HCSGD entry for IL15
1. General information
Official gene symbol | IL15 |
---|---|
Entrez ID | 3600 |
Gene full name | interleukin 15 |
Other gene symbols | IL-15 |
Links to Entrez Gene | Links to Entrez Gene |
2. Neighbors in the network
3. Gene ontology annotation
GO ID | GO term | Evidence | Category |
---|---|---|---|
GO:0001779 | Natural killer cell differentiation | IEA | biological_process |
GO:0001866 | NK T cell proliferation | IEA | biological_process |
GO:0005125 | Cytokine activity | IEA | molecular_function |
GO:0005126 | Cytokine receptor binding | IEA | molecular_function |
GO:0005515 | Protein binding | IPI | molecular_function |
GO:0005576 | Extracellular region | NAS | cellular_component |
GO:0005615 | Extracellular space | IEA | cellular_component |
GO:0005634 | Nucleus | IEA | cellular_component |
GO:0005737 | Cytoplasm | TAS | cellular_component |
GO:0005768 | Endosome | TAS | cellular_component |
GO:0005794 | Golgi apparatus | TAS | cellular_component |
GO:0005887 | Integral component of plasma membrane | TAS | cellular_component |
GO:0006954 | Inflammatory response | IEA | biological_process |
GO:0006955 | Immune response | IEA | biological_process |
GO:0007165 | Signal transduction | TAS | biological_process |
GO:0007267 | Cell-cell signaling | TAS | biological_process |
GO:0007568 | Aging | IEA | biological_process |
GO:0008284 | Positive regulation of cell proliferation | TAS | biological_process |
GO:0009986 | Cell surface | IEA | cellular_component |
GO:0014732 | Skeletal muscle atrophy | IEA | biological_process |
GO:0016020 | Membrane | TAS | cellular_component |
GO:0030212 | Hyaluronan metabolic process | IEA | biological_process |
GO:0032740 | Positive regulation of interleukin-17 production | IDA | biological_process |
GO:0032819 | Positive regulation of natural killer cell proliferation | IEA | biological_process |
GO:0032825 | Positive regulation of natural killer cell differentiation | IEA | biological_process |
GO:0034105 | Positive regulation of tissue remodeling | IC | biological_process |
GO:0042102 | Positive regulation of T cell proliferation | IEA | biological_process |
GO:0042517 | Positive regulation of tyrosine phosphorylation of Stat3 protein | IEA | biological_process |
GO:0045062 | Extrathymic T cell selection | IEA | biological_process |
GO:0045580 | Regulation of T cell differentiation | IEA | biological_process |
GO:0048469 | Cell maturation | IEA | biological_process |
GO:0048535 | Lymph node development | IEA | biological_process |
GO:0048662 | Negative regulation of smooth muscle cell proliferation | IEA | biological_process |
GO:0050691 | Regulation of defense response to virus by host | IEA | biological_process |
GO:0050729 | Positive regulation of inflammatory response | IC | biological_process |
GO:0050778 | Positive regulation of immune response | IEA | biological_process |
GO:0071305 | Cellular response to vitamin D | IEA | biological_process |
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4. Expression levels in datasets
- Meta-analysis result
p-value up | p-value down | FDR up | FDR down |
---|---|---|---|
0.9567958778 | 0.0019299457 | 0.9999902473 | 0.0846848435 |
- Individual experiment result
( "-" represent NA in the specific microarray platform )
( "-" represent NA in the specific microarray platform )
Data source | Up or down | Log fold change |
---|---|---|
GSE11954 | Down | -0.1971718086 |
GSE13712_SHEAR | Down | -0.1808977797 |
GSE13712_STATIC | Up | 0.1715331475 |
GSE19018 | Up | 0.2517450662 |
GSE19899_A1 | Down | -0.6393808197 |
GSE19899_A2 | Down | -3.2281972553 |
PubMed_21979375_A1 | Down | -1.5963216186 |
PubMed_21979375_A2 | Down | -4.2484845528 |
GSE35957 | Down | -0.5652922309 |
GSE36640 | Down | -0.6045107888 |
GSE54402 | Down | -1.6265171534 |
GSE9593 | Down | -0.1287428298 |
GSE43922 | Down | -0.3572316487 |
GSE24585 | Down | -0.0933767437 |
GSE37065 | Up | 0.1266260413 |
GSE28863_A1 | Down | -0.1591529819 |
GSE28863_A2 | Up | 0.2787076403 |
GSE28863_A3 | Down | -0.1031148632 |
GSE28863_A4 | Down | -0.0651383934 |
GSE48662 | Down | -0.1571202848 |
5. Regulation relationships with compounds/drugs/microRNAs
- Compounds
Not regulated by compounds
- Drugs
Not regulated by drugs
- MicroRNAs
- mirTarBase
MiRNA_name | mirBase ID | miRTarBase ID | Experiment | Support type | References (Pubmed ID) |
---|---|---|---|---|---|
hsa-miR-215-5p | MIMAT0000272 | MIRT024918 | Microarray | Functional MTI (Weak) | 19074876 |
hsa-miR-192-5p | MIMAT0000222 | MIRT026532 | Microarray | Functional MTI (Weak) | 19074876 |
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- mirRecord
No target information from mirRecord
6. Text-mining results about the gene
Gene occurances in abstracts of cellular senescence-associated articles: 4 abstracts the gene occurs.
