13 research outputs found

    A Muscle-Specific p38 MAPK/Mef2/MnSOD Pathway Regulates Stress, Motor Function, and Life Span in Drosophila

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    SummaryMolecular mechanisms that concordantly regulate stress, life span, and aging remain incompletely understood. Here, we demonstrate that in Drosophila, a p38 MAP kinase (p38K)/Mef2/MnSOD pathway is a coregulator of stress and life span. Hence, overexpression of p38K extends life span in a MnSOD-dependent manner, whereas inhibition of p38K causes early lethality and precipitates age-related motor dysfunction and stress sensitivity, that is rescued through muscle-restricted (but not neuronal) add-back of p38K. Additionally, mutations in p38K are associated with increased protein carbonylation and Nrf2-dependent transcription, while adversely affecting metabolic response to hypoxia. Mechanistically, p38K modulates expression of the mitochondrial MnSOD enzyme through the transcription factor Mef2, and predictably, perturbations in MnSOD modify p38K-dependent phenotypes. Thus, our results uncover a muscle-restricted p38K-Mef2-MnSOD signaling module that influences life span and stress, distinct from the insulin/JNK/FOXO pathway. We propose that potentiating p38K might be instrumental in restoring the mitochondrial detoxification machinery and combating stress-induced aging

    Glossary on atmospheric electricity and its effects on biology

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    [EN] There is an increasing interest to study the interactions between atmospheric electrical parameters and living organisms at multiple scales. So far, relatively few studies have been published that focus on possible biological effects of atmospheric electric and magnetic fields. To foster future work in this area of multidisciplinary research, here we present a glossary of relevant terms. Its main purpose is to facilitate the process of learning and communication among the different scientific disciplines working on this topic. While some definitions come from existing sources, other concepts have been re-defined to better reflect the existing and emerging scientific needs of this multidisciplinary and transdisciplinary area of research.This paper is based upon work from the COST Action "Atmospheric Electricity Network: coupling with the Earth System, climate and biological systems (ELECTRONET)," supported by COST (European Cooperation in Science and Technology). AO received funding from Poland Ministry of Science and Higher Education for statutory research of the Institute of Geophysics, Polish Academy of Sciences (Grant No 3841/E-41/S/2019).Fdez-Arroyabe, P.; Kourtidis, K.; Haldoupis, C.; Savoska, S.; Matthews, J.; Mir, LM.; Kassomenos, P.... (2021). Glossary on atmospheric electricity and its effects on biology. International Journal of Biometeorology. 65(1):5-29. https://doi.org/10.1007/s00484-020-02013-9S529651Adrovic F (2012) Editor, Gamma radiation, IntechOpen.Alberts B (2014). Molecular biology of the cell (6th ed.). New York. ISBN 9780815344322Ambus Per, (2015) Sophie Zechmeister-Boltenstern Sophie, in Biology of the Nitrogen Cycle, 2007.G.P. Robertson1, P.M. Groffman2, in Soil Microbiology, Ecology and Biochemistry (4th Edition)Apollonio F, Liberti M, Paffi A, Merla C, Marracino P, Denzi A, Marino C, d’Inzeo G (2013) Feasibility for microwaves energy to affect biological systems via nonthermal mechanisms: a systematic approach. 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    THE STUDY OF THE NEUROMUSCULAR SYSTEM WHICH CONTROLS THE MOVEMENT OF THE ABDOMEN IN THE INSECT D. ALBIFRONS

