Diversity of Central Oxytocinergic Projections
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Transferrin Variants and Conjugates
(19) TZZ Z ¥ T (11) EP 2 604 623 A2 (12) EUROPEAN PATENT APPLICATION (43) Date of publication: (51) Int Cl.: 19.06.2013 Bulletin 2013/25 C07K 14/79 (2006.01) A61K 47/48 (2006.01) A61K 38/40 (2006.01) C12N 5/10 (2006.01) (21) Application number: 12189421.6 (22) Date of filing: 08.08.2008 (84) Designated Contracting States: • Friis, Esben Peter AT BE BG CH CY CZ DE DK EE ES FI FR GB GR 2730 Herlev (DK) HR HU IE IS IT LI LT LU LV MC MT NL NO PL PT • Hay, Joanna RO SE SI SK TR Nottingham, Nottinghamshire NG2 6QW (GB) • Finnis, Christopher John Arthur (30) Priority: 08.08.2007 EP 07114012 Nottingham, Nottinghamshire NG7 1JB (GB) 02.04.2008 EP 08153938 (74) Representative: Williams, Rachel Clare (62) Document number(s) of the earlier application(s) in Novozymes Biopharma UK Limited accordance with Art. 76 EPC: Castle Court 08787067.1 / 2 201 036 59 Castle Boulevard Nottingham (71) Applicant: Novozymes Biopharma DK A/S Nottinghamshire NG7 1FD (GB) 2880 Bagsvaerd (DK) Remarks: (72) Inventors: This application was filed on 22-10-2012 as a • Sleep, Darrell divisional application to the application mentioned Nottingham, Nottinghamshire NG2 5DS (GB) under INID code 62. (54) Transferrin variants and conjugates (57) Based on the three-dimensional structure of "thiotransferrin"). The variant polypeptide may be conju- transferrin, the inventors have designed variant polypep- gated through the sulphur atom of the Cysteine residue tides (muteins) which have one or more Cysteine resi- to a bioactive compound. dues with a free thiol group (hereinafter referred to as EP 2 604 623 A2 Printed by Jouve, 75001 PARIS (FR) EP 2 604 623 A2 Description Reference to sequence listing 5 [0001] This application contains a Sequence Listing in computer readable form. -
Endocrinology
Endocrinology INTRODUCTION Endocrinology 1. Endocrinology is the study of the endocrine system secretions and their role at target cells within the body and nervous system are the major contributors to the flow of information between different cells and tissues. 2. Two systems maintain Homeostasis a. b 3. Maintain a complicated relationship 4. Hormones 1. The endocrine system uses hormones (chemical messengers/neurotransmitters) to convey information between different tissues. 2. Transport via the bloodstream to target cells within the body. It is here they bind to receptors on the cell surface. 3. Non-nutritive Endocrine System- Consists of a variety of glands working together. 1. Paracrine Effect (CHEMICAL) Endocrinology Spring 2013 Page 1 a. Autocrine Effect i. Hormones released by cells that act on the membrane receptor ii. When a hormone is released by a cell and acts on the receptors located WITHIN the same cell. Endocrine Secretions: 1. Secretions secreted Exocrine Secretion: 1. Secretion which come from a gland 2. The secretion will be released into a specific location Nervous System vs tHe Endocrine System 1. Nervous System a. Neurons b. Homeostatic control of the body achieved in conjunction with the endocrine system c. Maintain d. This system will have direct contact with the cells to be affected e. Composed of both the somatic and autonomic systems (sympathetic and parasympathetic) Endocrinology Spring 2013 Page 2 2. Endocrine System a. b. c. 3. Neuroendocrine: a. These are specialized neurons that release chemicals that travel through the vascular system and interact with target tissue. b. Hypothalamus à posterior pituitary gland History of tHe Endocrine System Bertold (1849)-FATHER OF ENDOCRINOLOGY 1. -
Atrazine and Cell Death Symbol Synonym(S)
Supplementary Table S1: Atrazine and Cell Death Symbol Synonym(s) Entrez Gene Name Location Family AR AIS, Andr, androgen receptor androgen receptor Nucleus ligand- dependent nuclear receptor atrazine 1,3,5-triazine-2,4-diamine Other chemical toxicant beta-estradiol (8R,9S,13S,14S,17S)-13-methyl- Other chemical - 6,7,8,9,11,12,14,15,16,17- endogenous decahydrocyclopenta[a]phenanthrene- mammalian 3,17-diol CGB (includes beta HCG5, CGB3, CGB5, CGB7, chorionic gonadotropin, beta Extracellular other others) CGB8, chorionic gonadotropin polypeptide Space CLEC11A AW457320, C-type lectin domain C-type lectin domain family 11, Extracellular growth factor family 11, member A, STEM CELL member A Space GROWTH FACTOR CYP11A1 CHOLESTEROL SIDE-CHAIN cytochrome P450, family 11, Cytoplasm enzyme CLEAVAGE ENZYME subfamily A, polypeptide 1 CYP19A1 Ar, ArKO, ARO, ARO1, Aromatase cytochrome P450, family 19, Cytoplasm enzyme subfamily A, polypeptide 1 ESR1 AA420328, Alpha estrogen receptor,(α) estrogen receptor 1 Nucleus ligand- dependent nuclear receptor estrogen C18 steroids, oestrogen Other chemical drug estrogen receptor ER, ESR, ESR1/2, esr1/esr2 Nucleus group estrone (8R,9S,13S,14S)-3-hydroxy-13-methyl- Other chemical - 7,8,9,11,12,14,15,16-octahydro-6H- endogenous cyclopenta[a]phenanthren-17-one mammalian G6PD BOS 25472, G28A, G6PD1, G6PDX, glucose-6-phosphate Cytoplasm enzyme Glucose-6-P Dehydrogenase dehydrogenase GATA4 ASD2, GATA binding protein 4, GATA binding protein 4 Nucleus transcription TACHD, TOF, VSD1 regulator GHRHR growth hormone releasing -
