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辐射诱导的少突胶质细胞谱系的神经病理学变化及其相关临床表现和治疗策略。

Radiation-induced neuropathological changes in the oligodendrocyte lineage with relevant clinical manifestations and therapeutic strategies.

机构信息

Radiation Physiology Laboratory, Singapore Nuclear Research and Safety Initiative, National University of Singapore, Singapore, Singapore.

出版信息

Int J Radiat Biol. 2022;98(10):1519-1531. doi: 10.1080/09553002.2022.2055804. Epub 2022 Apr 6.

Abstract

PURPOSE

With technological advancements in radiation therapy for tumors of the central nervous system (CNS), high doses of ionizing radiation can be delivered to the tumors with improved accuracy. Despite the reduction of ionizing radiation-induced toxicity to surrounding tissues of the CNS, a wide array of side effects still occurs, particularly late-delayed changes. These alterations, such as white matter damages and neurocognitive impairments, are often debilitative and untreatable, significantly affecting the quality of life of these patients, especially children. Oligodendrocytes, a major class of glial cells, have been identified to be one of the targets of radiation toxicity and are recognized be involved in late-delayed radiation-induced neuropathological changes. These cells are responsible for forming the myelin sheaths that surround and insulate axons within the CNS. Here, the effects of ionizing radiation on the oligodendrocyte lineage as well as the common clinical manifestations resulting from radiation-induced damage to oligodendrocytes will be discussed. Potential prophylactic and therapeutic strategies against radiation-induced oligodendrocyte damage will also be considered.

CONCLUSION

Oligodendrocytes and oligodendrocyte progenitor cells (OPCs) are radiosensitive cells of the CNS. Here, general responses of these cells to radiation exposure have been outlined. However, several findings have not been consistent across various studies. For instance, cognitive decline in irradiated animals was observed to be accompanied by obvious demyelination or white matter changes in several studies but not in others. Hence, further studies have to be conducted to elucidate the level of contribution of the oligodendrocyte lineage to the development of late-delayed effects of radiation exposure, as well as to classify the dose and brain region-specific responses of the oligodendrocyte lineage to radiation. Several potential therapeutic approaches against late-delayed changes have been discussed, such as the transplantation of OPCs into irradiated regions and implementation of exercise. Many of these approaches show promising results. Further elucidation of the mechanisms involved in radiation-induced death of oligodendrocytes and OPCs would certainly aid in the development of novel protective and therapeutic strategies against the late-delayed effects of radiation.

摘要

目的

随着中枢神经系统(CNS)肿瘤放射治疗技术的进步,可以更精确地向肿瘤提供高剂量的电离辐射。尽管 CNS 周围组织的电离辐射诱导毒性有所降低,但仍会发生广泛的副作用,特别是迟发性改变。这些改变,如白质损伤和神经认知障碍,常常使人衰弱且无法治疗,严重影响这些患者的生活质量,尤其是儿童。少突胶质细胞是一种主要的神经胶质细胞,已被确定为辐射毒性的靶标之一,并且被认为与迟发性辐射诱导的神经病理学变化有关。这些细胞负责形成围绕和隔离中枢神经系统内轴突的髓鞘。在这里,将讨论电离辐射对少突胶质细胞谱系的影响,以及辐射对少突胶质细胞损伤引起的常见临床表现。还将考虑针对辐射诱导的少突胶质细胞损伤的潜在预防和治疗策略。

结论

少突胶质细胞和少突胶质前体细胞(OPC)是中枢神经系统的辐射敏感细胞。在这里,概述了这些细胞对辐射暴露的一般反应。然而,在各种研究中,有几项发现并不一致。例如,在几项研究中,观察到照射动物的认知能力下降伴随着明显的脱髓鞘或白质变化,但在其他研究中则没有。因此,必须进行进一步的研究以阐明少突胶质细胞谱系对辐射暴露后迟发性影响的发展的贡献程度,以及对少突胶质细胞谱系对辐射的剂量和脑区特异性反应进行分类。已经讨论了几种针对迟发性变化的潜在治疗方法,例如将 OPC 移植到照射区域和进行运动。其中许多方法显示出有希望的结果。进一步阐明辐射诱导少突胶质细胞和 OPC 死亡的机制肯定有助于开发针对辐射迟发性效应的新型保护和治疗策略。

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