Cell and Molecular Biology Graduate Group, University of Pennsylvania, Philadelphia, PA 19104, USA.
Dev Dyn. 2013 Feb;242(2):108-21. doi: 10.1002/dvdy.23906.
Histone deacetylases (HDACs) regulate multiple developmental processes and cellular functions. However, their roles in blood development have not been determined, and in Xenopus laevis a specific function for HDACs has yet to be identified. Here, we employed the class I selective HDAC inhibitor, valproic acid (VPA), to show that HDAC activity is required for primitive hematopoiesis.
VPA treatment during gastrulation resulted in a complete absence of red blood cells (RBCs) in Xenopus tadpoles, but did not affect development of other mesodermal tissues, including myeloid and endothelial lineages. These effects of VPA were mimicked by Trichostatin A (TSA), a well-established pan-HDAC inhibitor, but not by valpromide, which is structurally similar to VPA but does not inhibit HDACs. VPA also caused a marked, dose-dependent loss of primitive erythroid progenitors in mouse yolk sac explants at clinically relevant concentrations. In addition, VPA treatment inhibited erythropoietic development downstream of bmp4 and gata1 in Xenopus ectodermal explants.
These findings suggest an important role for class I HDACs in primitive hematopoiesis. Our work also demonstrates that specific developmental defects associated with exposure to VPA, a significant teratogen in humans, arise through inhibition of class I HDACs.
组蛋白去乙酰化酶(HDACs)调节多种发育过程和细胞功能。然而,它们在血液发育中的作用尚未确定,在非洲爪蟾中尚未确定 HDACs 的特定功能。在这里,我们使用了 I 类选择性 HDAC 抑制剂丙戊酸(VPA),表明 HDAC 活性是原始造血所必需的。
VPA 在原肠胚形成期间的处理导致非洲爪蟾幼体中完全没有红细胞(RBCs),但不影响其他中胚层组织的发育,包括髓样和内皮谱系。VPA 的这些作用被 Trichostatin A(TSA)模拟,TSA 是一种成熟的泛 HDAC 抑制剂,但不被丙戊酸钠模拟,丙戊酸钠结构上与 VPA 相似,但不抑制 HDACs。VPA 还在临床相关浓度下引起小鼠卵黄囊外植体中原始红细胞祖细胞的明显、剂量依赖性丧失。此外,VPA 处理抑制了非洲爪蟾外胚层外植体中 bmp4 和 gata1 下游的红系发育。
这些发现表明 I 类 HDACs 在原始造血中起重要作用。我们的工作还表明,与 VPA 暴露相关的特定发育缺陷,VPA 是人类的一种重要致畸剂,是通过抑制 I 类 HDACs 引起的。