Human Neurophysin II Antibody
Human Neurophysin II Antibody Monoclonal Mouse IgG2B Clone # 62865 Catalog Number: MAB009 DESCRIPTION Species Reactivity Human Specificity Detects human Neurophysin II in direct ELISAs. Source Monoclonal Mouse IgG2B Clone # 62865 Purification Protein A or G purified from ascites Immunogen Synthetic peptide containing human Neurophysin II Accession # P01186 Formulation Lyophilized from a 0.2 μm filtered solution in PBS with Trehalose. See Certificate of Analysis for details. *Small pack size (-SP) is supplied either lyophilized or as a 0.2 μm filtered solution in PBS. APPLICATIONS Please Note: Optimal dilutions should be determined by each laboratory for each application. General Protocols are available in the Technical Information section on our website. Recommended Sample Concentration Immunohistochemistry 5-25 µg/mL See Below DATA Immunohistochemistry Neurophysin II in Human Brain Hippocampus Tissue. Neurophysin II was detected in immersion fixed paraffin- embedded sections of human brain hippocampus tissue using Mouse Anti- Human Neurophysin II Monoclonal Antibody (Catalog # MAB009) at 5 µg/mL for 1 hour at room temperature followed by incubation with the Anti-Mouse IgG VisUCyte™ HRP Polymer Antibody (Catalog # VC001). Before incubation with the primary antibody, tissue was subjected to heat-induced epitope retrieval using Antigen Retrieval Reagent- Basic (Catalog # CTS013). Tissue was stained using DAB (brown) and counterstained with hematoxylin (blue). Specific staining was localized to neurons. View our protocol for IHC Staining with VisUCyte HRP Polymer Detection Reagents. PREPARATION AND STORAGE Reconstitution Reconstitute at 0.5 mg/mL in sterile PBS. Shipping The product is shipped at ambient temperature. Upon receipt, store it immediately at the temperature recommended below. *Small pack size (-SP) is shipped with polar packs. -
Pnas11138correction 14002..14003
Corrections MEDICAL SCIENCES Correction for “Regulation of bone remodeling by vasopressin New, Alberta Zallone, and Mone Zaidi, which appeared in issue 46, explains the bone loss in hyponatremia,” by Roberto Tamma, November 12, 2013, of Proc Natl Acad Sci USA (110:18644–18649; Li Sun, Concetta Cuscito, Ping Lu, Michelangelo Corcelli, first published October 28, 2013; 10.1073/pnas.1318257110). Jianhua Li, Graziana Colaianni, Surinder S. Moonga, Adriana The authors note that Fig. 1 appeared incorrectly. The cor- Di Benedetto, Maria Grano, Silvia Colucci, Tony Yuen, Maria I. rected figure and its legend appear below. Fig. 1. Bone cells express Avprs. Immunofluorescence micrographs (A) and Western immunoblotting (B) show the expression of Avpr1α in osteoblasts and osteoclasts, and as a function of osteoblast (mineralization) and osteoclast (with Rankl) differentiation. The expression of Avp (ligand) and Avpr1α (receptor) in osteoblasts is regulated by 17β-estradiol, as determined by quantitative PCR (C) and Western immunoblotting (D). (Magnification: A,63×.) Because Avp is a small peptide, its precursor neurophysin II is measured. Statistics: Student t test, P values shown compared with 0 h. Stimulation of Erk phosphorylation − (p-Erk) as a function of total Erk (t-Erk) by Avp (10 8 M) in osteoclast precursors (preosteoclasts), osteoclasts (OC), and osteoblasts establishes functionality of − the Avpr1α in the presence or absence of the receptor inhibitor SR49059 (10 8 M) (E). Western immunoblotting showing the expression of Avpr2 in pre- −/− osteoclasts, OCs (F), and osteoblasts (G) isolated from Avpr1α mice, as well as in MC3T3.E1 osteoblast precursors (G). Functionality of Avpr2 was confirmed −/− by the demonstration that cells from Avpr1α mice remained responsive to AVP in reducing the expression of osteoblast differentiation genes, namely Runx2, Osx, Bsp, Atf4, Opn, and Osteocalcin (quantitative PCR, P values shown) (H). -
Oxytocin-Functions: an Overview
MOJ Anatomy & Physiology Review Article Open Access Oxytocin-functions: an overview Abstract Volume 6 Issue 4 - 2019 Oxytocin is a neuropeptide containing nine amino acids produced by paraventricular and supraoptic nuclei of hypothalamus. Oxytocin is derived from a Greek word ‘oxutokia’ Roopasree B, Jophy Joseph, Mukkadan JK meaning sudden delivery and it is well known for its role in parturition and lactation. In Department of Physiology, Little Flower Institute of Medical addition oxytocin performs a wide spectrum of functions. Oxytocin is a hormone with great Sciences and Research, India potential and it is a great facilitator of life. The purpose of this review is to cover almost all the functions of oxytocin - reproductive functions, social functions, role