TNF Receptor Superfamily Members RANK, RANKL, OPG Pathway As
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Signaling TNF-Like Ligand 1A/Death Receptor 3 the Adaptor Protein
The Adaptor Protein TRADD Is Essential for TNF-Like Ligand 1A/Death Receptor 3 Signaling This information is current as Yelena L. Pobezinskaya, Swati Choksi, Michael J. Morgan, of September 27, 2021. Xiumei Cao and Zheng-gang Liu J Immunol 2011; 186:5212-5216; Prepublished online 18 March 2011; doi: 10.4049/jimmunol.1002374 http://www.jimmunol.org/content/186/9/5212 Downloaded from Supplementary http://www.jimmunol.org/content/suppl/2011/03/18/jimmunol.100237 Material 4.DC1 http://www.jimmunol.org/ References This article cites 29 articles, 13 of which you can access for free at: http://www.jimmunol.org/content/186/9/5212.full#ref-list-1 Why The JI? Submit online. • Rapid Reviews! 30 days* from submission to initial decision by guest on September 27, 2021 • No Triage! Every submission reviewed by practicing scientists • Fast Publication! 4 weeks from acceptance to publication *average Subscription Information about subscribing to The Journal of Immunology is online at: http://jimmunol.org/subscription Permissions Submit copyright permission requests at: http://www.aai.org/About/Publications/JI/copyright.html Email Alerts Receive free email-alerts when new articles cite this article. Sign up at: http://jimmunol.org/alerts The Journal of Immunology is published twice each month by The American Association of Immunologists, Inc., 1451 Rockville Pike, Suite 650, Rockville, MD 20852 All rights reserved. Print ISSN: 0022-1767 Online ISSN: 1550-6606. The Journal of Immunology The Adaptor Protein TRADD Is Essential for TNF-Like Ligand 1A/Death Receptor 3 Signaling Yelena L. Pobezinskaya, Swati Choksi, Michael J. Morgan, Xiumei Cao, and Zheng-gang Liu TNFR-associated death domain protein (TRADD) is a key effector protein of TNFR1 signaling. -
The TNF and TNF Receptor Review Superfamilies: Integrating Mammalian Biology
Cell, Vol. 104, 487±501, February 23, 2001, Copyright 2001 by Cell Press The TNF and TNF Receptor Review Superfamilies: Integrating Mammalian Biology Richard M. Locksley,*²³k Nigel Killeen,²k The receptors and ligands in this superfamily have and Michael J. Lenardo§k unique structural attributes that couple them directly to *Department of Medicine signaling pathways for cell proliferation, survival, and ² Department of Microbiology and Immunology differentiation. Thus, they have assumed prominent ³ Howard Hughes Medical Institute roles in the generation of tissues and transient microen- University of California, San Francisco vironments. Most TNF/TNFR SFPs are expressed in the San Francisco, California 94143 immune system, where their rapid and potent signaling § Laboratory of Immunology capabilities are crucial in coordinating the proliferation National Institute of Allergy and Infectious Diseases and protective functions of pathogen-reactive cells. National Institutes of Health Here, we review the organization of the TNF/TNFR SF Bethesda, Maryland 20892 and how these proteins have been adapted for pro- cesses as seemingly disparate as host defense and or- ganogenesis. In interpreting this large and highly active Introduction area of research, we have focused on common themes that unite the actions of these genes in different tissues. Three decades ago, lymphotoxin (LT) and tumor necro- We also discuss the evolutionary success of this super- sis factor (TNF) were identified as products of lympho- familyÐsuccess that we infer from its expansion across cytes and macrophages that caused the lysis of certain the mammalian genome and from its many indispens- types of cells, especially tumor cells (Granger et al., able roles in mammalian biology. -
