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Increased expression of connective tissue growth factor (CTGF) in multiple organs after exposure of non-human primates (NHP) to lethal doses of radiation

机译:非人类灵长类动物(NHP)暴露于致命剂量的辐射后多个器官中结缔组织生长因子(CTGF)的表达增加

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摘要

Exposure to sufficiently high doses of ionizing radiation is known to cause fibrosis in many different organs and tissues. Connective tissue growth factor (CTGF/CCN2), a member of the CCN family of matricellular proteins, plays an important role in the development of fibrosis in multiple organs. The aim of the present study was to quantify the gene and protein expression of CTGF in a variety of organs from non-human primates (NHP) that were previously exposed to potentially lethal doses of radiation. Tissues from non-irradiated NHP, and NHP exposed to whole thoracic lung irradiation (WTLI) or partial-body irradiation with 5% bone marrow sparing (PBI/BM5) were examined by real-time quantitative reverse transcription PCR, western blot, and immunohistochemistry. Expression of CTGF was elevated in the lung tissues of NHP exposed to WTLI relative to the lung tissues of the non-irradiated NHP. Increased expression of CTGF was also observed in multiple organs from NHP exposed to PBI/BM5 compared to non-irradiated NHP; these included the lung, kidney, spleen, thymus and liver. These irradiated organs also exhibited histological evidence of increased collagen deposition compared to the control tissues. There was significant correlation of CTGF expression with collagen deposition in the lung and spleen of NHP exposed to PBI/BM5. Significant correlations were observed between spleen and multiple organs on CTGF expression and collagen deposition respectively, suggesting possible crosstalk between spleen and other organs. Our data suggest that CTGF levels are increased in multiple organs after radiation exposure and that inflammatory cell infiltration may contribute to the elevated levels of CTGF in multiple organs.
机译:已知暴露于足够高剂量的电离辐射会在许多不同的器官和组织中引起纤维化。结缔组织生长因子(CTGF / CCN2)是母细胞蛋白CCN家族的成员,在多器官纤维化的发展中起重要作用。本研究的目的是量化先前暴露于潜在致命剂量的非人类灵长类动物(NHP)的各种器官中CTGF的基因和蛋白质表达。通过实时定量逆转录PCR,Western印迹和免疫组织化学检查未辐照的NHP和暴露于全胸肺照射(WTLI)或部分身体照射并保留5%骨髓的NHP(PBI / BM5)的组织。相对于未照射的NHP的肺组织,在暴露于WTLI的NHP的肺组织中CTGF的表达升高。与未辐照的NHP相比,在暴露于PBI / BM5的NHP的多个器官中也观察到CTGF的表达增加;这些包括肺,肾,脾,胸腺和肝脏。与对照组织相比,这些受辐照的器官还表现出胶原沉积增加的组织学证据。暴露于PBI / BM5的NHP的肺和脾脏中CTGF的表达与胶原沉积密切相关。脾脏和多个器官之间分别观察到CTGF表达和胶原沉积的显着相关性,表明脾脏与其他器官之间可能存在串扰。我们的数据表明,辐射暴露后,多个器官的CTGF水平升高,炎症细胞浸润可能导致多个器官CTGF的水平升高。

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