Priority Research Papers: Immunology:

Zbtb1 prevents default myeloid differentiation of lymphoid-primed multipotent progenitors

Xianyu Zhang, Ying Lu, Xin Cao, Tao Zhen and Damian Kovalovsky _

PDF  |  HTML  |  How to cite

Oncotarget. 2016; 7:58768-58778. https://doi.org/10.18632/oncotarget.11356

Metrics: PDF 1806 views  |   HTML 2424 views  |   ?  


Xianyu Zhang1, Ying Lu1, Xin Cao2, Tao Zhen3 and Damian Kovalovsky1

1 Experimental Immunology Branch, NCI, NIH, Maryland, USA

2 College of Life Science and Engineering, Northwest University for Nationalities, Gansu Engineering Research Center for Animal Cell, Lanzhou, China

3 Oncogenesis and Development Section, National Human Genome Research Institute, NIH, Maryland, USA

Correspondence to:

Damian Kovalovsky, email:

Keywords: Zbtb1, lymphoid, development, myeloid, differentiation, Immunology and Microbiology Section, Immune response, Immunity

Received: June 18, 2016 Accepted: August 02, 2016 Published: August 17, 2016


Zbtb1 is a transcription factor that prevents DNA damage and p53-mediated apoptosis in replicating immune progenitors, affecting lymphoid as well as myeloid development when hematopoietic progenitors are in competition in mixed bone marrow chimeras. However, Zbtb1-deficient mice do not have an apparent myeloid deficiency. We report here that Zbtb1-deficient lymphoid-primed multipotent progenitors (LMPPs) are biased to develop towards the myeloid fate in detriment of lymphoid development, contributing to the apparent unaffected myeloid development. Zbtb1 expression was maintained during lymphoid development of LMPP cells but downregulated during myeloid development. Deficiency of Zbtb1 in LMPP cells was sufficient to direct a myeloid fate in lymphoid-inducing conditions and in the absence of myeloid cytokines as shown by upregulation of a myeloid gene signature and the generation of myeloid cells in vitro. Finally, biased myeloid differentiation of Zbtb1-deficient LMPP cells was not due to increased p53-dependent apoptosis as it was not reverted by transgenic Bcl2 expression or p53 deficiency. Altogether, our results show that Zbtb1 expression prevents activation of a default myeloid program in LMPP cells, ensuring the generation of lymphoid cells.

Creative Commons License All site content, except where otherwise noted, is licensed under a Creative Commons Attribution 4.0 License.
PII: 11356