scholarly journals Polychlorinated biphenyl toxicity in the thyroid gland of wild ungulates: an in vitro model

2020 ◽  
Vol 89 (2) ◽  
pp. 151-162
Author(s):  
Ehdaa Eltayeb Eltigani Abdelsalam ◽  
Hana Banďouchová ◽  
Tomáš Heger ◽  
Miroslava Kaňová ◽  
Kateřina Kobelková ◽  
...  
Keyword(s):  
Polychlorinated Biphenyl ◽  
Roe Deer ◽  
Three Dimensional ◽  
Fallow Deer ◽  
Target Cells ◽  
Wild Ungulates ◽  
Iodide Uptake ◽  
Significant Drop ◽  
Test Species

Polychlorinated biphenyls (PCBs) are carcinogens causing endocrine disruption. While production of PCBs is now banned, wildlife exposure still occurs due to environmental contamination. We investigated thyroid toxicity in wild ungulates using three-dimensional primary thyrocyte cultures exposed to PCB 138 for 24, 48, and 72 h at concentrations ranging within 0–3000 ng/ml. Thyrocyte viability ranged within 78.71–118.34%, 98.14–104.45%, and 84.16–106.70% in fallow deer-, mouflon-, and roe deer-derived cells, respectively. Viability decreased significantly in fallow deer (P = 0.012) and roe deer (P = 0.002) thyrocytes exposed for 48 h at 30 ng/ml. While cytotoxicity ranged within 2.36–16.37%, 3.19–9.85%, and 2.76–11.21% in fallow deer, mouflon, and roe deer, respectively, only roe deer displayed significantly higher cytotoxicity at a 3 ng/ml exposure (P < 0.05) and lower cytotoxicity at 30 ng/ml (P < 0.01). Exposure to 30 ng/ml for 24 and 48 h induced reactive oxygen species in fallow deer. Iodide uptake at 30 ng/ml exposure increased after 24 h in fallow and roe deer, but showed a significant drop after 48 and 72 h in fallow deer, mouflon, and roe deer. Thyroxine T4 release at 30 ng/ml exposure decreased significantly after 48 and 72 h; 24, 48 and 72 h; and 48 h in fallow deer, mouflon, and roe deer, respectively. Our findings indicate time- and species-dependent effects of PCB on performance and thyrocyte function. Use of cell culture models reduces the number of experimental specimens, increases test species welfare and replaces whole organisms with specific target cells.

scholarly journals Diesel Particulate Matter 2.5 Induces Epithelial-to-Mesenchymal Transition and Upregulation of SARS-CoV-2 Receptor during Human Pluripotent Stem Cell-Derived Alveolar Organoid Development

2020 ◽  
Vol 17 (22) ◽  
pp. 8410
Author(s):  
Jung-Hyun Kim ◽  
Jeeyoung Kim ◽  
Woo Jin Kim ◽  
Yung Hyun Choi ◽  
Se-Ran Yang ◽  
...  
Keyword(s):  
Particulate Matter ◽  
Epithelial To Mesenchymal Transition ◽  
Alveolar Epithelial Cell ◽  
Developmental Toxicity ◽  
Three Dimensional ◽  
Nicotinamide Adenine Dinucleotide Phosphate ◽  
The Body ◽  
Target Cells ◽  
Mesenchymal Transition

