Cd79a Percp-Cy5.5 Noto Anche Come: Mb-1 Catalog Number(S): 9045-0792-025 (25 Tests), 9045-0792-120 (120 Tests)

Total Page:16

File Type:pdf, Size:1020Kb

Cd79a Percp-Cy5.5 Noto Anche Come: Mb-1 Catalog Number(S): 9045-0792-025 (25 Tests), 9045-0792-120 (120 Tests) Page 1 of 2 CD79a PerCP-Cy5.5 Noto anche come: mb-1 Catalog Number(s): 9045-0792-025 (25 tests), 9045-0792-120 (120 tests) Profili di fluorescenza di normali linfociti del sangue periferico umano non colorati (istogramma blu) o colorati a livello intracellulare con CD79a coniugati con PerCP-Cy5.5 (istogramma viola). Informazioni sul prodotto Indice: CD79a PerCP-Cy5.5 Storage Conditions: Conservare a 2-8 °C. Catalog Number(s): 9045-0792-025 (25 tests), Non congelare. 9045-0792-120 (120 tests) Materiale fotosensibile. Clone: HM47 Attenzione: contiene azide Concentrazione: 5 µl (0,03 µg)/test (un test viene Manufacturer: eBioscience, Inc., 10255 Science definito come la quantità in grado di colorare Center Drive, San Diego, CA 92121, USA 1x10e6 cellule in 100 μl) Authorized Representative: Bender MedSystems Ospite/isotipo: IgG1 di topo, kappa GmbH, an eBioscience Company Campus Vienna Workshop HLDA: V Biocenter 2 A-1030 Vienna Austria Formulazione: Tampone acquoso, 0,09% di sodio azide; può contenere proteina carrier/stabilizzante. Uso previsto Descrizione L'anticorpo monoclonale HM47 coniugato con fluorocromo L'anticorpo monoclonale HM47 riconosce il dominio reagisce con l'antigene CD79a umano. Il CD79a può essere citoplasmatico del CD79a, chiamato anche mb-1. Il CD79a è rilevato in campioni biologici umani mediante tecniche una glicoproteina di membrana da 47 kDa che si unisce al immunologiche. CD79b con cui forma il recettore eterodimerico per i linfociti Principi del test B (BCR). Questo recettore è responsabile della segnalazione La citometria a flusso è uno strumento utile per la misurazione dei linfociti B e causa la loro attivazione, apoptosi o anergia. simultanea delle diverse proprietà fisiche di singole particelle L'espressione del CD79a si verifica durante tutto lo sviluppo, (come ad es., le cellule). Le cellule attraversano un raggio laser dalle prime cellule pre-linfociti B alle plasmacellule. Il CD79 allineate una dietro l'altra. Per ogni cellula che attraversa il viene espresso sulle neoplasie dei linfociti B e su alcuni raggio laser il citometro registra il modo in cui la cellula o la tumori maligni senza linfociti B, come la leucemia mieloide particella disperdono la luce laser incidente ed emettono acuta. A differenza degli altri anticorpi che possono risultare fluorescenza. Mediante questo protocollo di analisi con nascosti nei linfociti B neoplastici, il HM47 è un anticorpo citometria a flusso è possibile eseguire l'analisi simultanea delle affidabile che permette il riconoscimento del CD79a e di molecole di superficie a livello della singola cellula. conseguenza, è un ottimo marker dei linfociti B. Document # 30778_03_it • Effective date: 1/25/2011 Not for further distribution without written consent. Copyright © 2000-2010 eBioscience, Inc. www.eBioscience.com ORDER INQUIRIES • +43 1 796 40 40-120 TECH • +43 1 796 40 40-0 [email protected] Page 2 of 2 Istruzioni per il prelievo e la conservazione dei campioni 8. Risospendere il pellet di cellule colorate in 1 ml di Flow Prelevare un campione di sangue venoso mediante venipuntura Cytometry Staining Buffer e analizzare i campioni con in una provetta sterile per la raccolta del sangue, utilizzando un un citometro a flusso. anticoagulante appropriato (si consiglia di utilizzare EDTA). Limiti Conservare i campioni a temperatura ambiente (18-25 °C). 