Dixon Katherine, Chen Jihong, Li Qiao
Department of Cellular and Molecular Medicine, Faculty of Medicine, University of Ottawa, 451 Smyth Road, Room 2537, Ottawa, ON K1H 8M5 Canada.
Department of Pathology and Laboratory Medicine, Faculty of Medicine, University of Ottawa, Ottawa, ON Canada.
Cell Biosci. 2017 May 2;7:23. doi: 10.1186/s13578-017-0150-x. eCollection 2017.
Regulation of lineage specification and differentiation in embryonic stem (ES) cells can be achieved through the activation of endogenous signaling, an avenue for potential application in regenerative medicine. During vertebrate development, retinoic acid (RA) plays an important role in body axis elongation and mesoderm segmentation in that graded exposure to RA provides cells with positional identity and directs commitment to specific tissue lineages. Nevertheless, bexarotene, a clinically approved rexinoid, enhances the specification and differentiation of ES cells into skeletal myocytes more effectively than RA. Thus profiling the transcriptomes of ES cells differentiated with bexarotene or RA permits the identification of different genetic targets and signaling pathways that may contribute to the difference of bexarotene and RA in efficiency of myogenesis. Interestingly, bexarotene induces the early expression of a myogenic progenitor marker, , while the expression of many RA targets is also enhanced by bexarotene. Several signaling molecules involved in the progression of myogenic specification and commitment are differentially regulated by bexarotene and RA, suggesting that early targets of rexinoid allow the coordinated regulation of molecular events which leads to efficient myogenic differentiation in ES cells.
胚胎干细胞(ES细胞)谱系特化和分化的调控可通过激活内源性信号来实现,这是再生医学中潜在的应用途径。在脊椎动物发育过程中,视黄酸(RA)在体轴延长和中胚层分割中起重要作用,因为分级暴露于RA为细胞提供位置身份并指导其向特定组织谱系的定向分化。然而,贝沙罗汀是一种临床批准的类视黄醇X受体激动剂,它比RA更有效地增强ES细胞向骨骼肌细胞的特化和分化。因此,对用贝沙罗汀或RA分化的ES细胞的转录组进行分析,可以识别出不同的基因靶点和信号通路,这些可能导致贝沙罗汀和RA在成肌效率上的差异。有趣的是,贝沙罗汀诱导一种成肌祖细胞标志物的早期表达,而贝沙罗汀也增强了许多RA靶点的表达。几种参与成肌特化和定向分化进程的信号分子受到贝沙罗汀和RA的不同调节,这表明类视黄醇X受体激动剂的早期靶点允许对分子事件进行协调调节,从而导致ES细胞中高效的成肌分化。