Kikuchi H, Amano H, Yamada S
Department of Pharmacology, School of Dentistry, Showa University, Tokyo, Japan.
Cell Tissue Res. 2001 Jan;303(1):93-107. doi: 10.1007/s004410000279.
In a new culture-conditioning system of agar-coated mesenchyme of isolated incisor dental papillae, dentinogenesis has been induced adjacent to an agar substratum that functions as a foothold for cell immobilisation. To elucidate the role of the basement membrane (BM) in dentinogenesis, we have examined the way in which dentinogenesis depends upon BM components or transforming growth factor (TGF)-beta1 in this system. At the mesenchymal-epithelial junction of odontogenic organs (cut incisor tooth germs), TGF-beta1 visibly increased in the BM during incubation. In isolated dental papillae, BM components were synthesised and deposited at aligned peripheral cells of the explants, together with an increasing amount of TGF-beta1. These components were not assembled into extracellular matrix (ECM)-absorbed agar adjacent to explants, although dentinogenesis proceeded in the presence of pericellular BM components associated with TGF-beta1. When signalling via TGF-beta type II receptors was blocked, neither ECM production nor dentinogenesis was observed but explants partially detached from the agar surface, presumably as a result of the suppressed production of ECM, since attachment was retained by pre-coating explants with artificial matrices. Rescue experiments showed that TGF-beta1 regulated dentinogenesis through ECM production. With regard to BM components, inducible dentinogenesis was Arg-Gly-Asp (RGD)-dependent. Thus, pericellular BM components associated with TGF-beta1 and an ECM-absorbed agar substratum, which affects dentinogenesis, synergistically play a role similar to that of BM components in vivo. The BM therefore serves as a structural meshwork that acts as a foothold for cell immobilisation; its components act as ligands for RGD-dependent cell adhesion and it stores TGF-beta1, which regulates ECM production.
在一种新的培养条件系统中,该系统用于培养分离的切牙牙乳头的琼脂包被间充质,牙本质形成已在琼脂基质附近被诱导,该琼脂基质起到细胞固定的支撑作用。为了阐明基底膜(BM)在牙本质形成中的作用,我们研究了在该系统中牙本质形成如何依赖于BM成分或转化生长因子(TGF)-β1。在牙源性器官(切牙牙胚)的间充质-上皮交界处,孵育期间BM中的TGF-β1明显增加。在分离的牙乳头中,BM成分在外植体排列的外周细胞中合成并沉积,同时TGF-β1的量也在增加。尽管在与TGF-β1相关的细胞周围BM成分存在的情况下牙本质形成仍在进行,但这些成分并未组装到与外植体相邻的细胞外基质(ECM)吸收琼脂中。当通过TGF-β II型受体的信号传导被阻断时,既未观察到ECM产生也未观察到牙本质形成,但外植体部分从琼脂表面脱离,推测这是由于ECM产生受抑制所致,因为通过用人造基质预包被外植体可保留附着。拯救实验表明,TGF-β1通过ECM产生调节牙本质形成。关于BM成分,诱导性牙本质形成是依赖精氨酸-甘氨酸-天冬氨酸(RGD)的。因此,与TGF-β1相关的细胞周围BM成分和影响牙本质形成的ECM吸收琼脂基质协同发挥类似于体内BM成分的作用。因此,BM作为一种结构网络,起到细胞固定的支撑作用;其成分作为RGD依赖性细胞黏附的配体,并且它储存调节ECM产生的TGF-β1。