Rongish B J, Hinchman G, Doty M K, Baldwin H S, Tomanek R J
Department of Anatomy, University of Iowa, Iowa City, USA.
J Mol Cell Cardiol. 1996 Oct;28(10):2203-15. doi: 10.1006/jmcc.1996.0212.
The main goal of this study was to determine the temporal and spatial relationship of several components of the extracellular matrix (ECM) to coronary vascularization during prenatal and early postnatal development. Rat microvessels were visualized by immunolabeling for platelet endothelial cell adhesion molecule (PECAM-1), and by exposure to the lectin from Griffonia simplicifolia I. Coronary vasculogenesis, which first occurs in gestation day 13 (E13) hearts, was preceded by the deposition of fibronectin. The onset of laminin immunoreactivity in basement membranes coincided with tube formation and was followed by the appearance of collagen IV. Discontinuous collagen IV staining of basement membranes typified early tube formation but progressed to completely encircle capillaries. Sparse staining of collagen I and III was observed in prenatal hearts, but increased after birth. Staining for both molecules was limited mainly to the adventitia of vessels larger than capillaries, and as a component of septa and the epicardium. To determine the effects of loading conditions on key ECM molecules relating to neovascularization, avascular E12 rat hearts were grafted to the anterior eye chamber of adult hosts. In these hearts, which are hemodynamically unloaded, the appearance and distribution of ECM components were similar to hearts developing in utero. It was concluded that during heart development: (1) fibronectin may provide a primary scaffolding for the migration of primordial endothelial cells/angioblasts; (2) tube formation coincides with lamin deposition and is closely followed by the appearance of collagen IV; (3) collagens I and III are not related to tube formation in the prenatal heart; and (4) the relationship of the ECM to vessel formation is not notably altered in the absence of a ventricular load. Furthermore the early onset of PECAM-1 immunoreactivity suggests that it is a useful endothelial marker and may play a role in tube formation.
本研究的主要目的是确定细胞外基质(ECM)的几个成分在产前和产后早期发育过程中与冠状动脉血管形成的时空关系。通过对血小板内皮细胞黏附分子(PECAM-1)进行免疫标记以及用来自西非豆(Griffonia simplicifolia I)的凝集素处理,使大鼠微血管可视化。冠状动脉血管生成首先发生在妊娠第13天(E13)的心脏中,在此之前有纤连蛋白的沉积。基底膜中层粘连蛋白免疫反应性的出现与血管形成同时发生,随后出现IV型胶原。基底膜IV型胶原的间断染色是早期血管形成的典型特征,但随后发展为完全环绕毛细血管。在产前心脏中观察到I型和III型胶原的稀疏染色,但出生后增加。这两种分子的染色主要局限于大于毛细血管的血管外膜,以及作为间隔和心外膜的组成部分。为了确定负荷条件对与新生血管形成相关的关键ECM分子的影响,将无血管的E12大鼠心脏移植到成年宿主的前房。在这些血液动力学上无负荷的心脏中,ECM成分的出现和分布与子宫内发育的心脏相似。得出的结论是,在心脏发育过程中:(1)纤连蛋白可能为原始内皮细胞/成血管细胞的迁移提供主要支架;(2)血管形成与层粘连蛋白沉积同时发生,随后紧接着出现IV型胶原;(3)I型和III型胶原与产前心脏中的血管形成无关;(4)在没有心室负荷的情况下,ECM与血管形成的关系没有明显改变。此外,PECAM-1免疫反应性的早期出现表明它是一种有用的内皮标记物,可能在血管形成中起作用。