1. Per una performance ottimale degli anticorpi coniugati Prima dell'uso, miscelare i campioni agitandoli delicatamente. con il fluorocromo, conservare le fiale al buio a 2-8 °C. Materiali necessari ma non forniti Non congelarle. Provette da 12 x 75 mm 2. Centrifugare la fiala con gli anticorpi per recuperare il Tamponi (si consiglia eBioscience Flow Cytometry massimo volume possibile. Staining Buffer, N. cat. 00-4222) 3. Tranne quando riportato nel protocollo, tutte le Tampone di lisi (si consiglia eBioscience 1X RBC Lysis colorazioni devono essere eseguite su ghiaccio oppure Buffer, N. cat. 00-4333 o eBioscience 1-step Fix/Lyse a 2-8 °C con una minima esposizione alla luce. Solution (10X), N. cat. 00-5333) Caratteristiche della performance Per la colorazione intracellulare utilizzare IC Fixation La costanza della performance dei reagenti di alta qualità Buffer e Permeabilization Buffer, N. cat. 88-8823 viene assicurata mediante l'analisi di ciascun lotto di (colorazione per le citochine intracellulari o per le anticorpi monoclonali per eseguire il confronto tra la loro proteine citoplasmatiche) o Foxp3 Buffer Set, conformità e le caratteristiche di un reagente standard. N. cat. 00-5523 (colorazione delle proteine nucleari). Quando ritenuto idoneo, vengono inclusi i dati Fare riferimento alla sezione Best Protocols del sito rappresentativi della citometria a flusso. web di eBioscience per i protocolli "Staining Segni di deterioramento Intracellular Antigens for Flow Cytometry". Per qualsiasi domanda o dubbio riguardanti la performance Colorazione di vitalità (si consiglia 7-AAD Viability o la qualità dei prodotti ricevuti, contattare l'assistenza Staining Solution, N. cat. 00-6993 o Propidium Iodide tecnica di eBioscience (vedere di seguito). Staining Solution, N. cat. 00-6990) Pipette automatiche Bibliografia Centrifuga Procedures for the Collection of Diagnostic Blood Specimens Miscelatore Vortex by Venipuncture (H3-A6), 3rd Edition published by the Secchio con ghiaccio o frigorifero National Committee for Clinical Laboratory Standards. Citometro a flusso Schlossman SF, Boumsell L, Gilks W, et al, eds. Leucocyte Typing V: White Cell Differentiation Antigens. Oxford Protocollo del test University Press. New York. 1995. NOTA: per la colorazione intracellulare, fare riferimento alla Sakaguchi N, et al. B lymphocyte lineage-restricted sezione Best Protocols del sito web di eBioscience per i expression of mb-1, a gene with CD3-like structural protocolli "Staining Intracellular Antigens for Flow Cytometry". properties. EMBO J. 1988;7:3457-3464. 1. Erogare 100 µl del campione di analisi nelle provette. Nota legale 2. Aggiungere 5 µl dell'anticorpo appropriato in ciascuna FOR RESEARCH (NOT TO INCLUDE IN VIVO RESEARCH) AND/OR IN VITRO DIAGNOSTIC USE ONLY. provetta. THE ONLY PERMITTED COMMERCIAL USE IS PROVISION OF RESEARCH (NOT TO INCLUDE IN VIVO 3. Incubare per 30-60 minuti a 2-8 °C. In alternativa, RESEARCH) SERVICES AND/OR IN VITRO DIAGNOSTIC SERVICES. NOT FOR THERAPEUTIC OR IN i campioni possono essere incubati al buio a VIVO APPLICATIONS. OTHER USE NEEDS LICENSES WHICH ARE AVAILABLE FROM GE HEALTHCARE temperatura ambiente per 15-30 minuti. BIO-SCIENCES CORP. UNDER U.S. PATENT NOS. NOS 5,268,486, 5,569,587 AND 5,627,027 AND 4. Aggiungere 2 ml di 1X RBC Lysis Buffer (a temperatura FOREIGN EQUIVALENTS AND PENDING