An evolutionarily conserved serine protease network mediates melanization and Toll activation in Drosophila

被引:5
|
作者
Shan, Tisheng [1 ]
Wang, Yang [1 ]
Bhattarai, Krishna [1 ]
Jiang, Haobo [1 ]
机构
[1] Oklahoma State Univ, Dept Entomol & Plant Pathol, Stillwater, OK 74078 USA
来源
SCIENCE ADVANCES | 2023年 / 9卷 / 51期
基金
美国国家卫生研究院;
关键词
INNATE IMMUNE-RESPONSE; MANDUCA-SEXTA HEMOLYMPH; GRAM-POSITIVE BACTERIA; HIGH-MOLECULAR-WEIGHT; PROPHENOLOXIDASE ACTIVATION; RECOGNITION PROTEIN; PROTEOLYTIC CASCADE; PATHWAY; PEPTIDOGLYCAN; INSECT;
D O I
10.1126/sciadv.adk2756
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Melanization and Toll pathway activation are essential innate immune mechanisms in insects, which result in the generation of reactive compounds and antimicrobial peptides, respectively, to kill pathogens. These two processes are mediated by phenoloxidase (PO) and Spatzle (Spz) through an extracellular network of serine proteases. While some proteases have been identified in Drosophila melanogaster in genetic studies, the exact order of proteolytic activation events remains controversial. Here, we reconstituted the serine protease framework in Drosophila by biochemical methods. This system comprises 10 proteases, i.e., ModSP, cSP48, Grass, Psh, Hayan-PA, Hayan-PB, Sp7, MP1, SPE and Ser7, which form cascade pathways that recognize microbial molecular patterns and virulence factors, and generate PO1, PO2, and Spz from their precursors. Furthermore, the serpin Necrotic negatively regulates the immune response progression by inhibiting ModSP and Grass. The biochemical approach, when combined with genetic analysis, is crucial for addressing problems that long stand in this important research field.
引用
收藏
页数:16
相关论文
共 30 条
  • [1] Activation of Drosophila Toll during fungal infection by a blood serine protease
    Ligoxygakis, P
    Pelte, N
    Hoffmann, JA
    Reichhart, JM
    [J]. SCIENCE, 2002, 297 (5578) : 114 - 116
  • [2] Activation of Drosophila toll during fungal infection by a blood serine protease
    Ligoxygakis, P
    Pelte, N
    Hoffmann, JA
    Reichart, JM
    [J]. NATURE REVIEWS IMMUNOLOGY, 2002, 2 (08) : 545 - 545
  • [3] More Than Black or White: Melanization and Toll Share Regulatory Serine Proteases in Drosophila
    Dudzic, Jan Paul
    Hanson, Mark Austin
    Iatsenko, Igor
    Kondo, Shu
    Lemaitre, Bruno
    [J]. CELL REPORTS, 2019, 27 (04): : 1050 - +
  • [4] A serpin mutant links Toll activation to melanization in the host defence of Drosophila
    Ligoxygakis, P
    Pelte, N
    Ji, CY
    Leclerc, V
    Duvic, B
    Belvin, M
    Jiang, HB
    Hoffmann, JA
    Reichhart, JM
    [J]. EMBO JOURNAL, 2002, 21 (23): : 6330 - 6337
  • [5] Structure-Function Analysis of Grass Clip Serine Protease Involved in Drosophila Toll Pathway Activation
    Kellenberger, Christine
    Leone, Philippe
    Coquet, Laurent
    Jouenne, Thierry
    Reichhart, Jean-Marc
    Roussel, Alain
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2011, 286 (14) : 12300 - 12307
  • [6] Serine protease activation of the epidermal wound response in Drosophila
    Patterson, Rachel
    McGinnis, William J.
    [J]. DEVELOPMENTAL BIOLOGY, 2010, 344 (01) : 489 - 489
  • [7] The serine protease Sp7 is expressed in blood cells and regulates the melanization reaction in Drosophila
    Castillejo-López, C
    Häcker, U
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2005, 338 (02) : 1075 - 1082
  • [8] Serine Protease MP2 Activates Prophenoloxidase in the Melanization Immune Response of Drosophila melanogaster
    An, Chunju
    Zhang, Mingming
    Chu, Yuan
    Zhao, Zhangwu
    [J]. PLOS ONE, 2013, 8 (11):
  • [9] INVOLVEMENT OF A SERINE PROTEASE IN THE ACTIVATION OF PROPHENOLOXIDASE IN DROSOPHILA-MELANOGASTER
    YONEMURA, M
    KASATANI, K
    ASADA, N
    OHNISHI, E
    [J]. ZOOLOGICAL SCIENCE, 1991, 8 (05) : 865 - 867
  • [10] Serine protease activation of epidermal wound response genes in Drosophila
    Patterson, Rachel
    Juarez, Michelle T.
    McGinnis, William J.
    [J]. DEVELOPMENTAL BIOLOGY, 2009, 331 (02) : 441 - 441