoxynucleotidyl transferase (TdT) activity was found. The findings support the hypothesis that the primary cell involved in CML is a stem cell with pluripotential characteristics; frequently the blast cell proliferative phase terminates in acute myeloblastic leukemia, but it may also terminate in ALL. The TdT activity may be evidence of leukemic transformation and not necessarily related to the thymic origin of the lymphocytes.


2000 ◽  
Vol 74 (23) ◽  
pp. 11398-11406 ◽  
Author(s):  
Karl W. Boehme ◽  
Vsevolod L. Popov ◽  
Hans W. Heidner

ABSTRACT The Sindbis virus variant NE2G216 is a PE2-containing host range mutant that is growth restricted in cultured mosquito cells (C6/36) due to inefficient release of virions from this cell type. The maturation defect of NE2G216 has been linked to the structures of N-linked oligosaccharides synthesized by arthropod cells. Analysis of C6/36 cells infected with NE2G216 by transmission electron microscopy revealed the presence of dense virus aggregates within cytoplasmic vacuoles and virus aggregates adhered to the cell surface. The virus aggregation phenotype of NE2G216 was reproduced in vertebrate cells (Pro-5) by the addition of 1-deoxymannojirimycin, an inhibitor of carbohydrate processing which limits the processing of N-linked oligosaccharides to structures that are structurally similar, albeit not identical, to those synthesized in C6/36 cells. We conclude that defective maturation of NE2G216 in mosquito cells is due to virion aggregation and retention on the cell surface and that this phenotype is directly linked to the carbohydrate-processing properties of these cells.


2017 ◽  
Vol 12 (1) ◽  
Author(s):  
Mariko Ogawa ◽  
Fuminori Saitoh ◽  
Norihiro Sudou ◽  
Fumi Sato ◽  
Hiroki Fujieda

2012 ◽  
Vol 18 (3) ◽  
pp. 377-387 ◽  
Author(s):  
Zhe Jing ◽  
Rajendra K. Gangalum ◽  
Josh Z. Lee ◽  
Dennis Mock ◽  
Suraj P. Bhat
Keyword(s):  

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