Whitehead Institute for Biomedical Research, Cambridge, MA 02142, USA.
J Cell Sci. 2011 Apr 1;124(Pt 7):999-1006. doi: 10.1242/jcs.081513.
Maintenance of appropriate cell adhesion is crucial for normal cellular and organismal homeostasis. Certain microRNAs have recently been found capable of regulating molecules that oversee the fundamental cell biological events that drive cellular adhesion. It is now apparent that microRNAs play crucial roles in the great majority of biochemical pathways that contribute to normal cell adhesion. In this Commentary, we describe the latest advances within this still-emerging field, and highlight connections between the deregulation of microRNAs that affect cell-adhesion-associated molecules and the pathogenesis of several human diseases. Current evidence suggests that the ability of certain microRNAs--notably miR-17, miR-29, miR-31, miR-124 and miR-200--to pleiotropically regulate multiple molecular components of the cell adhesion machinery endows these microRNAs with the capacity to function as key modulators of adhesion-associated processes. This, in turn, holds important implications for our understanding of both the basic biology of cell adhesion and the etiology of multiple pathological conditions.
维持适当的细胞黏附对于正常的细胞和机体稳态至关重要。最近发现某些 microRNAs 能够调节负责驱动细胞黏附的基本细胞生物学事件的分子。现在很明显,microRNAs 在大多数参与正常细胞黏附的生化途径中发挥着关键作用。在这篇评论中,我们描述了这一仍在发展中的领域的最新进展,并强调了影响细胞黏附相关分子的 microRNAs 失调与几种人类疾病发病机制之间的联系。目前的证据表明,某些 microRNAs(尤其是 miR-17、miR-29、miR-31、miR-124 和 miR-200)能够多效性地调节细胞黏附机制的多个分子组成部分,这使这些 microRNAs 具有作为黏附相关过程关键调节剂的能力。这反过来又对我们理解细胞黏附的基础生物学和多种病理状况的病因学具有重要意义。