Temporal specificity and heterogeneity of Drosophila immune cells

被引:83
作者
Cattenoz, Pierre B. [1 ,2 ,3 ,4 ]
Sakr, Rosy [1 ,2 ,3 ,4 ]
Pavlidaki, Alexia [1 ,2 ,3 ,4 ]
Delaporte, Claude [1 ,2 ,3 ,4 ]
Riba, Andrea [1 ,2 ,3 ,4 ]
Molina, Nacho [1 ,2 ,3 ,4 ]
Hariharan, Nivedita [5 ,6 ]
Mukherjee, Tina [5 ]
Giangrande, Angela [1 ,2 ,3 ,4 ]
机构
[1] Inst Genet & Biol Mol & Cellulaire, Illkirch Graffenstaden, France
[2] CNRS, UMR7104, Illkirch Graffenstaden, France
[3] INSERM, U1258, Illkirch Graffenstaden, France
[4] Univ Strasbourg, Illkirch Graffenstaden, France
[5] Inst Stem Cell Sci & Regenerat Med InStem, Bangalore, Karnataka, India
[6] Univ Transdisciplinary Hlth Sci & Technol, Bangalore, Karnataka, India
关键词
Drosophila melanogaster; immune cells; single-cell RNA-seq; wasp infestation; APOPTOTIC CELLS; LIFE-SPAN; TRANSMEMBRANE PROTEIN; GENETIC MANIPULATION; HEMOCYTE LINEAGES; CELLULAR-IMMUNITY; NERVOUS-SYSTEM; MATRIX PROTEIN; PHAGOCYTOSIS; EXPRESSION;
D O I
10.15252/embj.2020104486
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Immune cells provide defense against non-self and have recently been shown to also play key roles in diverse processes such as development, metabolism, and tumor progression. The heterogeneity ofDrosophilaimmune cells (hemocytes) remains an open question. Using bulk RNA sequencing, we find that the hemocytes display distinct features in the embryo, a closed and rapidly developing system, compared to the larva, which is exposed to environmental and metabolic challenges. Through single-cell RNA sequencing, we identify fourteen hemocyte clusters present in unchallenged larvae and associated with distinct processes, e.g., proliferation, phagocytosis, metabolic homeostasis, and humoral response. Finally, we characterize the changes occurring in the hemocyte clusters upon wasp infestation, which triggers the differentiation of a novel hemocyte type, the lamellocyte. This first molecular atlas of hemocytes provides insights and paves the way to study the biology of theDrosophilaimmune cells in physiological and pathological conditions.
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页数:25
相关论文
共 158 条
[31]   Drosophila innate immunity: regional and functional specialization of prophenoloxidases [J].
Dudzic, Jan P. ;
Kondo, Shu ;
Ueda, Ryu ;
Bergman, Casey M. ;
Lemaitre, Bruno .
BMC BIOLOGY, 2015, 13
[32]   Aerobic glycolysis tunes YAP/TAZ transcriptional activity [J].
Enzo, Elena ;
Santinon, Giulia ;
Pocaterra, Arianna ;
Aragona, Mariaceleste ;
Bresolin, Silvia ;
Forcato, Mattia ;
Grifoni, Daniela ;
Pession, Annalisa ;
Zanconato, Francesca ;
Guzzo, Giulia ;
Bicciato, Silvio ;
Dupont, Sirio .
EMBO JOURNAL, 2015, 34 (10) :1349-1370
[33]   SWI/SNF Complex Prevents Lineage Reversion and Induces Temporal Patterning in Neural Stem Cells [J].
Eroglu, Elif ;
Burkard, Thomas R. ;
Jiang, Yanrui ;
Saini, Nidhi ;
Homem, Catarina C. F. ;
Reichert, Heinrich ;
Knoblich, Juergen A. .
CELL, 2014, 156 (06) :1259-1273
[34]   Sensing infection in Drosophila:: Toll and beyond [J].
Ferrandon, D ;
Imler, JL ;
Hoffmann, JA .
SEMINARS IN IMMUNOLOGY, 2004, 16 (01) :43-53
[35]   Adaptive evolution of metabolic pathways in Drosophila [J].
Flowers, J. M. ;
Sezgin, E. ;
Kumagai, S. ;
Duvernell, D. D. ;
Matzkin, L. M. ;
Schmidt, P. S. ;
Eanes, W. F. .
MOLECULAR BIOLOGY AND EVOLUTION, 2007, 24 (06) :1347-1354
[36]  
FOGERTY FJ, 1994, DEVELOPMENT, V120, P1747
[37]   Croquemort, a novel Drosophila hemocyte/macrophage receptor that recognizes apoptotic cells [J].
Franc, NC ;
Dimarcq, JL ;
Lagueux, M ;
Hoffmann, J ;
Ezekowitz, RAB .
IMMUNITY, 1996, 4 (05) :431-443
[38]   Requirement for croquemort in phagocytosis of apoptotic cells in Drosophila [J].
Franc, NC ;
Heitzler, P ;
Ezekowitz, RAB ;
White, K .
SCIENCE, 1999, 284 (5422) :1991-1994
[39]   The cis-Golgi Drosophila GMAP has a role in anterograde transport and Golgi organization in vivo, similar to its mammalian ortholog in tissue culture cells [J].
Friggi-Grelin, Florence ;
Rabouille, Catherine ;
Therond, Pascal .
EUROPEAN JOURNAL OF CELL BIOLOGY, 2006, 85 (11) :1155-1166
[40]   The Drosophila kinesin-like protein KLP67A is essential for mitotic and male meiotic spindle assembly [J].
Gandhi, R ;
Bonaccorsi, S ;
Wentworth, D ;
Doxsey, S ;
Gatti, M ;
Pereira, A .
MOLECULAR BIOLOGY OF THE CELL, 2004, 15 (01) :121-131