Department of Dermatology, University Hospital of Cologne, 50937 Cologne, Germany.
J Biol Chem. 2011 Jan 21;286(3):1911-8. doi: 10.1074/jbc.M110.149864. Epub 2010 Nov 17.
The nidogen-laminin interaction is proposed to play a key role in basement membrane (BM) assembly. However, though there are similarities, the phenotypes in mice lacking nidogen 1 and 2 (nidogen double null) differ to those of mice lacking the nidogen binding module (γ1III4) of the laminin γ1 chain. This indicates different cell- and tissue-specific functions for nidogens and their interaction with laminin and poses the question of whether the phenotypes in nidogen double null mice are caused by the loss of the laminin-nidogen interaction or rather by other unknown nidogen functions. To investigate this, we analyzed BMs, in particular those in the skin of mice lacking the nidogen binding module. In contrast to nidogen double null mice, all skin BMs in γ1III4-deficient mice appeared normal. Furthermore, although nidogen 1 deposition was strongly reduced, nidogen 2 appeared unchanged. Mice with additional deletion of the laminin γ3 chain, which contains a γ1-like nidogen binding module, showed a further reduction of nidogen 1 in the dermoepidermal BM; however, this again did not affect nidogen 2. This demonstrates that in vivo only nidogen 1 deposition is critically dependent on the nidogen binding modules of the laminin γ1 and γ3 chains, whereas nidogen 2 is independently recruited either by binding to an alternative site on laminin or to other BM proteins.
内格根-层粘连蛋白相互作用被认为在基底膜(BM)组装中起关键作用。然而,尽管存在相似之处,但缺乏内格根 1 和 2(内格根双重缺失)的小鼠表型与缺乏层粘连蛋白γ1 链的内格根结合模块(γ1III4)的小鼠表型不同。这表明内格根及其与层粘连蛋白的相互作用具有不同的细胞和组织特异性功能,并提出了内格根双重缺失小鼠的表型是由层粘连蛋白-内格根相互作用的丧失引起的,还是由其他未知的内格根功能引起的问题。为了研究这一点,我们分析了基底膜,特别是缺乏内格根结合模块的小鼠皮肤中的基底膜。与内格根双重缺失的小鼠相反,γ1III4 缺陷小鼠的所有皮肤 BM 似乎都正常。此外,尽管内格根 1 的沉积明显减少,但内格根 2 似乎没有变化。另外缺失含有γ1 样内格根结合模块的层粘连蛋白 γ3 链的小鼠,在真皮表皮 BM 中内格根 1 的沉积进一步减少;然而,这也没有影响内格根 2。这表明,在体内只有内格根 1 的沉积严重依赖于层粘连蛋白 γ1 和 γ3 链的内格根结合模块,而内格根 2 则通过与层粘连蛋白的替代结合位点或其他 BM 蛋白结合而被独立募集。