兰州大学机构库
IL-7 promoted the development of thymic DN3 cells in aged mice via DNA demethylation of Bcl2 and c-Myc genes
Han, Jiangyuan1,2,6; Ma, Yanlin1,2,6; Lv, Wei1,2,6; Wang, Juan1,2,6; Wu, Yu4; Niu, Hongxia1,2,6; Mi, Youjun1,3,6; Li, Fei1,2,6; Zhu, Bingdong1,2,5,6
2022-07-01
Online publication date2022-04
Source PublicationMOLECULAR IMMUNOLOGY   Impact Factor & Quartile
ISSN0161-5890
EISSN1872-9142
Volume147Pages:21-29
page numbers9
AbstractIL-7 promotes the development of thymic double negative (DN) T cells during beta-selection, which might contribute to the remission of aging-associated thymic involution. Methylation levels of CpG sites is correlated with aging and modulates the development. To determine the involvement of DNA methylation/demethylation instructed by IL-7 signaling during the expansion of double negative (DN) T cells, the aged mice were treated with recombinant Adeno-Associated Virus 2-mediated IL-7 (rAAV2-IL-7) and the DNA methylation/demethylation modifications in this process were analyzed. The results showed that rAAV2-IL-7 increased the number of thymocytes, especially the DN3 thymocytes during beta-selection in aged mice. With aging, the methylation levels of Bcl2 and c-Myc promoter regions were increased in DN3 cells. Following rAAV2-IL-7 treatment, DNA methyl-transferase Dnmt3a and Dnmt3b decreased, DNA demethylation factors TET2 and TET3 increased, and the methylation levels of Bcl2 and c-Myc in DN3 cells were reduced during DN3 stage in aged mice, consequently, resulting in the upregulation of Bcl2 and c-Myc and the larger increase of DN3 cells in thymus. In conclusion, these findings showed that Bcl2 and c-Myc genes of DN3 cells had an increased DNA methylation levels in aged mice compared to the young, and the hypermethylation in aged mice could be restored following rAAV2-IL-7 treatment.
KeywordIL-7 Ageing DNA demethylation DN3 cells Bcl2 c-Myc
PublisherPERGAMON-ELSEVIER SCIENCE LTD
DOI10.1016/j.molimm.2022.04.013
Indexed BySCIE
Language英语
WOS Research AreaBiochemistry & Molecular Biology ; Immunology
WOS SubjectBiochemistry & Molecular Biology ; Immunology
WOS IDWOS:000797833900003
Original Document TypeArticle
PMID 3550051
Citation statistics
Cited Times:1[WOS]   [WOS Record]     [Related Records in WOS]
Document Type期刊论文
Identifierhttps://ir.lzu.edu.cn/handle/262010/479907
Collection兰州大学
Corresponding AuthorZhu, Bingdong
Affiliation
1.Lanzhou Univ, Sch Basic Med Sci, Gansu Prov Key Lab Evidence Based Med & Clin Trans, Lanzhou 730000, Peoples R China;
2.Lanzhou Univ, Inst Pathogen Biol, Sch Basic Med Sci, Lanzhou 730000, Peoples R China;
3.Lanzhou Univ, Inst Pathophysiol, Sch Basic Med Sci, Lanzhou 730000, Peoples R China;
4.Gansu Prov Hosp, Inst Clin Res & Translat Med, Lanzhou 730000, Peoples R China;
5.Lanzhou Univ, Inst Pathogen Biol, Sch Basic Med Sci, 199 West Donggang Rd, Lanzhou 730000, Peoples R China;
6.Lanzhou Univ, Lanzhou Ctr TB Res, Sch Basic Med Sci, Lanzhou 730000, Peoples R China
Recommended Citation
GB/T 7714
Han, Jiangyuan,Ma, Yanlin,Lv, Wei,et al. IL-7 promoted the development of thymic DN3 cells in aged mice via DNA demethylation of Bcl2 and c-Myc genes[J]. MOLECULAR IMMUNOLOGY,2022,147:21-29.
APA Han, Jiangyuan.,Ma, Yanlin.,Lv, Wei.,Wang, Juan.,Wu, Yu.,...&Zhu, Bingdong.(2022).IL-7 promoted the development of thymic DN3 cells in aged mice via DNA demethylation of Bcl2 and c-Myc genes.MOLECULAR IMMUNOLOGY,147,21-29.
MLA Han, Jiangyuan,et al."IL-7 promoted the development of thymic DN3 cells in aged mice via DNA demethylation of Bcl2 and c-Myc genes".MOLECULAR IMMUNOLOGY 147(2022):21-29.
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