Robert Anny Waloski, Pereira Isabela Tiemy, Dallagiovanna Bruno, Stimamiglio Marco Augusto
Laboratório de Biologia Básica de Células-Tronco, Instituto Carlos Chagas - Fiocruz-Paraná, Curitiba, Brazil.
Front Cell Dev Biol. 2020 Feb 7;8:49. doi: 10.3389/fcell.2020.00049. eCollection 2020.
Human pluripotent stem cells are an important tool for the study of developmental processes, such as cardiomyogenic differentiation. Despite the advances made in this field, the molecular and cellular signals involved in the commitment of embryonic stem cells to the cardiac phenotype are still under investigation. Therefore, this study focuses on identifying the extracellular signals involved in cardiac differentiation of human embryonic stem cells. Using a three-dimensional cardiomyogenic differentiation protocol, the conditioned medium and the extracellular matrix (ECM) of embryoid body cultures were collected and characterized at four specific time points. Mass spectrometry (MS) and antibody array analysis of the secretome identified a number of secreted proteins related to signaling pathways, such as Wnt and TGFβ, as well as many ECM proteins. When comparing the proteins identified at selected time points, our data pointed out protein interactions and biological process related to cardiac differentiation. Interestingly, the great changes in secretome profile occurred during the cardiac progenitor specification. The secretome results were also compared with our previous RNAseq data, indicating that the secreted proteins undergo some level of gene regulation. During cardiac commitment it was observed an increase in complexity of the ECM, and some proteins as IGFBP7, FN1, HSPG2, as well as other members of the basal lamina could be highlighted. Thus, these findings contribute valuable information about essential microenvironmental signals working on cardiomyogenic differentiation that may be used in future strategies for cardiac differentiation, cardiomyocyte maturation, and in advances for future acellular therapies.
人类多能干细胞是研究发育过程(如心肌分化)的重要工具。尽管该领域已取得进展,但胚胎干细胞向心脏表型定向分化所涉及的分子和细胞信号仍在研究之中。因此,本研究聚焦于鉴定参与人类胚胎干细胞心脏分化的细胞外信号。采用三维心肌分化方案,在四个特定时间点收集并表征了胚状体培养物的条件培养基和细胞外基质(ECM)。对分泌蛋白组进行质谱(MS)和抗体阵列分析,鉴定出许多与信号通路(如Wnt和TGFβ)相关的分泌蛋白以及许多ECM蛋白。在比较选定时间点鉴定出的蛋白质时,我们的数据指出了与心脏分化相关的蛋白质相互作用和生物学过程。有趣的是,分泌蛋白组图谱的巨大变化发生在心脏祖细胞特化过程中。还将分泌蛋白组结果与我们之前的RNAseq数据进行了比较,表明分泌蛋白经历了一定程度的基因调控。在心脏定向分化过程中,观察到ECM的复杂性增加,一些蛋白质如IGFBP7、FN1、HSPG2以及基底层的其他成员尤为突出。因此,这些发现为参与心肌分化的重要微环境信号提供了有价值的信息,可用于未来心脏分化、心肌细胞成熟的策略以及未来无细胞疗法的进展。