Literature DB >> 16140148

Transcriptional regulation of hematopoietic stem cell development in zebrafish.

Nelson Hsia1, Leonard I Zon.   

Abstract

The zebrafish (Danio rerio) is a well-established vertebrate model for studying hematopoiesis. The major advantages of this system include robust experimental techniques in both genetics and embryology, which have been utilized to model many aspects of human development and disease. Although much is known about the transcription factors involved in the terminal differentiation of peripheral blood lineages, little is known about the development and maintenance of the hematopoietic stem cell (HSC). This review will focus on the current knowledge of the transcriptional regulation of the HSC in the context of the zebrafish. Future studies using new technologies in the zebrafish model will enhance our understanding of the molecular networks regulating HSC pluripotency and differentiation.

Entities:  

Mesh:

Substances:

Year:  2005        PMID: 16140148     DOI: 10.1016/j.exphem.2005.06.013

Source DB:  PubMed          Journal:  Exp Hematol        ISSN: 0301-472X            Impact factor:   3.084


  26 in total

1.  The role of meis1 in primitive and definitive hematopoiesis during zebrafish development.

Authors:  Ana Cvejic; Jovana Serbanovic-Canic; Derek L Stemple; Willem H Ouwehand
Journal:  Haematologica       Date:  2010-11-03       Impact factor: 9.941

2.  Distinct regulation of the anterior and posterior myeloperoxidase expression by Etv2 and Gata1 during primitive Granulopoiesis in zebrafish.

Authors:  Nicole O Glenn; Jennifer A Schumacher; Hyon J Kim; Emma J Zhao; Jurate Skerniskyte; Saulius Sumanas
Journal:  Dev Biol       Date:  2014-06-20       Impact factor: 3.582

3.  Critical role of connexin43 in zebrafish late primitive and definitive hematopoiesis.

Authors:  Qiu Jiang; Dong Liu; Shuna Sun; Jingying Hu; Li Tan; Yuexiang Wang; Yonghao Gui; Min Yu; Houyan Song
Journal:  Fish Physiol Biochem       Date:  2009-12-18       Impact factor: 2.794

4.  Zebrafish miR-462-731 regulates hematopoietic specification and pu.1-dependent primitive myelopoiesis.

Authors:  Chun-Xiao Huang; Yan Huang; Xue-Ke Duan; Mu Zhang; Jia-Peng Tu; Jing-Xia Liu; Hong Liu; Tian-Sheng Chen; Wei-Min Wang; Huan-Ling Wang
Journal:  Cell Death Differ       Date:  2018-11-20       Impact factor: 15.828

5.  Definitive hematopoiesis initiates through a committed erythromyeloid progenitor in the zebrafish embryo.

Authors:  Julien Y Bertrand; Albert D Kim; Emily P Violette; David L Stachura; Jennifer L Cisson; David Traver
Journal:  Development       Date:  2007-10-24       Impact factor: 6.868

Review 6.  Hematopoiesis.

Authors:  Madhumita Jagannathan-Bogdan; Leonard I Zon
Journal:  Development       Date:  2013-06       Impact factor: 6.868

7.  Differential requirement for Gata1 DNA binding and transactivation between primitive and definitive stages of hematopoiesis in zebrafish.

Authors:  Christiane L Belele; Milton A English; Jagman Chahal; Anthony Burnetti; Steven M Finckbeiner; Gretchen Gibney; Martha Kirby; Raman Sood; P Paul Liu
Journal:  Blood       Date:  2009-12-10       Impact factor: 22.113

8.  C/EBPalpha initiates primitive myelopoiesis in pluripotent embryonic cells.

Authors:  Yaoyao Chen; Ricardo M B Costa; Nick R Love; Ximena Soto; Martin Roth; Roberto Paredes; Enrique Amaya
Journal:  Blood       Date:  2009-05-06       Impact factor: 22.113

9.  Essential role of spi-1-like (spi-1l) in zebrafish myeloid cell differentiation.

Authors:  Alex Bukrinsky; Kevin J P Griffin; Yan Zhao; Shuo Lin; Utpal Banerjee
Journal:  Blood       Date:  2009-01-08       Impact factor: 22.113

10.  Zebrafish microRNA miR-210-5p inhibits primitive myelopoiesis by silencing foxj1b and slc3a2a mRNAs downstream of gata4/5/6 transcription factor genes.

Authors:  Wenshuang Jia; Dong Liang; Nan Li; Meijing Liu; Zhangji Dong; Jingyun Li; Xiaohua Dong; Yunyun Yue; Ping Hu; Jihua Yao; Qingshun Zhao
Journal:  J Biol Chem       Date:  2018-12-28       Impact factor: 5.157

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.