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1.
J Vis Exp ; (183)2022 05 27.
Article in English | MEDLINE | ID: mdl-35695523

ABSTRACT

Caenorhabditis elegans is a powerful model organism used in many research laboratories to understand the consequences of exposure to chemical pollutants, pesticides, and a wide variety of toxic substances. These nematodes are easy to work with and can be used to generate novel research findings, even in the undergraduate biology laboratory. A multi-week laboratory series of authentic, student-driven research projects trains students in a toolkit of techniques and approaches in behavioral measurements, cell biology, and microscopy that they then apply to their projects. One technique in that toolkit is quantifying the percentage of neurons exhibiting neurodegenerative damage following exposure to a chemical toxicant like a pesticide. Young adult C. elegans nematodes can be exposed to different concentrations of commercially available pesticides or other types of toxicants for 2-24 h. Then, undergraduate students can visualize different neuron subtypes using fluorescent-expressing strains of C. elegans. These techniques do not require sophisticated image processing software and are effective at even low magnifications, making the need for expensive confocal microscopy unnecessary. This paper demonstrates how to treat the nematodes with pesticides and how to image and score the neurons. It also provides a straightforward protocol for the microscopy and analysis of neuron morphology. The materials used for this technique are inexpensive and readily available in most undergraduate biology departments. This technique can be combined with behavioral measures like locomotion, basal slowing, or egg-laying to conduct a potentially publishable series of experiments and give undergraduate students an authentic research experience at a very low cost.


Subject(s)
Environmental Pollutants , Pesticides , Animals , Caenorhabditis elegans/metabolism , Humans , Locomotion , Neurons/metabolism , Pesticides/toxicity
2.
PLoS One ; 15(9): e0238637, 2020.
Article in English | MEDLINE | ID: mdl-32903270

ABSTRACT

Neonicotinoids, a class of insecticides structurally similar to nicotine that target biting and sucking insects, are the most widely used insecticides today, in part due to their supposed low toxicity in other organisms. However, a growing body of research has found that even low doses of neonicotinoids can induce unexpected negative effects on the physiology and survival of a wide range of non-target organisms. Importantly, no work has been done on the commercial formulations of pesticides that include imidacloprid as the active ingredient, but that also contain many other components. The present study examines the sublethal effects of "Tree and Shrub"™ ("T+S"), a commercial insecticide containing the neonicotinoid imidacloprid as its active ingredient, on Caenorhabditis elegans. We discovered that "T+S" significantly stunted the overall growth in wildtype nematodes, an effect that was exacerbated by concurrent exposure to heat stress. "T+S" also negatively impacted fecundity as measured by increased germline apoptosis, a decrease in egg-laying, and fewer viable offspring. Lastly, exposure to "T+S" resulted in degenerative changes in nicotinic cholinergic neurons in wildtype nematodes. As a whole, these findings demonstrate widespread toxic effects of neonicotinoids to critical functions in nematodes.


Subject(s)
Caenorhabditis elegans/growth & development , Caenorhabditis elegans/physiology , Insecticides/toxicity , Locomotion/drug effects , Neonicotinoids/toxicity , Animals , Apoptosis/drug effects , Caenorhabditis elegans/drug effects , Cholinergic Neurons/drug effects , Cholinergic Neurons/metabolism , Chromosome Aberrations , Fertility/drug effects , Germ Cells/cytology , Germ Cells/drug effects , Heat-Shock Response , Nerve Degeneration/pathology , Oviposition/drug effects , Reproduction/drug effects
3.
Environ Pollut ; 250: 447-455, 2019 Jul.
Article in English | MEDLINE | ID: mdl-31026691

