Thalamic Integration of Social Stimuli Regulating
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Searching for Novel Peptide Hormones in the Human Genome Olivier Mirabeau
Searching for novel peptide hormones in the human genome Olivier Mirabeau To cite this version: Olivier Mirabeau. Searching for novel peptide hormones in the human genome. Life Sciences [q-bio]. Université Montpellier II - Sciences et Techniques du Languedoc, 2008. English. tel-00340710 HAL Id: tel-00340710 https://tel.archives-ouvertes.fr/tel-00340710 Submitted on 21 Nov 2008 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. UNIVERSITE MONTPELLIER II SCIENCES ET TECHNIQUES DU LANGUEDOC THESE pour obtenir le grade de DOCTEUR DE L'UNIVERSITE MONTPELLIER II Discipline : Biologie Informatique Ecole Doctorale : Sciences chimiques et biologiques pour la santé Formation doctorale : Biologie-Santé Recherche de nouvelles hormones peptidiques codées par le génome humain par Olivier Mirabeau présentée et soutenue publiquement le 30 janvier 2008 JURY M. Hubert Vaudry Rapporteur M. Jean-Philippe Vert Rapporteur Mme Nadia Rosenthal Examinatrice M. Jean Martinez Président M. Olivier Gascuel Directeur M. Cornelius Gross Examinateur Résumé Résumé Cette thèse porte sur la découverte de gènes humains non caractérisés codant pour des précurseurs à hormones peptidiques. Les hormones peptidiques (PH) ont un rôle important dans la plupart des processus physiologiques du corps humain. -
Diversity of Central Oxytocinergic Projections
Cell and Tissue Research (2019) 375:41–48 https://doi.org/10.1007/s00441-018-2960-5 REVIEW Diversity of central oxytocinergic projections Gustav F. Jirikowski1 Received: 21 September 2018 /Accepted: 6 November 2018 /Published online: 29 November 2018 # Springer-Verlag GmbH Germany, part of Springer Nature 2018 Abstract Localization and distribution of hypothalamic neurons expressing the nonapeptide oxytocin has been extensively studied. Their projections to the neurohypophyseal system release oxytocin into the systemic circulation thus controlling endocrine events associated with reproduction in males and females. Oxytocinergic neurons seem to be confined to the ventral hypothalamus in all mammals. Groups of such cells located outside the supraoptic and the paraventricular nuclei are summarized as Baccessory neurons.^ Although evolutionary probably associated with the classical magocellular nuclei, accessory oxytocin neurons seem to consist of rather heterogenous groups: Periventricular oxytocin neurons may gain contact to the third ventricle to secrete the peptide into the cerebrospinal fluid. Perivascular neurons may be involved in control of cerebral blood flow. They may also gain access to the portal circulation of the anterior pituitary lobe. Central projections of oxytocinergic neurons extend to portions of the limbic system, to the mesencephalon and to the brain stem. Such projections have been associated with control of behaviors, central stress response as well as motor and vegetative functions. Activity of the different oxytocinergic systems seems to be malleable to functional status, strongly influenced by systemic levels of steroid hormones. Keywords Hypothalamo neurohypophyseal system . Circumventricular organs . Liquor contacting neurons . Perivascular system . Limbic system Introduction been shown to occur in prostate, gonads, or skin, OTexpression in the brain seems to be confined to the hypothalamus. -
Role of Amylase in Ovarian Cancer Mai Mohamed University of South Florida, [email protected]
University of South Florida Scholar Commons Graduate Theses and Dissertations Graduate School July 2017 Role of Amylase in Ovarian Cancer Mai Mohamed University of South Florida, [email protected] Follow this and additional works at: http://scholarcommons.usf.edu/etd Part of the Pathology Commons Scholar Commons Citation Mohamed, Mai, "Role of Amylase in Ovarian Cancer" (2017). Graduate Theses and Dissertations. http://scholarcommons.usf.edu/etd/6907 This Dissertation is brought to you for free and open access by the Graduate School at Scholar Commons. It has been accepted for inclusion in Graduate Theses and Dissertations by an authorized administrator of Scholar Commons. For more information, please contact [email protected]. Role of Amylase in Ovarian Cancer by Mai Mohamed A dissertation submitted in partial fulfillment of the requirements for the degree of Doctor of Philosophy