APPLICATIONS. ambiente) ad ogni provetta. Miscelare delicatamente. THIS PRODUCT IS SUBJECT TO PROPRIETARY RIGHTS OF GE HEALTHCARE BIO-SCIENCES (In alternativa, è possibile incubare i campioni con 2 ml CORP. ("GE HEALTHCARE") AND CARNEGIE MELLON UNIVERSITY ("CMU") AND MADE AND di 1-step Fix/Lyse Solution). SOLD UNDER LICENSE FROM GE HEALTHCARE. THE PRODUCT BEARING THIS LABEL IS 5. Incubare i campioni al buio e a temperatura ambiente LICENSED FOR SALE ONLY FOR RESEARCH (NOT TO INCLUDE IN VIVO RESEARCH) AND IN per 10 minuti. Con l'RBC Lysis Buffer non superare ADDITION MAY BE USED TO PERFORM RESEARCH (NOT TO INCLUDE IN VIVO RESEARCH) 15 minuti di incubazione. AND/OR IN VITRO DIAGNOSTIC SERVICES FOR THIRD PARTIES. IT IS NOT LICENSED NOR ARE 6. Centrifugare i campioni a 300-400 x g per 5 minuti a THERE ANY IMPLIED LICENSES FOR ANY OTHER USE INCLUDING, WITHOUT LIMITATION, temperatura ambiente, decantare/aspirare il surnatante e COMMERCIAL USES UNLESS EXPRESSLY AUTHORIZED BY GE HEALTHCARE IN WRITING. IF lavare 1 volta con 2 ml di Flow Cytometry Staining Buffer. YOU INTEND TO USE THIS PRODUCT COMMERCIALLY AND YOU DO NOT HAVE A LICENSE 7. Centrifugare i campioni a 300-400 x g per 5 minuti a TO USE THIS PRODUCT FOR THE INTENDED COMMERCIAL PURPOSE, RETURN THIS temperatura ambiente, decantare/aspirare il surnatante. PRODUCT, UNOPENED TO EBIOSCIENCE, INC. 10255 SCIENCE CENTER DRIVE, SAN DIEGO, CALIFORNIA 92121 USA AND ANY MONEY PAID FOR THE PRODUCT WILL BE REFUNDED. Document # 30778_03_it • Effective date: 1/25/2011 Not for further distribution without written consent. Copyright © 2000-2010 eBioscience, Inc. www.eBioscience.com ORDER INQUIRIES • +43 1 796 40 40-120 TECH • +43 1 796 40 40-0 [email protected] .
Recommended publications
  • Germ-Line Regulation of the Caenorhabditis Elegans Sex-Determining Gene Tra-2
    DEVELOPMENTAL BIOLOGY 204, 251–262 (1998) ARTICLE NO. DB989062 Germ-Line Regulation of the Caenorhabditis elegans Sex-Determining Gene tra-2 Patricia E. Kuwabara,* Peter G. Okkema,† and Judith Kimble‡ *MRC Laboratory of Molecular Biology, Hills Road, Cambridge CB2 2QH, United Kingdom; †Laboratory for Molecular Biology, University of Illinois at Chicago, Chicago, Illinois 60607; and ‡Howard Hughes Medical Institute, Laboratory of Molecular Biology, Department of Biochemistry, and Department of Medical Genetics, University of Wisconsin, Madison, Wisconsin 53706 The Caenorhabditis elegans sex-determining gene tra-2 promotes female development of the XX hermaphrodite soma and germ line. We previously showed that a 4.7-kb tra-2 mRNA, which encodes the membrane protein TRA-2A, provides the primary feminizing activity of the tra-2 locus. This paper focuses on the germ-line activity and regulation of tra-2. First, we characterize a 1.8-kb tra-2 mRNA, which is hermaphrodite-specific and germ-line-dependent. This mRNA encodes TRA-2B, a protein identical to a predicted intracellular domain of TRA-2A. We show that the 1.8-kb mRNA is oocyte-specific, suggesting that it is involved in germ-line or embryonic sex determination. Second, we identify a tra-2 maternal effect on brood size that may be associated with the 1.8-kb mRNA. Third, we investigate seven dominant tra-2(mx) (for mixed character) mutations that sexually transform hermaphrodites to females by eliminating hermaphrodite spermatogenesis. Each of the tra-2(mx) mutants possesses a nonconserved missense change in a 22-amino-acid region common to both TRA-2A and TRA-2B, called the MX region.