Growing evidence links prenatal exposure to particulate matter (PM2.5) with reduced lung function and incidence of pulmonary diseases in infancy and childhood. However, the underlying biological mechanisms of how prenatal PM2.5 exposure affects the lungs are incompletely understood, which explains the lack of an ideal in vitro lung development model. Human pluripotent stem cells (hPSCs) have been successfully employed for in vitro developmental toxicity evaluations due to their unique ability to differentiate into any type of cell in the body. In this study, we investigated the developmental toxicity of diesel fine PM (dPM2.5) exposure during hPSC-derived alveolar epithelial cell (AEC) differentiation and three-dimensional (3D) multicellular alveolar organoid (AO) development. We found that dPM2.5 (50 and 100 μg/mL) treatment disturbed the AEC differentiation, accompanied by upregulation of nicotinamide adenine dinucleotide phosphate oxidases and inflammation. Exposure to dPM2.5 also promoted epithelial-to-mesenchymal transition during AEC and AO development via activation of extracellular signal-regulated kinase signaling, while dPM2.5 had no effect on surfactant protein C expression in hPSC-derived AECs. Notably, we provided evidence, for the first time, that angiotensin-converting enzyme 2, a receptor to mediate the severe acute respiratory syndrome coronavirus clade 2 (SARS-CoV-2) entry into target cells, and the cofactor transmembrane protease serine 2 were significantly upregulated in both hPSC-AECs and AOs treated with dPM2.5. In conclusion, we demonstrated the potential alveolar development toxicity and the increase of SARS-Cov-2 susceptibility of PM2.5. Our findings suggest that an hPSC-based 2D and 3D alveolar induction system could be a useful in vitro platform for evaluating the adverse effects of environmental toxins and for virus research.

scholarly journals Wild ungulates in Jordan: past, present, and forthcoming opportunities

2021 ◽  
Vol 13 (9) ◽  
pp. 19338-19351
Author(s):  
Ehab Eid ◽  
David Mallon
Keyword(s):  
Cervus Elaphus ◽  
Roe Deer ◽  
Capreolus Capreolus ◽  
Fallow Deer ◽  
Current Status ◽  
Wild Ungulates ◽  
Equus Hemionus ◽  
Wild Ass ◽  
In The Wild ◽  
Arabian Oryx

Twelve species of ungulates are reported from the wild in Jordan. Three of these, Addax nasomaculatus (Addax), Bos primigenius (Aurochs), and Cervus elaphus (Red Deer) are known only from archaeological excavations. Dama mesopotamica (Mesopotamian Fallow Deer), Oryx leucoryx (Arabian Oryx) and Equus hemionus hemippus (Syrian Wild Ass) have been regionally extirpated in the wild. A semi-captive population of Persian Onager (E. h. hemionus) is held in Shumari Wildlife Reserve. The Arabian Oryx is also managed in semi-captive conditions in two reserves. Except the commonly occurring Wild Boar (Sus scrofa), other surviving ungulate species continue to be under serious threat. Gazella gazella (Palestinian Mountain Gazelle), Capreolus capreolus (European Roe Deer), Gazella marica (Arabian Sand Gazelle), and Gazella dorcas (Dorcas Gazelle) are Critically Endangered, and Capra nubiana (Nubian Ibex) is Endangered in the region. This paper provides a review of the historical and current status of wild ungulates in Jordan, listing the threats and conservation measures and provides recommendations for management and conservation in the future.

IN-VITRO STUDIES OF NORMAL HUMAN THYROID CELLS: RESPONSES TO THYROTROPHIN AND DIBUTYRYL CYCLIC AMP

1977 ◽  
Vol 72 (1) ◽  
pp. 87-96 ◽  
Author(s):  
S. P. BIDEY ◽  
P. MARSDEN ◽  
J. ANDERSON ◽  
C. G. McKERRON ◽  
H. BERRY
Keyword(s):  
Cyclic Amp ◽  
Thyroid Tissue ◽  
Three Dimensional ◽  
Human Thyroid ◽  
Dibutyryl Cyclic Amp ◽  
Iodide Uptake ◽  
Thyroid Cells ◽  
Normal Human

SUMMARY Follicular cells isolated from normal human thyroid tissue have been cultured for up to 140 h with bovine thyrotrophin (TSH) or dibutyryl cyclic AMP (DBcAMP). Both compounds induced marked reorganization of the cells into three-dimensional follicular structures, whilst non-supplemented cells assumed a monolayer form. Cultures treated initially with TSH or DBcAMP showed a greater iodide uptake capacity, in comparison with unsupplemented cultures, in which iodide uptake was markedly diminished after 24 h. The release of tri-iodothyronine (T3) and thyroxine (T4) into the medium was determined by radioimmunoassay. Both TSH- and DBcAMP-treated cells showed a significant increase in iodothyronine output compared with unsupplemented control cells. In contrast to the 'classical' TSH-induced depression of the T4:T3 ratio in vivo, an increase in the ratio was observed for both TSH- and DBcAMP-supplemented cells in vitro. The ratio was also significantly greater after TSH than after DBcAMP, and possible implications of this finding are discussed.

