Mecham R P, Lange G, Madaras J, Starcher B
J Cell Biol. 1981 Aug;90(2):332-8. doi: 10.1083/jcb.90.2.332.
Fetal bovine ligamentum nuchae fibroblasts maintained in culture synthesized soluble elastin but were unable to form the insoluble elastic fiber. Secreted elastin precursors accumulated in culture medium and were measured using a radioimmunoassay for elastin. When elastin production was examined in ligament tissue from fetal calves of various gestational ages, cells from tissue taken during the last trimester of development produced significantly more elastin than did cells from younger fetal tissue, with maximal elastin synthesis occurring shortly before birth. Soluble elastin was detected in ligament cells plated at low density until proliferation began to be density inhibited and the cells became quiescent. Also, soluble elastin production per cell declined with increasing population doubling or with age in culture. Cells grown in the presence of 5% fetal calf serum produced approximately four times as much soluble elastin as cells grown in serum-free medium. The addition of dexamethasone (0.1 microM) and bleomycin (1 microgram/ml) increased soluble elastin production by cultured cells 180% and 50%, respectively, whereas theophylline (5 micrograms/ml) depressed production 50% and antagonized stimulation by dexamethasone. Ascorbate (50 micrograms/ml), soybean trypsin inhibitor (1 mg/ml), insulin (100 microunits/ml), and aminoacetonitrile (50 micrograms/ml) had no effect, but cycloheximide at 10(-4) M completely inhibited soluble elastin production. In contrast to cells in culture, ligament tissue minces (ligament cells surrounded by in vivo extracellular matrix) efficiently incorporated soluble elastin precursors into insoluble, cross-linked elastin. In addition, soluble elastin production per cell (per microgram of DNA) was higher in tissue minces than elastin production by cells maintained on plastic. These results suggest a role for extracellular matrix in formation of the elastic fiber and in stabilizing elastin phenotypic expression by ligament fibroblasts. Fibroblasts from the bovine ligamentum nuchae present an excellent model for in vitro studies of elastin biosynthesis.
培养的胎牛项韧带成纤维细胞可合成可溶性弹性蛋白,但无法形成不溶性弹性纤维。分泌的弹性蛋白前体在培养基中积累,可使用弹性蛋白放射免疫测定法进行测量。当检测不同胎龄胎牛韧带组织中的弹性蛋白生成情况时,取自发育最后三个月组织的细胞产生的弹性蛋白明显多于较年轻胎儿组织的细胞,弹性蛋白合成量在出生前不久达到最大值。低密度接种的韧带细胞在增殖开始受到密度抑制且细胞进入静止期之前可检测到可溶性弹性蛋白。此外,每个细胞的可溶性弹性蛋白产量会随着群体倍增次数的增加或培养时间的延长而下降。在含5%胎牛血清的培养基中生长的细胞产生的可溶性弹性蛋白约为无血清培养基中生长细胞的四倍。添加地塞米松(0.1微摩尔/升)和博来霉素(1微克/毫升)可使培养细胞的可溶性弹性蛋白产量分别增加180%和50%,而氨茶碱(5微克/毫升)可使产量降低50%并拮抗地塞米松的刺激作用。抗坏血酸盐(50微克/毫升)、大豆胰蛋白酶抑制剂(1毫克/毫升)、胰岛素(100微单位/毫升)和氨基乙腈(50微克/毫升)无作用,但10⁻⁴摩尔/升的环己酰亚胺可完全抑制可溶性弹性蛋白的产生。与培养的细胞不同,韧带组织碎块(被体内细胞外基质包围的韧带细胞)可有效地将可溶性弹性蛋白前体整合到不溶性的交联弹性蛋白中。此外,组织碎块中每个细胞(每微克DNA)的可溶性弹性蛋白产量高于培养在塑料上的细胞的弹性蛋白产量。这些结果表明细胞外基质在弹性纤维形成以及维持韧带成纤维细胞弹性蛋白表型表达稳定方面发挥作用。牛项韧带成纤维细胞是弹性蛋白生物合成体外研究的理想模型。