Signaling by IL-2 and related cytokines: JAKs, STATs, and relationship to immunodeficiency
Cytokines that bind to the interleukin‐2 (IL‐2) receptor common gamma chain (γc), including IL‐2, IL‐4, IL‐7, IL‐9, and IL‐15, are important for the growth and differentiation of T and B lymphocytes, natural killer cells, macrophages, and monoctyes. These cytokines have overlapping biological effect...
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Veröffentlicht in: | Journal of leukocyte biology 1996-10, Vol.60 (4), p.441-452 |
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creator | Johnston, James A. Bacon, Chris M. Riedy, M. C. O'Shea, John J. |
description | Cytokines that bind to the interleukin‐2 (IL‐2) receptor common gamma chain (γc), including IL‐2, IL‐4, IL‐7, IL‐9, and IL‐15, are important for the growth and differentiation of T and B lymphocytes, natural killer cells, macrophages, and monoctyes. These cytokines have overlapping biological effects that in part result from the use of the shared receptor subunit γc. Recently it has become clear that these cytokines activate a number of important intracellular signaling molecules, including the Janus kinases JAK1 and JAK3 and members of the transcription factor family of signal transducers and activators of transcription (STATs). The discovery of these signaling pathways has led to important new insights into their role in lymphocyte maturation, as it has emerged that mutations in the genes encoding both γc and JAK3 result in similar forms of severe combined immunodeficiency (SCID). In this review we examine the structure and function of cytokine receptors and the signaling pathways involved in their regulation of gene expression. Furthermore, we discuss recent advances that have led to a better understanding of how cytokines elicit intracellular responses, as well as their role in normal lymphoid development. J. Leukoc. Biol. 60: 441–452; 1996. |
doi_str_mv | 10.1002/jlb.60.4.441 |
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The discovery of these signaling pathways has led to important new insights into their role in lymphocyte maturation, as it has emerged that mutations in the genes encoding both γc and JAK3 result in similar forms of severe combined immunodeficiency (SCID). In this review we examine the structure and function of cytokine receptors and the signaling pathways involved in their regulation of gene expression. Furthermore, we discuss recent advances that have led to a better understanding of how cytokines elicit intracellular responses, as well as their role in normal lymphoid development. J. Leukoc. Biol. 60: 441–452; 1996.</description><identifier>ISSN: 0741-5400</identifier><identifier>EISSN: 1938-3673</identifier><identifier>DOI: 10.1002/jlb.60.4.441</identifier><identifier>PMID: 8864127</identifier><language>eng</language><publisher>United States: Society for Leukocyte Biology</publisher><subject>Cell Transformation, Neoplastic - genetics ; Chromosome Mapping ; cytokine signaling ; DNA-Binding Proteins - physiology ; Enzyme Precursors - physiology ; Genes ; Humans ; IL‐12 ; IL‐15 ; IL‐4 ; Interleukin-12 - physiology ; Interleukin-2 - physiology ; Intracellular Signaling Peptides and Proteins ; JAK3 ; Janus ; Janus Kinase 3 ; Lymphocyte Specific Protein Tyrosine Kinase p56(lck) ; Lymphocytes - physiology ; Phosphotyrosine - physiology ; Protein-Tyrosine Kinases - physiology ; receptor ; Receptors, Cytokine - physiology ; severe combined immunodeficiency ; Severe Combined Immunodeficiency - physiopathology ; Signal Transduction ; src Homology Domains ; src-Family Kinases - physiology ; STAT1 Transcription Factor ; STAT5 ; Syk Kinase ; Trans-Activators - physiology</subject><ispartof>Journal of leukocyte biology, 1996-10, Vol.60 (4), p.441-452</ispartof><rights>1996 Society for Leukocyte Biology</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3891-b8b1ee8d2607be0042455302d9ce0cb9a9d6cf69d163b18f914cf10db93c4c643</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8864127$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Johnston, James A.