Centre for Stem Cells and Regenerative Medicine, King's College London, London, UK.
Centre for Craniofacial and Regenerative Biology, King's College London, London, UK.
J Cell Biol. 2021 Apr 5;220(4). doi: 10.1083/jcb.202005095.
To coordinate cell fate with changes in spatial organization, stem cells (SCs) require specific and adaptable systems of signal exchange and cell-to-cell communication. Pluripotent embryonic stem cells (ESCs) use cytonemes to pair with trophoblast stem cells (TSCs) and form synthetic embryonic structures in a Wnt-dependent manner. How these interactions vary with pluripotency states remains elusive. Here we show that ESC transition to an early primed ESC (pESC) state reduces their pairing with TSCs and impairs synthetic embryogenesis. pESCs can activate the Wnt/β-catenin pathway in response to soluble Wnt ligands, but their cytonemes form unspecific and unstable interactions with localized Wnt sources. This is due to an impaired crosstalk between Wnt and glutamate receptor activity and reduced generation of Ca2+ transients on the cytonemes upon Wnt source contact. Induced iGluR activation can partially restore cytoneme function in pESCs, while transient overexpression of E-cadherin improves pESC-TSC pairing. Our results illustrate how changes in pluripotency state alter the mechanisms SCs use to self-organize.
为了协调细胞命运与空间组织变化,干细胞 (SCs) 需要特定且适应性强的信号交换和细胞间通讯系统。多能胚胎干细胞 (ESCs) 使用纤毛与滋养层干细胞 (TSCs) 配对,并以 Wnt 依赖的方式形成合成胚胎结构。这些相互作用如何随多能状态而变化仍然难以捉摸。在这里,我们表明 ESC 向早期初始 ESC (pESC) 状态的转变会减少与 TSCs 的配对,并损害合成胚胎发生。pESCs 可以响应可溶性 Wnt 配体激活 Wnt/β-catenin 途径,但它们的纤毛与局部 Wnt 源形成非特异性和不稳定的相互作用。这是由于 Wnt 和谷氨酸受体活性之间的串扰受损,以及 Wnt 源接触时纤毛上 Ca2+ 瞬变的生成减少。诱导性 iGluR 激活可以部分恢复 pESC 中的纤毛功能,而瞬时过表达 E-钙粘蛋白可改善 pESC-TSC 配对。我们的研究结果说明了多能状态的变化如何改变 SC 自我组织的机制。