ABSTRACT

Recent studies have demonstrated the occurrence of microplastic fibers (MFs) in soil environments. To determine whether MFs are harmful for soil biota, we evaluated toxic effects on terrestrial snails (Achatina fulica) after 28 d exposure to polyethylene terephthalate MFs at concentrations of 0.01-0.71 g kg-1 (dry soil weight). Digestion kinetics experiments on 24 snails showed that MFs can be ingested and excreted within 48 h. We found the appearance of cracks and deterioration on the surface of MFs after depuration by the digestive system. Prolonged exposure to 40 snails showed that 0.14-0.71 g kg-1 MFs caused an average reduction of 24.7-34.9% food intake and 46.6-69.7% excretion. 0.71 g kg-1 MFs induced significant villi damage in the gastrointestinal walls of 40% snails, but did not influence the histology of the liver and kidney. Moreover, 0.71 g kg-1 MFs exposure reduced glutathione peroxidase (59.3 ±â€¯13.8%) and total antioxidant capacity (36.7 ±â€¯8.5%), but elevated malondialdehyde level (58.0 ±â€¯6.4%) in the liver, which indicates oxidative stress is involved in the toxic mechanism. Our results suggest that MFs have adverse impacts on the fitness of soil organisms, and highlight the ecological risks of microplastic pollution in terrestrial ecosystems.


Subject(s)
Polyethylene Terephthalates/metabolism , Snails/physiology , Soil Pollutants/metabolism , Animals , Biota , Ecosystem , Environmental Pollution , Glutathione , Malondialdehyde/metabolism , Oxidative Stress , Peroxidases , Plastics , Polyethylene Terephthalates/toxicity , Soil/chemistry , Soil Pollutants/toxicity
4.
Ecotoxicol Environ Saf ; 153: 8-15, 2018 May 30.
Article in English | MEDLINE | ID: mdl-29407742

ABSTRACT

The decline in amphibian populations is a critical threat to global biodiversity, and pesticide pollution is considered as one of the major factors. Although effects of single pesticides on amphibians have been documented, toxicological interactions prevailing in mixtures of pesticides have not been well elucidated. Strobilurin and succinate dehydrogenase inhibitor (SDHI) fungicides are new types of commonly used pesticides. In this study, effects of three strobilurins (pyraclostrobin, trifloxystrobin and azoxystrobin), two SDHIs (isopyrazam and bixafen), and their mixtures on X. tropicalis embryos were fully investigated. Results showed that exposure to individual fungicides induced lethal and teratogenetic effects; and malformed embryos displayed similar phenotypes including microcephaly, hypopigmentation, somite segmentation and narrow fin. Exposure to two strobilurins or two SDHIs at equitoxic concentrations caused additive or synergetic effects at environmentally relevant concentrations. TU for mixtures of isopyrazam and bixafen was 0.53 and 0.30 for lethal and teratogenic toxicity, respectively. Finally, binary mixtures of strobilurins and SDHIs also exhibited additive or synergetic effects on amphibian embryos. Overall, these results reveal that the mixtures of multiple fungicides caused a higher incidence of lethality and teratogenicity of amphibian embryos, compared to a single fungicide at the corresponding doses. Our findings provide important data about the ecotoxicology of agricultural fungicides on non-target organisms, which is useful for guiding management practices for pesticides.


Subject(s)
Embryo, Nonmammalian/drug effects , Enzyme Inhibitors/toxicity , Fungicides, Industrial/toxicity , Strobilurins/toxicity , Succinate Dehydrogenase/antagonists & inhibitors , Teratogens/toxicity , Animals , Drug Synergism , Ecotoxicology , Embryo, Nonmammalian/abnormalities , Xenopus
5.
Sci Total Environ ; 619-620: 1-8, 2018 Apr 01.
Article in English | MEDLINE | ID: mdl-29136530

ABSTRACT

Microplastics have been frequently detected in aquatic environments, and there are increasing concerns about potential effects on biota. In this study, zebrafish Danio rerio and nematode Caenorhabditis elegans were used as model organisms for microplastic exposure in freshwater pelagic (i.e. water column) and benthic (i.e. sediment) environments. We investigated the toxic effects of five common types of microplastics: polyamides (PA), polyethylene (PE), polypropylene (PP), polyvinyl chloride (PVC) and polystyrene (PS) particles. Results showed no or low lethality in D. rerio after exposure for 10d at 0.001-10.0mgL-1 microplastics. The PA, PE, PP and/or PVC microplastics with ~70µm size caused intestinal damage including cracking of villi and splitting of enterocytes. Exposure to 5.0mgm-2 microplastics for 2d significantly inhibited survival rates, body length and reproduction of C. elegans. Moreover, exposure to microplastics reduced calcium levels but increased expression of the glutathione S-transferase 4 enzyme in the intestine, which indicates intestinal damage and oxidative stress are major effects of microplastic exposure. Among 0.1, 1.0 and 5.0µm sizes of fluorescently labeled PS, 1.0µm particles caused the highest lethality, the maximum accumulation, the lowest Ca2+ level in the intestine and the highest expression of glutathione S-transferase 4 in nematodes. Taken together, these findings suggest that intestinal damage is a key effect of microplastics; and that the toxicity of microplastics is closely dependent on their size, rather than their composition.


