Stem Cell and Regenerative Medicine Lab, Beijing Institute of Transfusion Medicine, Beijing 100850, China.
Tissue Engineering Lab, Beijing Institute of Transfusion Medicine, Beijing 100850, China.
Sci Rep. 2016 Nov 22;6:37388. doi: 10.1038/srep37388.
Gap junction-mediated cell-cell interactions are highly conserved and play essential roles in cell survival, proliferation, differentiation and patterning. We report that Connexin 32 (Cx32)-mediated gap junctional intercellular communication (GJIC) is necessary for human embryonic stem cell-derived hepatocytes (hESC-Heps) during step-wise hepatic lineage restriction and maturation. Vitamin K2, previously shown to promote Cx32 expression in mature hepatocytes, up-regulated Cx32 expression and GJIC activation during hepatic differentiation and maturation, resulting in significant increases of hepatic markers expression and hepatocyte functions. In contrast, negative Cx32 regulator 2-aminoethoxydiphenyl borate blocked hESC-to-hepatocyte maturation and muted hepatocyte functions through disruption of GJIC activities. Dynamic gap junction organization and internalization are phosphorylation-dependent and the p38 mitogen-activated protein kinases pathway (MAPK) can negatively regulate Cxs through phosphorylation-dependent degradation of Cxs. We found that p38 MAPK inhibitor SB203580 improved maturation of hESC-Heps correlating with up-regulation of Cx32; by contrast, the p38 MAPK activator, anisomycin, blocked hESC-Heps maturation correlating with down-regulation of Cx32. These results suggested that Cx32 is essential for cell-cell interactions that facilitate driving hESCs through hepatic-lineage maturation. Regulators of both Cx32 and other members of its pathways maybe used as a promising approach on regulating hepatic lineage restriction of pluripotent stem cells and optimizing their functional maturation.
缝隙连接介导的细胞间相互作用高度保守,在细胞存活、增殖、分化和模式形成中发挥着重要作用。我们报告说,缝隙连接蛋白 32(Cx32)介导的缝隙连接细胞间通讯(GJIC)对于人胚胎干细胞来源的肝细胞(hESC-Heps)在逐步肝系限制和成熟过程中是必需的。维生素 K2 先前被证明能促进成熟肝细胞中 Cx32 的表达,在肝分化和成熟过程中上调 Cx32 的表达和 GJIC 激活,导致肝标志物表达和肝细胞功能显著增加。相比之下,负性 Cx32 调节剂 2-氨基乙氧基二苯硼酸盐通过破坏 GJIC 活性,阻断 hESC 向肝细胞成熟,并使肝细胞功能减弱。动态缝隙连接组织和内化是磷酸化依赖性的,p38 丝裂原激活蛋白激酶途径(MAPK)可以通过磷酸化依赖性 Cxs 降解负调控 Cxs。我们发现 p38 MAPK 抑制剂 SB203580 改善了 hESC-Heps 的成熟,与 Cx32 的上调相关;相比之下,p38 MAPK 激活剂anisomycin 阻断了 hESC-Heps 的成熟,与 Cx32 的下调相关。这些结果表明,Cx32 对于促进 hESC 通过肝系成熟的细胞间相互作用是必需的。Cx32 及其途径的其他成员的调节剂可作为调节多能干细胞肝系限制和优化其功能成熟的有前途的方法。