RANKL

TNFSF11
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesTNFSF11, CD254, ODF, OPGL, OPTB2, RANKL, TRANCE, hRANKL2, sOdf, TNLG6B, tumor necrosis factor superfamily member 11, TNF superfamily member 11
External IDsOMIM: 602642; MGI: 1100089; HomoloGene: 2744; GeneCards: TNFSF11; OMA:TNFSF11 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_003701
NM_033012

NM_011613

RefSeq (protein)

NP_003692
NP_143026

NP_035743

Location (UCSC)Chr 13: 42.56 – 42.61 MbChr 14: 78.51 – 78.55 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Receptor activator of nuclear factor kappa-Β ligand (RANKL), also known as tumor necrosis factor ligand superfamily member 11 (TNFSF11), TNF-related activation-induced cytokine (TRANCE), osteoprotegerin ligand (OPGL), and osteoclast differentiation factor (ODF), is a protein that in humans is encoded by the TNFSF11 gene.[5][6]

RANKL is known as a type II membrane protein and is a member of the tumor necrosis factor (TNF) superfamily.[7] RANKL has been identified to affect the immune system and control bone regeneration and remodeling. RANKL is an apoptosis regulator gene, a binding partner of osteoprotegerin (OPG), a ligand for the receptor RANK and controls cell proliferation by modifying protein levels of Id4, Id2 and cyclin D1.[8][9] RANKL is expressed in several tissues and organs including: skeletal muscle, thymus, liver, colon, small intestine, adrenal gland, osteoblast, mammary gland epithelial cells, prostate and pancreas.[9] Variation in concentration levels of RANKL throughout several organs reconfirms the importance of RANKL in tissue growth (particularly bone growth) and immune functions within the body.

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000120659Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000022015Ensembl, 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. ^ Wong BR, Rho J, Arron J, Robinson E, Orlinick J, Chao M, et al. (October 1997). "TRANCE is a novel ligand of the tumor necrosis factor receptor family that activates c-Jun N-terminal kinase in T cells". The Journal of Biological Chemistry. 272 (40): 25190–25194. doi:10.1074/jbc.272.40.25190. PMID 9312132.
  6. ^ Anderson DM, Maraskovsky E, Billingsley WL, Dougall WC, Tometsko ME, Roux ER, et al. (November 1997). "A homologue of the TNF receptor and its ligand enhance T-cell growth and dendritic-cell function". Nature. 390 (6656): 175–179. Bibcode:1997Natur.390..175A. doi:10.1038/36593. PMID 9367155. S2CID 4373990.
  7. ^ Hanada R, Hanada T, Sigl V, Schramek D, Penninger JM (July 2011). "RANKL/RANK-beyond bones". Journal of Molecular Medicine. 89 (7): 647–656. doi:10.1007/s00109-011-0749-z. PMID 21445556. S2CID 25285776.
  8. ^ Mueller CG, Hess E (2012). "Emerging Functions of RANKL in Lymphoid Tissues". Frontiers in Immunology. 3: 261. doi:10.3389/fimmu.2012.00261. PMC 3432452. PMID 22969763.
  9. ^ a b Wada T, Nakashima T, Hiroshi N, Penninger JM (January 2006). "RANKL-RANK signaling in osteoclastogenesis and bone disease". Trends in Molecular Medicine. 12 (1): 17–25. doi:10.1016/j.molmed.2005.11.007. PMID 16356770.