DDIT4介导IL-34对人单核细胞白血病细胞增殖的促进作用

IF 1.5 Q3 HEMATOLOGY
血液科学(英文) Pub Date : 2021-04-27 eCollection Date: 2021-04-01 DOI:10.1097/BS9.0000000000000069
Xiaoqian Lv, Yuting Hu, Lina Wang, Dongyue Zhang, Hao Wang, Yibo Dai, Xiaoxi Cui, Guoguang Zheng
{"title":"DDIT4介导IL-34对人单核细胞白血病细胞增殖的促进作用","authors":"Xiaoqian Lv, Yuting Hu, Lina Wang, Dongyue Zhang, Hao Wang, Yibo Dai, Xiaoxi Cui, Guoguang Zheng","doi":"10.1097/BS9.0000000000000069","DOIUrl":null,"url":null,"abstract":"<p><p><i>Interleukin 34 (IL-34) is a cytokine that shares the receptor with colony-stimulating factor 1 (CSF-1).</i> IL-34 is involved in a broad range of <i>pathologic processes including</i> cancer. <i>We previously demonstrated</i> that IL-34 promoted the proliferation and colony formation of human acute monocytic leukemia (AMoL) cells. However, the mechanism has not been elucidated. Here, by analyzing the gene profiles of Molm13 and THP1 cells overexpressing IL-34 <i>(Molm13-IL-34 and THP1-IL-34)</i>, upregulation of the DNA damage-inducible transcript 4 (DDIT4) was detected in both series. Knockdown of DDIT4 <i>effectively inhibited the proliferation, promoted apoptosis and colony formation in Molm13-IL-34 and THP1-IL-34</i> cells. Our results suggest that DDIT4 mediates the proliferation-promotive effect of IL-34 whereas does not mediate the promotive effect of IL-34 on colony formation in AMoL cells.</p>","PeriodicalId":67343,"journal":{"name":"血液科学(英文)","volume":"3 1","pages":"48-56"},"PeriodicalIF":1.5000,"publicationDate":"2021-04-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8975083/pdf/","citationCount":"0","resultStr":"{\"title\":\"DDIT4 mediates the proliferation-promotive effect of IL-34 in human monocytic leukemia cells.\",\"authors\":\"Xiaoqian Lv, Yuting Hu, Lina Wang, Dongyue Zhang, Hao Wang, Yibo Dai, Xiaoxi Cui, Guoguang Zheng\",\"doi\":\"10.1097/BS9.0000000000000069\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p><i>Interleukin 34 (IL-34) is a cytokine that shares the receptor with colony-stimulating factor 1 (CSF-1).</i> IL-34 is involved in a broad range of <i>pathologic processes including</i> cancer. <i>We previously demonstrated</i> that IL-34 promoted the proliferation and colony formation of human acute monocytic leukemia (AMoL) cells. However, the mechanism has not been elucidated. Here, by analyzing the gene profiles of Molm13 and THP1 cells overexpressing IL-34 <i>(Molm13-IL-34 and THP1-IL-34)</i>, upregulation of the DNA damage-inducible transcript 4 (DDIT4) was detected in both series. Knockdown of DDIT4 <i>effectively inhibited the proliferation, promoted apoptosis and colony formation in Molm13-IL-34 and THP1-IL-34</i> cells. Our results suggest that DDIT4 mediates the proliferation-promotive effect of IL-34 whereas does not mediate the promotive effect of IL-34 on colony formation in AMoL cells.</p>\",\"PeriodicalId\":67343,\"journal\":{\"name\":\"血液科学(英文)\",\"volume\":\"3 1\",\"pages\":\"48-56\"},\"PeriodicalIF\":1.5000,\"publicationDate\":\"2021-04-27\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8975083/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"血液科学(英文)\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1097/BS9.0000000000000069\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2021/4/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"Q3\",\"JCRName\":\"HEMATOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"血液科学(英文)","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1097/BS9.0000000000000069","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2021/4/1 0:00:00","PubModel":"eCollection","JCR":"Q3","JCRName":"HEMATOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

摘要白细胞介素34(IL-34)是一种与集落刺激因子1(CSF-1)共受体的细胞因子。IL-34参与广泛的病理过程,包括癌症。我们先前证明IL-34促进人类急性单核细胞白血病(AMoL)细胞的增殖和集落形成。然而,其机制尚未阐明。在此,通过分析过表达IL-34的Molm13和THP1细胞(Molm13-IL-34和THP1-IL-34)的基因图谱,在两个系列中都检测到DNA损伤诱导型转录物4(DDIT4)的上调。敲除DDIT4可有效抑制Molm13-IL-34和THP1-IL-34细胞的增殖,促进细胞凋亡和集落形成。我们的结果表明,DDIT4介导IL-34对AMoL细胞中集落形成的增殖促进作用,而不介导IL-4对集落形成形成的促进作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
DDIT4 mediates the proliferation-promotive effect of IL-34 in human monocytic leukemia cells.

Interleukin 34 (IL-34) is a cytokine that shares the receptor with colony-stimulating factor 1 (CSF-1). IL-34 is involved in a broad range of pathologic processes including cancer. We previously demonstrated that IL-34 promoted the proliferation and colony formation of human acute monocytic leukemia (AMoL) cells. However, the mechanism has not been elucidated. Here, by analyzing the gene profiles of Molm13 and THP1 cells overexpressing IL-34 (Molm13-IL-34 and THP1-IL-34), upregulation of the DNA damage-inducible transcript 4 (DDIT4) was detected in both series. Knockdown of DDIT4 effectively inhibited the proliferation, promoted apoptosis and colony formation in Molm13-IL-34 and THP1-IL-34 cells. Our results suggest that DDIT4 mediates the proliferation-promotive effect of IL-34 whereas does not mediate the promotive effect of IL-34 on colony formation in AMoL cells.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
CiteScore
1.70
自引率
0.00%
发文量
0
审稿时长
10 weeks
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信