Wewer U M, Wayner E A, Hoffstrom B G, Lan F, Meyer-Nielsen B, Engvall E, Albrechtsen R
Laboratory of Molecular Pathology, University Institute of Pathological Anatomy, Copenhagen, Denmark.
Lab Invest. 1994 Nov;71(5):719-30.
The laminins are heterotrimeric basement membrane glycoproteins. Eight subunits that can be assembled into laminins have been characterized and are known as: A, B1, B2, S, M, K, B2t, B1k laminin chains. Although many neoplastic cells secrete laminins and some of them even assemble basement membranes, the pattern of production of various laminin subunits remains to be explored.
The expression of laminin was examined in several human carcinoma cells using a panel of specific cDNA probes as well as polyclonal and chain specific monoclonal antibodies. For this purpose a human laminin S chain 2 kb cDNA was isolated and characterized and used together with existing probes for laminin chains.
All carcinoma cell lines had a high level of expression of three light chains (B1, S and B2) mRNA. In contrast, the heavy chains of laminin, A and M, were expressed in negligible amounts as detected by Northern blotting and PCR. The only exception was the HU-1 lung adenocarcinoma cell line which expressed significant quantities of laminin M chain mRNA and lower levels of laminin A chain mRNA. The presence in the HU-1 cells of translated polypeptides was demonstrated by immunofluorescence staining. The cells contained both B1 and S chain laminin in the cell layer, but preferentially secreted the B1 chain into the culture supernatant as shown by Western blotting. The 300 to 400 kDa M chain immunoreactive band was found in laminin secreted into the culture medium of HU-1 cells. Immunoprecipitation of biosynthetically labeled proteins showed that the M chain was synthesized as a complex with B chains. Little or no A chain laminin was detected in the culture medium supernatant. HU-1 cells also synthesized the newly described laminin variant, epiligrin which was secreted into the medium. Thus, the HU-1 cells secreted two laminin variants: M-B1-B12 laminin and epiligrin into the culture medium. Immunostaining of HU-1 nude mice tumors showed that tumor basement membranes contained M, B1, and B2 laminin and epiligrin immunoreactivity but apparently no S chain.
All human carcinoma cell lines produced laminin chains B1, B2 and S, but no or little A or M. The only exception was the lung carcinoma cell line HU-1. Human HU-1 carcinoma cells in culture synthesize several homologous laminin chains and regulate the process of assembly, secretion and deposition of laminin variants into tumor basement membranes. These data indicate that the tumor cells vary among themselves with regards to laminin production and that some of them, like HU-1 may produce essentially all laminin chains simultaneously.
层粘连蛋白是异源三聚体基底膜糖蛋白。已鉴定出可组装成层粘连蛋白的8个亚基,分别称为:A、B1、B2、S、M、K、B2t、B1k层粘连蛋白链。尽管许多肿瘤细胞分泌层粘连蛋白,其中一些甚至能组装基底膜,但各种层粘连蛋白亚基的产生模式仍有待探索。
使用一组特异性cDNA探针以及多克隆和链特异性单克隆抗体,检测了几种人癌细胞中层粘连蛋白的表达。为此,分离并鉴定了一个2kb的人层粘连蛋白S链cDNA,并将其与现有的层粘连蛋白链探针一起使用。
所有癌细胞系中三种轻链(B1、S和B2)mRNA均有高水平表达。相比之下,通过Northern印迹法和PCR检测发现,层粘连蛋白的重链A和M表达量极低。唯一的例外是HU-1肺腺癌细胞系,其表达大量层粘连蛋白M链mRNA和较低水平的层粘连蛋白A链mRNA。免疫荧光染色证明HU-1细胞中存在翻译后的多肽。细胞层中同时含有B1链和S链层粘连蛋白,但如Western印迹所示,细胞优先将B1链分泌到培养上清液中。在HU-1细胞培养基分泌的层粘连蛋白中发现了300至400kDa的M链免疫反应带。对生物合成标记蛋白的免疫沉淀显示,M链是与B链形成复合物合成的。在培养基上清液中几乎检测不到或未检测到A链层粘连蛋白。HU-1细胞还合成了新描述的层粘连蛋白变体表皮整联配体蛋白,并分泌到培养基中。因此,HU-1细胞向培养基中分泌了两种层粘连蛋白变体:M-B1-B12层粘连蛋白和表皮整联配体蛋白。对HU-1裸鼠肿瘤的免疫染色显示,肿瘤基底膜含有M、B1和B2层粘连蛋白以及表皮整联配体蛋白免疫反应性,但显然没有S链。
所有人癌细胞系均产生层粘连蛋白链B1、B2和S,但不产生或很少产生A或M。唯一的例外是肺癌细胞系HU-1。培养的人HU-1癌细胞合成几种同源层粘连蛋白链,并调节层粘连蛋白变体组装、分泌和沉积到肿瘤基底膜的过程。这些数据表明,肿瘤细胞在层粘连蛋白产生方面彼此不同,其中一些细胞,如HU-1,可能同时产生基本上所有的层粘连蛋白链。