Repetitive Elements Trigger RIG-I-like Receptor Signaling that Regulates the Emergence of Hematopoietic Stem and Progenitor Cells

被引:46
|
作者
Lefkopoulos, Stylianos [1 ,2 ,3 ]
Polyzou, Aikaterini [1 ,2 ]
Derecka, Marta [1 ]
Bergo, Veronica [1 ,4 ]
Clapes, Thomas [1 ]
Cauchy, Pierre [1 ]
Jerez-Longres, Carolina [1 ,9 ,10 ]
Onishi-Seebacher, Megumi [5 ]
Yin, Na [1 ]
Martagon-Calderoen, Natalia-Adriana [1 ]
Potts, Kathryn S. [6 ]
Klaeyle, Lheanna [1 ]
Liu, Feng [7 ]
Bowman, Teresa, V [6 ]
Jenuwein, Thomas [5 ]
Mione, Maria Caterina [4 ]
Trompouki, Eirini [1 ,8 ]
机构
[1] Max Planck Inst Immunobiol & Epigenet, Dept Cellular & Mol Immunol, D-79108 Freiburg, Germany
[2] Univ Freiburg, Fac Biol, D-79104 Freiburg, Germany
[3] Int Max Planck Res Sch Mol & Cellular Biol IMPRS, D-79108 Freiburg, Germany
[4] Univ Trento, Dept Cellular Computat & Integrat Biol, Via Sommar 9, I-38123 Trento, Italy
[5] Max Planck Inst Immunobiol & Epigenet, Dept Epigenet, D-79108 Freiburg, Germany
[6] Albert Einstein Coll Med, Dept Dev & Mol Biol, 1300 Morris Pk Ave, Bronx, NY 10467 USA
[7] Chinese Acad Sci, Inst Zool, State Key Lab Membrane Biol, Beijing 100101, Peoples R China
[8] Univ Freiburg, CIBSS Ctr Integrat Biol Signaling Studies, Freiburg, Germany
[9] Univ Freiburg, Fac Biol, Spemann Grad Sch Biol & Med SGBM, D-79104 Freiburg, Germany
[10] BIOSS Ctr Biol Signalling Studies, CIBSS Ctr Integrat Biol Signaling Studies, Freiburg, Germany
关键词
NF-KAPPA-B; DIFFERENTIAL EXPRESSION ANALYSIS; PATTERN-RECOGNITION RECEPTORS; READ ALIGNMENT; STRUCTURAL BASIS; CANCER CELLS; SELF-RENEWAL; RNA; ZEBRAFISH; ACTIVATION;
D O I
10.1016/j.immuni.2020.10.007
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Inflammatory signaling is required for hematopoietic stem and progenitor cell (HSPC) development. Here, we studied the involvement of RIG-I-like receptors (RLRs) in HSPC formation. Rig-I or Mda5 deficiency impaired, while Lgp2 deficiency enhanced, HSPC emergence in zebrafish embryos. Rig-I or Mda5 deficiency reduced HSPC numbers by inhibiting inflammatory signals that were in turn enhanced in Lgp2 deficient embryos. Simultaneous reduction of Lgp2 and either Rig-I or Mda5 rescued inflammatory signals and HSPC numbers. Modulating the expression of the signaling mediator Traf6 in RLR deficient embryos restored HSPC numbers. Repetitive element transcripts could be detected in hemogenic endothelial cells and HSPCs, suggesting a role as RLR ligands. Indeed, ectopic expression of repetitive elements enhanced HSPC formation in wild-type, but not in Rig-I or Mda5 deficient embryos. Manipulation of RLR expression in mouse fetal liver HSPCs indicated functional conservation among species. Thus, repetitive elements transcribed during development drive RLR-mediated inflammatory signals that regulate HSPC formation.
引用
收藏
页码:934 / +
页数:27
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