Happe Cassandra L, Engler Adam J
From the Department of Bioengineering, University of California, San Diego, La Jolla; and Sanford Consortium for Regenerative Medicine, La Jolla, CA.
Circ Res. 2016 Jan 22;118(2):296-310. doi: 10.1161/CIRCRESAHA.115.305139.
Soluble morphogen gradients have long been studied in the context of heart specification and patterning. However, recent data have begun to challenge the notion that long-standing in vivo observations are driven solely by these gradients alone. Evidence from multiple biological models, from stem cells to ex vivo biophysical assays, now supports a role for mechanical forces in not only modulating cell behavior but also inducing it de novo in a process termed mechanotransduction. Structural proteins that connect the cell to its niche, for example, integrins and cadherins, and that couple to other growth factor receptors, either directly or indirectly, seem to mediate these changes, although specific mechanistic details are still being elucidated. In this review, we summarize how the wingless (Wnt), transforming growth factor-β, and bone morphogenetic protein signaling pathways affect cardiomyogenesis and then highlight the interplay between each pathway and mechanical forces. In addition, we will outline the role of integrins and cadherins during cardiac development. For each, we will describe how the interplay could change multiple processes during cardiomyogenesis, including the specification of undifferentiated cells, the establishment of heart patterns to accomplish tube and chamber formation, or the maturation of myocytes in the fully formed heart.
可溶性形态发生素梯度长期以来一直是在心脏特化和模式形成的背景下进行研究的。然而,最近的数据开始对长期以来的体内观察结果仅由这些梯度单独驱动这一观点提出挑战。从干细胞到体外生物物理分析等多种生物学模型的证据,现在支持了机械力不仅在调节细胞行为方面,而且在一个称为机械转导的过程中从头诱导细胞行为方面所起的作用。例如,将细胞与其微环境连接起来的结构蛋白,如整合素和钙黏着蛋白,它们直接或间接地与其他生长因子受体偶联,似乎介导了这些变化,尽管具体的机制细节仍在阐明之中。在这篇综述中,我们总结了无翅型(Wnt)、转化生长因子-β和骨形态发生蛋白信号通路如何影响心肌发生,然后强调了每条通路与机械力之间的相互作用。此外,我们将概述整合素和钙黏着蛋白在心脏发育过程中的作用。对于每一种,我们将描述这种相互作用如何在心肌发生过程中改变多个过程,包括未分化细胞的特化、实现管腔形成的心脏模式的建立,或在完全形成的心脏中肌细胞的成熟。