TRAIL and Cardiovascular Disease—A Risk Factor Or Risk Marker: a Systematic Review
Journal of Clinical Medicine Review TRAIL and Cardiovascular Disease—A Risk Factor or Risk Marker: A Systematic Review Katarzyna Kakareko 1,* , Alicja Rydzewska-Rosołowska 1 , Edyta Zbroch 2 and Tomasz Hryszko 1 1 2nd Department of Nephrology and Hypertension with Dialysis Unit, Medical University of Białystok, 15-276 Białystok, Poland; [email protected] (A.R.-R.); [email protected] (T.H.) 2 Department of Internal Medicine and Hypertension, Medical University of Białystok, 15-276 Białystok, Poland; [email protected] * Correspondence: [email protected] Abstract: Tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) is a pro-apoptotic protein showing broad biological functions. Data from animal studies indicate that TRAIL may possibly contribute to the pathophysiology of cardiomyopathy, atherosclerosis, ischemic stroke and abdomi- nal aortic aneurysm. It has been also suggested that TRAIL might be useful in cardiovascular risk stratification. This systematic review aimed to evaluate whether TRAIL is a risk factor or risk marker in cardiovascular diseases (CVDs) focusing on major adverse cardiovascular events. Two databases (PubMed and Cochrane Library) were searched until December 2020 without a year limit in accor- dance to the PRISMA guidelines. A total of 63 eligible original studies were identified and included in our systematic review. Studies suggest an important role of TRAIL in disorders such as heart failure, myocardial infarction, atrial fibrillation, ischemic stroke, peripheral artery disease, and pul- monary and gestational hypertension. Most evidence associates reduced TRAIL levels and increased TRAIL-R2 concentration with all-cause mortality in patients with CVDs. It is, however, unclear Citation: Kakareko, K.; whether low TRAIL levels should be considered as a risk factor rather than a risk marker of CVDs. -
Role of ADAM10 and ADAM17 in Regulating CD137 Function
International Journal of Molecular Sciences Article Role of ADAM10 and ADAM17 in Regulating CD137 Function Jana Seidel 1, Sinje Leitzke 1, Björn Ahrens 1, Maria Sperrhacke 1, Sucharit Bhakdi 2 and Karina Reiss 1,* 1 Department of Dermatology, University of Kiel, 24105 Kiel, Germany; [email protected] (J.S.); [email protected] (S.L.); [email protected] (B.A.); [email protected] (M.S.) 2 Independent Researcher, 24105 Kiel, Germany; [email protected] * Correspondence: [email protected] Abstract: Human CD137 (4-1BB), a member of the TNF receptor family, and its ligand CD137L (4-1BBL), are expressed on immune cells and tumor cells. CD137/CD137L interaction mediates bidirectional cellular responses of potential relevance in inflammatory diseases, autoimmunity and oncology. A soluble form of CD137 exists, elevated levels of which have been reported in patients with rheumatoid arthritis and various malignancies. Soluble CD137 (sCD137) is considered to represent a splice variant of CD137. In this report, however, evidence is presented that A Disintegrin and Metalloproteinase (ADAM)10 and potentially also ADAM17 are centrally involved in its generation. Release of sCD137 by transfected cell lines and primary T cells was uniformly inhibitable by ADAM10 inhibition. The shedding function of ADAM10 can be blocked through inhibition of its interaction with surface exposed phosphatidylserine (PS), and this effectively inhibited sCD137 generation. The phospholipid scramblase Anoctamin-6 (ANO6) traffics PS to the outer membrane and thus modifies ADAM10 function. Overexpression of ANO6 increased stimulated shedding, and hyperactive ANO6 led to maximal constitutive shedding of CD137. -
