Spib is required for primitive myeloid development in Xenopus

Blood

Volumn 112, Issue 6, 2008, Pages 2287-2296

  Costa, Ricardo M B ^a   Soto, Ximena ^a   Chen, Yaoyao ^a   Zorn, Aaron M ^b   Amaya, Enrique ^a  

^a UNIVERSITY OF MANCHESTER   (United Kingdom)

^b CINCINNATI CHILDREN S HOSPITAL RESEARCH FOUNDATION   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

TRANSCRIPTION FACTOR; TRANSCRIPTION FACTOR SPIB; UNCLASSIFIED DRUG; SPIB PROTEIN, XENOPUS; TRANSCRIPTION FACTOR ETS; XENOPUS PROTEIN;

ANIMAL EXPERIMENT; ARTICLE; BONE MARROW CELL; CELL DIFFERENTIATION; CELL FUNCTION; CELL MATURATION; CELL MIGRATION; CONTROLLED STUDY; EMBRYO; FLUORESCENCE MICROSCOPY; HEMANGIOBLASTOMA; HEMATOPOIESIS; NONHUMAN; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; PROTEIN ISOLATION; XENOPUS; YOLK SAC; ANIMAL; ANIMAL EMBRYO; CELL LINEAGE; CELL MOTION; CYTOLOGY; ISOLATION AND PURIFICATION; MICROSCOPY; PHYSIOLOGY; PRENATAL DEVELOPMENT; WOUND HEALING; XENOPUS LAEVIS;

ANIMALS; CELL DIFFERENTIATION; CELL LINEAGE; CELL MOVEMENT; EMBRYO, NONMAMMALIAN; MICROSCOPY, VIDEO; MYELOID CELLS; PROTO-ONCOGENE PROTEINS C-ETS; TRANSCRIPTION FACTORS; WOUND HEALING; XENOPUS LAEVIS; XENOPUS PROTEINS;

EID: 55249087503     PISSN: 00064971     EISSN: 15280020     Source Type: Journal    
DOI: 10.1182/blood-2008-04-150268     Document Type: Article

References (47)