    [Show full text]
  • And Crry, the Two Genetic Homologues of Human CR1 by Hector Molina,* Winnie Wong,~ Taroh Kinoshita,$ Carol Brenner,* Sharon Foley,* and V
    View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by PubMed Central Disfin_ct Receptor and Regulatory Properties of Recombinant Mouse Complement Receptor 1 (CR1) and Crry, the Two Genetic Homologues of Human CR1 By Hector Molina,* Winnie Wong,~ Taroh Kinoshita,$ Carol Brenner,* Sharon Foley,* and V. Michael Holers* From the *Howard Hughes Medical Institute Laboratories and Department of Medicine, Division of Rheumatology, Washington University School of Medicine, St. Louis, Missouri 63110; the *BASF Bioresearch Corporation, Cambridge, Massachusetts 02139; and the SDepartraent of Immunoregulation, Research Institute for Microbial Diseases, Osaka University, Osaka 565, Japan Summary The relationship between the characterized mouse regulators of complement activation (RCA) genes and the 190-kD mouse complement receptor 1 (MCK1), 155-kD mouse complement receptor 2 (MCR2), and mouse p65 is unclear. One mouse RCA gene, designatedMCR2 (or Cr2), encodes alternatively spliced 21 and 15 short consensus repeat (SCR)-containing transcripts that crosshybridize with cDNAs of both human CR2 and CR1, or CR2 alone, respectively. A five SCR-containing transcript derived from a second unique gene, designated Crry, also crosshybridizes with human CR1. We have previously shown that the 155-kD MCR2 is encoded by the 15 SCR-containing transcript. To analyze the protein products of the other transcripts, which are considered the genetic homologues of human CRI, we have expressed the 21 and the 5 SCR-containing cDNAs in the human K562 erythroleukemia cell line. We demonstrate that cells expressing the 21 SCK transcript express the 190-kD MCR1 protein. These cells react with five unique rat anti-MCR1 monodonal antibodies, including the 8C12 antibody considered to be monospecific for MCK1.
    [Show full text]
  • Research Article Microarray Analysis of the Molecular Mechanism Involved in Parkinson’S Disease
    Hindawi Parkinson’s Disease Volume 2018, Article ID 1590465, 12 pages https://doi.org/10.1155/2018/1590465 Research Article Microarray Analysis of the Molecular Mechanism Involved in Parkinson’s Disease Cheng Tan, Xiaoyang Liu, and Jiajun Chen Department of Neurology, China-Japan Union Hospital of Jilin University, Changchun, Jilin 130033, China Correspondence should be addressed to Jiajun Chen; [email protected] Received 24 May 2017; Revised 21 August 2017; Accepted 18 October 2017; Published 1 March 2018 Academic Editor: Amnon Sintov Copyright © 2018 Cheng Tan et al. )is is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Purpose. )is study aimed to investigate the underlying molecular mechanisms of Parkinson’s disease (PD) by bioinformatics. Methods. Using the microarray dataset GSE72267 from the Gene Expression Omnibus database, which included 40 blood samples from PD patients and 19 matched controls, differentially expressed genes (DEGs) were identified after data preprocessing, followed by Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment analyses. Protein-protein interaction (PPI) network, microRNA- (miRNA-) target regulatory network, and transcription factor- (TF-) target regulatory networks were constructed. Results. Of 819 DEGs obtained, 359 were upregulated and 460 were downregulated. Two GO terms, “rRNA processing” and “cytoplasm,” and two KEGG pathways, “metabolic pathways” and “TNF signaling pathway,” played roles in PD development. Intercellular adhesion molecule 1 (ICAM1) was the hub node in the PPI network; hsa- miR-7-5p, hsa-miR-433-3p, and hsa-miR-133b participated in PD pathogenesis.