scholarly journals Spatiotemporal patterns of wolf, mesocarnivores and prey in a Mediterranean area

2021 ◽  
Vol 75 (2) ◽  
Author(s):  
Mariana Rossa ◽  
Sandro Lovari ◽  
Francesco Ferretti
Keyword(s):  
Wild Boar ◽  
Red Fox ◽  
Roe Deer ◽  
Fallow Deer ◽  
Apex Predator ◽  
Wild Ungulates ◽  
Apex Predators ◽  
Predator Prey ◽  
Behavioural Interactions ◽  
Temporal Overlap

Abstract Spatial and temporal occurrence can mediate behavioural interactions between apex predators, mesocarnivores and herbivores. Predators should adapt their activity to that of prey, whereas predator avoidance would be expected to influence activity patterns and space use of prey and smaller competitors. We evaluated interspecific spatiotemporal relationships in a prey-rich community including an apex predator (the wolf), three wild ungulates and several smaller herbivores/mesocarnivores, through camera trapping. All considered species (i.e. wolves and potential prey/smaller competitors: wild boar, fallow deer, roe deer, crested porcupine, red fox and European badger) were active especially at night and/or twilight. Among wild ungulates, the wolf showed the greatest temporal overlap with the wild boar and the lowest one with the least abundant and used of them, i.e. the roe deer. The main prey (i.e. the fallow deer) showed more diurnal activity and a lower temporal overlap with the predator in sites with high wolf activity than in low-activity ones. Among mesocarnivores, the red fox showed extensive temporal overlap with the wolf: the overlap between the two canids was greater in sites intensively used by this apex predator than in sites with low wolf activity, supporting a concurrent study which suggested a potential for facilitative—rather than competitive—interactions. Spatiotemporal relationships suggest complex interactions between the apex predator, prey and smaller carnivores, for which a substantial temporal or spatial association was often supported. Significance statement There is a growing interest in the influence of apex predators on ecosystems through their effects on the behaviour of prey and smaller carnivores, especially in the light of the ongoing recovery of large carnivores in temperate areas. Predators should synchronise their activity to that of prey; conversely, prey and smaller carnivores would be expected to avoid predators. In a rich community including the wolf, three wild ungulates and several mesomammals, we detected (i) a substantial temporal overlap between wolves and wild boar, porcupines and mesocarnivores; (ii) a negative temporal association between the predator and its main prey (i.e. the fallow deer) and (iii) a great temporal overlap between the wolf and the red fox. We provide a baseline to evaluate temporal changes of predator-prey-mesocarnivore behavioural interactions along with variations of carnivore-prey densities.

scholarly journals Human Embryonic Stem Cell-derived Lung Organoids: a Model for SARS-CoV-2 Infection and Drug Test

2020 ◽  
Author(s):  
Rongjuan Pei ◽  
Jianqi Feng ◽  
Yecheng Zhang ◽  
Hao Sun ◽  
Lian Li ◽  
...  
Keyword(s):  
Stem Cell ◽  
Cell Lines ◽  
Three Dimensional ◽  
Embryonic Stem ◽  
Target Cells ◽  
Alveolar Type ◽  
Physiological Conditions ◽  
Self Organized ◽  
Respiratory Droplets