Subject(s)
Caenorhabditis elegans , Intestines/injuries , Plastics/adverse effects , Water Pollutants, Chemical/adverse effects , Zebrafish , Animals , Calcium , Environmental Monitoring , Glutathione Transferase , Oxidative Stress
6.
PLoS One ; 12(12): e0189341, 2017.
Article in English | MEDLINE | ID: mdl-29283995

ABSTRACT

We report the results of in vivo studies in Caenorhabditis elegans nematodes in which addition of extra virgin olive oil (EVOO) to their diet significantly increased their life span with respect to the control group. Furthermore, when nematodes were exposed to the pesticide paraquat, they started to die after two days, but after the addition of EVOO to their diet, both survival percentage and lifespans of paraquat-exposed nematodes increased. Since paraquat is associated with superoxide radical production, a test for scavenging this radical was performed using cyclovoltammetry and the EVOO efficiently scavenged the superoxide. Thus, a linear correlation (y = -0.0838x +19.73, regression factor = 0.99348) was observed for superoxide presence (y) in the voltaic cell as a function of aliquot (x) additions of EVOO, 10 µL each. The originally generated supoeroxide was approximately halved after 10 aliquots (100 µL total). The superoxide scavenging ability was analyzed, theoretically, using Density Functional Theory for tyrosol and hydroxytyrosol, two components of EVOO and was also confirmed experimentally for the galvinoxyl radical, using Electron Paramagnetic Resonance (EPR) spectroscopy. The galvinoxyl signal disappeared after adding 1 µL of EVOO to the EPR cell in 10 minutes. In addition, EVOO significantly decreased the proliferation of human leukemic THP-1 cells, while it kept the proliferation at about normal levels in rat L6 myoblasts, a non-tumoral skeletal muscle cell line. The protection due to EVOO was also assessed in L6 cells and THP-1 exposed to the radical generator cumene hydroperoxide, in which cell viability was reduced. Also in this case the oxidative stress was ameliorated by EVOO, in line with results obtained with tetrazolium dye reduction assays, cell cycle analysis and reactive oxygen species measurements. We ascribe these beneficial effects to EVOO antioxidant properties and our results are in agreement with a clear health benefit of EVOO use in the Mediterranean diet.


Subject(s)
Diet, Mediterranean , Olive Oil/pharmacology , Oxidative Stress/drug effects , Animals , Caenorhabditis elegans/drug effects , Caenorhabditis elegans/metabolism , Cell Cycle/drug effects , Cell Line , Electron Spin Resonance Spectroscopy , Humans , In Vitro Techniques , Olive Oil/chemistry , Paraquat/toxicity , Rats , Reactive Oxygen Species/metabolism
7.
J Vis Exp ; (127)2017 09 13.
Article in English | MEDLINE | ID: mdl-28930977