    [Show full text]
  • Analyzing the Phenotypic and Functional Complexity of Lymphocytes Using Cytof (Cytometry by Time-Of-Flight)
    Cellular & Molecular Immunology (2012) 9, 322–323 ß 2012 CSI and USTC. All rights reserved 1672-7681/12 $32.00 www.nature.com/cmi RESEARCH HIGHLIGHT Analyzing the phenotypic and functional complexity of lymphocytes using CyTOF (cytometry by time-of-flight) Guobing Chen and Nan-ping Weng Cellular & Molecular Immunology (2012) 9, 322–323; doi:10.1038/cmi.2012.16; published online 28 May 2012 he human immune system is equipped antigen peptide-MHC tetramers on human status of cytokines, cytotoxic granule T with vast numbers of lymphocytes pos- CD81 T cells. These parameters covered components and CD107, a degranulation sessing distinct antigen specificities. The nine functional attributes and distinguished marker. A shift in the proportions of enormous repertoire and heterogeneity of all reported CD81 T-cell subsets, such as cells with each phenotype was identified after lymphocytes ensures their ability to effec- naive, central memory, effector memory, in vitro stimulation with either PMA/ tively fight against external microbial inva- terminal effector, long-lived memory pre- ionomycin or anti-CD36anti-CD28. PMA/ ders, as well as internal aberrant cells. cursor effector cells and short-lived effector ionomycin induced a greater number of dis- However, the understanding of the specific cells. The authors used principal compon- tinct functional types of CD81 T cells than phenotypes and functions of lymphocytes is ent analysis (PCA) to analyze the large did anti-CD36anti-CD28. However, because hindered by the lack of tools that can be used CyTOF datasets and presented their results these studies were performed at the same to visualize this complexity. Fluorescent dye- either in two-dimensional PCA or in com- timepoint after stimulation, it is not clear based flow cytometry, which can simulta- bination with a protein structure program whether the observed difference in the num- 1 neously analyze 8–10 parameters of a single (PyMOL) as three-dimensional PCA.
    [Show full text]
  • A Possible Approach for Oral Drug Delivery of Nanoparticles
    COSMOS, Vol. 10, No. 1 (2014) 1–4 © World Scienti¯c Publishing Company DOI: 10.1142/S0219607714400035 A POSSIBLE APPROACH FOR ORAL DRUG DELIVERY OF NANOPARTICLES RABI'ATUL `ADAWIYAH BINTE MINHAT and THILO HAGEN Department of Biochemistry, Yong Loo Lin School of Medicine National University of Singapore, 117599 Singapore Received 12 February 2014 Revised 26 March 2014 Accepted 10 April 2014 Published 13 February 2015 Keywords: Oral drug delivery; nanoparticles; neonatal Fc receptor. Advances in biotechnology have led to numerous nanoparticles relative to the total atom number.2 discoveries and development of proteins and other These special properties are the reason why nano- macromolecules as pharmaceutical drugs.2 The particles have a wide variety of potential applica- production of macromolecules as therapeutics has tions in various ¯elds such as medicine, energy and improved treatment options in many areas in electronics industries. Thus, the development of an medicine. However, delivery of these macromolecule oral delivery system using nanoparticles is advan- COSMOS Downloaded from www.worldscientific.com drugs has mostly been restricted to parenteral tageous. If successful, the method could be combined methods of administration. The development of a with other techniques, such as a nanoparticle-based more convenient oral delivery system still faces many chemotherapy free of the debilitating side-e®ects,7,9 challenges. to further improve available treatment options. by NATIONAL UNIVERSITY OF SINGAPORE on 03/30/15. For personal use only. Many macromolecule drugs are vulnerable to the There have been several attempts to develop a pH variation and enzymatic degradation in the method for oral drug delivery using nanoparticles,2 gastrointestinal tract.2 One way to protect the drugs but these attempts have mostly had undesirable from degradation is by encapsulation.4 In particular, drawbacks.
