4.6 Article

Toll pathway modulates TNF-induced JNK-dependent cell death in Drosophila

期刊

OPEN BIOLOGY
卷 5, 期 7, 页码 -

出版社

ROYAL SOC
DOI: 10.1098/rsob.140171

关键词

cell death; Drosophila; Eiger; c-Jun N-terminal kinase; Toll

资金

  1. National Basic Research Program of China (973 Program) [2011CB943903]
  2. National Natural Science Foundation of China [31071294, 31171413, 31371490]
  3. Specialized Research Fund for the Doctoral Program of Higher Education of China [20120072110023]
  4. Shanghai Committee of Science and Technology [09DZ2260100, 14JC1406000]
  5. National Nature Science Foundation of China [31371459]
  6. Tsinghua Initiative Program [20131089281]
  7. 1000 Talents award

向作者/读者索取更多资源

Signalling networks that control the life or death of a cell are of central interest in modern biology. While the defined roles of the c-Jun N-terminal kinase (JNK) pathway in regulating cell death have been well-established, additional factors that modulate JNK-mediated cell death have yet to be fully elucidated. To identify novel regulators of JNK-dependent cell death, we performed a dominant-modifier screen in Drosophila and found that the Toll pathway participates in JNK-mediated cell death. Loss of Toll signalling suppresses ectopically and physiologically activated JNK signalling-induced cell death. Our epistasis analysis suggests that the Toll pathway acts as a downstream modulator for JNK-dependent cell death. In addition, gain of JNK signalling results in Toll pathway activation, revealed by stimulated transcription of Drosomycin (Drs) and increased cytoplasm-to-nucleus translocation of Dorsal. Furthermore, the Spatzle (Spz) family ligands for the Toll receptor are transcriptionally upregulated by activated JNK signalling in a non-cell-autonomous manner, providing a molecular mechanism for JNK-induced Toll pathway activation. Finally, gain of Toll signalling exacerbates JNK-mediated cell death and promotes cell death independent of caspases. Thus, we have identified another important function for the evolutionarily conserved Toll pathway, in addition to its well-studied roles in embryonic dorso-ventral patterning and innate immunity.

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