Inefficient megakaryopoiesis in mouse hematopoietic stem–progenitor cells lacking T-bet

• Published in: Experimental hematology Vol. 44; no. 3; pp. 194 - 206.e17
• Main Authors: Furusawa, Aki, Sadashivaiah, Kavitha, Singh, Zeba N, Civin, Curt I, Banerjee, Arnob
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier Inc 01-03-2016
• Subjects: Advanced Basic Science; Animals; Cell Differentiation; Cell Proliferation; Cell Survival; Erythrocytes - cytology; Erythrocytes - metabolism; Hematology, Oncology and Palliative Medicine; Hematopoietic Stem Cells - cytology; Hematopoietic Stem Cells - metabolism; Integrin beta3 - biosynthesis; Integrin beta3 - genetics; Megakaryocytes - cytology; Megakaryocytes - metabolism; Mice; Mice, Mutant Strains; Platelet Membrane Glycoprotein IIb - biosynthesis; Platelet Membrane Glycoprotein IIb - genetics; T-Box Domain Proteins - deficiency
• ISSN: 0301-472X; 1873-2399
• DOI: 10.1016/j.exphem.2015.11.003

Differentiation of hematopoietic stem–progenitor cells (HSPCs) into mature blood lineages results from the translation of extracellular signals into changes in the expression levels of transcription factors controlling cell fate decisions. Multiple transcription factor families are known to be involved in hematopoiesis. Although the T-box transcription factor family is known to be involved in the differentiation of multiple tissues, and expression of T-bet, a T-box family transcription factor, has been observed in HSPCs, T-box family transcription factors do not have a described role in HSPC differentiation. In the current study, we address the functional consequences of T-bet expression in mouse HSPCs. T-bet protein levels differed among HSPC subsets, with highest levels observed in megakaryo-erythroid progenitor cells (MEPs), the common precursor to megakaryocytes and erythrocytes. HSPCs from T-bet-deficient mice exhibited a defect in megakaryocytic differentiation when cultured in the presence of thrombopoietin. In contrast, erythroid differentiation in culture in the presence of erythropoietin was not substantially altered in T-bet-deficient HSPCs. Differences observed with respect to megakaryocyte number and maturity, as assessed by level of expression of CD41 and CD61, and megakaryocyte ploidy, in T-bet-deficient HSPCs were not associated with altered proliferation or survival in culture. Gene expression micro-array analysis of MEPs from T-bet-deficient mice exhibited diminished expression of multiple genes associated with the megakaryocyte lineage. These data advance our understanding of the transcriptional regulation of megakaryopoiesis by supporting a new role for T-bet in the differentiation of MEPs into megakaryocytes.