Osteoprotegerin: a Novel Secreted Protein Involved in the Regulation of Bone Density
Cell, Vol. 89, 309±319, April 18, 1997, Copyright 1997 by Cell Press Osteoprotegerin: A Novel Secreted Protein Involved in the Regulation of Bone Density W. S. Simonet,2 D. L. Lacey,7 C. R. Dunstan,7 during normal bone remodeling that occurs throughout M. Kelley,3 M.-S. Chang,4 R. LuÈ thy,4 life. In contrast, osteoclasts differentiate from hemato- H. Q. Nguyen,2 S. Wooden,5 L. Bennett,6 poietic precursors of the monocyte±macrophage lin- T. Boone,10 G. Shimamoto,10 M. DeRose,2 eage and resorb bone matrix. Both these cell types are R. Elliott,1 A. Colombero,1 H.-L. Tan,7 influenced by a wide variety of hormones, inflammatory G. Trail,5 J. Sullivan,8 E. Davy,3 N. Bucay,2 mediators, and growth factors (Suda et al., 1992; Mundy, L. Renshaw-Gegg,5 T. M. Hughes,2 D. Hill,7 1993a, 1993b). An imbalance of osteoblast and osteo- W. Pattison,4 P. Campbell,6 S. Sander,5 clast functions can result in skeletal abnormalities char- G. Van,7 J. Tarpley,7 P. Derby,9 R. Lee,10 acterized by increased (osteopetrosis) or decreased (os- Amgen EST Program, and W. J. Boyle1 teoporosis) bone mass. 1 Department of Cell Biology The study of osteopetrosis in mutant mice has led to 2 Department of Molecular Genetics significant advances in the understanding of the pro- 3 Department of Protein Chemistry cesses that regulate bone mass (Marks, 1989). From 4 Department of Computational Biology these studies we have learned the following: (i) genetic 5 Department of Mammalian Cell Molecular Biology defects in osteoclast development, maturation, and/or 6 Department of Immunology activation lead to decreased bone resorption and uni- 7 Department of Pathology formly result in severe osteopetrosis (Marks, 1989); (ii) 8 Department of Bacterial Expression the stromal microenvironment plays an essential role in osteoclast differentiation (Udagawa et al., 1989); (iii) 9 Department of Protein Structure signal transduction from the cell membrane through Src 10 Department of Process Science tyrosine kinase is necessary for osteoclast-mediated Amgen Inc. -
TNFR2 Signaling Regulates the Immunomodulatory Function of Oligodendrocyte Precursor Cells
cells Article TNFR2 Signaling Regulates the Immunomodulatory Function of Oligodendrocyte Precursor Cells Haritha L. Desu 1, Placido Illiano 1, James S. Choi 1, Maureen C. Ascona 1, Han Gao 1,2, Jae K. Lee 1 and Roberta Brambilla 1,3,4,* 1 The Miami Project to Cure Paralysis, Department of Neurological Surgery, University of Miami Miller School of Medicine, Miami, FL 33136, USA; [email protected] (H.L.D.); [email protected] (P.I.); [email protected] (J.S.C.); [email protected] (M.C.A.); [email protected] (H.G.); [email protected] (J.K.L.) 2 Department of Spine Surgery, The Third Affiliated Hospital of Sun Yat-Sen University, Guangzhou 510630, China 3 Department of Neurobiology Research, Institute of Molecular Medicine, and BRIDGE—Brain Research Inter Disciplinary Guided Excellence, 5000 Odense, Denmark 4 Department of Clinical Research, University of Southern Denmark, 5000 Odense, Denmark * Correspondence: [email protected]; Tel.: +305-243-3567 Abstract: Multiple sclerosis (MS) is a neuroimmune disorder characterized by inflammation, CNS demyelination, and progressive neurodegeneration. Chronic MS patients exhibit impaired remyeli- nation capacity, partly due to the changes that oligodendrocyte precursor cells (OPCs) undergo in response to the MS lesion environment. The cytokine tumor necrosis factor (TNF) is present in the MS-affected CNS and has been implicated in disease pathophysiology. Of the two active forms of TNF, transmembrane (tmTNF) and soluble (solTNF), tmTNF signals via TNFR2 mediating protective and reparative effects, including remyelination, whereas solTNF signals predominantly via TNFR1 Citation: Desu, H.L.; Illiano, P.; Choi, promoting neurotoxicity. -