Department of Pathology and Cell Biology Morsani College of Medicine University of South Florida Major Professor: Patricia Kruk, Ph.D. Paula C. Bickford, Ph.D. Meera Nanjundan, Ph.D. Marzenna Wiranowska, Ph.D. Lauri Wright, Ph.D. Date of Approval: June 29, 2017 Keywords: ovarian cancer, amylase, computational analyses, glycocalyx, cellular invasion Copyright © 2017, Mai Mohamed Dedication This dissertation is dedicated to my parents, Ahmed and Fatma, who have always stressed the importance of education, and, throughout my education, have been my strongest source of encouragement and support. They always believed in me and I am eternally grateful to them. I would also like to thank my brothers, Mohamed and Hussien, and my sister, Mariam. I would also like to thank my husband, Ahmed. -
Regulation of Hypothalamic Signaling by Tuberoinfundibular Peptide of 39
18166 • The Journal of Neuroscience, December 7, 2011 • 31(49):18166–18179 Behavioral/Systems/Cognitive Regulation of Hypothalamic Signaling by Tuberoinfundibular Peptide of 39 Residues Is Critical for the Response to Cold: A Novel Peptidergic Mechanism of Thermoregulation Eugene L. Dimitrov, Yoon Yi Kim, and Ted B. Usdin Section On Fundamental Neuroscience, National Institute Of Mental Health, National Institutes Of Health, Bethesda, Maryland 20892 Euthermia is critical for mammalian homeostasis. Circuits within the preoptic hypothalamus regulate temperature, with fine control exerted via descending GABAergic inhibition of presympathetic motor neurons that control brown adipose tissue (BAT) thermogenesis and cutaneous vascular tone. The thermoregulatory role of hypothalamic excitatory neurons is less clear. Here we report peptidergic regulation of preoptic glutamatergic neurons that contributes to temperature regulation. Tuberoinfundibular peptide of 39 residues (TIP39) is a ligand for the parathyroid hormone 2 receptor (PTH2R). Both peptide and receptor are abundant in the preoptic hypothal- amus. Based on PTH2R and vesicular glutamate transporter 2 (VGlut2) immunolabeling in animals with retrograde tracer injection, PTH2R-containing glutamatergic fibers are presynaptic to neurons projecting from the median preoptic nucleus (MnPO) to the dorso- medial hypothalamus. Transneuronal retrograde pathway tracing with pseudorabies virus revealed connectivity between MnPO VGlut2 and PTH2R neurons and BAT. MnPO injection of TIP39 increased body temperature by 2°C for several hours. Mice lacking TIP39 signaling, either because of PTH2R-null mutation or brain delivery of a PTH2R antagonist had impaired heat production upon cold exposure, but no change in basal temperature and no impairment in response to a hot environment. Thus, TIP39 appears to act on PTH2Rs present on MnPO glutamatergic terminals to regulate their activation of projection neurons and subsequent sympathetic BAT activation. -
Quantitative Magnetic Resonance Imaging in Optic Neuritis
Quantitative magnetic resonance imaging in optic neuritis Simon James Hickman A thesis submitted to the University of London for the degree of Doctor of Philosophy 2004 NMR Research Unit Department of Neuroinflammation Institute of Neurology University College London Queen Square London WC1N3BG United Kingdom UMI Number: U602525 All rights reserved INFORMATION TO ALL USERS The quality of this reproduction is dependent upon the quality of the copy submitted. In the unlikely event that the author did not send a complete manuscript and there are missing pages, these will be noted. Also, if material had to be removed, a note will indicate the deletion. Dissertation Publishing UMI U602525 Published by ProQuest LLC 2014. Copyright in the Dissertation held by the Author. Microform Edition © ProQuest LLC. All rights reserved. This work is protected against unauthorized copying under Title 17, United States Code. ProQuest LLC 789 East Eisenhower Parkway P.O. Box 1346 Ann Arbor, Ml 48106-1346 i Abstract The major event in relapsing remitting multiple sclerosis (MS) is the acute relapse. The majority of patients with MS present with such an event. Most early relapses are followed by complete or near complete recovery, however partial recovery or significant disability can result from an individual relapse. Study of relapses in vivo is therefore desirable. Magnetic resonance imaging (MRI) is very sensitive at detecting MS lesions. Unfortunately, in the brain and spinal cord, it has been difficult to reliably identify the lesion that is responsible for the symptoms of an individual relapse and most new brain lesions which are apparent on MRI are clinically silent. -