ABSTRACT

This manuscript describes how to classify nematodes using temporal far-field diffraction signatures. A single C. elegans is suspended in a water column inside an optical cuvette. A 632 nm continuous wave HeNe laser is directed through the cuvette using front surface mirrors. A significant distance of at least 20-30 cm traveled after the light passes through the cuvette ensures a useful far-field (Fraunhofer) diffraction pattern. The diffraction pattern changes in real time as the nematode swims within the laser beam. The photodiode is placed off-center in the diffraction pattern. The voltage signal from the photodiode is observed in real time and recorded using a digital oscilloscope. This process is repeated for 139 wild type and 108 "roller" C. elegans. Wild type worms exhibit a rapid oscillation pattern in solution. The "roller" worms have a mutation in a key component of the cuticle that interferes with smooth locomotion. Time intervals that are not free of saturation and inactivity are discarded. It is practical to divide each average by its maximum to compare relative intensities. The signal for each worm is Fourier transformed so that the frequency pattern for each worm emerges. The signal for each type of worm is averaged. The averaged Fourier spectra for the wild type and the "roller" C. elegans are distinctly different and reveal that the dynamic worm shapes of the two different worm strains can be distinguished using Fourier analysis. The Fourier spectra of each worm strain match an approximate model using two different binary worm shapes that correspond to locomotory moments. The envelope of the averaged frequency distribution for actual and modeled worms confirms the model matches the data. This method can serve as a baseline for Fourier analysis for many microscopic species, as every microorganism will have its unique Fourier spectrum.


Subject(s)
Caenorhabditis elegans/anatomy & histology , X-Ray Diffraction/methods , Animals
8.
Bull Environ Contam Toxicol ; 97(1): 119-23, 2016 Jul.
Article in English | MEDLINE | ID: mdl-27095033

ABSTRACT

Perfluorooctane sulfonate (PFOS) is a persistent organic pollutant. Although multiple adverse effects of PFOS have been demonstrated, whether PFOS can accelerate aging and affect animal longevity remains unknown. In Caenorhabditis elegans, we found that a 50 h exposure to 0.2-200 µM PFOS reduced lifespan in a concentration dependent manner. In transgenic nematodes, lifespans are affected by mutations of daf-16, daf-2 or age-1 genes, which are related to the Insulin/IGF-1 Signaling pathway (IIS). PFOS exposure caused an additional reduction in average lifespan in daf-2(e1370) and daf-16b(KO) nematodes. In contrast, daf-16(mu86) nematodes showed no additional reduction with PFOS exposure and age-1(hx546) mutants did not exhibit a reduction in lifespan with PFOS exposure, compared with wildtype nematodes. Overall, our findings demonstrate that PFOS exposure accelerates aging and shortens longevity of animals. The PFOS-induced effect may involve genes of the IIS pathway, particularly daf-16 and age-1.


Subject(s)
Alkanesulfonic Acids/toxicity , Caenorhabditis elegans Proteins/physiology , Caenorhabditis elegans/drug effects , Environmental Pollutants/toxicity , Fluorocarbons/toxicity , Insulin-Like Growth Factor I/physiology , Insulin/physiology , Animals , Caenorhabditis elegans/physiology , Caenorhabditis elegans Proteins/genetics , Genes, Helminth , Insulin-Like Growth Factor I/genetics , Longevity/drug effects , Mutation , Signal Transduction
9.
J Esthet Restor Dent ; 28(2): 102-9, 2016.
Article in English | MEDLINE | ID: mdl-26880426

ABSTRACT

BACKGROUND: This study evaluated the preferences of dental professionals and lay persons with respect to the Recurring Esthetic Dental (RED) Proportion, an objective mathematical tool used in treatment planning the "apparent" widths of maxillary anterior teeth. MATERIALS AND METHODS: Stock dentofacial and facial images of a prototypical smiling male and female were digitally altered to demonstrate five different RED proportion relationships (0.62, 0.65, 0.70, 0.75, and 0.80). Four sets of the five altered images were presented to dental professionals and lay persons using a web-based survey site. The professional group included dentists and dental laboratory technicians. The lay group included anyone without previous dental education or experience. Study participants were asked to rank each series from most to least esthetic and their preferences were extracted from the data. RESULTS: Preference data from the five RED proportion relationships was consolidated into two categories: a narrow group including 0.62, 0.65, and 0.70 and a broad group including 0.75 and 0.80. Analysis shows that the level of professional training or experience does not play a significant role in the RED proportion preferences of study participants. Only in the prototypical male facial views was there any significant difference between professional and lay groups. For that view, a greater percentage of the layperson group preferred the narrow RED proportions. However, for the male dentofacial views that difference disappeared and both participant groups showed a slight preference for the broad proportion category. This may be due to the traditional esthetic stereotype for males to have broader, more vigorous appearing anterior teeth. For the prototypical female images, all participants expressed a clear, statistically significant preference for the narrower RED proportions in both full face and close up views. CONCLUSIONS: Based on the results above, dental professionals who are developing a treatment plan should attempt to utilize a RED proportion ≤ 0.70 for both male and female patients. CLINICAL SIGNIFICANCE: The RED proportion is an objective numeric tool for relating the apparent widths of maxillary anterior teeth. It may be used by dental professionals to help diagnose and develop an optimal esthetic treatment plan. This paper offers insight into whether there are specific RED proportions that are preferred, whether there is a difference in preference when considering the male or female smile and whether professional educational training changes those preferences.


