シック

関

Sykファミリー Syk family

[[造血系細胞に広く発現する細胞質内チロシンキナーゼ。リンパ球においては，T細胞・B細胞の抗原受容体の下流に位置し，抗原刺激特異的シグナルを細胞内に伝達する。Sykはspleen tyrosine kinaseの略で〈シック〉と読まれることが多い。]]

WordNet

the 19th letter of the Roman alphabet (同)s

PrepTutorEJDIC

sulfurの化学記号 / {略}South[ern]

Wikipedia preview

出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2016/02/22 05:22:32」(JST)

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[Wiki en表示]

Spleen tyrosine kinase, also known as Syk, is an enzyme which in humans is encoded by the SYK gene.^[1]^[2]^[3]

Function

SYK, along with Zap-70, is a member of the Syk family of tyrosine kinases. These non-receptor cytoplasmic tyrosine kinases share a characteristic dual SH2 domain separated by a linker domain.^[4]

While Syk and Zap-70 are primarily expressed in hematopoietic tissues, there is expression of Syk in a variety of tissues. Within B and T cells respectively, Syk and Zap-70 transmit signals from the B-Cell receptor and T-Cell receptor.^[5] Syk plays a similar role in transmitting signals from a variety of cell surface receptors including CD74, Fc Receptor, and integrins.

Function during development

Mice that lack Syk completely (Syk^−/−, Syk-knockout) die during embryonic development around midgestation. They show severe defects in the development of the lymphatic system. Normally, the lymphatic system and the blood system are strictly separated from each other. However, in Syk deficient mice the lymphatics and the blood vessels form abnormal shunts, leading to leakage of blood into the lymphatic system. The reason for this phenotype was identified by a genetic fate mapping approach, showing that Syk is expressed in myeloid cells which orchestrate the proper separation of lymphatics and blood system during embryogenesis and beyond. Thus, Syk is an essential regulator of the lymphatic system development in mice.^[6]

Clinical significance

Abnormal function of Syk has been implicated in several instances of hematopoeitic malignancies including translocations involving Itk and Tel. Constitutive Syk activity can transform B cells.^[7] Several transforming viruses contain "Immunoreceptor Tyrosine Activation Motifs" (ITAMs) which lead to activation of Syk including Epstein Barr virus, bovine leukemia virus, and mouse mammary tumor virus.

Given the central role of SYK in transmission of activating signals within B-cells, a suppression of this tyrosine kinase might aid in the treatment of B cell malignancies and autoimmune diseases.^[8] This has been demonstrated by the orally active inhibitor fostamatinib (R788) in the treatment of rheumatoid arthritis.^[9] The 6-month double-blind, placebo-controlled trial investigated clinical responses in 457 patients with rheumatoid arthritis who were not sufficiently responsive to methotrexate. The drug indeed caused a dose-dependent improvement in disease severity. The drug was however associated with an increase in the frequency in diarrhea, upper respiratory tract infections, neutropenia. Moreover R788 increased blood pressure and a concomitant increase in treatment with antihypertensive drugs. The drug is investigational and at present the final position within the broad set of antirheumatic drugs and its long-term safety are unknown.

Syk inhibition has also been proposed as a therapy for both lymphoma and chronic lymphocytic leukemia.<^[10] Other inhibitors of B-cell receptor (BCR) signaling including ibrutinib (PCI-32765) which inhibits BTK, and idelalisib (PI3K inhibitor - CAL-101 / GS-1101) showed activity in the diseases as well. Newer Syk inhibitors have entered the clinic and are also in clinical development (GS-9973).^[11]

The role of Syk in epithelial malignancies is controversial. Several authors have suggested that abnormal Syk function facilitates transformation in Nasopharyngeal carcinoma and head and neck cancer while other authors have suggested a tumor suppressor role in breast and gastric cancer.