    [Show full text]
  • A Role for the L-Selectin Adhesion System in Mediating Cytotrophoblast Emigration from the Placenta
    Developmental Biology 298 (2006) 107–117 www.elsevier.com/locate/ydbio A role for the L-selectin adhesion system in mediating cytotrophoblast emigration from the placenta ⁎ Akraporn Prakobphol a, Olga Genbacev a, Matthew Gormley a, Mirhan Kapidzic a, Susan J. Fisher a,b, a Department of Cell and Tissue Biology, University of California, San Francisco, CA 94143, USA b Departments of Anatomy and Pharmaceutical Chemistry, University of California, San Francisco, CA 94143, USA Received for publication 24 February 2006; revised 13 June 2006; accepted 13 June 2006 Available online 15 June 2006 Abstract Cytotrophoblast (CTB) aggregates that bridge the gap between the placenta and the uterus are suspended as cell columns in the intervillous space, where they experience significant amounts of shear stress generated by maternal blood flow. The proper formation of these structures is crucial to pregnancy outcome as they play a vital role in anchoring the embryo/fetus to the decidua. At the same time, they provide a route by which CTBs enter the uterine wall. The mechanism by which the integrity of the columns is maintained while allowing cell movement is unknown. Here, we present evidence that the interactions of L-selectin with its carbohydrate ligands, a specialized adhesion system that is activated by shear stress, play an important role. CTBs in cell columns, particularly near the distal ends, stained brightly for L-selectin and with the TRA-1-81 antibody, which recognizes carbohydrate epitopes that support binding of L-selectin chimeras in vitro. Function-perturbing antibodies that inhibited either receptor or ligand activity also inhibited formation of cell columns in vitro.
    [Show full text]
  • (CR1) and Crry, the Two Genetic Homologues of Human CR1 by Hector Molina,* Winnie Wong,~ Taroh Kinoshita,$ Carol Brenner,* Sharon Foley,* and V
    Disfin_ct Receptor and Regulatory Properties of Recombinant Mouse Complement Receptor 1 (CR1) and Crry, the Two Genetic Homologues of Human CR1 By Hector Molina,* Winnie Wong,~ Taroh Kinoshita,$ Carol Brenner,* Sharon Foley,* and V. Michael Holers* From the *Howard Hughes Medical Institute Laboratories and Department of Medicine, Division of Rheumatology, Washington University School of Medicine, St. Louis, Missouri 63110; the *BASF Bioresearch Corporation, Cambridge, Massachusetts 02139; and the SDepartraent of Immunoregulation, Research Institute for Microbial Diseases, Osaka University, Osaka 565, Japan Downloaded from http://rupress.org/jem/article-pdf/175/1/121/1267946/121.pdf by guest on 27 September 2021 Summary The relationship between the characterized mouse regulators of complement activation (RCA) genes and the 190-kD mouse complement receptor 1 (MCK1), 155-kD mouse complement receptor 2 (MCR2), and mouse p65 is unclear. One mouse RCA gene, designatedMCR2 (or Cr2), encodes alternatively spliced 21 and 15 short consensus repeat (SCR)-containing transcripts that crosshybridize with cDNAs of both human CR2 and CR1, or CR2 alone, respectively. A five SCR-containing transcript derived from a second unique gene, designated Crry, also crosshybridizes with human CR1. We have previously shown that the 155-kD MCR2 is encoded by the 15 SCR-containing transcript. To analyze the protein products of the other transcripts, which are considered the genetic homologues of human CRI, we have expressed the 21 and the 5 SCR-containing cDNAs in the human K562 erythroleukemia cell line. We demonstrate that cells expressing the 21 SCK transcript express the 190-kD MCR1 protein. These cells react with five unique rat anti-MCR1 monodonal antibodies, including the 8C12 antibody considered to be monospecific for MCK1.