G Protein‐Coupled Receptors
S.P.H. Alexander et al. The Concise Guide to PHARMACOLOGY 2019/20: G protein-coupled receptors. British Journal of Pharmacology (2019) 176, S21–S141 THE CONCISE GUIDE TO PHARMACOLOGY 2019/20: G protein-coupled receptors Stephen PH Alexander1 , Arthur Christopoulos2 , Anthony P Davenport3 , Eamonn Kelly4, Alistair Mathie5 , John A Peters6 , Emma L Veale5 ,JaneFArmstrong7 , Elena Faccenda7 ,SimonDHarding7 ,AdamJPawson7 , Joanna L Sharman7 , Christopher Southan7 , Jamie A Davies7 and CGTP Collaborators 1School of Life Sciences, University of Nottingham Medical School, Nottingham, NG7 2UH, UK 2Monash Institute of Pharmaceutical Sciences and Department of Pharmacology, Monash University, Parkville, Victoria 3052, Australia 3Clinical Pharmacology Unit, University of Cambridge, Cambridge, CB2 0QQ, UK 4School of Physiology, Pharmacology and Neuroscience, University of Bristol, Bristol, BS8 1TD, UK 5Medway School of Pharmacy, The Universities of Greenwich and Kent at Medway, Anson Building, Central Avenue, Chatham Maritime, Chatham, Kent, ME4 4TB, UK 6Neuroscience Division, Medical Education Institute, Ninewells Hospital and Medical School, University of Dundee, Dundee, DD1 9SY, UK 7Centre for Discovery Brain Sciences, University of Edinburgh, Edinburgh, EH8 9XD, UK Abstract The Concise Guide to PHARMACOLOGY 2019/20 is the fourth in this series of biennial publications. The Concise Guide provides concise overviews of the key properties of nearly 1800 human drug targets with an emphasis on selective pharmacology (where available), plus links to the open access knowledgebase source of drug targets and their ligands (www.guidetopharmacology.org), which provides more detailed views of target and ligand properties. Although the Concise Guide represents approximately 400 pages, the material presented is substantially reduced compared to information and links presented on the website. -
Selective Cell Deathin Glaucoma
BritishJournal ofOphthalmology 1994; 78: 875-880 875 PERSPECTIVE Br J Ophthalmol: first published as 10.1136/bjo.78.11.875 on 1 November 1994. Downloaded from Selective cell death in glaucoma: does it really occur? J E Morgan Glaucoma is associated with retinal ganglion cell death and preparations2148 where, away from the fovea, cell size consequent deterioration in visual field. However, the asso- histograms indicated a reduction in the number ofcells at the ciation between these events is not straightforward since a upper end of the cell diameter range. A similar effect was substantial proportion ofthe ganglion cell population may be subsequently observed in tissue taken from the macular zone lost before visual field defects can be detected using conven- and examined in the transverse plane."9 It seemed reasonable tional perimetric methods.'2 Clinically, ganglion cell loss to assume that these changes in the axon and cell diameter manifests as optic disc cupping and defects in the nerve fibre distributions would be reflected as a change in the proportion layer3 before the onset ofvisual field changes. In recent years a ofthe types of remaining ganglion cells. number of studies have suggested that some ganglion cells The first aspect ofthese cell size distributions to consider is may have a greater susceptibility to the damaging effects of whether they result from a mechanism of cell death that is glaucoma and this idea has become central to a number of influenced by cell size. Taken on its own, this point is strategies designed to detect the earliest changes in this important since it has implications for the mechanism of cell disease. -
SIX1 Mouse Monoclonal Antibody [Clone ID: OTI1H4] Product Data
