Chiu Gabriel S, Boukelmoune Nabila, Chiang Angie C A, Peng Bo, Rao Vikram, Kingsley Charles, Liu Ho-Ling, Kavelaars Annemieke, Kesler Shelli R, Heijnen Cobi J
Neuroimmunology Laboratory, Department of Symptom Research, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Department of Bioinformatics and Computational Biology, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Oncotarget. 2018 Oct 30;9(85):35581-35597. doi: 10.18632/oncotarget.26272.
Cognitive impairments are a common side effect of chemotherapy that often persists long after treatment completion. There are no FDA-approved interventions to treat these cognitive deficits also called 'chemobrain'. We hypothesized that nasal administration of mesenchymal stem cells (MSC) reverses chemobrain. To test this hypothesis, we used a mouse model of cognitive deficits induced by cisplatin that we recently developed. Mice were treated with two cycles of cisplatin followed by nasal administration of MSC. Cisplatin treatment induced deficits in the puzzle box, novel object/place recognition and Y-maze tests, indicating cognitive impairment. Nasal MSC treatment fully reversed these cognitive deficits in males and females. MSC also reversed the cisplatin-induced damage to cortical myelin. Resting state functional MRI and connectome analysis revealed a decrease in characteristic path length after cisplatin, while MSC treatment increased path length in cisplatin-treated mice. MSCs enter the brain but did not survive longer than 12-72 hrs, indicating that they do not replace damaged tissue. RNA-sequencing analysis identified mitochondrial oxidative phosphorylation as a top pathway activated by MSC administration to cisplatin-treated mice. Consistently, MSC treatment restored the cisplatin-induced mitochondrial dysfunction and structural abnormalities in brain synaptosomes. Nasal administration of MSC did not interfere with the peripheral anti-tumor effect of cisplatin. In conclusion, nasal administration of MSC may represent a powerful, non-invasive, and safe regenerative treatment for resolution of chemobrain.
认知障碍是化疗常见的副作用,常在治疗结束后长期持续存在。目前尚无美国食品药品监督管理局(FDA)批准的干预措施来治疗这些认知缺陷,即所谓的“化疗脑”。我们假设经鼻给予间充质干细胞(MSC)可逆转化疗脑。为验证这一假设,我们使用了我们最近建立的顺铂诱导的小鼠认知缺陷模型。小鼠接受两个周期的顺铂治疗,随后经鼻给予MSC。顺铂治疗导致在迷宫箱、新物体/新位置识别和Y迷宫测试中出现缺陷,表明存在认知障碍。经鼻给予MSC可完全逆转雄性和雌性小鼠的这些认知缺陷。MSC还可逆转顺铂诱导的皮质髓鞘损伤。静息态功能磁共振成像和连接组分析显示,顺铂处理后特征路径长度缩短,而MSC治疗可增加顺铂处理小鼠的路径长度。MSC进入大脑,但存活时间不超过12 - 72小时,表明它们不会替代受损组织。RNA测序分析确定线粒体氧化磷酸化是经鼻给予MSC处理的顺铂处理小鼠激活的首要通路。一致的是,MSC治疗可恢复顺铂诱导的脑突触体线粒体功能障碍和结构异常。经鼻给予MSC不干扰顺铂的外周抗肿瘤作用。总之,经鼻给予MSC可能是一种有效、非侵入性且安全的再生治疗方法,用于解决化疗脑问题。