Mosher D F, Fogerty F J, Chernousov M A, Barry E L
Department of Medicine, University of Wisconsin, Madison 53706.
Ann N Y Acad Sci. 1991;614:167-80. doi: 10.1111/j.1749-6632.1991.tb43701.x.
The results summarized above suggest that assembly of fibronectin is a fundamental biological process and that knowledge of the process of assembly may reveal new ways by which cells interact with extracellular molecules. Deposition of a fibronectin matrix seems to be regulated as tightly as synthesis of fibronectin or expression of adhesion receptors for fibronectin and is influenced profoundly by two products of blood coagulation--TGF-beta released from platelets and factor XIII activated by thrombin. Fibronectin assembly may be important in all sorts of physiological and pathophysiological processes. Cell A--for instance, a stromal cell--can influence the behavior of cell B--for instance, a lymphocyte--by assembling fibronectin made by cell C--for instance, a hepatocyte. We hope that the testable models of assembly presented in this paper will lead to new understanding of the process of assembly and suggest new modalities for treatment of diseases that result in fibrosis, damaged tissues, and neoplastic growth.
上述总结的结果表明,纤连蛋白的组装是一个基本的生物学过程,而对组装过程的了解可能会揭示细胞与细胞外分子相互作用的新方式。纤连蛋白基质的沉积似乎与纤连蛋白的合成或纤连蛋白黏附受体的表达一样受到严格调控,并且受到血液凝固的两种产物——血小板释放的转化生长因子-β和凝血酶激活的因子 XIII 的深刻影响。纤连蛋白的组装在各种生理和病理生理过程中可能都很重要。例如,细胞 A(如基质细胞)可以通过组装细胞 C(如肝细胞)产生的纤连蛋白来影响细胞 B(如淋巴细胞)的行为。我们希望本文中提出的可测试的组装模型将有助于对组装过程有新的理解,并为治疗导致纤维化、组织损伤和肿瘤生长的疾病提出新的治疗方式。