1. Zon LI. Hematopoiesis. New York, NY: Oxford University Press; 2001.
2. de Jong J, Zon L. Use of the zebrafish system to study primitive and definitive hematopoiesis. Annu Rev Genet. 2005;39:481-501.
3. Baron MH. Developmental Hematopoiesis. Vol 105. Totowa, NJ: Humana Press; 2005.
4. Lane MC, Smith WC. The origins of primitive blood in Xenopus: implications for axial patterning. Development. 1999;126:423-434.
5. Lane MC, Sheets MD. Primitive and definitive blood share a common origin in Xenopus: a comparison of lineage techniques used to construct fate maps. Dev Biol. 2002;248:52-67.
6. Ciau-UitzA, Walmsley M, Patient R. Distinct origins of adult and embryonic blood in Xenopus. Cell. 2000;102:787-796.
7. Patterson L, Gering M, Patient R. Scl is required for dorsal aorta as well as blood formation in zebrafish embryos. Blood. 2005;105:3502-3511.
8. Patterson L Gering M, Eckfeldt C, et al. The transcription factors Scl and Lmo2 act together during development of the hemangioblast in zebrafish. Blood. 2007;109:2389-2398.
9. Robb L Elwood NJ, ElefantyAG, et al. The scl gene product is required for the generation of all hematopoietic lineages in the adult mouse. EMBO J. 1996;15:4123-4129.
10. Porcher C, Swat W, Rockwell K, Fujiwara Y, Alt FW. Orkin SH. The T cell leukemia oncoprotein SCL/tal-1 is essential for development of all hematopoietic lineages. Cell. 1996;86:47-57.
11. Mead P, Kelley C, Hahn P, Piedad O, Zon L. SCL specifies hematopoietic mesoderm in Xenopus embryos. Development. 1998;125:2611-2620.
12. Walmsley M, Cleaver D, Patient R. FGF controls the timing of Scl, Lmo2 and Runxl expression during embryonic blood development. Blood. 2008;111:1157-1166.
13. Walmsley M, Ciau-Uitz A, Patient R. Adult and embryonic blood and endothelium derive from distinct precursor populations which are differentially programmed by BMP in Xenopus. Development. 2002;129:5683-5695.
14. Vogeli K, Jin S, Martin G, Stainier D. A common progenitor for haematopoietic and endothelial lineages in the zebrafish gastrula. Nature. 2006; 443:337-339.
15. Dieterlen-Lièvre F, Le Douarin NM. From the hemangioblast to self-tolerance: a series of innovations gained from studies on the avian embryo. Mech Dev. 2004;121:1117-1128.
16. Rhodes J, Hagen A, Hsu K. et al. Interplay of pu. 1 and gata1 determines myelo-erythroid progenitor cell fate in zebrafish. Dev Cell. 2005;8:97-108.
17. Joint Genome Institute. Xenopus tropicalis v4.1. http://genome.jgi-psf. org/Xentr4. Accessed July 29, 2008.
18. Wellcome Trust Sanger. Ensembl. http://www.ensembl.org. Accessed July 29, 2008.
19. University of California. Metazome. http://www.metazome.net. Accessed July 29, 2008.
20. European Bioinformatics Institute. Clustal W. http://www.ebi.ac.uk/Tools/ clustalw2/index.html. Accessed July 29, 2008.
21. University of Glasgow. TreeView X. http://darwin. zoology.gla.ac.uk/- rpage/treeviewx. Accessed July 29, 2008.
22. EMBnet Austria. PESTfind. https://emb1.bcc.univie. ac.at/toolbox/ pestfind/. Accessed July 29, 2008.
23. University of Calgary. Xenbase. http://www.xenbase.org/gene/static/ geneNomenclature.jsp. Accessed July 29, 2008.
24. Ohinata H, Tochinal S, Katagiri C. Ontogeny and tissue distribution of Leukocyte-common antigen bearing cells during early development of Xenopus laevis. Development. 1989; 107:445-452.
25. Herbomel P, Levraud J P. Imaging early macrophage differentiation, migration, and behaviors in live zebrafish embryos. Methods Mol Med. 2005; 105:199-214.
26. Sive HLGR, Harland RM. Early Development of Xenopus laevis: A Laboratory Manual. Cold Spring, NY: Cold Spring Harbor Press; 2000.
27. Smith S, Kotecha S, Towers N, Latinkic B, Mohun T. XPOX2-peroxidase expression and the XLURP-1 promoter reveal the site of embryonic myeloid cell development in Xenopus. Mech Dev. 2002;117:173-186.
28. TraceyW, Pepling M, Horb M, Thomsen G, Gergen J. A Xenopus homologue of aml-1 reveals unexpected patterning mechanisms leading to the formation of embryonic blood. Development. 1998;125:1371-1380.
29. Costa RM, Mason J, Lee M, Amaya E, Zorn AM. Novel gene expression domains reveal early patterning of the Xenopus endoderm. Gene Expr Patterns. 2003;3:509-519.
30. Harrison M, Abu-Elmagd M, Grocott T, Yates C, Gavrilovic J, Wheeler G. Matrix metalloproteinase genes in Xenopus development. Dev Dyn. 2004; 231:214-220.
31. Tashiro S, Sedohara A, Asashima M, Izutsu Y, Maeno M. Characterization of myeloid cells derived from the anterior ventral mesoderm in the Xenopus laevis embryo. Dev Growth Differ. 2006; 48:499-512.
32. Ohinata H, Tochinai S, Katagiri C. Ontogeny and tissue distribution of leukocyte-common antigen bearing cells during early development of Xenopus laevis. Development. 1989;107:445-452.
33. Herbomel P, Levraud J P. Imaging early macrophage differentiation, migration, and behaviors in live zebrafish embryos. Methods Mol Med. 2005; 105:199-214.
34. Le Guyader D, Redd M, Colucci-Guyon E, et al. Origins and unconventional behavior of neutrophils in developing zebrafish. Blood. 2008:111: 132-141.
35. Hsu K, Traver D. Kutok J. et al. The pu.1 promoter drives myeloid gene expression in zebrafish. Blood. 2004;104:1291-1297.
36. Lieschke GJ, Gates AC, Paw BH, et al. Zebrafish SPI-1 (PU.1) marks a site of myeloid development independent of primitive erythropoiesis: implications for axial patterning. Dev Biol. 2002;246: 274-295.
37. Ward A, McPhee D, Condron M, et al. The zebrafish spi1 promoter drives myeloid-specific expression in stable transgenic fish. Blood. 2003; 102:3238-3240.
38. Lieschke G, Oates A, Crowhurst M, Ward A, Layton J. Morphologic and functional characterization of granulocytes and macrophages in embryonic and adult zebrafish. Blood. 2001;98: 3087-3096.
39. Herbomel P. Thisse B, Thisse C. Ontogeny and behaviour of early macrophages in the zebrafish embryo. Development. 1999;126:3735-3745.
40. Page-McGaw A, Ewald AJ, Werb Z. Matrix metalloproteinases and the regulation of tissue remodelling. Nat Rev Mol Cell Biol. 2007;8:221-233.
41. Lichanska A, Browne C, Henkel G, et al. Differentiation of the mononuclear phagocyte system during mouse embryogenesis: the role of transcription factor PU. 1. Blood. 1999;94:127-138.
42. LevineAJ, Munoz-Sanjuan I, Bell E, North AJ, Brivanlou AH. Fluorescent labeling of endothelial cells allows in vivo, continuous characterization of the vascular development of Xenopus laevis. Dev Biol. 2003;254:50-67.
43. Schotte R, Nagasawa M, Weijer K, Spits H, Blom B. The ETS transcription factor Spi-B is required for human plasmacytoid dendritic cell development. J Exp Med. 2004;200:1503-1509.
44. Su G, Chen H, Muthusamy N, et al. Defective B cell receptor-mediated responses in mice lacking the Ets protein, Spi-B. EMBO J. 1997;16:7118-7129.
45. McKercher S, Torbett B, Anderson K, et al. Targeted disruption of the PU. 1 gene results in multiple hematopoietic abnormalities. EMBO J. 1996; 15:5647-5658.
46. Scott EW, Simon MC, Anastasi J, Singh H. Requirement of transcription factor PU. 1 in the development of multiple hematopoietic lineages. Science. 1994;265:1573-1577.
47. Olson MC, Scott EW, HackAA, et al. PU. 1 is not essential for early myeloid gene expression but is required for terminal myeloid differentiation. Immunity. 1995;3:703-714.