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Quantitative assessment of the age of fibrotic lesions using polarized light microscopy and digital image analysis.

机译:使用偏光显微镜和数字图像分析定量评估纤维化病变的年龄。

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摘要

Reliable histologic methods for gauging the maturity of fibrotic lesions are limited, making interventions in the healing process difficult to assess. As collagen ages there is enhanced birefringence due to increased molecular and fibrillar organization. The purpose of this study was to develop a microscopal technique to quantify this process and to determine its ability to distinguish scars of varying ages. Fibrosis in the rat gracilis muscle was studied 5 to 63 days after superficial injury. Sections were stained with picrosirius red and illuminated with monochromatic, polarized light. The microscope fields were digitized using a computer-video system yielding an image in which noncollagenous material was dark (gray level 0) and collagen was depicted by grey levels 1 to 255. In the fibrosis model used, the collagen area fraction plateaued at 80% by day 21. The median collagen grey level increased progressively as the scar aged. It is concluded that this histologic, nondestructive technique can reliably quantify age-related optical properties of fibrotic collagen and that this could be used to determine the maturity of fibrotic lesions.
机译:测量纤维化病变成熟度的可靠组织学方法是有限的,这使得难以评估愈合过程中的干预措施。随着胶原蛋白的老化,由于分子和原纤维组织的增加,双折射增强。这项研究的目的是开发一种显微技术,以量化该过程并确定其区分不同年龄疤痕的能力。浅表损伤后5至63天研究了大鼠腹肌的纤维化。切片用picrosirius红色染色,并用单色偏振光照射。使用计算机视频系统对显微镜视野进行数字化处理,得到的图像中非胶原材料较暗(灰色级别0),而胶原蛋白的灰度级别为1至255。在所使用的纤维化模型中,胶原蛋白面积分数稳定在80%到第21天,随着疤痕的老化,胶原蛋白的中位灰度值逐渐增加。结论是,这种组织学,非破坏性技术可以可靠地量化与年龄相关的纤维化胶原蛋白的光学特性,并且可以用于确定纤维化病变的成熟度。

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