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Two Independent Functions of Collier/Early B Cell Factor in the Control of Drosophila Blood Cell Homeostasis
Author(s) -
Justine Oyallon,
Nathalie Vanzo,
Joanna Krzemień,
Ismaël Morin-Poulard,
Alain Vincent,
Michèle Crozatier
Publication year - 2016
Publication title -
plos one
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.99
H-Index - 332
ISSN - 1932-6203
DOI - 10.1371/journal.pone.0148978
Subject(s) - biology , progenitor cell , haematopoiesis , microbiology and biotechnology , immunology , population , blood cell , homeostasis , cellular differentiation , stem cell , medicine , genetics , environmental health , gene
Blood cell production in the Drosophila hematopoietic organ, the lymph gland, is controlled by intrinsic factors and extrinsic signals. Initial analysis of Collier/Early B Cell Factor function in the lymph gland revealed the role of the Posterior Signaling Center (PSC) in mounting a dedicated cellular immune response to wasp parasitism. Further, premature blood cell differentiation when PSC specification or signaling was impaired, led to assigning the PSC a role equivalent to the vertebrate hematopoietic niche. We report here that Collier is expressed in a core population of lymph gland progenitors and cell autonomously maintains this population. The PSC contributes to lymph gland homeostasis by regulating blood cell differentiation, rather than by maintaining core progenitors. In addition to PSC signaling, switching off Collier expression in progenitors is required for efficient immune response to parasitism. Our data show that two independent sites of Collier/Early B Cell Factor expression, hematopoietic progenitors and the PSC, achieve control of hematopoiesis.

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