Literature DB >> 20381581

A potential activity of valproic acid in the stimulation of interleukin-3-mediated megakaryopoiesis and erythropoiesis.

Bing Liu1, Kohshi Ohishi, Kentaro Yamamura, Kei Suzuki, Fumihiko Monma, Kazuko Ino, Kazuhiro Nishii, Masahiro Masuya, Takao Sekine, Yuji Heike, Yoichi Takaue, Naoyuki Katayama.   

Abstract

OBJECTIVE: Although the anticancer activities of histone deacetylase (HDAC) inhibitors have been studied, a role for HDAC in normal hematopoiesis has not been clearly defined. Previous studies have shown that the potent HDAC inhibitor FK228 stimulates interleukin (IL)-3-mediated erythropoiesis. Here, we examined whether the widely used valproic acid (VPA) affects megakaryopoiesis as well as erythropoiesis.
MATERIALS AND METHODS: CD34(+) cells were incubated in serum-free or serum-containing cultures with cytokines, with or without VPA.
RESULTS: In the serum-free cultures containing IL-3+stem cell factor (SCF), VPA significantly increased generation of CD61(+)GPA(-) megakaryocytic and a CD61(+)GPA(+) mixture of megakaryocytic and erythroid precursors from CD34(+) hematopoietic precursors at a pharmacological concentration (100 microg/mL). The increase in generation of megakaryocytic and erythroid precursors by VPA was confirmed by replating cultured cells with thrombopoietin+SCF and erythropoietin+SCF, respectively. VPA was as potent as FK228. In cultures with granulocyte-macrophage colony-stimulating factor+SCF, where CD61(-)GPA(+) erythroid precursors were mostly developed, VPA mainly enhanced the generation of CD61(-)GPA(+) erythroid precursors. In serum-containing cultures, only low numbers of CD61(+) or GPA(+) cells were developed with IL-3+SCF. Nevertheless, a substantial number of these cells were generated with VPA. Furthermore, these stimulating effects of VPA were observed by incubating CD34(+) cells from patients with myelodysplastic syndrome. Quantitative reverse transcription polymerase chain reaction showed that VPA enhanced GATA-2, but not GATA-1, messenger RNA expression with IL-3+SCF.
CONCLUSIONS: These results indicate a novel role for VPA in enhancing the potential of IL-3 to stimulate megakaryopoiesis as well as erythropoiesis and suggest a new therapeutic approach of epigenetic therapy for hematological disease. 2010 ISEH - Society for Hematology and Stem Cells. Published by Elsevier Inc. All rights reserved.

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Year:  2010        PMID: 20381581     DOI: 10.1016/j.exphem.2010.03.019

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


  5 in total

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Journal:  J Surg Res       Date:  2014-02-04       Impact factor: 2.192

2.  SCL/TAL1-mediated transcriptional network enhances megakaryocytic specification of human embryonic stem cells.

Authors:  Miguel G Toscano; Oscar Navarro-Montero; Veronica Ayllon; Veronica Ramos-Mejia; Xiomara Guerrero-Carreno; Clara Bueno; Tamara Romero; Mar Lamolda; Marien Cobo; Francisco Martin; Pablo Menendez; Pedro J Real
Journal:  Mol Ther       Date:  2014-10-08       Impact factor: 11.454

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4.  A small-molecule/cytokine combination enhances hematopoietic stem cell proliferation via inhibition of cell differentiation.

Authors:  Lan Wang; Xin Guan; Huihui Wang; Bin Shen; Yu Zhang; Zhihua Ren; Yupo Ma; Xinxin Ding; Yongping Jiang
Journal:  Stem Cell Res Ther       Date:  2017-07-18       Impact factor: 6.832

5.  Megakaryocyte lineage development is controlled by modulation of protein acetylation.

Authors:  Marije Bartels; Anita Govers; Roel Polak; Stephin Vervoort; Ruben van Boxtel; Cornelieke Pals; Marc Bierings; Wouter van Solinge; Toine Egberts; Edward Nieuwenhuis; Michal Mokry; Paul James Coffer
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  5 in total

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