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血小板第4因子

出典: フリー百科事典『ウィキペディア(Wikipedia)』
CXCL4から転送)
PF4
PDBに登録されている構造
PDBオルソログ検索: RCSB PDBe PDBj
PDBのIDコード一覧

1RHP, 1DN3, 1F9Q, 1F9R, 1F9S, 1PFM, 1PFN, 4R9W, 4R9Y, 4RAU

識別子
記号PF4, CXCL4, PF-4, SCYB4, platelet factor 4
外部IDOMIM: 173460 MGI: 1888711 HomoloGene: 87791 GeneCards: PF4
遺伝子の位置 (ヒト)
4番染色体 (ヒト)
染色体4番染色体 (ヒト)[1]
4番染色体 (ヒト)

PF4遺伝子の位置

PF4遺伝子の位置

バンドデータ無し開始点73,980,811 bp[1]
終点73,982,027 bp[1]
遺伝子の位置 (マウス)
5番染色体 (マウス)
染色体5番染色体 (マウス)[2]
5番染色体 (マウス)

PF4遺伝子の位置

PF4遺伝子の位置

バンドデータ無し開始点90,920,294 bp[2]
終点90,921,242 bp[2]
RNA発現パターン
さらなる参照発現データ
遺伝子オントロジー
分子機能 cytokine activity
heparin binding
CXCR3 chemokine receptor binding
chemokine activity
血漿タンパク結合
細胞の構成要素 細胞外領域
platelet alpha granule lumen
細胞外空間
細胞質
collagen-containing extracellular matrix
生物学的プロセス サイトカイン媒介シグナル伝達経路
chemokine-mediated signaling pathway
positive regulation of macrophage differentiation
platelet degranulation
negative regulation of megakaryocyte differentiation
positive regulation of cAMP-mediated signaling
negative regulation of MHC class II biosynthetic process
leukocyte chemotaxis
走化性
リポ多糖への反応
positive regulation of macrophage derived foam cell differentiation
positive regulation of gene expression
regulation of cell population proliferation
免疫応答
positive regulation of tumor necrosis factor production
negative regulation of angiogenesis
negative regulation of extrinsic apoptotic signaling pathway in absence of ligand
炎症反応
positive regulation of transcription by RNA polymerase II
negative regulation of cytolysis
platelet activation
防衛反応
positive regulation of neutrophil chemotaxis
antimicrobial humoral immune response mediated by antimicrobial peptide
regulation of megakaryocyte differentiation
regulation of signaling receptor activity
Gタンパク質共役受容体シグナル伝達経路
adenylate cyclase-activating G protein-coupled receptor signaling pathway
neutrophil chemotaxis
cellular response to lipopolysaccharide
出典:Amigo / QuickGO
オルソログ
ヒトマウス
Entrez
Ensembl
UniProt
RefSeq
(mRNA)

NM_002619
NM_001363352

NM_019932

RefSeq
(タンパク質)

NP_002610
NP_001350281

NP_064316

場所
(UCSC)
Chr 4: 73.98 – 73.98 MbChr 4: 90.92 – 90.92 Mb
PubMed検索[3][4]
ウィキデータ
閲覧/編集 ヒト閲覧/編集 マウス

44: platelet factor 4: PF4CXCchemokine (C-X-C motif) ligand 4CXCL4α[5]

[]


4PF44[6]

[]


470α4CXCR3BCXCR3[5][7][8]

[]


HIT:PF4[9]PF4HIT[10]

PF4[11]

4[12]

出典[編集]

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000163737 - Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000029373 - Ensembl, May 2017
  3. ^ Human PubMed Reference:
  4. ^ Mouse PubMed Reference:
  5. ^ a b “Structural and functional comparison of the genes for human platelet factor 4 and PF4alt”. Blood 76 (2): 336–44. (July 1990). PMID 1695112. 
  6. ^ “Physical mapping of the CXC chemokine locus on human chromosome 4”. Cytogenet Cell Genet 84 (1–2): 39–42. (1999). doi:10.1159/000015209. PMID 10343098. 
  7. ^ Entrez Gene: PF4 platelet factor 4 (chemokine (C-X-C motif) ligand 4)”. 2020年5月2日閲覧。
  8. ^ “An alternatively spliced variant of CXCR3 mediates the inhibition of endothelial cell growth induced by IP-10, Mig, and I-TAC, and acts as functional receptor for platelet factor 4”. J Exp Med 197 (11): 1537–1549. (2003). doi:10.1084/jem.20021897. PMC 2193908. PMID 12782716. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2193908/. 
  9. ^ Warkentin TE (March 2007). “Drug-induced immune-mediated thrombocytopenia--from purpura to thrombosis”. N. Engl. J. Med. 356 (9): 891–893. doi:10.1056/NEJMp068309. PMID 17329695. http://content.nejm.org/cgi/content/full/356/9/891. 
  10. ^ “A spontaneous prothrombotic disorder resembling heparin-induced thrombocytopenia”. Am. J. Med. 121 (7): 632–636. (July 2008). doi:10.1016/j.amjmed.2008.03.012. PMID 18589060. 
  11. ^ “Changes in plasma CXCL4 levels are associated with improvements in lung function in patients receiving immunosuppressive therapy for systemic sclerosis-related interstitial lung disease”. Arthritis Research & Therapy 18 (1): 305. (2016). doi:10.1186/s13075-016-1203-y. PMC 5203703. PMID 28038680. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5203703/. 
  12. ^ “Platelet Factor 4 Activity against P. falciparum and Its Translation to Nonpeptidic Mimics as Antimalarials”. Cell Host Microbe 12 (6): 815–23. (December 2012). doi:10.1016/j.chom.2012.10.017. PMC 3638032. PMID 23245326. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3638032/. 

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