Interleukin 9

IL9
Identifiers
Aliases	IL9, HP40, IL-9, P40, interleukin 9
External IDs	OMIM: 146931; MGI: 96563; HomoloGene: 492; GeneCards: IL9; OMA:IL9 - orthologs
Gene location (Human) Chr. Chromosome 5 (human)[1] Band 5q31.1 Start 135,892,246 bp[1] End 135,895,841 bp[1]
Gene location (Mouse) Chr. Chromosome 13 (mouse)[2] Band 13 B1|13 30.06 cM Start 56,627,090 bp[2] End 56,630,059 bp[2]
RNA expression pattern Bgee Human Mouse (ortholog) Top expressed in tibial nerve sural nerve amygdala caudate nucleus Brodmann area 9 substantia nigra putamen cingulate gyrus hippocampus proper hypothalamus Top expressed in entorhinal cortex inferior colliculus spermatocyte uterus gonad male reproductive system testicle embryo More reference expression data BioGPS More reference expression data
Gene ontology Molecular function interleukin-9 receptor binding cytokine activity growth factor activity cytokine receptor binding Cellular component extracellular region extracellular space Biological process positive regulation of cell growth inflammatory response immune response positive regulation of cell population proliferation regulation of signaling receptor activity interleukin-9-mediated signaling pathway Sources:Amigo / QuickGO
Orthologs Species Human Mouse Entrez 3578 16198 Ensembl ENSG00000145839 ENSMUSG00000021538 UniProt P15248 P15247 RefSeq (mRNA) NM_000590 NM_008373 RefSeq (protein) NP_000581 NP_032399 Location (UCSC) Chr 5: 135.89 – 135.9 Mb Chr 13: 56.63 – 56.63 Mb PubMed search [3] [4]
Wikidata
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Interleukin 9, also known as IL-9, is a pleiotropic cytokine (cell signalling molecule) belonging to the group of interleukins.^[5] IL-9 is produced by variety of cells like mast cells, NKT cells, Th2, Th17, Treg, ILC2, and Th9 cells in different amounts. Among them, Th9 cells are regarded as the major CD4+ T cells that produce IL-9.^[6]

Functions

Il-9 is a cytokine secreted by CD4+ helper cells that acts as a regulator of a variety of hematopoietic cells.^[7] This cytokine stimulates cell proliferation and prevents apoptosis. It functions through the interleukin-9 receptor (IL9R), which activates different signal transducer and activator (STAT) proteins namely STAT1, STAT3 and STAT5 and thus connects this cytokine to various biological processes. The gene encoding this cytokine has been identified as a candidate gene for asthma. Genetic studies on a mouse model of asthma demonstrated that this cytokine is a determining factor in the pathogenesis of bronchial hyperresponsiveness.^[5]

Interleukin-9 has also shown to inhibit melanoma growth in mice. ^[8]

Additionally, it gives rise to the multiplication of hematologic neoplasias and also Hodgkin's lymphoma in humans but IL-9 also has antitumor properties in solid tumors, for example melanoma.^[6]

Discovery

IL-9 was first described in the late 1980s as a member of a growing number of cytokines that had pleiotropic functions in the immune system.IL-9 remains an understudied cytokine even though it has been allocated with many biological functions. It was first purified and characterized as a T cell and mast cell growth factor and termed as P40, based on their molecular weight, or Mast cell growth-enhancing activity (MEA).The cloning and complete amino acid sequencing of P40 disclosed that it is structurally different from other T cells growth factors. So, it was named IL-9 based on its biological effects on both myeloid and lymphoid cells.^[9]

The identification and cloning was first done by Yang and colleagues as a mitogenic factor for a human megakaryoblastic leukemia. The same human cDNA was isolated again by cross-hybridization with the mouse IL-9 probe.^[10]

Gene location

The human IL-9 gene is located on the long arm of human chromosome 5 at band 5q31-32, a region which is not found in a number of patients with acquired chromosome 5q deletion syndrome.^[11]

Protein structure

Human IL-9 protein sequence contains 144 residues with a typical signal peptide of 18 amino acids. There is also the presence of 9 cysteines in mature polypeptide and 4 N-linked glycosylation sites.^[10] Until recently, IL-9 was thought to be evolutionary related to IL-7.^[12] However, we know now that IL-9 is closer to IL-2 and IL-15 than to IL-7,^[13] at both the tertiary and amino acid sequence levels.

Production

Interleukin 33 (IL-33) induces IL-9 expression and secretion in T cells, which was confirmed by the results obtained in mice by using Human in vitro system.^[14] Whereas the report of others confirms that TGF-β is an essential factor for IL-9 induction.^[15] For the first time (Lars Blom, Britta C. Poulsen, Bettina M. Jensen, Anker Hansen and Lars K. Poulsen published a journal online in 2011 Jul 6),indicating that TGF-β may be important for production of IL-9 but it is not only the definite requirement for IL-9 induction, since cultures with IL-33 without TGF-β have noticeably increased secretion of IL-9, suggesting an important role of IL-33, even though that the effect was not found significant on the gene level.^[16]

IL-9 expression

The analysis of IL-9 expression in different types of tumours such as Large cell anaplastic lymphoma (LCAL) and Hodgkin's Disease (HD) by Northern blot analysis and in situ hybridization has showed that IL-9 is not involved as an autocrine growth factor in the pathogenesis of most B and T-cell lymphomas, but it may have a part in HD and LCAL autocrine growth.

The further investigation could be done to conclude another probability, that, the in vivo overexpression of IL-9 might show the unique symptoms related to eosinophilia which was recently reported for Interleukin 5 positive cases of HD.^[17]

IL-9 was found to be the first physiological stimulus triggering BCL3 expression in T cells and mast cells by the analysis done in mouse.^[18]

References

Further reading