Fontijn R D, Favre J, Naaijkens B A, Meinster E, Paauw N J, Ragghoe S L, Nauta T D, van den Broek M A, Weijers E M, Niessen H W, Koolwijk P, Horrevoets A J
Department of Molecular Cell Biology and Immunology, VU University Medical Center, van der Boechorststraat 7, 1081 BT Amsterdam, The Netherlands.
Department of Pathology and Cardiac Surgery, VU University Medical Center, de Boelelaan 117, 1081 HV Amsterdam, The Netherlands.
Stem Cell Res. 2014 Nov;13(3 Pt A):367-78. doi: 10.1016/j.scr.2014.09.004. Epub 2014 Sep 28.
Adipose tissue-derived stromal cells (ASC) form a rich source of autologous cells for use in regenerative medicine. In vitro induction of an endothelial phenotype may improve performance of ASCs in cardiovascular repair. Here, we report on an in vitro strategy using direct reprogramming of ASCs by means of ectopic expression of the endothelial-specific transcription factor SRY (sex determining region Y)-box18 (SOX18). SOX18 induces ASCs to express a set of genes involved in vascular patterning: MMP7, KDR, EFNB2, SEMA3G and CXCR4. Accordingly, SOX18 transduced ASCs reorganize under conditions of shear stress, display VEGF-induced chemotaxis and form tubular structures in 3D matrices in an MMP7-dependent manner. These in vitro findings provide insight into molecular and cellular processes downstream of SOX18 and show that reprogramming using SOX18 is sufficient to induce several endothelial-like features in ASCs.
脂肪组织来源的基质细胞(ASC)构成了再生医学中丰富的自体细胞来源。体外诱导内皮细胞表型可能会改善ASC在心血管修复中的性能。在此,我们报告一种体外策略,即通过异位表达内皮特异性转录因子SRY(性别决定区Y)-盒18(SOX18)对ASC进行直接重编程。SOX18诱导ASC表达一组参与血管形成的基因:MMP7、KDR、EFNB2、SEMA3G和CXCR4。因此,SOX18转导的ASC在剪切应力条件下会重新组织,表现出VEGF诱导的趋化性,并以MMP7依赖的方式在三维基质中形成管状结构。这些体外研究结果为深入了解SOX18下游的分子和细胞过程提供了线索,并表明使用SOX18进行重编程足以在ASC中诱导出几种内皮样特征。