Subject(s)
Dentists , Esthetics, Dental , Patient Preference , Female , Humans , Male
10.
J Vis Exp ; (86)2014 Apr 18.
Article in English | MEDLINE | ID: mdl-24798818

ABSTRACT

This study demonstrates an inexpensive and straightforward technique that allows the measurement of physical properties such as position, velocity, acceleration and forces involved in the locomotory behavior of nematodes suspended in a column of water in response to single wavelengths of light. We demonstrate how to evaluate the locomotion of a microscopic organism using Single Wavelength Shadow Imaging (SWSI) using two different examples. The first example is a systematic and statistically viable study of the average descent of C. elegans in a column of water. For this study, we used living and dead wildtype C. elegans. When we compared the velocity and direction of nematode active movement with the passive descent of dead worms within the gravitational field, this study showed no difference in descent-times. The average descent was 1.5 mm/sec ± 0.1 mm/sec for both the live and dead worms using 633 nm coherent light. The second example is a case study of select individual C. elegans changing direction during the descent in a vertical water column. Acceleration and force are analyzed in this example. This case study demonstrates the scope of other physical properties that can be evaluated using SWSI while evaluating the behavior using single wavelengths in an environment that is not accessible with traditional microscopes. Using this analysis we estimated an individual nematode is capable of thrusting with a force in excess of 28 nN. Our findings indicate that living nematodes exert 28 nN when turning, or moving against the gravitational field. The findings further suggest that nematodes passively descend in a column of water, but can actively resist the force of gravity primarily by turning direction.


Subject(s)
Caenorhabditis elegans/physiology , Image Enhancement/methods , Locomotion/physiology , Optics and Photonics/methods , Animals , Biomechanical Phenomena , Swimming
11.
Neurotoxicology ; 34: 74-81, 2013 Jan.
Article in English | MEDLINE | ID: mdl-23103283

ABSTRACT

Manganese-containing fungicides like Mancozeb have been associated with neurodegenerative conditions like Parkinson's disease. We examined the behavioral damage and differential neuronal vulnerability resulting from Mancozeb exposure using Caenorhabditis elegans, an important mid-trophic level soil organism that is also a powerful model for studying mechanisms of environmental pollutant-induced neurodegenerative disease. The dopamine-mediated swim to crawl locomotory transition behavior is exquisitely vulnerable to Mancozeb, with functional impairment preceding markers of neuronal structural damage. The damage is partially rescued in mutants lacking the divalent metal transporter, SMF-1, demonstrating that some, but not all, of the damage is mediated by manganese. Increasing concentrations of Mancozeb recruit additional behavioral dysfunction, notably serotonin-mediated egg-laying behavior, but without evident serotonergic neuronal structural damage. Thus, measurements of behavioral dysfunction are a sensitive early marker of fungicide toxicity that could be exploited to examine further mechanisms of neuron damage and possible therapeutic interventions. These results also provide important insight into the consequences of fungicide use on the ecological behavior of nematodes.


