Wang Junru, Zheng Huaien, Ou Xuemei, Fink Louis M, Hauer-Jensen Martin
Department of Surgery, University of Arkansas for Medical Sciences and Central Arkansas Veterans Healthcare System, Little Rock, Arkansas 72205, USA.
Am J Pathol. 2002 Jun;160(6):2063-72. doi: 10.1016/S0002-9440(10)61156-X.
Microvascular injury is believed to be mechanistically involved in radiation fibrosis, but direct molecular links between endothelial dysfunction and radiation fibrosis have not been established in vivo. We examined radiation-induced changes in endothelial thrombomodulin (TM) and protease-activated receptor-1 (PAR-1) in irradiated intestine, and their relationship to structural, cellular, and molecular aspects of radiation injury. Rat small intestine was locally exposed to fractionated X-radiation. Structural injury was assessed 24 hours and 2, 6, and 26 weeks after the last radiation fraction using quantitative histology and morphometry. TM, neutrophils, transforming growth factor-beta, and collagens I and III were assessed by quantitative immunohistochemistry. PAR-1 protein was localized immunohistochemically, and cells expressing TM or PAR-1 transcript were identified by in situ hybridization. Steady-state PAR-1 mRNA levels in intestinal smooth muscle were determined using laser capture microdissection and competitive reverse transcriptase-polymerase chain reaction. Radiation caused a sustained, dose-dependent decrease in microvascular TM. The number of TM-positive vessels correlated with all parameters of radiation enteropathy and, after adjusting for radiation dose and observation time in a statistical model, remained independently associated with neutrophil infiltration, intestinal wall thickening, and collagen I accumulation. PAR-1 immunoreactivity and transcript increased in vascular and intestinal smooth muscle cells in irradiated intestine. PAR-1 mRNA increased twofold in irradiated intestinal smooth muscle. Intestinal irradiation up-regulates PAR-1 and causes a dose-dependent, sustained deficiency of microvascular TM that is independently associated with the severity of radiation toxicity. Interventions aimed at preserving or restoring endothelial TM or blocking PAR-1 should be explored as strategies to increase the therapeutic ratio in clinical radiation therapy.
微血管损伤被认为在机制上与放射性纤维化有关,但内皮功能障碍与放射性纤维化之间的直接分子联系尚未在体内得到证实。我们研究了辐射诱导的受照肠道内皮血栓调节蛋白(TM)和蛋白酶激活受体-1(PAR-1)的变化,以及它们与辐射损伤的结构、细胞和分子方面的关系。将大鼠小肠局部暴露于分次X射线辐射。在最后一次辐射分次后24小时、2周、6周和26周,使用定量组织学和形态计量学评估结构损伤。通过定量免疫组织化学评估TM、中性粒细胞、转化生长因子-β以及I型和III型胶原蛋白。通过免疫组织化学定位PAR-1蛋白,并通过原位杂交鉴定表达TM或PAR-1转录本的细胞。使用激光捕获显微切割和竞争性逆转录聚合酶链反应测定肠道平滑肌中PAR-1 mRNA的稳态水平。辐射导致微血管TM持续、剂量依赖性降低。TM阳性血管的数量与放射性肠炎的所有参数相关,并且在统计模型中调整辐射剂量和观察时间后,仍与中性粒细胞浸润、肠壁增厚和I型胶原蛋白积累独立相关。PAR-1免疫反应性和转录本在受照肠道的血管和平滑肌细胞中增加。受照肠道平滑肌中PAR-1 mRNA增加了两倍。肠道辐射上调PAR-1并导致微血管TM剂量依赖性、持续性缺乏,这与放射毒性的严重程度独立相关。应探索旨在保留或恢复内皮TM或阻断PAR-1的干预措施,作为提高临床放射治疗治疗增益比的策略。