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    THE NEUROMUSCULAR SYSTEM OF THE PREGENITAL ABDOMINAL SEGMENTS OF D.ALBIFRONS, HAS BEEN DESCRIBED IN DETAIL. TWELVE PAIRS OF MUSCLES HAVE BEEN FOUND IN THE TYPICAL ABDOMINAL SEGMENTS (4TH TO 8TH). FIVE OF THESE PAIRS ARE LOCATED IN THE VENTRAL REGION OF THE SEGMENTS, FIVE PAIRS IN THE LATERAL REGIONS AND TWO PAIRS OF MUSCLES IN THE DORSAL REGION OF THE SEGMENTS. THE VENTRAL NERVE CORD CONSISTS OF SIX ABDOMINAL GANGLIA. THE FIRST "REAL" ABDOMINAL GANGLION IS FUSED AND CONSISTS OF THE 2ND AND 3RD NEUROMERES, INNERVATING THE 2ND AND 3RD ABDOMINAL SEGMENTS. THE FIRST SEGMENT IS INNERVATED BY NERVES (N7, N8) ARISING FROM THE METATHORACIC GANGLION. THERE IS ONLY ONE PAIR OF MAIN NERVE ROOTS (N1)WHICH INNERVATES THE MOST OF THE SEGMENTAL MUSCLES, WHILE MEDIAN NERVES SUPPLY THE SPIRACULAR MUSCLES. FROM THE LARGE GROUP OF THE ABDOMINAL SEGMENTAL MUSCLES, THE ANATOMICAL AND ELECTROPHYSIOLOGICAL PROPERTIES OF TWO MAIN MUSCLESHAVE BEEN STUDIED. DURING VENTILATION MOST OF THE ABDOMINAL VENTILATORY MUSCLES CONTRACT SIMULTANEOUSLY IN PHACE WITH EXPIRATION. IT IS WELL KNOWN THAT, THIS BEHAVIOURAL MOTOR PATTERN IS CONTROLLED BY A CENTRAL PATTERN GENERATOR (CPG), WHICH IN OTHER ORTHOPTERA IS LOCATED IN THE FUSED METATHORACIC GANGLION. IND.ALBIFRONS LESSION EXPERIMENTS OF NERVE CORD HAVE SHOWN THAT THE CPG IS LOCATED IN THE FIRST ABDOMINAL GANGLION. THIS GANGLION IS ALSO FUSED BUT CONTAINS A SMALLER NUMBER OF NEURONS, A FACT WHICH ALLOWS FURTHER STUDIES OF ELECTROPHYSIOLOGICAL PROPERTIES OF CPG.ΟΙ ΜΥΕΣ ΤΩΝ ΠΡΟΓΕΝΝΗΤΙΚΩΝ ΜΕΤΑΜΕΡΩΝ ΤΗΣ ΚΟΙΛΙΑΣ, ΤΗΣ ΑΚΡΙΔΑΣ DECTICUS ALBIFRONS, ΣΥΜΜΕΤΕΧΟΥΝ ΣΤΗΝ ΑΝΑΠΝΕΥΣΤΙΚΗ ΔΙΑΔΙΚΑΣΙΑ ΑΦΟΥ ΕΝΕΡΓΟΠΟΙΟΥΝΤΑΙ ΚΑΤΑ ΤΗ ΦΑΣΗ ΤΗΣ ΕΚΠΝΟΗΣ. ΣΤΟ ΕΝΤΟΜΟ ΑΥΤΟ ΔΕΝ ΥΠΑΡΧΟΥΝ ΕΙΣΠΝΕΥΣΤΙΚΟΙ ΜΥΕΣ. Η ΜΟΡΦΟΛΟΓΙΚΗΜΕΛΕΤΗ ΤΟΥ ΜΥΙΚΟΥ ΣΥΣΤΗΜΑΤΟΣ, ΑΥΤΩΝ ΤΩΝ ΜΕΤΑΜΕΡΩΝ, ΕΔΕΙΞΕ ΟΤΙ ΔΩΔΕΚΑ ΖΕΥΓΗ ΜΥΩΝ ΔΙΕΥΘΕΤΟΥΝΤΑΙ ΣΤΙΣ ΤΡΕΙΣ ΠΕΡΙΟΧΕΣ ΚΑΘΕ ΜΕΤΑΜΕΡΟΥΣ. ΠΕΝΤΕ ΖΕΥΓΗ ΜΥΩΝ ΕΝΤΟΠΙΣΤΗΚΑΝ ΤΟΣΟ ΣΤΗΝ ΚΟΙΛΙΑΚΗ ΟΣΟ ΚΑΙ ΣΤΙΣ ΠΛΕΥΡΙΚΕΣ ΠΕΡΙΟΧΕΣ ΕΝΩ ΔΥΟ ΖΕΥΓΗ ΜΥΩΝ ΒΡΕΘΗΚΑΝ ΣΤΙΣ ΡΑΧΙΑΙΕΣ ΠΕΡΙΟΧΕΣ ΤΩΝ ΜΕΤΑΜΕΡΩΝ. Η ΚΟΙΛΙΑΚΗ ΝΕΥΡΙΚΗ ΧΟΡΔΗ ΑΠΟΤΕΛΕΙΤΑΙ ΑΠΟ ΕΞΙ ΓΑΓΓΛΙΑ, ΕΚ ΤΩΝ ΟΠΟΙΩΝ ΤΟ ΠΡΩΤΟ ΓΑΓΓΛΙΟ ΕΙΝΑΙ ΠΡΟΙΟΝ ΣΥΜΦΥΣΗΣ ΔΥΟ ΓΑΓΓΛΙΩΝ. ΕΝΑ ΖΕΥΓΟΣ ΝΕΥΡΙΚΩΝ ΟΔΩΝ (Ν1), ΠΟΥ ΔΙΑΚΛΑΔΙΖΟΝΤΑΙ, ΝΕΥΡΩΝΕΙ ΤΟΥΣ ΠΕΡΙΣΣΟΤΕΡΟΥΣ ΜΥΣ ΤΟΥ ΚΑΘΕ ΜΕΤΑΜΕΡΟΥΣ. ΔΥΟ ΟΜΑΔΕΣ ΑΝΑΠΝΕΥΣΤΙΚΩΝ ΜΥΩΝ ΤΗΣ ΚΟΙΛΙΑΣ, ΟΙ ΡΑΧΑΙΟΙ ΔΙΑΤΜΗΜΑΤΙΚΟΙ ΚΑΙ ΟΙ ΕΓΚΑΡΣΙΟΙ ΚΟΙΛΙΑΚΟΙ ΜΥΕΣ, ΕΞΕΤΑΣΤΗΚΑΝ ΩΣ ΠΡΟΣ ΤΑ ΜΟΡΦΟΛΟΓΙΚΑ ΚΑΙ ΤΑ ΦΥΣΙΟΛΟΓΙΚΑ ΤΟΥΣ ΧΑΡΑΚΤΗΡΙΣΤΙΚΑ. ΤΟ ΤΕΛΕΥΤΑΙΟ ΤΜΗΜΑΤΗΣ ΠΑΡΟΥΣΑΣ ΕΡΓΑΣΙΑΣ ΑΦΟΡΟΥΣΕ ΤΟΝ ΕΝΤΟΠΙΣΜΟ ΤΟΥ ΑΝΑΠΝΕΥΣΤΙΚΟΥ ΚΕΝΤΡΟΥ (ΑΚ) ΣΤΟ D.ALBIFRONS. ΤΟ ΚΥΡΙΟ ΑΝΑΠΝΕΥΣΤΙΚΟ ΚΕΝΤΡΟ ΕΝΤΟΠΙΣΤΗΚΕ ΣΤΟ ΠΡΩΤΟ ΚΟΙΛΙΑΚΟ ΓΑΓΓΛΙΟ. Ο ΑΝΑΠΝΕΥΣΤΙΚΟΣ ΡΥΘΜΟΣ ΠΟΥ ΔΗΜΙΟΥΡΓΕΙΤΑΙ ΣΤΟ ΠΡΩΤΕΥΟΝ ΑΝΑΠΝΕΥΣΤΙΚΟ ΚΕΝΤΡΟ ΜΕΤΑΦΕΡΕΤΑΙ ΣΤΑ ΔΕΥΤΕΡΕΥΟΝΤΑ ΑΝΑΠΝΕΥΣΤΙΚΑ ΚΕΝΤΡΑ ΠΟΥ ΕΝΤΟΠΙΖΟΝΤΑΙ ΣΕ ΚΑΘΕ ΓΑΓΓΛΙΟ ΧΩΡΙΣΤΑ. ΟΙ ΑΝΑΠΝΕΥΣΤΙΚΕΣ ΕΝΤΟΛΕΣ ΜΕΤΑ ΤΗΝ ΕΠΕΞΕΡΓΑΣΙΑ ΠΟΥ ΥΦΙΣΤΑΝΤΑΙ ΣΤΑ ΔΕΥΤΕΡΕΥΟΝΤΑ ΑΝΑΠΝΕΥΣΤΙΚΑ ΚΕΝΤΡΑ ΜΕΤΑΦΕΡΟΝΤΑΙ ΤΕΛΙΚΑ ΣΤΟΥΣ ΜΥΣ ΟΛΩΝ ΤΩΝΜΕΤΑΜΕΡΩΝ. (ΠΕΡΙΚΟΠΗ ΠΕΡΙΛΗΨΗΣ