AbstractThe coronavirus disease 2019 (COVID-19) pandemic is caused by infection with the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), which is spread primary via respiratory droplets and infects the lungs. Currently widely used cell lines and animals are unable to accurately mimic human physiological conditions because of the abnormal status of cell lines (transformed or cancer cells) and species differences between animals and humans. Organoids are stem cell-derived self-organized three-dimensional culture in vitro and model the physiological conditions of natural organs. Here we demonstrated that SARS-CoV-2 infected and extensively replicated in human embryonic stem cells (hESCs)-derived lung organoids, including airway and alveolar organoids. Ciliated cells, alveolar type 2 (AT2) cells and rare club cells were virus target cells. Electron microscopy captured typical replication, assembly and release ultrastructures and revealed the presence of viruses within lamellar bodies in AT2 cells. Virus infection induced more severe cell death in alveolar organoids than in airway organoids. Additionally, RNA-seq revealed early cell response to SARS-CoV-2 infection and an unexpected downregulation of ACE2 mRNA. Further, compared to the transmembrane protease, serine 2 (TMPRSS2) inhibitor camostat, the nucleotide analog prodrug Remdesivir potently inhibited SARS-CoV-2 replication in lung organoids. Therefore, human lung organoids can serve as a pathophysiological model for SARS-CoV-2 infection and drug discovery.

scholarly journals Mapping of a dengue virus neutralizing epitope critical for the infectivity of all serotypes: insight into the neutralization mechanism

2001 ◽  
Vol 82 (8) ◽  
pp. 1885-1892 ◽  
Author(s):  
Philippe Thullier ◽  
Caroline Demangel ◽  
Hugues Bedouelle ◽  
Françoise Mégret ◽  
Alain Jouan ◽  
...  
Keyword(s):  
Amino Acids ◽  
Dengue Virus ◽  
Three Dimensional ◽  
Phage Clone ◽  
Health Concern ◽  
Target Cells ◽  
Virus Infections ◽  
Three Dimensional Model ◽  
Virus Envelope

Dengue virus infections are a growing public health concern and strategies to control the spread of the virus are urgently needed. The murine monoclonal antibody 4E11 might be of interest, since it neutralizes dengue viruses of all serotypes by binding to the 296–400 segment of the major dengue virus envelope glycoprotein (DE). When phage-displayed peptide libraries were screened by affinity for 4E11, phage clone C1 was selected with a 50% frequency. C1 shared three of nine residues with DE306–314 and showed significant reactivity to 4E11 in ELISA. C1-induced antibodies cross-reacted with DE296–400 in mice, suggesting that it was a structural equivalent of the native epitope of 4E11 on DE. Accordingly, 4E11 bound to the DE306–314 synthetic peptide and this reaction was inhibited by DE296–400. Moreover, DE306–314 could block dengue virus infection of target cells in an in vitro assay. A three-dimensional model of DE revealed that the three amino acids shared by DE296–400 and C1 were exposed to the solvent and suggested that most of the amino acids comprising the 4E11 epitope were located in the DE306–314 region. Since 4E11 blocked the binding of DE296–400 to heparin, which is a highly sulfated heparan sulfate (HSHS) molecule, 4E11 may act by neutralizing the interaction of DE306–314 with target cell-displayed HSHS. Our data suggest that the DE306–314 segment is critical for the infectivity of all dengue virus serotypes and that molecules that block the binding of DE306–314 to HSHS may be antiviral reagents of therapeutic interest.

Ultrastructural Investigations of the Contractile Filaments of Amoebae

1974 ◽  
Vol 32 ◽  
pp. 188-189
Author(s):  
P.L. Moore
Keyword(s):  
Cytoplasmic Streaming ◽  
Three Dimensional ◽  
Freeze Fracture ◽  
Amoeboid Movement ◽  
Different Types ◽  
Chemical Conditions ◽  
Complete Interpretation

Previous freeze fracture results on the intact giant, amoeba Chaos carolinensis indicated the presence of a fibrillar arrangement of filaments within the cytoplasm. A complete interpretation of the three dimensional ultrastructure of these structures, and their possible role in amoeboid movement was not possible, since comparable results could not be obtained with conventional fixation of intact amoebae. Progress in interpreting the freeze fracture images of amoebae required a more thorough understanding of the different types of filaments present in amoebae, and of the ways in which they could be organized while remaining functional.The recent development of a calcium sensitive, demembranated, amoeboid model of Chaos carolinensis has made it possible to achieve a better understanding of such functional arrangements of amoeboid filaments. In these models the motility of demembranated cytoplasm can be controlled in vitro, and the chemical conditions necessary for contractility, and cytoplasmic streaming can be investigated. It is clear from these studies that “fibrils” exist in amoeboid models, and that they are capable of contracting along their length under conditions similar to those which cause contraction in vertebrate muscles.

