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收缩性胶原晶格中细胞生物合成活性的调节

Modulation of cellular biosynthetic activity in the retracting collagen lattice.

作者信息

Paye M, Nusgens B V, Lapière C M

机构信息

Institute of Pathology, University of Liège, Belgium.

出版信息

Eur J Cell Biol. 1987 Dec;45(1):44-50.

PMID:3443111
Abstract

When included in a free floating collagen lattice, several types of cells and fibroblasts attach to the collagen polymers, retract the gel, and their biosynthetic activity is repressed. Under similar conditions transformed pulmonary epithelial rat (PER) cells are unable to attach to the fibers and to significantly retract the lattice. Retraction can be induced by adding fibronectin (fn) and factor XIII (FXIII) together. This effect is fibronectin dose dependent and observed with a maximum efficiency for FXIII concentrations of 0.1 U/ml and above. Fibronectin or FXIII alone has only a limited effect on retraction. This experimental model allowed us to study the biosynthetic activity of PER cells under various degrees of cell interaction (control less than FXIII less than fn less than fn + FXIII) with their three-dimensional collagen support. The more the cells interacted with their support and retracted the gel, the more protein and collagen synthesis were reduced. This effect was observed for the products deposited in the cell layer and for those released in the medium. Increasing collagen concentration in a nonretracting lattice to a final density obtained in a maximally retracted lattice resulted in a much lower repression of biosynthetic activity. Fn and FXIII added at the same concentrations in monolayer cultures did not produce significant modification in biosynthetic activities. We propose that the regulation of the biosynthetic activity of adherent cells contracting the lattice is related to mechanical information resulting from the interactions between the cells and their support.

摘要

当包含在自由漂浮的胶原晶格中时,几种类型的细胞和成纤维细胞会附着在胶原聚合物上,使凝胶收缩,并且它们的生物合成活性受到抑制。在类似条件下,转化的大鼠肺上皮(PER)细胞无法附着在纤维上,也无法使晶格显著收缩。通过同时添加纤连蛋白(fn)和凝血因子 XIII(FXIII)可诱导收缩。这种效应呈纤连蛋白剂量依赖性,在 FXIII 浓度为 0.1 U/ml 及以上时观察到最大效率。单独的纤连蛋白或 FXIII 对收缩的影响有限。这个实验模型使我们能够研究 PER 细胞在与三维胶原支架不同程度的细胞相互作用(对照<FXIII<fn<fn + FXIII)下的生物合成活性。细胞与支架相互作用并使凝胶收缩的程度越大,蛋白质和胶原合成减少得就越多。在细胞层中沉积的产物以及在培养基中释放的产物都观察到了这种效应。将非收缩晶格中的胶原浓度增加到最大收缩晶格中获得的最终密度,导致生物合成活性的抑制要低得多。在单层培养中以相同浓度添加的 fn 和 FXIII 对生物合成活性没有产生显著影响。我们提出,收缩晶格的贴壁细胞生物合成活性的调节与细胞与其支架之间相互作用产生的机械信息有关。

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