Without Syk, the protein it makes, and genetic disruption in a panel of 55 genes thought also to be controlled by Syk, breast ductal carcinoma in situ (breast DCIS, which can become invasive), it is believed that the cancer has a markedly increased tendency to invade and metastasize.^[12]

Interactions

Syk has been shown to interact with:

Cbl gene^[13]^[14]^[15]
CRKL,^[16]
FCGR2A,^[17]^[18]
FYN,^[19]^[20]
Grb2,^[21]^[22]
Lck,^[23]
LYN,^[24]
PTK2,^[25]
PTPN6,^[21]^[26] and
VAV1.^[27]^[28]^[13]

References

^ "Entrez Gene: SYK Spleen tyrosine kinase".
^ Chan AC, Iwashima M, Turck CW, Weiss A (November 1992). "ZAP-70: a 70 kd protein-tyrosine kinase that associates with the TCR zeta chain". Cell 71 (4): 649–62. doi:10.1016/0092-8674(92)90598-7. PMID 1423621.
^ Ku G, Malissen B, Mattei MG (1994). "Chromosomal location of the Syk and ZAP-70 tyrosine kinase genes in mice and humans". Immunogenetics 40 (4): 300–2. doi:10.1007/BF00189976. PMID 8082894.
^ Seda, V; Mraz, M (2014). "B cell receptor (BCR) signalling and its crosstalk with other pathways in normal and malignant cells". European Journal of Haematology: n/a. doi:10.1111/ejh.12427. PMID 25080849.
^ Seda, V; Mraz, M (2014). "B cell receptor (BCR) signalling and its crosstalk with other pathways in normal and malignant cells". European Journal of Haematology: n/a. doi:10.1111/ejh.12427. PMID 25080849.
^ Böhmer R, Neuhaus B, Bühren S, Zhang D, Stehling S, Böck B and Friedemann Kiefer (2010). "Regulation of Developmental Lymphangiogenesis by Syk⁺ Leukocytes". Dev. Cell 18 (3): 437–49. doi:10.1016/j.devcel.2010.01.009. PMID 20230750.
^ Seda, V; Mraz, M (2014). "B cell receptor (BCR) signalling and its crosstalk with other pathways in normal and malignant cells". European Journal of Haematology: n/a. doi:10.1111/ejh.12427. PMID 25080849.
^ Seda, V; Mraz, M (2014). "B cell receptor (BCR) signalling and its crosstalk with other pathways in normal and malignant cells". European Journal of Haematology: n/a. doi:10.1111/ejh.12427. PMID 25080849.
^ Weinblatt ME, Kavanaugh A, Genovese MC, Musser TK, Grossbard EB, Magilavy DB. (September 2010). "An oral spleen tyrosine kinase (Syk) inhibitor for rheumatoid arthritis.". N Engl J Med. 363 (14): 1303–12. doi:10.1056/NEJMoa1000500. PMID 20879879.
^ Seda, V; Mraz, M (2014). "B cell receptor (BCR) signalling and its crosstalk with other pathways in normal and malignant cells". European Journal of Haematology: n/a. doi:10.1111/ejh.12427. PMID 25080849.
^ Seda, V; Mraz, M (2014). "B cell receptor (BCR) signalling and its crosstalk with other pathways in normal and malignant cells". European Journal of Haematology: n/a. doi:10.1111/ejh.12427. PMID 25080849.
^ http://explore.georgetown.edu/news/?ID=74635&PageTemplateID=295
^ ^a ^b Bertagnolo V, Marchisio M, Brugnoli F, Bavelloni A, Boccafogli L, Colamussi ML, Capitani S (April 2001). "Requirement of tyrosine-phosphorylated Vav for morphological differentiation of all-trans-retinoic acid-treated HL-60 cells". Cell Growth Differ. 12 (4): 193–200. PMID 11331248.
^ Lupher ML, Rao N, Lill NL, Andoniou CE, Miyake S, Clark EA, Druker B, Band H (December 1998). "Cbl-mediated negative regulation of the Syk tyrosine kinase. A critical role for Cbl phosphotyrosine-binding domain binding to Syk phosphotyrosine 323". J. Biol. Chem. 273 (52): 35273–81. doi:10.1074/jbc.273.52.35273. PMID 9857068.
^ Melander F, Andersson T, Dib K (March 2003). "Fgr but not Syk tyrosine kinase is a target for beta 2 integrin-induced c-Cbl-mediated ubiquitination in adherent human neutrophils". Biochem. J. 370 (Pt 2): 687–94. doi:10.1042/BJ20021201. PMC 1223185. PMID 12435267.
