Carson D D, Tang J P, Julian J, Glasser S R
Department of Biochemistry and Molecular Biology, University of Texas, M. D. Anderson Hospital and Tumor Institute, Houston.
J Cell Biol. 1988 Dec;107(6 Pt 1):2425-35. doi: 10.1083/jcb.107.6.2425.
We have studied proteoglycan secretion using a recently developed system for the preparing of polarized primary cultures of rat uterine epithelial cells. To mimic their native environment better and provide a system for discriminating apical from basolateral compartments, we cultured cells on semipermeable supports impregnated with biomatrix. Keratan sulfate proteoglycans (KSPG) as well as heparan sulfate-containing molecules (HS[PG]) were the major sulfated products synthesized and secreted by these cells. The ability of epithelial cells to secrete KSPG greatly increased in parallel with the development of cell polarity. Furthermore, KSPG secretion occurred preferentially to the apical medium in highly polarized cultures. In contrast, HS(PG) secretion did not increase along with development of polarity, although most HS(PG) (85%) were secreted apically as well. Pulse-chase studies indicated that highly polarized cultures secreted 80-90% of the sulfated macromolecules they synthesized, predominantly to the apical secretory compartment. The half-lives for KSPG and HS(PG) secretion were approximately 3 and 4 h, respectively. Parallel studies of cells cultured on tissue culture plastic-coated with biomatrix indicated that neither the state of confluency nor the biomatrix was primarily responsible for inducing the KSPG secretion observed in polarizing cultures. Experiments with uterine strips indicated that the steroid hormone, 17-beta-estradiol, markedly stimulated synthesis and secretion of sulfated macromolecules, but had no preferential effect on KSPG production. The ratio of KSPG to HS(PG) secretion from uterine strips was similar to that found in the apical medium of highly polarized cell cultures. Thus, the pattern of proteoglycan secretion observed in polarized cell cultures mimicked that observed for uterine cells, although the preferential increase in KSPG production by polarized cells could not be attributed to an estrogen response. Collectively, these studies describe the major sulfated molecules secreted by rat uterine epithelial cells under varying conditions and provide evidence for a novel influence of cell polarity on the cell's ability to secrete sulfated glycoconjugates.
我们使用最近开发的一种系统来制备大鼠子宫上皮细胞的极化原代培养物,以此研究蛋白聚糖的分泌情况。为了更好地模拟其天然环境,并提供一种区分顶端和基底外侧区室的系统,我们将细胞培养在浸渍有生物基质的半透性支持物上。硫酸角质素蛋白聚糖(KSPG)以及含硫酸乙酰肝素的分子(HS[PG])是这些细胞合成和分泌的主要硫酸化产物。上皮细胞分泌KSPG的能力随着细胞极性的发展而大幅增加。此外,在高度极化的培养物中,KSPG优先分泌到顶端培养基中。相比之下,HS(PG)的分泌并未随着极性的发展而增加,尽管大多数HS(PG)(85%)也分泌到顶端。脉冲追踪研究表明,高度极化的培养物分泌了它们合成的80 - 90%的硫酸化大分子,主要分泌到顶端分泌区室。KSPG和HS(PG)分泌的半衰期分别约为3小时和4小时。对培养在涂有生物基质的组织培养塑料上的细胞进行的平行研究表明,汇合状态和生物基质都不是极化培养物中观察到的KSPG分泌的主要诱导因素。对子宫条带的实验表明,类固醇激素17-β-雌二醇显著刺激硫酸化大分子的合成和分泌,但对KSPG的产生没有优先影响。子宫条带中KSPG与HS(PG)分泌之比与高度极化细胞培养物顶端培养基中的情况相似。因此,在极化细胞培养物中观察到的蛋白聚糖分泌模式与子宫细胞中观察到的模式相似,尽管极化细胞中KSPG产生的优先增加不能归因于雌激素反应。总的来说,这些研究描述了大鼠子宫上皮细胞在不同条件下分泌的主要硫酸化分子,并为细胞极性对细胞分泌硫酸化糖缀合物能力的新影响提供了证据。