Human Colon Cancer Primer Library
Human Colon Cancer Primer Library Catalog No: HCCR-1 Supplier: RealTimePrimers Lot No: XXXXX Supplied as: solid Stability: store at -20°C Description Contains 88 primer sets directed against cytokine and chemokine receptor genes and 8 housekeeping gene primer sets. Provided in a 96-well microplate (20 ul - 10 uM). Perform up to 100 PCR arrays (based on 20 ul assay volume per reaction). Just add cDNA template and SYBR green master mix. Gene List: • CCR1 chemokine (C-C motif) receptor 1 • IL11RA interleukin 11 receptor, alpha • CCR2 chemokine (C-C motif) receptor 2 • IL11RB interleukin 11 receptor, beta • CCR3 chemokine (C-C motif) receptor 3 • IL12RB1 interleukin 12 receptor, beta 1 • CCR4 chemokine (C-C motif) receptor 4 • IL12RB2 interleukin 12 receptor, beta 2 • CCR5 chemokine (C-C motif) receptor 5 • IL13RA1 interleukin 13 receptor, alpha 1 • CCR6 chemokine (C-C motif) receptor 6 • IL13RA2 interleukin 13 receptor, alpha 2 • CCR7 chemokine (C-C motif) receptor 7 • IL15RA interleukin 15 receptor, alpha • CCR8 chemokine (C-C motif) receptor 8 • IL15RB interleukin 15 receptor, beta • CCR9 chemokine (C-C motif) receptor 9 • IL17RA interleukin 17 receptor A • CCR10 chemokine (C-C motif) receptor 10 • IL17RB interleukin 17 receptor B • CX3CR1 chemokine (C-X3-C motif) receptor 1 • IL17RC interleukin 17 receptor C • CXCR1 chemokine (C-X-C motif) receptor 1 • IL17RD interleukin 17 receptor D • CXCR2 chemokine (C-X-C motif) receptor 2 • IL17RE interleukin 17 receptor E • CXCR3 chemokine (C-X-C motif) receptor 3 • IL18R1 interleukin 18 receptor -
Belantamab Mafodotin to Treat Multiple Myeloma: a Comprehensive Review of Disease, Drug Efficacy and Side Effects
Review Belantamab Mafodotin to Treat Multiple Myeloma: A Comprehensive Review of Disease, Drug Efficacy and Side Effects Grace Lassiter 1,*, Cole Bergeron 2, Ryan Guedry 2, Julia Cucarola 2, Adam M. Kaye 3 , Elyse M. Cornett 4, Alan D. Kaye 4 , Giustino Varrassi 5, Omar Viswanath 4,6,7,8 and Ivan Urits 4,9 1 School of Medicine, Georgetown University, Washington, DC 20007, USA 2 School of Medicine, Louisiana State University Shreveport, Shreveport, LA 71103, USA; [email protected] (C.B.); [email protected] (R.G.); [email protected] (J.C.) 3 Department of Pharmacy Practice, Thomas J. Long School of Pharmacy and Health Sciences, University of the Pacific, Stockton, CA 95211, USA; akaye@pacific.edu 4 Department of Anesthesiology, Louisiana State University Shreveport, Shreveport, LA 71103, USA; [email protected] (E.M.C.); [email protected] (A.D.K.); [email protected] (O.V.); [email protected] (I.U.) 5 Paolo Procacci Foundation, Via Tacito 7, 00193 Roma, Italy; [email protected] 6 College of Medicine-Phoenix, University of Arizona, Phoenix, AZ 85724, USA 7 Department of Anesthesiology, School of Medicine, Creighton University, Omaha, NE 68124, USA 8 Valley Anesthesiology and Pain Consultants—Envision Physician Services, Phoenix, AZ 85004, USA 9 Southcoast Health, Southcoast Physicians Group Pain Medicine, Wareham, MA 02571, USA * Correspondence: [email protected] Received: 14 December 2020; Accepted: 18 January 2021; Published: 21 January 2021 Abstract: Multiple myeloma (MM) is a hematologic malignancy characterized by excessive clonal proliferation of plasma cells. The treatment of multiple myeloma presents a variety of unique challenges due to the complex molecular pathophysiology and incurable status of the disease at this time. -
