Valcourt Ulrich, Alcaraz Lindsay B, Exposito Jean-Yves, Lethias Claire, Bartholin Laurent
a Inserm U1052, Centre de Recherche en Cancérologie de Lyon , Lyon , France.
Cell Adh Migr. 2015;9(1-2):154-65. doi: 10.4161/19336918.2014.994893.
Tenascin-X is the largest member of the tenascin (TN) family of evolutionary conserved extracellular matrix glycoproteins, which also comprises TN-C, TN-R and TN-W. Among this family, TN-X is the only member described so far to exert a crucial architectural function as evidenced by a connective tissue disorder (a recessive form of Ehlers-Danlos syndrome) resulting from a loss-of-function of this glycoprotein in humans and mice. However, TN-X is more than an architectural protein, as it displays features of a matricellular protein by modulating cell adhesion. However, the cellular functions associated with the anti-adhesive properties of TN-X have not yet been revealed. Recent findings indicate that TN-X is also an extracellular regulator of signaling pathways. Indeed, TN-X has been shown to regulate the bioavailability of the Transforming Growth Factor (TGF)-β and to modulate epithelial cell plasticity. The next challenges will be to unravel whether the signaling functions of TN-X are functionally linked to its matricellular properties.
腱生蛋白-X是腱生蛋白(TN)家族中最大的成员,该家族是进化保守的细胞外基质糖蛋白家族,还包括TN-C、TN-R和TN-W。在这个家族中,TN-X是迄今为止描述的唯一发挥关键结构功能的成员,这一点在人类和小鼠中因这种糖蛋白功能丧失导致的结缔组织疾病(埃勒斯-当洛综合征的隐性形式)中得到了证明。然而,TN-X不仅仅是一种结构蛋白,因为它通过调节细胞黏附表现出基质细胞蛋白的特征。然而,与TN-X抗黏附特性相关的细胞功能尚未被揭示。最近的研究结果表明,TN-X也是信号通路的细胞外调节因子。事实上,TN-X已被证明可调节转化生长因子(TGF)-β的生物利用度并调节上皮细胞可塑性。接下来的挑战将是弄清楚TN-X的信号功能是否在功能上与其基质细胞特性相关联。