Krieg T, Müller P K
Exp Cell Biol. 1977;45(3-4):207-21.
Tissue specimen of the aorta was obtained from a patient with Marfan's syndrome after heart surgery. Media and adventitia were carefully separated and subsequently used for biochemical characterization. Aortas from an embryonic calf and from a human adult were used as internal controls. The data clearly indicated that an insufficient synthesis of type I collagen rather than a defect in the formation of cross-links may be the prime cause in this inherited connective tissue disorder. Such a disturbance in the regulation of the genes coding for the different collagen chains may explain the weakness and enhanced extensibility of the blood vessels finally resulting in an aneurysm.
取自一名马凡氏综合征患者心脏手术后的主动脉组织标本。仔细分离中膜和外膜,随后用于生化特性分析。取自胚胎小牛和成年人类的主动脉用作内部对照。数据清楚地表明,I型胶原蛋白合成不足而非交联形成缺陷可能是这种遗传性结缔组织疾病的主要原因。编码不同胶原链的基因调控中的这种紊乱可能解释血管的脆弱性和增强的伸展性,最终导致动脉瘤。