TP53 缺失通过上调 NF-κB-IFN-β-MHC-Ia 信号促进骨肉瘤对 NK 细胞的抵抗
TP53 Loss Elevates NF-κB-IFN-β-MHC-Ia Signaling to Promote NK Cell Resistance in Osteosarcoma.
英文原题:Dysbiosis of gut microbiota and metabolites is associated with radiation-induced colorectal fibrosis and is restored by adipose-derived mesenchymal stem cell therapy.
Dysbiosis of gut microbiota and metabolites is associated with radiation-induced colorectal fibrosis and is restored by adipose-derived mesenchymal stem cell therapy.
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本研究旨在探讨脂肪间充质干细胞(ADSCs)对放射性结直肠纤维化(RICF)的作用及其相关的肠道菌群和代谢物失调。主要方法:通过16S rRNA基因测序评估粪便菌群,并利用液相色谱-质谱联用和气相色谱-质谱联用对粪便代谢组进行表征。探索了菌群与代谢组数据之间的相关性。
ADSC注射在体内显著恢复了辐射诱导的肠道损伤。在门水平上,受照射大鼠表现出拟杆菌门和弯曲菌门增加,厚壁菌门和脱硫杆菌门减少,与ADSC治疗组形成对比。代谢组学分析显示,与空白组相比,辐射组通过气相色谱-质谱法鉴定出72种差异表达代谢物(DEMs),通过液相色谱-质谱法鉴定出284种DEMs。在ADSC治疗组与辐射组比较中,通过气相色谱-质谱法鉴定出36种DEMs,通过液相色谱-质谱法鉴定出341种DEMs。KEGG富集分析涉及类固醇激素生物合成、间隙连接、初级胆汁酸生物合成、柠檬酸循环、cAMP信号通路以及丙氨酸、天冬氨酸和谷氨酸代谢等通路,在RICF进展过程中及ADSC治疗之后。相关性分析突出了ADSC在调节粪便拟杆菌中Camelledionol代谢过程中的作用。意义:这些发现强调了ADSC在RICF背景下逆转菌群失调和恢复正常结肠菌群的潜力,为针对辐射诱导并发症的治疗干预提供了有价值的见解。
AIMS: This study aimed to investigate the effects of adipose-derived mesenchymal stem cells (ADSCs) on radiation-induced colorectal fibrosis (RICF) along with the associated dysbiosis of gut microbiota and metabolites. MAIN METHODS: Fecal microbiota were assessed through 16S rRNA gene sequencing, and the fecal metabolome was characterized using liquid chromatography-mass spectrometry and gas chromatography-mass spectrometry. The correlation between microbiota and metabolome data was explored. KEY FINDINGS: ADSC injection demonstrated a significant restoration of radiation-induced intestinal damage in vivo. At the phylum level, irradiated rats exhibited an increase in Bacteroidota and Campilobacterota, and a decrease in Firmicutes and Desulfobacterota, contrasting with the ADSC treatment group. Metabolomic analysis revealed 72 differently expressed metabolites (DEMs) from gas chromatography-mass spectrometry and 284 DEMs from liquid chromatography-mass spectrometry in the radiation group compared to the blank group.
In the ADSC treatment group versus the radiation group, 36 DEMs from gas chromatography-mass spectrometry and 341 DEMs from liquid chromatography-mass spectrometry were identified. KEGG enrichment analysis implicated pathways such as steroid hormone biosynthesis, gap junction, primary bile acid biosynthesis, citrate cycle, cAMP signaling pathway, and alanine, aspartate, and glutamate metabolism during RICF progression and after treated with ADSCs.
Correlation analysis highlighted the role of ADSCs in modulating the metabolic process of Camelledionol in fecal Bacteroides. SIGNIFICANCE: These findings underscore the potential of ADSCs in reversing dysbiosis and restoring normal colonic flora in the context of RICF, offering valuable insights for therapeutic interventions targeting radiation-induced complications.
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