Dubin D, Peters J H, Brown L F, Logan B, Kent K C, Berse B, Berven S, Cercek B, Sharifi B G, Pratt R E
Department of Pathology, Beth Israel Hospital, Boston, MA 02215, USA.
Arterioscler Thromb Vasc Biol. 1995 Nov;15(11):1958-67. doi: 10.1161/01.atv.15.11.1958.
Fibronectins (FNs) comprise a family of adhesive extracellular matrix proteins that arise by alternative splicing in three regions: V (IIICS), EIIIA (ED-A), and EIIIB (ED-B). FNs bearing the EIIIA and EIIIB segments are prevalent during embryogenesis, expressed to lesser degrees in normal adult tissues, and may be locally reexpressed at adult tissue injury. RNase mapping shows that normal rat arteries express low levels of FNs that are predominantly EIIIA- and EIIIB-. Following balloon injury, arterial walls produce increased total levels of FN transcripts that preferentially include both the EIIIA and EIIIB segments. However, despite inducing increased total FN mRNA, balloon injury does not alter the relative composition of V120+, V95+, AND V0 spliced forms. In situ hybridization reveals that as early as 4 days after injury medial cells express increased total FN mRNA, and by 7 days substantial neointimal and focal medial synthesis of EIIIA+, EIIIB+, and V120+ FNs occurs; macrophages do not significantly contribute to this observed vascular FN synthesis. Consistent with the mRNA data, immunofluorescence microscopic analysis reveals increased deposition of EIIIB+ and V+ FN protein forms in injured arterial walls, particularly within the neointima. Our results suggest that local synthesis of specific FN isoforms is important to the neointimal formation that ensues after balloon injury.
纤连蛋白(FNs)是一类具有黏附性的细胞外基质蛋白家族,通过在三个区域(V区(IIICS)、EIIIA区(ED - A)和EIIIB区(ED - B))进行可变剪接产生。带有EIIIA和EIIIB片段的FNs在胚胎发育过程中普遍存在,在正常成年组织中表达程度较低,并且在成年组织损伤时可能会局部重新表达。核糖核酸酶图谱分析显示,正常大鼠动脉表达低水平的FNs,主要是EIIIA - 和EIIIB - 型。球囊损伤后,动脉壁产生的FN转录本总水平增加,且优先包含EIIIA和EIIIB片段。然而,尽管球囊损伤诱导了FN mRNA总水平的增加,但并未改变V120 +、V95 +和V0剪接形式的相对组成。原位杂交显示,损伤后最早4天,中膜细胞表达的FN mRNA总量增加,到7天时,新内膜和局部中膜大量合成EIIIA +、EIIIB +和V120 +型FNs;巨噬细胞对观察到的血管FN合成没有显著贡献。与mRNA数据一致,免疫荧光显微镜分析显示,损伤动脉壁中EIIIB +和V +型FN蛋白形式的沉积增加,特别是在新内膜内。我们的结果表明,特定FN异构体的局部合成对球囊损伤后随之而来的新内膜形成很重要。