^ Oda A, Ochs HD, Lasky LA, Spencer S, Ozaki K, Fujihara M, Handa M, Ikebuchi K, Ikeda H (May 2001). "CrkL is an adapter for Wiskott-Aldrich syndrome protein and Syk". Blood 97 (9): 2633–9. doi:10.1182/blood.V97.9.2633. PMID 11313252.
^ Ibarrola I, Vossebeld PJ, Homburg CH, Thelen M, Roos D, Verhoeven AJ (July 1997). "Influence of tyrosine phosphorylation on protein interaction with FcgammaRIIa". Biochim. Biophys. Acta 1357 (3): 348–58. doi:10.1016/S0167-4889(97)00034-7. PMID 9268059.
^ Kim MK, Pan XQ, Huang ZY, Hunter S, Hwang PH, Indik ZK, Schreiber AD (January 2001). "Fc gamma receptors differ in their structural requirements for interaction with the tyrosine kinase Syk in the initial steps of signaling for phagocytosis". Clin. Immunol. 98 (1): 125–32. doi:10.1006/clim.2000.4955. PMID 11141335.
^ Deckert M, Elly C, Altman A, Liu YC (April 1998). "Coordinated regulation of the tyrosine phosphorylation of Cbl by Fyn and Syk tyrosine kinases". J. Biol. Chem. 273 (15): 8867–74. doi:10.1074/jbc.273.15.8867. PMID 9535867.
^ Chung J, Gao AG, Frazier WA (June 1997). "Thrombspondin acts via integrin-associated protein to activate the platelet integrin alphaIIbbeta3". J. Biol. Chem. 272 (23): 14740–6. doi:10.1074/jbc.272.23.14740. PMID 9169439.
^ ^a ^b Ganju RK, Brubaker SA, Chernock RD, Avraham S, Groopman JE (June 2000). "Beta-chemokine receptor CCR5 signals through SHP1, SHP2, and Syk". J. Biol. Chem. 275 (23): 17263–8. doi:10.1074/jbc.M000689200. PMID 10747947.
^ Saci A, Liu WQ, Vidal M, Garbay C, Rendu F, Bachelot-Loza C (May 2002). "Differential effect of the inhibition of Grb2-SH3 interactions in platelet activation induced by thrombin and by Fc receptor engagement". Biochem. J. 363 (Pt 3): 717–25. doi:10.1042/0264-6021:3630717. PMC 1222524. PMID 11964172.
^ Thome M, Duplay P, Guttinger M, Acuto O (June 1995). "Syk and ZAP-70 mediate recruitment of p56lck/CD4 to the activated T cell receptor/CD3/zeta complex". J. Exp. Med. 181 (6): 1997–2006. doi:10.1084/jem.181.6.1997. PMC 2192070. PMID 7539035.
^ Sidorenko SP, Law CL, Chandran KA, Clark EA (January 1995). "Human spleen tyrosine kinase p72Syk associates with the Src-family kinase p53/56Lyn and a 120-kDa phosphoprotein". Proc. Natl. Acad. Sci. U.S.A. 92 (2): 359–63. doi:10.1073/pnas.92.2.359. PMC 42739. PMID 7831290.
^ Sada K, Minami Y, Yamamura H (September 1997). "Relocation of Syk protein-tyrosine kinase to the actin filament network and subsequent association with Fak". Eur. J. Biochem. 248 (3): 827–33. doi:10.1111/j.1432-1033.1997.00827.x. PMID 9342235.
^ Dustin LB, Plas DR, Wong J, Hu YT, Soto C, Chan AC, Thomas ML (March 1999). "Expression of dominant-negative src-homology domain 2-containing protein tyrosine phosphatase-1 results in increased Syk tyrosine kinase activity and B cell activation". J. Immunol. 162 (5): 2717–24. PMID 10072516.
^ Deckert M, Tartare-Deckert S, Couture C, Mustelin T, Altman A (December 1996). "Functional and physical interactions of Syk family kinases with the Vav proto-oncogene product". Immunity 5 (6): 591–604. doi:10.1016/S1074-7613(00)80273-3. PMID 8986718.
^ Song JS, Gomez J, Stancato LF, Rivera J (October 1996). "Association of a p95 Vav-containing signaling complex with the FcepsilonRI gamma chain in the RBL-2H3 mast cell line. Evidence for a constitutive in vivo association of Vav with Grb2, Raf-1, and ERK2 in an active complex". J. Biol. Chem. 271 (43): 26962–70. doi:10.1074/jbc.271.43.26962. PMID 8900182.