OriGene Technologies, Inc. 9620 Medical Center Drive, Ste 200 Rockville, MD 20850, US Phone: +1-888-267-4436 [email protected] EU: [email protected] CN: [email protected] Product datasheet for CF504057 SIX1 Mouse Monoclonal Antibody [Clone ID: OTI1H4] Product data: Product Type: Primary Antibodies Clone Name: OTI1H4 Applications: WB Recommended Dilution: WB 1:2000 Reactivity: Human, Mouse, Rat Host: Mouse Isotype: IgG1 Clonality: Monoclonal Immunogen: Human recombinant protein fragment corresponding to amino acids 1-284 of human SIX1(NP_005973) produced in E.coli. Formulation: Lyophilized powder (original buffer 1X PBS, pH 7.3, 8% trehalose) Reconstitution Method: For reconstitution, we recommend adding 100uL distilled water to a final antibody concentration of about 1 mg/mL. To use this carrier-free antibody for conjugation experiment, we strongly recommend performing another round of desalting process. (OriGene recommends Zeba Spin Desalting Columns, 7KMWCO from Thermo Scientific) Purification: Purified from mouse ascites fluids or tissue culture supernatant by affinity chromatography (protein A/G) Conjugation: Unconjugated Storage: Store at -20°C as received. Stability: Stable for 12 months from date of receipt. Predicted Protein Size: 32 kDa Gene Name: Homo sapiens SIX homeobox 1 (SIX1), mRNA. Database Link: NP_005973 Entrez Gene 20471 MouseEntrez Gene 114634 RatEntrez Gene 6495 Human Q15475 This product is to be used for laboratory only. Not for diagnostic or therapeutic use. View online » ©2021 OriGene Technologies, Inc., 9620 Medical Center Drive, Ste 200, Rockville, MD 20850, US 1 / 2 SIX1 Mouse Monoclonal Antibody [Clone ID: OTI1H4] – CF504057 Background: The protein encoded by this gene is a homeobox protein that is similar to the Drosophila 'sine oculis' gene product. -
Arginine Vasotocin Neuronal Phenotypes Among Congeneric Territorial and Shoaling Reef Butterflyfishes: Species, Sex and Reproductive Season Comparisons
Journal of Neuroendocrinology From Molecular to Translational Neurobiology Journal of Neuroendocrinology 20, 1382À1394 ORIGINAL ARTICLE ª 2008 The Authors. Journal Compilation ª 2008 Blackwell Publishing Ltd Arginine Vasotocin Neuronal Phenotypes among Congeneric Territorial and Shoaling Reef Butterflyfishes: Species, Sex and Reproductive Season Comparisons A. K. Dewan, K. P. Maruska and T. C. Tricas Department of Zoology, University of Hawai’i at Manoa, Honolulu and Hawai’i Institute of Marine Biology, Kaneohe, HI, USA. Journal of Arginine vasotocin (AVT) and the homologous arginine vasopressin (AVP) neuropeptides are involved in the control of aggression, spacing behaviour and mating systems in vertebrates, but Neuroendocrinology the function of AVT in the regulation of social behaviour among closely-related fish species needs further clarification. We used immunocytochemical techniques to test whether AVT neuro- nes show species, sex or seasonal differences in two sympatric butterflyfish sister species: the territorial monogamous multiband butterflyfish, Chaetodon multicinctus, and the shoaling polyg- amous milletseed butterflyfish, Chaetodon miliaris. The territorial species had larger AVT-immu- noreactive (-ir) somata within the preoptic area, and higher AVT fibre densities within but not limited to the ventral telencephalon, medial and dorsal nucleus of the dorsal telencephalon, torus semicircularis, and tectum compared to the shoaling nonterritorial species. Furthermore, AVT-ir somata size and number did not differ among sexes or spawning periods in the territorial species, and showed only limited variation within the shoaling species. The distinct difference in AVT neuronal characteristics among species is likely to be independent of body size differences, and the lack of sex and seasonal variability is consistent with their divergent but stable social and mating systems. -
The Evolution of Cell Communication: the Road Not Taken
UCLA UCLA Previously Published Works Title The Evolution of Cell Communication: The Road not Taken. Permalink https://escholarship.org/uc/item/2fx0d60p Authors Torday, JS Rehan, VK Publication Date 2009-09-01 DOI 10.4137/cci.s2776 Peer reviewed eScholarship.org Powered by the California Digital Library University of California HHS Public Access Author manuscript Author ManuscriptAuthor Manuscript Author Cell Commun Manuscript Author Insights. Manuscript Author manuscript; available in PMC 2015 April 15. Published in final edited form as: Cell Commun Insights. ; 2: 17–25. The Evolution of Cell Communication: The Road not Taken J.S. Torday and V.K. Rehan Department of Pediatrics, Los Angeles Biomedical Research Institute at Harbor-UCLA Medical Center, Torrance, California, U.S Abstract In the post-genomic era the complex problem of evolutionary biology can be tackled from the top- down, the bottom-up, or from the middle-out. Given the emergent and contingent nature of this process, we have chosen to take the latter approach, both as a mechanistic link to developmental biology and as a rational means