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肺胶原异质性。培养的兔和人肺细胞合成I型和III型胶原。

Lung collagen heterogeneity. Synthesis of type I and type III collagen by rabbit and human lung cells in culture.

作者信息

Hance A J, Bradley K, Crystal R G

出版信息

J Clin Invest. 1976 Jan;57(1):102-11. doi: 10.1172/JCI108250.

Abstract

The fetal and adult lung have a constant level of collagen synthesis that represents 4-5% of the total amino acids incorporated into lung protein. Prior studies have demonstrated that this collagen is not homogeneous but rather is composed of at least two collagen types, I and II, each localized to specific lung structures. Although it is known that explants of rabit lung parenchyma and blood vessels synthesize type I collagen and that rabbit lung tracheobronchial tree synthesizes type II collagen, it has been suggested that other collagen types are present in lung. It is not known which cells are responsible for the synthesis of any lung collagen type. To approach the problem of additional lung collagen heterogeneity and the identification of the cells responsible for lung collagen synthesis, techniques were developed to examine collagen synthesized by lung cells in culture. 10-15% of the proteins synthesized by confluent cultures of rabbit lung cells and fetal human lung fibroblasts are collagen. Separation and purification of this collagen by ion-exchange chromatography and cyanogen bromide (CNBr) peptide mapping techniques indicate that collagen secreted by these cells is composed of two collagen types, I and III. The CNBr peptides of type I collagen secreted by these cells are identical to the CNBr peptides of type I collagen synthesized by lung parenchyma and blood vessels. The peptides of type III collagen secreted by these cells are identical to fetal skin type III collagen CNBr peptides. The existence of 40 cell types and the insolubility of lung collagen increase the complexity of identifying the types of collagen in lung and the cells responsible for the synthesis of each type. The techniques described here should eventually lead to a complete description of the synthesis and composition of lung collagen, thus providing a probe to understand the role of collagen in lung development and structure in health and disease.

摘要

胎儿和成人肺中的胶原蛋白合成水平恒定,占掺入肺蛋白的总氨基酸的4-5%。先前的研究表明,这种胶原蛋白并非均质,而是至少由两种胶原蛋白类型组成,即I型和II型,每种类型都定位于特定的肺结构。虽然已知兔肺实质和血管外植体合成I型胶原蛋白,兔肺气管支气管树合成II型胶原蛋白,但有人提出肺中还存在其他胶原蛋白类型。目前尚不清楚哪种细胞负责合成任何一种肺胶原蛋白类型。为了解决肺胶原蛋白额外的异质性问题以及确定负责肺胶原蛋白合成的细胞,人们开发了一些技术来检测培养的肺细胞合成的胶原蛋白。兔肺细胞和胎儿人肺成纤维细胞汇合培养物合成的蛋白质中有10-15%是胶原蛋白。通过离子交换色谱法和溴化氰(CNBr)肽图谱技术对这种胶原蛋白进行分离和纯化表明,这些细胞分泌的胶原蛋白由两种胶原蛋白类型组成,即I型和III型。这些细胞分泌的I型胶原蛋白的CNBr肽与肺实质和血管合成的I型胶原蛋白的CNBr肽相同。这些细胞分泌的III型胶原蛋白的肽与胎儿皮肤III型胶原蛋白的CNBr肽相同。肺中存在40种细胞类型以及肺胶原蛋白的不溶性增加了确定肺中胶原蛋白类型以及负责每种类型合成的细胞的复杂性。这里描述的技术最终应该能够完整地描述肺胶原蛋白的合成和组成,从而为理解胶原蛋白在肺发育以及健康和疾病状态下的结构中的作用提供一个探究工具。

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The biosynthesis of collagen.胶原蛋白的生物合成。
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Lung collagen heterogeneity.肺胶原异质性。
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