Phillips G D, Whitehead R A, Stone A M, Ruebel M W, Goodkin M L, Knighton D R
Department of Surgery, University of Minnesota, Minneapolis.
J Submicrosc Cytol Pathol. 1993 Apr;25(2):149-55.
The object of this study was to examine the initiation and pattern of corneal angiogenesis stimulated by transforming growth factor beta (TGF-B) using scanning electron microscopy (SEM) of vascular corrosion casts and transmission electron microscopy (TEM). Fifty nanograms of TGF-B was combined with the slow release polymer Hydron and implanted in the rabbit cornea as an assay for angiogenic activity. Two and 7 days after implantation, the corneas were removed for TEM. At the same time intervals the limbal vasculature was filled with Mercox, an acrylic monomer. After the Mercox hardened, the tissue was digested with alternating immersions in 40% KOH and distilled water. The resulting casts were air-dried, sputter coated with gold and viewed with the scanning electron microscope. TEM revealed that 2 days after implantation, TGF-B elicited an influx of a vast number of inflammatory cells, which at two days were predominantly neutrophils. By 7 days the inflammation had subsided and typical capillaries were seen between the collagenous laminae of the normally avascular corneal stroma. SEM of vascular corrosion casts showed evidence of margination/diapedesis of leukocytes from the limbal venules 2 days post-implantation. In addition, the casts from the 7 day time point showed that new vessels arose solely from limbal venules.
本研究的目的是利用血管铸型扫描电子显微镜(SEM)和透射电子显微镜(TEM)来检测转化生长因子β(TGF-B)刺激角膜血管生成的起始过程和模式。将50纳克TGF-B与缓释聚合物Hydron混合,并植入兔角膜中作为血管生成活性的检测方法。植入后2天和7天,取出角膜进行TEM检查。在相同的时间间隔,用丙烯酸单体Mercox填充角膜缘血管系统。Mercox硬化后,组织交替浸泡在40%氢氧化钾和蒸馏水中进行消化。将得到的铸型空气干燥,溅射镀上金,并用扫描电子显微镜观察。TEM显示,植入后2天,TGF-B引发大量炎性细胞流入,此时主要是中性粒细胞。到7天时,炎症消退,在正常无血管的角膜基质胶原板层之间可见典型的毛细血管。血管铸型的SEM显示,植入后2天有白细胞从角膜缘小静脉游出/渗出的迹象。此外,7天时间点的铸型显示新血管仅起源于角膜缘小静脉。