    Evidence for cell autonomous AP1 function in regulation of Drosophila motor-neuron plasticity

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    BACKGROUND:The transcription factor AP1 mediates long-term plasticity in vertebrate and invertebrate central nervous systems. Recent studies of activity-induced synaptic change indicate that AP1 can function upstream of CREB to regulate both CREB-dependent enhancement of synaptic strength as well as CREB-independent increase in bouton number at the Drosophila neuromuscular junction (NMJ). However, it is not clear from this study if AP1 functions autonomously in motor neurons to directly modulate plasticity.RESULTS:Here, we show that Fos and Jun, the two components of AP1, are abundantly expressed in motor neurons. We further combine immunohistochemical and electrophysiological analyses with use of a collection of enhancers that tightly restrict AP1 transgene expression within the nervous system to show that AP1 induction or inhibition in, but not outside of, motor neurons is necessary and sufficient for its modulation of NMJ size and strength.CONCLUSION:By arguing against the possibility that AP1 effects at the NMJ occur via a polysynaptic mechanism, these observations support a model in which AP1 directly modulates NMJ plasticity processes through a cell autonomous pathway in the motor neuron. The approach described here may serve as a useful experimental paradigm for analyzing cell autonomy of genes found to influence structure and function of Drosophila motor neurons.This item is part of the UA Faculty Publications collection. For more information this item or other items in the UA Campus Repository, contact the University of Arizona Libraries at [email protected]