    [Show full text]
  • Download Slides
    PEARLS OF LABORATORY MEDICINE Pearl Title: Immunoglobulin and T Cell Receptor Genetics Name of Presenter: Bing Melody Zhang Affiliation: Stanford University School of Medicine DOI: 10.15428/CCTC.2020.318055 © Clinical Chemistry Outline • Structure of Immunoglobulin (Ig) and TCR (T cell receptor) • TCR/Ig genetics • T/B cell development and TCR/Ig gene rearrangement • Molecular testing of TCR/Ig rearrangement • Clinical utility of molecular TCR/Ig rearrangement analysis in lymphoid malignancies 2 Immunoglobulin (Ig) and T Cell Receptor (TCR) 3 TCR/Ig Genetics • Each receptor chain is encoded in the germline genome as different gene segments (V, D, J). • During T/B lymphocyte development, the gene segments undergo random somatic DNA recombination (VDJ or VJ) to form a complete variable region sequence, known as gene rearrangement. • Non-templated insertion and deletion of random nucleotides at the junctional regions. • Somatic hypermutation: high rate of point mutations in V region of Ig genes (mature B cells). 4 IGH Gene Rearrangement V genes D genes J genes Constant region Germline V-N-D-N-J 5 B cell development and BCR/Ig gene rearrangement Large pre- Small pre- Immature B Mature B Stem cells Early pro-B Late pro-B cell cell B cell B cell cell cell IgH: germline D-J joining V-DJ joining VDJ rearranged VDJ rearranged VDJ rearranged VDJ rearranged IgK/L: germline germline germline germline V-J joining VJ rearranged VJ rearranged Order of gene rearrangements: IGH → IGK If IGK rearrangement fails → IGL gene rearrangement The Immune System,
    [Show full text]
  • Inventories of Naive and Tolerant Mouse CD4 T Cell Repertoires Reveal a Hierarchy of Deleted and Diverted T Cell Receptors
    Inventories of naive and tolerant mouse CD4 T cell repertoires reveal a hierarchy of deleted and diverted T cell receptors Tobias Hasslera, Emanuel Urmanna, Sebastian Teschnera, Christine Federlea, Thamotharampillai Dileepanb, Kilian Schoberc, Marc K. Jenkinsb, Dirk H. Buschc,d, Maria Hinterbergera,1, and Ludger Kleina,1,2 aInstitute for Immunology, Faculty of Medicine, Ludwig-Maximilians-University, 82152 Planegg-Martinsried, Germany; bCenter for Immunology, University of Minnesota, Minneapolis, MN 55455; cInstitute for Medical Microbiology, Immunology and Hygiene, Technische Universität München, 81675 Munich, Germany; and dGerman Center for Infection Research, 81675 Munich, Germany Edited by Shimon Sakaguchi, WPI Immunology Frontier Research Center, Osaka University, Osaka, Japan, and approved August 5, 2019 (received for review May 2, 2019) – Deletion or Treg cell differentiation are alternative fates of autore- deletional tolerance (14 17), also shapes the Treg cell repertoire active MHCII-restricted thymocytes. How these different modes (18–20). of tolerance determine the size and composition of polyclonal co- MHCII tetramers were employed to trace minute cohorts of horts of autoreactive T cells with shared specificity is poorly un- CD4 T cells when their cognate antigens were transgenically derstood. We addressed how tolerance to a naturally expressed expressed to emulate a ubiquitous or TRA-like expression pat- autoantigen of the central nervous system shapes the CD4 T cell tern (21, 22). Widespread antigen expression was associated with repertoire. Specific cells in the tolerant peripheral repertoire either deletion, whereas a more restricted TRA-like expression ensued + + were Foxp3 or displayed anergy hallmarks and, surprisingly, in the emergence of Foxp3 Treg cells. While these findings were at least as frequent as in the nontolerant repertoire.
    [Show full text]
  • TITLE: Immunoglobulin and T Cell Receptor Genetics PRESENTER: Bing Melody Zhang
    TITLE: Immunoglobulin and T Cell Receptor Genetics PRESENTER: Bing Melody Zhang Slide 1: Hello, my name is Bing Melody Zhang. I am an Assistant professor (Clinical) of Pathology at Stanford University. Welcome to this Pearl of Laboratory Medicine on “Immunoglobulin and T Cell Receptor Genetics.” Slide 2: Here is the outline of this talk. I will cover the structure and genetics of Ig and TCR, T/B cell development and TCR/Ig gene rearrangements, molecular testing and clinical utility of TCR/Ig rearrangement analysis. Slide 3: Let’s first review the structure of Ig and TCR. B and T lymphocytes are characterized by their antigen-specific receptors, which are the primary effector molecules of the adaptive immune system. For B cells, there are the membrane-bound form of the immunoglobulin as main component of the B cell receptor (BCR), and the soluble form of Ig secreted by plasma cells. Both forms of Ig have the identical Y- shaped structure, composed of 2 heavy and 2 light chains. © 2016 Clinical Chemistry Pearls of Laboratory Medicine Title On the other hand, T cell receptors are heterodimeric cell surface molecules responsible for recognizing antigens presented to T cells in context of MHC molecules. In the circulation, majority (95%) of T cells express alpha beta chains and a minority of T cells express gamma- delta chains, as part of the TCR complex. Gamma-delta T cells are dominant subtype of T cells found in epithelial tissues. Both TCR and Ig molecules consist of variable and constant regions. Each lymphocyte receptor has a unique antigen-specificity determined by the structure of antigen-binding site primarily from the variable amino acid sequences.