Trailblazing Strategies for Cancer Treatment
cancers Review TRAILblazing Strategies for Cancer Treatment Anna-Laura Kretz 1, Anna Trauzold 2,3, Andreas Hillenbrand 1, Uwe Knippschild 1, Doris Henne-Bruns 1, Silvia von Karstedt 4,5 and Johannes Lemke 1,* 1 Department of General and Visceral Surgery, Ulm University Hospital, Albert-Einstein-Allee 23, 89081 Ulm, Germany; [email protected] (A.-L.K.); [email protected] (A.H.); [email protected] (U.K.); [email protected] (D.H.-B.) 2 Institute for Experimental Cancer Research, University of Kiel, 24105 Kiel, Germany; [email protected] 3 Clinic for General Surgery, Visceral, Thoracic, Transplantation and Pediatric Surgery, University Hospital Schleswig-Holstein, 24105 Kiel, Germany 4 Department of Translational Genomics, University Hospital Cologne, Weyertal 115b, 50931 Cologne, Germany; [email protected] 5 Cologne Excellence Cluster on Cellular Stress Response in Aging-Associated Diseases (CECAD), University of Cologne, Joseph-Stelzmann Straße 26, 50931 Cologne, Germany * Correspondence: [email protected] Received: 11 March 2019; Accepted: 26 March 2019; Published: 30 March 2019 Abstract: In the late 1990s, tumor necrosis factor (TNF)-related apoptosis-inducing ligand (TRAIL), a member of the TNF-family, started receiving much attention for its potential in cancer therapy, due to its capacity to induce apoptosis selectively in tumour cells in vivo. TRAIL binds to its membrane-bound death receptors TRAIL-R1 (DR4) and TRAIL-R2 (DR5) inducing the formation of a death-inducing signalling complex (DISC) thereby activating the apoptotic cascade. The ability of TRAIL to also induce apoptosis independently of p53 makes TRAIL a promising anticancer agent, especially in p53-mutated tumour entities. -
Characterisation of Chicken OX40 and OX40L
Characterisation of chicken OX40 and OX40L von Stephanie Hanna Katharina Scherer Inaugural-Dissertation zur Erlangung der Doktorw¨urde der Tier¨arztlichenFakult¨at der Ludwig-Maximilians-Universit¨atM¨unchen Characterisation of chicken OX40 and OX40L von Stephanie Hanna Katharina Scherer aus Baunach bei Bamberg M¨unchen2018 Aus dem Veterin¨arwissenschaftlichenDepartment der Tier¨arztlichenFakult¨at der Ludwig-Maximilians-Universit¨atM¨unchen Lehrstuhl f¨urPhysiologie Arbeit angefertigt unter der Leitung von Univ.-Prof. Dr. Thomas G¨obel Gedruckt mit Genehmigung der Tier¨arztlichenFakult¨at der Ludwig-Maximilians-Universit¨atM¨unchen Dekan: Univ.-Prof. Dr. Reinhard K. Straubinger, Ph.D. Berichterstatter: Univ.-Prof. Dr. Thomas G¨obel Korreferenten: Priv.-Doz. Dr. Nadja Herbach Univ.-Prof. Dr. Bernhard Aigner Prof. Dr. Herbert Kaltner Univ.-Prof. Dr. R¨udiger Wanke Tag der Promotion: 27. Juli 2018 Meinen Eltern und Großeltern Contents List of Figures 11 Abbreviations 13 1 Introduction 17 2 Fundamentals 19 2.1 T cell activation . 19 2.1.1 The activation of T cells requires the presence of several signals 19 2.1.2 Costimulatory signals transmitted via members of the im- munoglobulin superfamily . 22 2.1.3 Costimulatory signals transmitted via members of the cy- tokine receptor family . 23 2.1.4 Costimulatory signals transmitted via members of the tumour necrosis factor receptor superfamily . 24 2.2 The tumour necrosis factor receptor superfamily . 26 2.2.1 The structure of tumour necrosis factor receptors . 26 2.2.2 Functional classification of TNFRSF members . 28 2.3 The tumour necrosis factor superfamily . 29 2.3.1 The structure of tumour necrosis factor ligands . -