    CORL Expression and Function in Insulin Producing Neurons Reversibly Influences Adult Longevity in Drosophila

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    CORL proteins (known as SKOR in mice, Fussel in humans and fussel in Flybase) are a family of CNS specific proteins related to Sno/Ski oncogenes. Their developmental and adult roles are largely unknown. A Drosophila CORL (dCORL) reporter gene is expressed in all Drosophila insulin-like peptide 2 (dILP2) neurons of the pars intercerebralis (PI) of the larval and adult brain. The transcription factor Drifter is also expressed in the PI in a subset of dCORL and dILP2 expressing neurons and in several non-dILP2 neurons. dCORL mutant virgin adult brains are missing all dILP2 neurons that do not also express Drifter. This phenotype is also seen when expressing dCORL-RNAi in neurosecretory cells of the PI. dCORL mutant virgin adults of both sexes have a significantly shorter lifespan than their parental strain. This longevity defect is completely reversed by mating (lifespan increases over 50% for males and females). Analyses of dCORL mutant mated adult brains revealed a complete rescue of dILP2 neurons without Drifter. Taken together, the data suggest that dCORL participates in a neural network connecting the insulin signaling pathway, longevity and mating. The conserved sequence and CNS specificity of all CORL proteins imply that this network may be operating in mammals

    Adult Movement Defects Associated with a CORL Mutation in Drosophila Display Behavioral Plasticity

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    The CORL family of CNS-specific proteins share a Smad-binding region with mammalian SnoN and c-Ski protooncogenes. In this family Drosophila CORL has two mouse and two human relatives. Roles for the mouse and human CORL proteins are largely unknown. Based on genome-wide association studies linking the human CORL proteins Fussel15 and Fussel18 with ataxia, we tested the hypothesis that dCORL mutations will cause adult movement disorders. For our initial tests, we conducted side by side studies of adults with the small deletion Df(4)dCORL and eight control strains. We found that deletion mutants exhibit three types of behavioral plasticity. First, significant climbing defects attributable to loss of dCORL are eliminated by age. Second, significant phototaxis defects due to loss of dCORL are partially ameliorated by age and are not due to faulty photoreceptors. Third, Df(4)dCORL males raised in groups have a lower courtship index than males raised as singles though this defect is not due to loss of dCORL. Subsequent tests showed that the climbing and phototaxis defects were phenocpied by dCORL21B and dCORL23C two CRISPR generated mutations. Overall, the finding that adult movement defects due to loss of dCORL are subject to age-dependent plasticity suggests new hypotheses for CORL functions in flies and mammals

    Development and Evaluation of Automated Tools for Auditory-Brainstem and Middle-Auditory Evoked Potentials Waves Detection and Annotation

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    Auditory evoked potentials (AEPs) are brain-derived electrical signals, following an auditory stimulus, utilised to examine any obstructions along the brain neural-pathways and to diagnose hearing impairment. The clinical evaluation of AEPs is based on the measurements of the latencies and amplitudes of waves of interest; hence, their identification is a prerequisite for AEP analysis. This process has proven to be complex, as it requires relevant clinical experience, and the existing software for this purpose has little practical use. The aim of this study was the development of two automated annotation tools for ABR (auditory brainstem response)- and AMLR (auditory middle latency response)-tests. After the acquisition of 1046 raw waveforms, appropriate pre-processing and implementation of a four-stage development process were performed, to define the appropriate logical conditions and steps for each algorithm. The tools’ detection and annotation results, regarding the waves of interest, were then compared to the clinicians’ manual annotation, achieving match rates of at least 93.86%, 98.51%, and 91.51% respectively, for the three ABR-waves of interest, and 93.21%, 92.25%, 83.35%, and 79.27%, respectively, for the four AMLR-waves. The application of such tools in AEP analysis is expected to assist towards an easier interpretation of these signals

    Supplemental Material for Tran et al., 2018

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    Table S1. <i>dCORL</i> mutant virgin and mated adult longevity defects compared to seven control lines.<div><br></div><div>Table S2. Mean & median longevity of <i>dCORL</i> virgin and mated adults with seven controls.<br></div><div><br></div><div>Table S3. Significant brain size reduction is present in <i>Df(4)dCORL</i> larvae but not adults.<br></div
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