Correlated Studies of Cellular Interactions Using TEM, Freeze Etching, and SEM

1974 ◽  
Vol 32 ◽  
pp. 320-321
Author(s):  
J. P. Revel
Keyword(s):  
Developmental Stages ◽  
Three Dimensional ◽  
Cell Movement ◽  
Cellular Interactions ◽  
Serial Sections ◽  
Cell Sheets ◽  
Freeze Etching ◽  
Early Developmental

Movement of individual cells or of cell sheets and complex patterns of folding play a prominent role in the early developmental stages of the embryo. Our understanding of these processes is based on three- dimensional reconstructions laboriously prepared from serial sections, and from autoradiographic and other studies. Many concepts have also evolved from extrapolation of investigations of cell movement carried out in vitro. The scanning electron microscope now allows us to examine some of these events in situ. It is possible to prepare dissections of embryos and even of tissues of adult animals which reveal existing relationships between various structures more readily than used to be possible vithout an SEM.

In vitro and in vivo polysaccharides assembly: ultrastructural and cytochemical study of growing plant cell wall components.

1978 ◽  
Vol 36 (2) ◽  
pp. 434-435
Author(s):  
D. Reis ◽  
B. Vian ◽  
J. C. Roland
Keyword(s):  
Cell Wall ◽  
Self Assembly ◽  
Plant Cell Wall ◽  
Higher Plants ◽  
Three Dimensional ◽  
Cytochemical Study ◽  
Wall Components

Wall morphogenesis in higher plants is a problem still open to controversy. Until now the possibility of a transmembrane control and the involvement of microtubules were mostly envisaged. Self-assembly processes have been observed in the case of walls of Chlamydomonas and bacteria. Spontaneous gelling interactions between xanthan and galactomannan from Ceratonia have been analyzed very recently. The present work provides indications that some processes of spontaneous aggregation could occur in higher plants during the formation and expansion of cell wall.Observations were performed on hypocotyl of mung bean (Phaseolus aureus) for which growth characteristics and wall composition have been previously defined.In situ, the walls of actively growing cells (primary walls) show an ordered three-dimensional organization (fig. 1). The wall is typically polylamellate with multifibrillar layers alternately transverse and longitudinal. Between these layers intermediate strata exist in which the orientation of microfibrils progressively rotates. Thus a progressive change in the morphogenetic activity occurs.

Ultrastructural Changes in Tumor Cells During Human Peripheral Blood Monocyte-Mediated Cytotoxicity

1981 ◽  
Vol 39 ◽  
pp. 452-453
Author(s):  
K. E. Muse ◽  
D. G. Fischer ◽  
H. S. Koren
Keyword(s):  
Target Cell ◽  
Human Peripheral Blood ◽  
Mononuclear Phagocytes ◽  
Ultrastructural Changes ◽  
Target Cells ◽  
Limited Information ◽  
Blood Monocytes ◽  
Tumoricidal Activity ◽  
Activated State

Mononuclear phagocytes, a pluripotential cell line, manifest an array of basic extracellular functions. Among these physiological regulatory functions is the expression of spontaneous cytolytic potential against tumor cell targets.The limited observations on human cells, almost exclusively blood monocytes, initially reported limited or a lack of tumoricidal activity in the absence of antibody. More recently, freshly obtained monocytes have been reported to spontaneously impair the biability of tumor target cells in vitro (Harowitz et al., 1979; Montavani et al., 1979; Hammerstrom, 1979). Although the mechanism by which effector cells express cytotoxicity is poorly understood, discrete steps can be distinguished in the process of cell mediated cytotoxicity: recognition and binding of effector to target cells,a lethal-hit stage, and subsequent lysis of the target cell. Other important parameters in monocyte-mediated cytotoxicity include, activated state of the monocyte, effector cell concentrations, and target cell suseptibility. However, limited information is available with regard to the ultrastructural changes accompanying monocyte-mediated cytotoxicity.

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