PubMed ID of the article | Sentenece the gene occurs |
---|---|
28123872 | IL-15 enhances the antitumor effect of human antigen-specific CD8+ T cells by cellular senescence delay |
28123872 | Optimal expansion protocols for adoptive human T-cell therapy often include interleukin (IL)-15; however, the mechanism by which IL-15 improves the in vivo antitumor effect of T cells remains to be elucidated |
28123872 | Using human T cells generated from HLA-A2+ donors against novel T-cell epitopes derived from the human U266 myeloma cell line Ig light chain V-region (idiotype) as a model, we found that T cells cultured with IL-15 provided superior resistance to tumor growth in vivo, compared with IL-2, after adoptive transfer into immunodeficient hosts |
28123872 | This effect of IL-15 was associated with delayed/reversed senescence in tumor antigen-specific memory CD8+ T cells mediated through downregulation of P21WAF1, P16INK4a, and P53 expression |
28123872 | Compared to IL-2, IL-15 stimulation dramatically activated JAK3-STAT5 signaling and inhibited the expression of DNA damage genes |
28123872 | Thus, our study elucidates a new mechanism for IL-15 in the regulation of STAT signaling pathways and CD8+ T-cell senescence |
26857736 | IL-15 boosts the function and migration of human terminally differentiated CD8+ T cells by inducing a unique gene signature |
26857736 | Human CCR7(low)CD45RA(high) effector memory CD8(+) T cells (terminally differentiated TEMRA) are reportedly a functionally compromised population with characteristics of cellular senescence when examined ex vivo Although their frequencies are increased in elderly subjects in association with declined immune competence, however, it remains unclear whether their impaired functions can be reversed so that they contribute to immune responses in vivo Here, I show that, in contrast to TCR stimulation, stimulation of TEMRA with IL-15 induced a unique transcriptional signature, promoted IFN-gamma production and cell cycle entry, and reduced chemotaxis toward sphingosine-1-phosphate (S1P) |
26857736 | These results suggest that TEMRA act as functional effector T cells in non-lymphoid tissues when IL-15 is abundant and that IL-15 treatment may be beneficial in enhancing vaccine efficacy in elderly people |
21635686 | IL-15 preferentially enhances functional properties and antigen-specific responses of CD4+CD28(null) compared to CD4+CD28+ T cells |
21635686 | Recent studies have shown that IL-15 does in fact play an appreciable role in CD4 memory T cells under physiological conditions |
21635686 | We found that treatment with IL-15 increased the frequency of elderly CD4+CD28(null) T cells by the preferential proliferation of these cells compared to CD4+CD28+ T cells |
21635686 | IL-15 induced an activated phenotype in CD4+CD28(null) T cells |
21635686 | Moreover, pretreatment of CD4+CD28(null) T cells with IL-15 displayed a synergistic effect on the IFN-gamma production in CMV-specific responses, which was not observed in CD4+CD28+ T cells |
21635686 | IL-15 could play a role enhancing the effector response of CD4+CD28(null) T cells against their specific chronic antigens |
15882354 | Interestingly, in vitro culture of these two subsets with interleukin-15 showed that similar gene expression changes occurred in both subsets |
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