External links

Syk kinase at the US National Library of Medicine Medical Subject Headings (MeSH)

Molecular and Cellular Biology portal

UpToDate Contents

全文を閲覧するには購読必要です。 To read the full text you will need to subscribe.

1. 慢性粘膜皮膚カンジダ症 chronic mucocutaneous candidiasis
2. リウマチ性疾患におけるサイトカインネットワーク：治療の意味 cytokine networks in rheumatic diseases implications for therapy
3. ZAP-70欠損症 zap 70 deficiency
4. 血小板生物学 platelet biology
5. T細胞受容体シグナル伝達 t cell receptor signaling

English Journal

Damnacanthal inhibits IgE receptor-mediated activation of mast cells.

Garcia-Vilas JA1, Medina MA1, Melo FR2, Pejler G3, Garcia-Faroldi G4.
Molecular immunology.Mol Immunol.2015 May;65(1):86-93. doi: 10.1016/j.molimm.2015.01.008. Epub 2015 Feb 2.
Damnacanthal, an anthraquinone obtained from the noni fruit (Morinda citrifolia L.), has been described to possess anti-cancer and anti-inflammatory properties. Since mast cells are key players in various inflammatory conditions as well as in cancer, we considered the possibility that the biological
PMID 25656801

T cell tyrosine phosphorylation response to transient redox stress.

Secchi C1, Carta M2, Crescio C2, Spano A2, Arras M3, Caocci G4, Galimi F1, La Nasa G4, Pippia P2, Turrini F5, Pantaleo A6.
Cellular signalling.Cell Signal.2015 Apr;27(4):777-88. doi: 10.1016/j.cellsig.2014.12.014. Epub 2015 Jan 6.
Reactive Oxygen Species (ROS) are crucial to multiple biological processes involved in the pathophysiology of inflammation, and are also involved in redox signaling responses. Although previous reports have described an association between oxidative events and the modulation of innate immunity, a ro
PMID 25572700

B-cell receptor signalling and its crosstalk with other pathways in normal and malignant cells.

Seda V1, Mraz M.
European journal of haematology.Eur J Haematol.2015 Mar;94(3):193-205. doi: 10.1111/ejh.12427. Epub 2014 Sep 13.
The physiology of B cells is intimately connected with the function of their B-cell receptor (BCR). B-cell lymphomas frequently (dys)regulate BCR signalling and thus take advantage of this pre-existing pathway for B-cell proliferation and survival. This has recently been underscored by clinical tria
PMID 25080849

Japanese Journal

World Wide View 海外情報企業関連ニュースバイオジェン・アイデック/ポルトラファーマシューティカルズ経口Syk阻害薬の開発と商業化に関するグローバル提携契約締結

国際医薬品情報 (949), 51-53, 2011-11-14
NAID 40019070718

A Novel Imidazo[1,5-b]isoquinolinone Derivative, U63A05, Inhibits Syk Activation in Mast Cells to Suppress IgE-Mediated Anaphylaxis in Mice

KIM Do Kyun,LEE Jun Ho,KIM Jie Wan,KIM Hyuk Soon,KIM A-Ram,KIM Bo Kyung,YI Kyu Yang,PARK Hye-Jin,PARK Dong Ki,CHOI Wahn Soo
Journal of pharmacological sciences 115(4), 500-508, 2011-04-20
NAID 10029893454