in human Correspondence: Mukkadan JK, Research Director, Department of Physiology, Little Flower Medical Research behaviour and other biologically significant functions.. Centre LFMRC, Angamaly, Kerala, India, Tel 91 9387518037, Fax Keywords: oxytocin, functions, neurophysin I, magnocellular neurons 0484 2452646, Email Received: July 24, 2019 | Published: August 16, 2019 Introduction (GPCR) family. It is coupled to phospholipase C through Gαq11.20,21 Once Oxytocin binds to its receptor, it gives rise to a cascade of Oxytocin is a non a-peptide hormone containing nine amino acids, reactions that finally activates the enzyme Phospholipase-C. This with one disulphide linkage between the 1st and 6th cysteine residue. enzyme produces ITP (inositol triphosphate) and DAG (1, 2-diacyl It is also called as α-Hypophamine. Half-life is found to be minutes. It glycerol) and also activates intracellular Ca++ release, which in turn is known to be the 1st polypeptide hormone that has been sequenced set off various cellular events.9 and synthesized biochemically. -
Review Article Mouse Homologues of Human Hereditary Disease
I Med Genet 1994;31:1-19 I Review article J Med Genet: first published as 10.1136/jmg.31.1.1 on 1 January 1994. Downloaded from Mouse homologues of human hereditary disease A G Searle, J H Edwards, J G Hall Abstract involve homologous loci. In this respect our Details are given of 214 loci known to be genetic knowledge of the laboratory mouse associated with human hereditary dis- outstrips that for all other non-human mam- ease, which have been mapped on both mals. The 829 loci recently assigned to both human and mouse chromosomes. Forty human and mouse chromosomes3 has now two of these have pathological variants in risen to 900, well above comparable figures for both species; in general the mouse vari- other laboratory or farm animals. In a previous ants are similar in their effects to the publication,4 102 loci were listed which were corresponding human ones, but excep- associated with specific human disease, had tions include the Dmd/DMD and Hprt/ mouse homologues, and had been located in HPRT mutations which cause little, if both species. The number has now more than any, harm in mice. Possible reasons for doubled (table 1A). Of particular interest are phenotypic differences are discussed. In those which have pathological variants in both most pathological variants the gene pro- the mouse and humans: these are listed in table duct seems to be absent or greatly 2. Many other pathological mutations have reduced in both species. The extensive been detected and located in the mouse; about data on conserved segments between half these appear to lie in conserved chromo- human and mouse chromosomes are somal segments. -
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. -
Recent Applications of Retro-Inverso Peptides
International Journal of Molecular Sciences Review Recent Applications of Retro-Inverso Peptides Nunzianna Doti 1, Mario Mardirossian 2, Annamaria Sandomenico 1 , Menotti Ruvo 1,* and Andrea Caporale 3,* 1 Institute of Biostructures and Bioimaging (IBB), National Research Council (CNR), 80134 Napoli, Italy; [email protected] (N.D.); [email protected] (A.S.) 2 Department of Medicine, Surgery and Health Sciences, University of Trieste, 34149 Trieste, Italy; [email protected] 3 Institute of Crystallography (IC), National Research Council (CNR), 34149 Trieste, Italy * Correspondence: [email protected] (M.R.); [email protected] (A.C.) Abstract: Natural and de novo designed peptides are gaining an ever-growing interest as drugs against several diseases. Their use is however limited by the intrinsic low bioavailability and poor stability. To overcome these issues retro-inverso analogues have been investigated for decades as more stable surrogates of peptides composed of natural amino acids. Retro-inverso peptides possess reversed sequences and chirality compared to the parent molecules maintaining at the same time an identical array of side chains and in some cases similar structure. The inverted chirality renders them less prone to degradation by endogenous proteases conferring enhanced half-lives and an increased potential as new drugs. However, given their general incapability to adopt the 3D structure of the parent peptides their application should be careful evaluated and investigated case by case. Here, we review the application of retro-inverso peptides in anticancer therapies, in immunology, in neurodegenerative diseases, and as antimicrobials, analyzing pros and cons of this interesting subclass of molecules. Keywords: retro-inverso peptides; anticancer peptides; drug delivery; peptide antigens; Aβ; IAPP; Citation: Doti, N.; Mardirossian, M.; antimicrobial peptides Sandomenico, A.; Ruvo, M.; Caporale, A. -
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. -
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. -
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.