Subject(s)
Behavior, Animal/drug effects , Caenorhabditis elegans/drug effects , Environmental Pollutants/toxicity , Fungicides, Industrial/toxicity , Maneb/toxicity , Nerve Degeneration , Neurons/drug effects , Zineb/toxicity , Animals , Caenorhabditis elegans/genetics , Caenorhabditis elegans/metabolism , Caenorhabditis elegans Proteins/genetics , Caenorhabditis elegans Proteins/metabolism , Cation Transport Proteins/genetics , Cation Transport Proteins/metabolism , Dopamine/metabolism , Dose-Response Relationship, Drug , Environmental Pollutants/metabolism , Fungicides, Industrial/metabolism , Locomotion/drug effects , Maneb/metabolism , Mechanotransduction, Cellular/drug effects , Mutation , Neurons/metabolism , Neurons/pathology , Oviposition/drug effects , Serotonin/metabolism , Touch , Zineb/metabolism
13.
J Undergrad Neurosci Educ ; 8(2): A108-15, 2010.
Article in English | MEDLINE | ID: mdl-23493645

ABSTRACT

In this paper, we describe and assess a laboratory module that we introduced into an intermediate-level undergraduate course in Neuroscience and Behavior (NEUR201) in order to expose students to the new and rapidly developing neurogenomic and bioinformatics approaches to neuroscience research. The laboratory accompanies a topics-based, highly process-oriented course that explores research methodologies and integrative approaches to particular topics in the field. The laboratory comprises multi-week modules that expand upon the topics being covered in class. In the class for which this module was developed, a key topic under discussion is the role played by the nervous system in aging and/or lifespan. This laboratory module focuses on the model organism, Caenorhabditis elegans (C. elegans), which has been studied extensively. There is a large and ongoing literature elucidating a number of genes involved in determining or modulating lifespan in C. elegans. Students choose a candidate gerontogene expressed in neurons in C. elegans from a provided list for which we have mutant strains. Students use available databases to become experts on their candidate gene and design, carry out and analyze a behavioral experiment. In addition, students use available bioinformatics and genomic tools to conduct a protein sequence phylogenetic analysis of their candidate protein across at least 10 different taxa of animals. The laboratory module thus focuses on the integration of behavioral, genetic and bioinformatics approaches, as well as on the evolutionary considerations of the role played by gerontogenes in different organisms.

14.
Mech Dev ; 126(5-6): 289-300, 2009.
Article in English | MEDLINE | ID: mdl-19303437

ABSTRACT

During Drosophila oogenesis, organized microtubule networks coordinate the localization of specific RNAs, the positioning of the oocyte nucleus, and ooplasmic streaming events. We used mutations in mini spindles (msps), a microtubule-associated protein, to disrupt microtubule function during mid- and late-oogenesis, and show that msps is required for these microtubule-based events. Since endoplasmic reticulum (ER) organization is influenced by microtubules in other systems, we hypothesized that using msps to alter microtubule dynamics might affect the structure and organization of the ER in nurse cells and the oocyte. ER organization was monitored using GFP-tagged versions of Reticulon-like1 and protein disulfide isomerase. Analyses of living cells indicate microtubule associations mediate the movement of ER components within the oocyte. Surprisingly, the distribution and behavior of tubular ER in the oocyte differs from general ER, suggesting these two compartments of the ER interact differently with microtubules. We find that the morphology of Exu particles is msps-dependent, and that Exu is specifically associated with tubular ER in msps mutants. Our results extend previous descriptions of sponge bodies and the fusome, suggesting both are manifestations of a dynamic structure that interacts with microtubules and persists throughout oogenesis.


Subject(s)
Drosophila Proteins/genetics , Drosophila Proteins/metabolism , Drosophila melanogaster/metabolism , Egg Proteins/metabolism , Endoplasmic Reticulum/metabolism , Microtubule-Associated Proteins/genetics , Microtubule-Associated Proteins/metabolism , Microtubules/metabolism , Mutation/genetics , RNA-Binding Proteins/metabolism , Animals , Cell Nucleus/metabolism , Cytoplasmic Streaming , Drosophila melanogaster/cytology , Green Fluorescent Proteins/metabolism , Oocytes/cytology , Oocytes/metabolism , Recombinant Fusion Proteins/metabolism
15.
Dev Genes Evol ; 218(10): 541-51, 2008 Oct.
Article in English | MEDLINE | ID: mdl-18807071

