Guerry-Force M L, Perkett E A, Brigham K L, Meyrick B
Department of Pathology, Vanderbilt University Medical Center, Nashville, Tennessee 37232.
Radiat Res. 1988 Apr;114(1):138-53.
Using a large animal model of radiation lung injury--the sheep exposed to bilateral thoracic irradiation--we have recently shown the development of sustained pulmonary hypertension during the first 4 weeks following radiation. This is the period prior to the onset of pneumonitis and pulmonary fibrosis. In the present study, we have examined biopsy and autopsy lung tissue from these same sheep and assessed the sequential changes in lung morphology. Six unanesthetized sheep received bilateral thoracic irradiation (a total of 15 Gy); control sheep were sham irradiated. Lung biopsy tissue was taken prior to and at weekly or biweekly intervals during the 4 weeks immediately following radiation. The lungs were also removed at autopsy for light and electron microscopic examination. Our results show early (Week 1) interstitial and progressive intraalveolar edema accompanied by endothelial and epithelial injury. A gradual increase in number of interstitial mononuclear cells was evident from Week 1, both in the lung tissue and in perivascular cuffs. The number of peripheral lung interstitial mononuclear cells was twice baseline from Week 3 and included accumulation of lymphocytes, fibroblasts, and intravascular macrophages. The increased numbers of mononuclear cells paralleled the development of chronic pulmonary hypertension, perhaps suggesting their involvement in the pathogenesis of this disease. Alternatively, it may be that increased mononuclear cell number represents a stage of lung repair.
利用辐射性肺损伤的大型动物模型——双侧胸部接受照射的绵羊,我们最近发现,在辐射后的前4周会出现持续性肺动脉高压。这是肺炎和肺纤维化发病之前的时期。在本研究中,我们检查了这些绵羊的活检和尸检肺组织,并评估了肺形态的连续变化。6只未麻醉的绵羊接受双侧胸部照射(共15 Gy);对照绵羊接受假照射。在辐射后的4周内,于辐射前以及每周或每两周的间隔时间采集肺活检组织。还在尸检时取出肺进行光镜和电镜检查。我们的结果显示,早期(第1周)出现间质性和进行性肺泡水肿,并伴有内皮和上皮损伤。从第1周开始,肺组织和血管周围袖套中间质单核细胞数量逐渐增加。从第3周起,肺外周间质单核细胞数量是基线的两倍,其中包括淋巴细胞、成纤维细胞和血管内巨噬细胞的积聚。单核细胞数量的增加与慢性肺动脉高压的发展平行,这或许表明它们参与了该疾病的发病机制。或者,单核细胞数量增加可能代表肺修复的一个阶段。