Related Pictures

Lagt inn av Penny Hui kl. 17.13 selv. Sånt kan en gjøre når en er syk SYK Lekser? Jeg er jo syk! Description Protein SYK PDB 1a81.png Syk :S Syk og dårlig bak SYK Eve

★リンクテーブル★

リンク元	「抗原受容体」
関連記事	「S」

「抗原受容体」

Spleen tyrosine kinase
	PDB rendering based on 1a81.
Available structures
PDB	Ortholog search: PDBe, RCSB
List of PDB id codes
	1A81, 1CSY, 1CSZ, 1XBA, 1XBB, 1XBC, 3BUW, 3EMG, 3FQE, 3FQH, 3FQS, 3SRV, 3TUB, 3TUC, 3TUD, 3VF8, 3VF9, 4DFL, 4DFN, 4F4P, 4FL1, 4FL2, 4FL3, 4FYN, 4FYO, 4FZ6, 4FZ7, 4GFG, 4I0R, 4I0S, 4I0T, 4PUZ, 4PV0, 4PX6, 4RX7, 4RX8, 4RX9
Identifiers
Symbols	SYK ; p72-Syk
External IDs	OMIM: 600085 MGI: 99515 HomoloGene: 2390 ChEMBL: 2599 GeneCards: SYK Gene
EC number	2.7.10.2
Gene ontology
Molecular function	• protein kinase activity; • protein serine/threonine kinase activity; • protein tyrosine kinase activity; • non-membrane spanning protein tyrosine kinase activity; • receptor signaling protein tyrosine kinase activity; • integrin binding; • protein binding; • ATP binding; • protein kinase binding;
Cellular component	• nucleus; • cytoplasm; • cytosol; • plasma membrane; • B cell receptor complex; • extrinsic component of cytoplasmic side of plasma membrane; • early phagosome; • T cell receptor complex; • protein complex;
Biological process	• angiogenesis; • lymph vessel development; • positive regulation of receptor internalization; • stimulatory C-type lectin receptor signaling pathway; • adaptive immune response; • macrophage activation involved in immune response; • neutrophil activation involved in immune response; • leukocyte activation involved in immune response; • serotonin secretion by platelet; • protein phosphorylation; • leukocyte cell-cell adhesion; • transmembrane receptor protein tyrosine kinase signaling pathway; • integrin-mediated signaling pathway; • activation of JUN kinase activity; • blood coagulation; • cell proliferation; • organ morphogenesis; • regulation of platelet activation; • regulation of tumor necrosis factor-mediated signaling pathway; • viral process; • peptidyl-serine phosphorylation; • leukotriene biosynthetic process; • cell differentiation; • platelet activation; • neutrophil chemotaxis; • positive regulation of type I interferon production; • regulation of superoxide anion generation; • positive regulation of cell adhesion mediated by integrin; • peptidyl-tyrosine autophosphorylation; • Fc-epsilon receptor signaling pathway; • Fc-gamma receptor signaling pathway involved in phagocytosis; • defense response to bacterium; • transcription factor import into nucleus; • positive regulation of mast cell degranulation; • regulation of neutrophil degranulation; • beta selection; • innate immune response; • positive regulation of interleukin-3 biosynthetic process; • positive regulation of granulocyte macrophage colony-stimulating factor biosynthetic process; • positive regulation of B cell differentiation; • positive regulation of gamma-delta T cell differentiation; • positive regulation of bone resorption; • positive regulation of alpha-beta T cell differentiation; • positive regulation of alpha-beta T cell proliferation; • blood vessel morphogenesis; • positive regulation of cytokine secretion; • positive regulation of peptidyl-tyrosine phosphorylation; • regulation of phagocytosis; • positive regulation of calcium-mediated signaling; • B cell receptor signaling pathway; • regulation of sequence-specific DNA binding transcription factor activity; • regulation of ERK1 and ERK2 cascade; • cellular response to molecule of fungal origin; • regulation of arachidonic acid secretion; • regulation of platelet aggregation;
	Sources: Amigo / QuickGO
RNA expression pattern
	More reference expression data
Orthologs
	v; t; e;

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