ABSTRACT

PTL-1, a microtubule-associated protein of the structural MAP2/tau family, is the sole member of this gene family in Caenorhabditis elegans. Sequence analysis of available invertebrate genomes revealed a number of single, putative tau-like genes with high similarity to ptl-1. The ptl-1 gene is expressed in a number of cells, most notably mechanosensory neurons. We examined the role of ptl-1 in C. elegans in adult neurons as well as during development. A ptl-1 knockout strain of worms exhibited an egg-hatching defect, as well as a reduced sensitivity to touch stimuli. In addition, the knockout allele ptl-1(ok621) acts as a dominant enhancer of several temperature-sensitive alleles of mec-7 and mec-12, which code the isoforms of beta-tubulin and alpha-tubulin that together form the unusual 15 protofilament microtubules involved in touch sensation. These results demonstrate for the first time a functional role for this microtubule-associated protein in nematodes and suggest that PTL-1 is involved in mechanosensation as well as some aspect of embryogenesis.


Subject(s)
Caenorhabditis elegans Proteins/metabolism , Caenorhabditis elegans/growth & development , Caenorhabditis elegans/metabolism , Mechanotransduction, Cellular , Microtubule-Associated Proteins/metabolism , Amino Acid Sequence , Animals , Caenorhabditis elegans/genetics , Caenorhabditis elegans Proteins/chemistry , Caenorhabditis elegans Proteins/genetics , Female , Gene Deletion , Gene Expression Regulation , Larva/cytology , Larva/metabolism , Microtubule-Associated Proteins/chemistry , Microtubule-Associated Proteins/genetics , Microtubules/metabolism , Molecular Sequence Data , Neurons/cytology , Neurons/metabolism , Ovum/cytology , Ovum/metabolism , RNA, Messenger/genetics , RNA, Messenger/metabolism , Sequence Homology, Amino Acid , Touch , tau Proteins/chemistry
16.
Brain Res ; 978(1-2): 38-50, 2003 Jul 18.
Article in English | MEDLINE | ID: mdl-12834896

ABSTRACT

MAP2 (microtubule-associated protein 2) is a cytoskeletal phosphoprotein that regulates the dynamic assembly characteristics of microtubules and appears to provide scaffolding for organelle distribution into the dendrites and for the localization of signal transduction apparatus in dendrites, particularly near spines. MAP2 is degraded after ischemia and other metabolic insults, but the time course and initial triggers of that breakdown are not fully understood. This study determined that MAP2 resides in a complex with the NMDA receptor, suggesting that spatially localized changes may be important in the mechanism of MAP2 redistribution and breakdown after oxygen-glucose deprivation (OGD). Using OGD in the adult rat hippocampal slice as a model system, this study demonstrated that MAP2 breakdown occurs very early after OGD, with the first statistical decrease in MAP2 levels within the first 30 min after the insult. There is a dramatic redistribution of MAP2 to the somata of pyramidal neurons, particularly neurons at the CA1-subiculum border. Free radicals and nitric oxide are not involved in the damage to MAP2. NMDA-receptor activation plays a prominent role in the MAP2 breakdown. In direct response to NMDA receptor activation, calcium influx, likely through the receptor ion channel complex, as well as release of calcium from the mitochondria through activation of the 2Na(+)-Ca(2+) exchanger of mitochondria, triggers MAP2 degradation. The proteolysis of MAP2 is limited by endogenous calpain activity, likely via the spatial access of calpain to MAP2.


Subject(s)
Glucose/metabolism , Hippocampus/cytology , Hypoxia/metabolism , Microtubule-Associated Proteins/metabolism , Neurons/metabolism , Receptors, N-Methyl-D-Aspartate/metabolism , Animals , Calcium/physiology , Calcium Channel Blockers/pharmacology , Dizocilpine Maleate/pharmacology , Dose-Response Relationship, Drug , Excitatory Amino Acid Agonists/pharmacology , Excitatory Amino Acid Antagonists/pharmacology , Glucose/deficiency , Glycoproteins/pharmacology , Hippocampus/metabolism , Immunoblotting/methods , Immunohistochemistry/methods , In Vitro Techniques , Male , N-Methylaspartate/pharmacology , Neurons/drug effects , Oxygen/metabolism , Precipitin Tests/methods , Protein Subunits/metabolism , Rats , Rats, Sprague-Dawley , Time Factors
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