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CXCL16

From Wikipedia, the free encyclopedia
CXCL16
Identifiers
AliasesCXCL16, CXCLG16, SR-PSOX, SRPSOX, C-X-C motif chemokine ligand 16
External IDsOMIM: 605398; MGI: 1932682; GeneCards: CXCL16
Orthologs
DatabasesNCBI: entry; OMA: entry
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_022059
NM_001100812
NM_001386809

NM_023158

RefSeq (protein)

NP_001094282
NP_071342

NP_075647

Location (UCSC)Chr 17: 4.73 – 4.74 MbChr 11: 70.34 – 70.35 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Chemokine (C-X-C motif) ligand 16 (CXCL16) is a small cytokine belonging to the CXC chemokine family. Larger than other chemokines (with 254 amino acids), CXCL16 is composed of a CXC chemokine domain, a mucin-like stalk, a transmembrane domain and a cytoplasmic tail containing a potential tyrosine phosphorylation site that may bind SH2.

[5] These are unusual features for a chemokine, allowing CXCL16 to be expressed as a cell surface bound molecule, as well as a soluble chemokine.[6] CXCL16 is produced by dendritic cells found in the T cell zones of lymphoid organs, and by cells found in the red pulp of the spleen.[5] Cells that bind and migrate in response to CXCL16 include several subsets of T cells, and natural killer T (NKT) cells.[5]

CXCL16 interacts with the chemokine receptor CXCR6, also known as Bonzo.[5][7] Expression of CXCL16 is induced by the inflammatory cytokines IFN-gamma and TNF-alpha.[6] The gene for human CXCL16 is located on chromosome 17.[5]

The administration of folinic acid, which forces the methylation of CXCL 16, induces high levels of methylation of the CXCL 16 gene promoter in colon, ileum and lung and causes iNKT cells accumulation in these tissues. Colonization of neonatal GF mice, but not in adult mice, with a conventional microbiota decreases hypermethylation levels of CXCL 16.[8]

References

[edit]
  1. 1 2 3 GRCh38: Ensembl release 89: ENSG00000161921 – Ensembl, May 2017
  2. 1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000018920 – Ensembl, May 2017
  3. ↑ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ↑ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. 1 2 3 4 5 Matloubian M, David A, Engel S, Ryan J, Cyster J (2000). "A transmembrane CXC chemokine is a ligand for HIV-coreceptor Bonzo". Nat Immunol. 1 (4): 298–304. doi:10.1038/79738. PMID 11017100. S2CID 22773861.
  6. 1 2 Abel S, Hundhausen C, Mentlein R, Schulte A, Berkhout T, Broadway N, Hartmann D, Sedlacek R, Dietrich S, Muetze B, Schuster B, Kallen K, Saftig P, Rose-John S, Ludwig A (2004). "The transmembrane CXC-chemokine ligand 16 is induced by IFN-gamma and TNF-alpha and shed by the activity of the disintegrin-like metalloproteinase ADAM10". J Immunol. 172 (10): 6362–72. doi:10.4049/jimmunol.172.10.6362. PMID 15128827.
  7. ↑ Wilbanks A, Zondlo S, Murphy K, Mak S, Soler D, Langdon P, Andrew D, Wu L, Briskin M (2001). "Expression cloning of the STRL33/BONZO/TYMSTRligand reveals elements of CC, CXC, and CX3C chemokines". J Immunol. 166 (8): 5145–54. doi:10.4049/jimmunol.166.8.5145. PMID 11290797.
  8. ↑ Olszak T, An D, Zeissig S, Vera MP, Richter J, Franke A, Glickman JN, Siebert R, Baron RM, Kasper DL, Blumberg RS (2012). "Microbial exposure during early life has persistent effects on natural killer T cell function". Science. 336 (6080): 489–493. Bibcode:2012Sci...336..489O. doi:10.1126/science.1219328. PMC 3437652. PMID 22442383.