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CXCL16 / SR-PSOX Protein, Antibody, ELISA Kit, cDNA Clone

Expression host: Human Cells
  • Slide 1
50142-M08H-20
50142-M08H-50
20 µg / $108
50 µg / $198
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Expression host: Human Cells
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80149-R08H-20
80149-R08H-50
20 µg / $108
50 µg / $198
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Expression host: Human Cells
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80149-R02H-20
80149-R02H-50
20 µg / $108
50 µg / $198
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Expression host: Human Cells
  • Slide 1
70060-D08H-20
70060-D08H-50
20 µg / $108
50 µg / $198
Add to Cart
Expression host: Human Cells
  • Slide 1
70060-D02H-20
70060-D02H-50
20 µg / $108
50 µg / $198
Add to Cart

CXCL16 / SR-PSOX Related Areas

CXCL16 / SR-PSOX Related Pathways

CXCL16 / SR-PSOX Related Product

CXCL16 / SR-PSOX Summary & Protein Information

CXCL16 / SR-PSOX Related Information

CXCL16 / SR-PSOX Background

Subcellular location: Cell membrane; Single-pass type I membrane protein (Potential). Secreted. Note=Also exists as a soluble form.
Tissue specificity: Expressed in T-cell areas. Expressed in spleen, lymph nodes, lung, kidney, small intestine and thymus. Weak expression in heart and liver and no expression in brain and bone marrow.
Post-translational: Glycosylated.
Sequence similarity: Belongs to the intercrine alpha (chemokine CxC) family.
General information above from UniProt

C-X-C motif chemokine 16, also known as Small-inducible cytokine B16, SR-PSOX, and CXCL16, is a single-pass type I membrane protein which belongs to the intercrine alpha (chemokine CxC) family. CXCL16 exists in transmembrane and soluble forms. The transmembrane form acts as a scavenger receptor for oxidised LDL whereas the soluble form acts a chemoattractant for mainly CD8+ T cells. CXCL16 is a protein which shares pattern recognition receptor functions, relevant for adhesion and phagocytosis of bacterial products, with the properties of an adhesion molecule and inflammatory chemokine. CXCL16/SR-PSOX is an interferon-gamma-regulated chemokine and scavenger receptor for oxidized low-density lipoprotein that is expressed in atherosclerotic lesions. Proteolytic cleavage of membrane-bound CXCL16 releases soluble CXCL16, which may promote migration of effector T cells and augment a proatherogenic inflammatory response. CXCL16/SR-PSOX can be a potential player in atherogenesis. Enhanced expression of CXCL16 has been demonstrated in atherosclerotic plaques and several properties have been attributed to CXCL16 that could influence the atherosclerotic process. Following in vitro studies suggested that as an adhesion molecule CXCL16/SR-PSOX might mediate T-cell adhesion to the endothelium, as a chemokine-drive T-cell migration, stimulate cell proliferation and elicit inflammatory phenotype in smooth muscle cells (SMC) and, finally, as a scavenger receptor-mediate uptake of atherogenic lipoproteins by macrophages and SMC. CXCR6 and its ligand CXCL16 in regulating metastasis and invasion of cancer. CXCR6 and CXCL16 are up-regulated in multiple cancer tissue types and cancer cell lines relative to normal tissues and cell lines. In addition, both CXCR6 and CXCL16 levels increase as tumor malignancy increases. Thus, CXCL16 and CXCR6 may mark cancers arising in an inflammatory milieu and mediate pro-tumorigenic effects of inflammation through direct effects on cancer cell growth and by inducing the migration and proliferation of tumor-associated leukocytes.

CXCL16 / SR-PSOX Alternative Name

CXCL16,CXCLG16,SRPSOX,SR-PSOX, [human]
0910001K24Rik,AV290116,BB024863,CXCL16,DN-491F10.6,SR-PSOX,Zmynd15, [mouse]

CXCL16 / SR-PSOX Related Studies

  • Sheikine Y, et al. (2008) CXCL16/SR-PSOX--a friend or a foe in atherosclerosis? Atherosclerosis. 197(2): 487-95.
  • Lehrke M, et al. (2008) CXCL16 is a surrogate marker of inflammatory bowel disease. Scand J Gastroenterol. 43(3): 283-8.
  • Jansson AM, et al. (2009) Soluble CXCL16 predicts long-term mortality in acute coronary syndromes. Circulation. 119(25): 3181-8.
  • Darash-Yahana M, et al. (2009) The chemokine CXCL16 and its receptor, CXCR6, as markers and promoters of inflammation-associated cancers. PLoS One. 4(8): e6695.
  • Deng L, et al. (2010) CXCR6/CXCL16 functions as a regulator in metastasis and progression of cancer. Biochim Biophys Acta. 1806(1): 42-9.
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