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多能间充质基质细胞对热应激敏感 - 对治疗性高热的潜在影响。

Multipotent mesenchymal stromal cells are sensitive to thermic stress - potential implications for therapeutic hyperthermia.

机构信息

Department of Radiation Oncology, Freiburg University Medical Center, Freiburg, Germany.

German Cancer Consortium (DKTK) Partner Site Freiburg, German Cancer Research Center (DKFZ), Heidelberg, Germany.

出版信息

Int J Hyperthermia. 2020;37(1):430-441. doi: 10.1080/02656736.2020.1758350.

Abstract

Hyperthermia demonstrated clinical efficacy in multimodal cancer treatment. Multipotent mesenchymal stromal cells (MSCs) as part of the tumor-supporting stroma modulate tumor response and tissue regeneration after hyperthermia. We aimed to investigate the effects of hyperthermia on the survival, stem cell characteristics and heat shock expression of human MSCs. Human MSCs and normal human dermal fibroblasts (NHDFs) were exposed to temperatures between 37 °C and 44 °C for 60 min, and hyperthermic sensitivity was examined by clonogenicity, proliferation and viability assays. The influence of 42 °C hyperthermia on the MSCs' adhesion potential, migratory capacity, surface marker expression and multi-lineage differentiation capability was investigated. Cell cycle distribution, apoptosis and senescence after 42 °C hyperthermia were determined by flow cytometry and β-galactosidase staining. Heat shock protein expression was determined by Western Blots. MSCs exhibited decreased clonogenic survival after 40 °C and 42 °C hyperthermia compared to NHDFs, while proliferative activity and viability were comparable after hyperthermia up to 44 °C. MSC adhesion was reduced after 42 °C hyperthermia, while the characteristic surface marker expression and the migratory ability remained unaffected in 42 °C hyperthermia-exposed MSCs. 42 °C hyperthermia diminished the adipogenic differential potential of all tested MSC samples. A pronounced G2/M arrest was found after 42 °C hyperthermia and was associated with increased apoptosis and senescence levels in MSCs. MSCs exhibited slightly lower heat shock protein levels compared to NHDFs. Human MSCs exhibit a thermosensitive phenotype which reduced the multipotent cells' regenerative abilities, resulting in impaired tissue regeneration after hyperthermia treatment or thermal injuries. On the other hand, tumor-associated MSCs may be efficiently targeted by hyperthermia treatment.

摘要

过热症在多模式癌症治疗中显示出临床疗效。多能间充质基质细胞(MSCs)作为肿瘤支持基质的一部分,调节过热症后的肿瘤反应和组织再生。我们旨在研究过热症对人 MSCs 的存活、干细胞特征和热休克表达的影响。将人 MSCs 和正常人类真皮成纤维细胞(NHDFs)暴露于 37°C 至 44°C 之间 60 分钟,并通过集落形成、增殖和活力测定来检查过热症的敏感性。研究了 42°C 过热症对 MSCs 黏附潜力、迁移能力、表面标志物表达和多谱系分化能力的影响。通过流式细胞术和β-半乳糖苷酶染色测定 42°C 过热症后的细胞周期分布、凋亡和衰老。通过 Western Blots 测定热休克蛋白表达。与 NHDFs 相比,40°C 和 42°C 过热症后 MSCs 的集落形成存活率降低,而在高达 44°C 的过热症后,增殖活性和活力相当。42°C 过热症后 MSC 黏附减少,而在 42°C 过热症暴露的 MSC 中,特征性表面标志物表达和迁移能力保持不变。42°C 过热症减弱了所有测试 MSC 样本的成脂分化潜力。在 42°C 过热症后发现明显的 G2/M 期阻滞,并且与 MSC 中的凋亡和衰老水平增加相关。与 NHDFs 相比,MSCs 表现出略低的热休克蛋白水平。人 MSCs 表现出热敏表型,降低了多能细胞的再生能力,导致过热症治疗或热损伤后组织再生受损。另一方面,肿瘤相关的 MSCs 可能会被过热症治疗有效地靶向。

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