    [Show full text]
  • Cells of the Immune System and Innate Immunity
    Harvard-MIT Division of Health Sciences and Technology HST.176: Cellular and Molecular Immunology Course Director: Dr. Shiv Pillai Cells of the Immune System and Innate Immunity Recommended reading: Abbas et al., 4th edition, Chapters 2 and 12 Janeway and Travers, 5th edition, Chapters 1 and 10 The innate immune system is made up of molecules and cellular processes that defend the host within minutes and hours after exposure to a noxious stimulus. It is the only immune system in plants and invertebrates. Innate immune responses may initiate acute inflammation, which basically involves the accumulation and activation of phagocytes (mainly polymorphonuclear cells in man) and of vascular endothelium at sites of injury. In vertebrates, the innate and adaptive immune systems talk to each other and there is an important reciprocal interplay that operates between these systems. In these animals the cells and molecules of the innate immune system provide immediate protection and then set in motion the activation of the adaptive immune response. The adaptive immune response in turn “revs” up innate immune mechanisms of host defense. The innate immune system uses non-clonal “pattern recognition” receptors (PRRs) which cannot recognize host structures but which do recognize patterns found on microbes.These are sometimes called PAMPs for Pathogen Associated Molecular Patterns. Pathogens/ microbes The most common organisms that cause disease are viruses, bacteria, fungi, protozoa, and worms. A microbe (a small invader) or a worm that does not cause disease in most people may generally be classified as non-pathogenic. Such an organism will provoke an immune response in a normal immunocompetent host.
    [Show full text]
  • Tetraspanin 3, As a Novel Regulator of Intracellular Β1 Integrin Recycling, Promotes Non-Small Cell Lung Cancer Cell Proliferation
    Tetraspanin 3, as a Novel Regulator of Intracellular β1 Integrin Recycling, Promotes Non-Small Cell Lung Cancer Cell Proliferation Hongbo Su China Medical University Yitong Xu China Medical University Yao Zhang China Medical University Xizi Jiang China Medical University Qingfu Zhang China Medical University Hongjiu Ren China Medical University Zifang Zou China Medical University Xueshan Qiu ( [email protected] ) China Medical University https://orcid.org/0000-0001-9481-8249 Research Keywords: beta 1 integrin, tetraspanin 3, non-small cell lung carcinoma, Rab11a Posted Date: June 9th, 2021 DOI: https://doi.org/10.21203/rs.3.rs-572884/v1 License: This work is licensed under a Creative Commons Attribution 4.0 International License. Read Full License Page 1/25 Abstract Background: The role of tetraspanins in cancer development has been widely reported. However, the expression and roles of tetraspanin 3 (TSPAN3) in solid tumors, including non-small cell lung cancer (NSCLC), have not yet been extensively investigated. In this study, we explored the role of TSPAN3 in NSCLC and its potential role in the tracking of integrin β1, which is highly expressed in this type of cancer. Methods: The expression of TSPAN3 in NSCLC tissue and NSCLC cell lines was evaluated, and the correlation between TSPAN3 expression and disease progression was assessed. Furthermore, loss- and gain-of-expression studies were conducted to determine the biological function of TSPAN3 both in vivo and vitro. The regulatory role of TSPAN3 in β1 integrin expression and intracellular recycling was studied through western blot, RT-PCR, and immunouorescence analyses. Results: TSPAN3 was found to be highly expressed in lung cancer cells and tissues.
    [Show full text]