Zebrafish granulocyte colony-stimulating factor receptor signaling promotes myelopoiesis and myeloid cell migration

被引:102
作者
Liongue, Clifford [1 ,2 ]
Hall, Chris J. [3 ]
O'Connell, Bree A. [1 ,2 ]
Crosier, Phil [3 ]
Ward, Alister C. [1 ]
机构
[1] Deakin Univ, Sch Med, Waurn Ponds, Vic 3217, Australia
[2] Deakin Univ, Sch Life & Environm Sci, Ctr Cellular & Mol Biol, Burwood, Australia
[3] Univ Auckland, Sch Med Sci, Dept Mol Med & Pathol, Auckland 1, New Zealand
关键词
G-CSF RECEPTOR; EXPRESSION PATTERN; TRANSCRIPTION FACTORS; PROGENITOR CELLS; TRANSGENIC FISH; BONE-MARROW; FACTOR GENE; ACTIVATION; HEMATOPOIESIS; BLOOD;
D O I
10.1182/blood-2008-07-171967
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Granulocyte colony-stimulating factor receptor (GCSFR) signaling participates in the production of neutrophilic granulocytes during normal hematopoietic development, with a particularly important role during emergency hematopoiesis. This study describes the characterization of the zebrafish gcsf and gcsfr genes, which showed broad conservation and similar regulation to their mammalian counterparts. Morpholino-mediated knockdown of gcsfr and overexpression of gcsf revealed the presence of an anterior population of myeloid cells during primitive hematopoiesis that was dependent on GCSF/GCSFR for development and migration. This contrasted with a posterior domain that was largely independent of this pathway. Definitive myelopoiesis was also partially dependent on a functional GCSF/GCSFR pathway. Injection of bacterial lipopolysaccharide elicited significant induction of gcsf expression and emergency production of myeloid cells, which was abrogated by gcsfr knockdown. Collectively, these data demonstrate GCSF/GCSFR to be a conserved signaling system for facilitating the production of multiple myeloid cell lineages in both homeostatic and emergency conditions, as well as for early myeloid cell migration, establishing a useful experimental platform for further dissection of this pathway. (Blood. 2009; 113:2535-2546)
引用
收藏
页码:2535 / 2546
页数:12
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