</creatorcontrib><creatorcontrib>Bacon, Chris M.</creatorcontrib><creatorcontrib>Riedy, M. C.</creatorcontrib><creatorcontrib>O'Shea, John J.</creatorcontrib><title>Signaling by IL-2 and related cytokines: JAKs, STATs, and relationship to immunodeficiency</title><title>Journal of leukocyte biology</title><addtitle>J Leukoc Biol</addtitle><description>Cytokines that bind to the interleukin‐2 (IL‐2) receptor common gamma chain (γc), including IL‐2, IL‐4, IL‐7, IL‐9, and IL‐15, are important for the growth and differentiation of T and B lymphocytes, natural killer cells, macrophages, and monoctyes. These cytokines have overlapping biological effects that in part result from the use of the shared receptor subunit γc. Recently it has become clear that these cytokines activate a number of important intracellular signaling molecules, including the Janus kinases JAK1 and JAK3 and members of the transcription factor family of signal transducers and activators of transcription (STATs). The discovery of these signaling pathways has led to important new insights into their role in lymphocyte maturation, as it has emerged that mutations in the genes encoding both γc and JAK3 result in similar forms of severe combined immunodeficiency (SCID). In this review we examine the structure and function of cytokine receptors and the signaling pathways involved in their regulation of gene expression. Furthermore, we discuss recent advances that have led to a better understanding of how cytokines elicit intracellular responses, as well as their role in normal lymphoid development. J. Leukoc. Biol. 60: 441–452; 1996.</description><subject>Cell Transformation, Neoplastic - genetics</subject><subject>Chromosome Mapping</subject><subject>cytokine signaling</subject><subject>DNA-Binding Proteins - physiology</subject><subject>Enzyme Precursors - physiology</subject><subject>Genes</subject><subject>Humans</subject><subject>IL‐12</subject><subject>IL‐15</subject><subject>IL‐4</subject><subject>Interleukin-12 - physiology</subject><subject>Interleukin-2 - physiology</subject><subject>Intracellular Signaling Peptides and Proteins</subject><subject>JAK3</subject><subject>Janus</subject><subject>Janus Kinase 3</subject><subject>Lymphocyte Specific Protein Tyrosine Kinase p56(lck)</subject><subject>Lymphocytes - physiology</subject><subject>Phosphotyrosine - physiology</subject><subject>Protein-Tyrosine Kinases - physiology</subject><subject>receptor</subject><subject>Receptors, Cytokine - physiology</subject><subject>severe combined immunodeficiency</subject><subject>Severe Combined Immunodeficiency - physiopathology</subject><subject>Signal Transduction</subject><subject>src Homology Domains</subject><subject>src-Family Kinases - physiology</subject><subject>STAT1 Transcription Factor</subject><subject>STAT5</subject><subject>Syk Kinase</subject><subject>Trans-Activators - physiology</subject><issn>0741-5400</issn><issn>1938-3673</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1996</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkE2P0zAQhi0EWsrCjSuSL3DalHHsOA63sgL2oxKHLRcuVmxPWi9OUuJWUf79GqXqcTnN4X3mndFDyHsGSwaQf34MZilhKZZCsBdkwSquMi5L_pIsoBQsKwTAa_ImxkcA4LmEC3KhlBQsLxfk94PfdnXw3Zaaid6us5zWnaMDhvqAjtrp0P_xHcYv9G51H6_ow2a1SePM-L6LO7-nh576tj12vcPGW4-dnd6SV00dIr47zUvy6_u3zfVNtv754_Z6tc4sVxXLjDIMUbn0WGkQQOSiKDjkrrII1lR15aRtZOWY5IappmLCNgycqbgVVgp-ST7Nvfuh_3vEeNCtjxZDqDvsj1GXSuSFTEL-B7JCFQzKIoFXM2iHPsYBG70ffFsPk2ag_znXybmWoIVOzhP-4dR7NC26M3ySnHI256MPOD3bpe_WX2Hu_Djv7Px2N_oBdWzrENKFXI_jeL79BCARl8U</recordid><startdate>199610</startdate><enddate>199610</enddate><creator>Johnston, James A.</creator><creator>Bacon, Chris M.</creator><creator>Riedy, M. 