Davis E C
Department of Anatomy, McGill University, Montreal, Quebec, Canada.
J Histochem Cytochem. 1995 Nov;43(11):1115-23. doi: 10.1177/43.11.7560894.
The growth and development of elastic laminae in the mouse aortic media were investigated by light and electron microscopic autoradiography after a single SC injection of L-[3,4-3H]-valine. Because of the remarkable stability of elastin, radiolabel incorporated into the elastic laminae during early stages of aortic development can be identified in the mature vessel. Light microscopic autoradiographs of aortae from mice injected with radiolabeled valine at 3, 14, or 21 days of postnatal age and sacrificed at 4 months of age showed silver grains evenly distributed around the circumference of the vessel, suggesting uniform elastic lamina growth. Electron microscopic autoradiographs of aortae from mice injected at 3 and 14 days' postnatal age and killed at 4 months of age showed the elastin initially deposited at 3 days to be in the center of the lamina, whereas the elastin deposited at 14 days remained peripherally located. These observations suggest that elastin deposited early in development does not undergo any significant redistribution during growth of the vessel. Because the aorta continues to increase in diameter after the elastic laminae are essentially complete, the fenestrations in the laminae were investigated as possible sites of further expansion of the laminae. In aortae from mice injected at 3 days and sacrificed at 4 days of postnatal age, the edges of the elastic lamina that border on fenestrations showed a large number of silver grains. Regions of the elastic lamina at some distance from the fenestration, however, appeared to be associated with fewer grains. Results from this study not only present unique observations of elastin deposition in developing elastic laminae but also provide evidence that the fenestrations in the elastic laminae may play a role in their continued expansion during later stages of aortic development.
单次皮下注射L-[3,4-³H]-缬氨酸后,通过光镜和电镜放射自显影术研究了小鼠主动脉中膜弹性板的生长和发育。由于弹性蛋白具有显著的稳定性,在主动脉发育早期掺入弹性板中的放射性标记物在成熟血管中仍可被识别。对出生后3天、14天或21天注射放射性标记缬氨酸并在4个月龄时处死的小鼠主动脉进行光镜放射自显影,结果显示银颗粒均匀分布在血管周围,提示弹性板生长均匀。对出生后3天和14天注射并在4个月龄时处死的小鼠主动脉进行电镜放射自显影,结果显示3天时最初沉积的弹性蛋白位于板层中央,而14天时沉积的弹性蛋白仍位于周边。这些观察结果表明,发育早期沉积的弹性蛋白在血管生长过程中不会发生任何显著的重新分布。由于在弹性板基本完成后主动脉直径仍会继续增加,因此对板层中的窗孔进行了研究,将其作为弹性板进一步扩张的可能部位。在出生后3天注射并在出生后4天处死的小鼠主动脉中,与窗孔相邻的弹性板边缘显示出大量银颗粒。然而,距离窗孔一定距离的弹性板区域似乎银颗粒较少。本研究结果不仅提供了发育中的弹性板中弹性蛋白沉积的独特观察结果,还提供了证据表明弹性板中的窗孔可能在主动脉发育后期的持续扩张中发挥作用。