of identifying signaling mechanisms based on their functional genomic significance. Using this approach, we have been able to configure a working model for lung evolution by reverse-engineering lung surfactant from the mammalian lung to the swim bladder of fish. Based on this archetypal cell-molecular model, we have reduced evolutionary biology to cell communication, starting with unicellular organisms communicating with the environment, followed by cell-cell communication to generate metazoa, culminating in the communication of genetic information between generations, i.e. reproduction. This model predicts the evolution of physiologic systems-including development, homeostasis, disease, regeneration/ repair, and aging- as a logical consequence of biology reducing entropy. -
Identifying Glaucomatous Vision Loss with Visual-Function–Specific
Identifying Glaucomatous Vision Loss with Visual-Function–Specific Perimetry in the Diagnostic Innovations in Glaucoma Study Pamela A. Sample, Felipe A. Medeiros, Lyne Racette, John P. Pascual, Catherine Boden, Linda M. Zangwill, Christopher Bowd, and Robert N. Weinreb PURPOSE. To compare the diagnostic results of four perimetric rameters at suggested criterion values provided good sensitiv- tests and to identify useful parameters from each for determin- ity and specificity. FDT showed the highest sensitivity overall, ing abnormality. with SAP performing better than in prior reports. Of note, the METHODS. One hundred eleven eyes with glaucomatous optic same area of the retina was identified as damaged in all tests. neuropathy (GON), 31 with progressive optic neuropathy (Invest Ophthalmol Vis Sci. 2006;47:3381–3389) DOI: (PGON) 53 with ocular hypertension, and 51 with no disease 10.1167/iovs.05-1546 were included (N ϭ 246). Visual field results were not used to classify the eyes. Short-wavelength automated perimetry ver the past several years, psychophysical tests of specific (SWAP), frequency-doubling technology perimetry (FDT), Ovisual functions have been used to measure visual perfor- high-pass resolution perimetry (HPRP), and standard auto- mance and to understand the underlying glaucomatous mated perimetry (SAP) were performed. Receiver operating changes in retinal ganglion cell function. Testing vision with characteristic (ROC) curves were used to compute the areas standard automated perimetry (SAP) is not selective for a par- under the curves (AUC) and sensitivity levels at given specific- ticular ganglion cell type. Any of the primary ganglion cell ities for a variety of abnormality criteria. The agreement among subtypes can respond to an achromatic incremental stimulus tests for abnormality, location, and extent of visual field deficit presented on an achromatic background. -
Anti-SIX1 Antibody (ARG59134)
Product datasheet [email protected] ARG59134 Package: 50 μg anti-SIX1 antibody Store at: -20°C Summary Product Description Rabbit Polyclonal antibody recognizes SIX1 Tested Reactivity Hu Tested Application WB Host Rabbit Clonality Polyclonal Isotype IgG Target Name SIX1 Antigen Species Human Immunogen Synthetic peptide corresponding to aa. 245-282 of Human SIX1. (NYSLPGLTASQPSHGLQTHQHQLQDSLLGPLTSSLVDL) Conjugation Un-conjugated Alternate Names Sine oculis homeobox homolog 1; Homeobox protein SIX1; DFNA23; TIP39; BOS3 Application Instructions Application table Application Dilution WB 0.1 - 0.5 µg/ml Application Note * The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist. Calculated Mw 32 kDa Properties Form Liquid Purification Affinity purification with immunogen. Buffer 0.9% NaCl, 0.2% Na2HPO4, 0.05% Sodium azide and 5% BSA. Preservative 0.05% Sodium azide Stabilizer 5% BSA Concentration 0.5 mg/ml Storage instruction For continuous use, store undiluted antibody at 2-8°C for up to a week. For long-term storage, aliquot and store at -20°C or below. Storage in frost free freezers is not recommended. Avoid repeated freeze/thaw cycles. Suggest spin the vial prior to opening. The antibody solution should be gently mixed before use. Note For laboratory research only, not for drug, diagnostic or other use. www.arigobio.com 1/2 Bioinformation Gene Symbol SIX1 Gene Full Name SIX homeobox 1 Background The protein encoded by this gene is a homeobox protein that is similar to the Drosophila 'sine oculis' gene product. This gene is found in a cluster of related genes on chromosome 14 and is thought to be involved in limb development.