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C. ; O'Shea, John J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3891-b8b1ee8d2607be0042455302d9ce0cb9a9d6cf69d163b18f914cf10db93c4c643</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1996</creationdate><topic>Cell Transformation, Neoplastic - genetics</topic><topic>Chromosome Mapping</topic><topic>cytokine signaling</topic><topic>DNA-Binding Proteins - physiology</topic><topic>Enzyme Precursors - physiology</topic><topic>Genes</topic><topic>Humans</topic><topic>IL‐12</topic><topic>IL‐15</topic><topic>IL‐4</topic><topic>Interleukin-12 - physiology</topic><topic>Interleukin-2 - physiology</topic><topic>Intracellular Signaling Peptides and Proteins</topic><topic>JAK3</topic><topic>Janus</topic><topic>Janus Kinase 3</topic><topic>Lymphocyte Specific Protein Tyrosine Kinase p56(lck)</topic><topic>Lymphocytes - physiology</topic><topic>Phosphotyrosine - physiology</topic><topic>Protein-Tyrosine Kinases - physiology</topic><topic>receptor</topic><topic>Receptors, Cytokine - physiology</topic><topic>severe combined immunodeficiency</topic><topic>Severe Combined Immunodeficiency - physiopathology</topic><topic>Signal Transduction</topic><topic>src Homology Domains</topic><topic>src-Family Kinases - physiology</topic><topic>STAT1 Transcription Factor</topic><topic>STAT5</topic><topic>Syk Kinase</topic><topic>Trans-Activators - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Johnston, James A.</creatorcontrib><creatorcontrib>Bacon, Chris M.</creatorcontrib><creatorcontrib>Riedy, M. 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C.</au><au>O'Shea, John J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Signaling by IL-2 and related cytokines: JAKs, STATs, and relationship to immunodeficiency</atitle><jtitle>Journal of leukocyte biology</jtitle><addtitle>J Leukoc Biol</addtitle><date>1996-10</date><risdate>1996</risdate><volume>60</volume><issue>4</issue><spage>441</spage><epage>452</epage><pages>441-452</pages><issn>0741-5400</issn><eissn>1938-3673</eissn><abstract>Cytokines that bind to the interleukin‐2 (IL‐2) receptor common gamma chain (γc), including IL‐2, IL‐4, IL‐7, IL‐9, and IL‐15, are important for the growth and differentiation of T and B lymphocytes, natural killer cells, macrophages, and monoctyes. These cytokines have overlapping biological effects that in part result from the use of the shared receptor subunit γc. Recently it has become clear that these cytokines activate a number of important intracellular signaling molecules, including the Janus kinases JAK1 and JAK3 and members of the transcription factor family of signal transducers and activators of transcription (STATs). The discovery of these signaling pathways has led to important new insights into their role in lymphocyte maturation, as it has emerged that mutations in the genes encoding both γc and JAK3 result in similar forms of severe combined immunodeficiency (SCID). In this review we examine the structure and function of cytokine receptors and the signaling pathways involved in their regulation of gene expression. Furthermore, we discuss recent advances that have led to a better understanding of how cytokines elicit intracellular responses, as well as their role in normal lymphoid development. J. Leukoc. Biol. 60: 441–452; 1996.</abstract><cop>United States</cop><pub>Society for Leukocyte Biology</pub><pmid>8864127</pmid><doi>10.1002/jlb.60.4.441</doi><tpages>12</tpages></addata></record> |
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source | Oxford University Press Journals All Titles (1996-Current); MEDLINE |
subjects | Cell Transformation, Neoplastic - genetics Chromosome Mapping cytokine signaling DNA-Binding Proteins - physiology Enzyme Precursors - physiology Genes Humans IL‐12 IL‐15 IL‐4 Interleukin-12 - physiology Interleukin-2 - physiology Intracellular Signaling Peptides and Proteins JAK3 Janus Janus Kinase 3 Lymphocyte Specific Protein Tyrosine Kinase p56(lck) Lymphocytes - physiology Phosphotyrosine - physiology Protein-Tyrosine Kinases - physiology receptor Receptors, Cytokine - physiology severe combined immunodeficiency Severe Combined Immunodeficiency - physiopathology Signal Transduction src Homology Domains src-Family Kinases - physiology STAT1 Transcription Factor STAT5 Syk Kinase Trans-Activators - physiology |
title | Signaling by IL-2 and related cytokines: JAKs, STATs, and relationship to immunodeficiency |
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