A Comparison of the Cytoplasmic Domains of the Fas Receptor and the P75 Neurotrophin Receptor
Cell Death and Differentiation (1999) 6, 1133 ± 1142 ã 1999 Stockton Press All rights reserved 13509047/99 $15.00 http://www.stockton-press.co.uk/cdd A comparison of the cytoplasmic domains of the Fas receptor and the p75 neurotrophin receptor 1,2 1,2 1 ,1 H Kong , AH Kim , JR Orlinick and MV Chao* Introduction 1 Molecular Neurobiology Program, Skirball Institute, New York University The p75 receptor is the founding member of the TNF Medical Center, 540 First Avenue, New York, NY 10016, USA receptor superfamily.1 Structural features shared by several 2 The ®rst two authors contributed equally to this study members of this family include a cysteine-rich extracellular * Corresponding author: MV Chao, Molecular Neurobiology Program, Skirball domain repeated two to six times and an intracellular motif Institute, New York University Medical Center, 540 First Avenue, New York, NY termed the `death domain'. The term `death domain' was 10016, USA. Tel: +1 212-263-0722; Fax: +1 212-263-0723; E-mail: [email protected] coined from its functional role in mediating apoptosis, particularly via the p55 TNF receptor and FasR.2,3 The Received 15.7.98; revised 20.8.99; accepted 23.8.99 death domain is a protein association motif4,5 that binds to Edited by C Thiele cytoplasmic proteins, which can trigger the caspase protease cascade or other signal transduction pathways. Multiple adaptor and death effector proteins that bind to the Abstract death domains of the p55 TNF and Fas receptors have The p75 neurotrophic receptor (p75) shares structural been identified. -
Alterations in the Immuno-Skeletal Interface Drive Bone Destruction in HIV-1 Transgenic Rats
Alterations in the immuno-skeletal interface drive bone destruction in HIV-1 transgenic rats Tatyana Vikulinaa,1, Xian Fanb,c,1, Masayoshi Yamaguchia, Susanne Roser-Pagec, Majd Zayzafoond, David M. Guidotb,c, Ighovwerha Ofotokune, and M. Neale Weitzmanna,c,f,2 Divisions of aEndocrinology and Metabolism and Lipids and bPulmonary, Allergy and Critical Care Medicine, Emory University School of Medicine, Atlanta, GA 30322; cAtlanta Veterans Affairs Medical Center, Decatur, GA 30033; dDepartment of Pathology, University of Alabama at Birmingham, Birmingham, AL 35294; eDivision of Infectious Diseases, Department of Medicine, Emory University School of Medicine, Atlanta, GA 30322; and fWinship Cancer Institute, Emory University School of Medicine, Atlanta, GA 30322 Edited* by Max D. Cooper, Emory University, Atlanta, GA, and approved June 24, 2010 (received for review March 10, 2010) Osteoporosis and bone fractures are increasingly recognized compli- capable of making RANKL and OPG, B cells are recognized as cations of HIV-1 infection. Although antiretroviral therapy itself has a significant source of RANKL when activated in vitro (13), in complex effects on bone turnover, it is now evident that the majority postmenopausal humans in vivo (3), and in inflammatory con- of HIV-infected individuals already exhibit reduced bone mineral ditions such as periodontitis (14). By contrast, both human (15) density before therapy. The mechanisms responsible are likely multi- and mouse B cells (1) are recognized producers of OPG, which is factorial and have been difficult to delineate in humans. The HIV-1 regulated, in part, by T cells through CD40/CD40 ligand (CD40L) transgenic rat recapitulates many key features of human AIDS.