Inserm, U1036, Grenoble, France.
J Cell Physiol. 2012 Nov;227(11):3593-602. doi: 10.1002/jcp.24063.
The lymphatic vasculature is essential for the maintenance of tissue fluid, immune surveillance, and dissemination of metastasis. Recently, several models for lymphatic vascular research and markers specific for lymphatic endothelium have been characterized. Despite these significant achievements, our understanding of the early lymphatic development is still rather limited. The purpose of the study was to further define early lymphatic differentiation regulatory pathways. In the present study, we have developed conditions leading to lymphatic endothelial cell differentiation under both serum-rich and serum-free conditions, using the coculture system of Flk-1-positive vascular precursors derived from murine embryonic stem (ES) cells grown on an OP9 stromal cell layer. In this work, we also identified Transforming Growth Factor-β1 (TGFβ1) as a negative regulator of lymphvasculogenesis from ES-derived vascular progenitors. Finally, we could show that TGFβ1 addition decreases COUP-TFII and Sox18 mRNA levels, which are two transcription factors known to be involved in early lymphatic endothelial differentiation. Taken together these findings support the concept that manipulating the TGFβ signaling pathway may represent an interesting target to favor lymphatic endothelial cell expansion for cell replacement strategies.
淋巴管系统对于维持组织液、免疫监视和转移扩散至关重要。最近,已经有几种用于淋巴管研究的模型和淋巴管内皮特异性标记物被鉴定出来。尽管取得了这些重大成就,但我们对早期淋巴管发育的理解仍然相当有限。本研究旨在进一步确定早期淋巴管分化的调节途径。在本研究中,我们利用源自鼠胚胎干细胞(ES 细胞)的 Flk-1 阳性血管前体细胞在 OP9 基质细胞层上的共培养系统,在富含血清和无血清条件下分别开发了诱导淋巴管内皮细胞分化的条件。在这项工作中,我们还鉴定出转化生长因子-β1(TGFβ1)是 ES 细胞衍生的血管祖细胞向淋巴管发生分化的负调节剂。最后,我们可以表明 TGFβ1 的添加会降低 COUP-TFII 和 Sox18 mRNA 水平,这两种转录因子已知参与早期淋巴管内皮细胞分化。综上所述,这些发现支持这样一种概念,即操纵 TGFβ 信号通路可能代表一个有趣的靶点,以有利于用于细胞替代策略的淋巴管内皮细胞的扩增。