Department of Neurosurgery, The Fourth Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Department of Endoscopic Center, The Fourth Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Neurol Res. 2024 Nov;46(11):1037-1045. doi: 10.1080/01616412.2024.2381160. Epub 2024 Jul 30.
To determine whether YTHDF1 and YTHDF3 play the same role in brain and gut damage after traumatic brain injury (TBI).
We generated YTHDF1-/- and YTHDF3-/- mice using CRISPR/Cas9 technology, established a mouse brain injury model through severe controlled cortical impact (CCI), and finally observed the different types of damage between YTHDF1-/- and YTHDF3-/- mice by analysing the levels of oedema proteins in cortical tissue and inflammatory proteins and histopathological lesions in brain and gut tissues in mice at 3 days after CCI.
Compared with WT mice, YTHDF1-/- mice had decreased levels of oedema in cortical tissue and inflammation and histopathological lesions in brain and gut tissues at 3 days post-CCI, but YTHDF3-/- mice did not.
Our results suggest that deletion of YTHDF1, but not YTHDF3, could reduce damage to the brain and gut following TBI.
确定 YTHDF1 和 YTHDF3 在创伤性脑损伤 (TBI) 后对脑和肠道损伤是否发挥相同作用。
我们使用 CRISPR/Cas9 技术生成 YTHDF1-/- 和 YTHDF3-/- 小鼠,通过严重的皮质控制冲击 (CCI) 建立小鼠脑损伤模型,最后通过分析 CCI 后 3 天小鼠皮质组织水肿蛋白水平以及脑和肠道组织中炎症蛋白和组织病理学损伤,观察 YTHDF1-/- 和 YTHDF3-/- 小鼠之间的不同类型损伤。
与 WT 小鼠相比,YTHDF1-/- 小鼠在 CCI 后 3 天,皮质组织水肿、脑和肠道组织炎症以及组织病理学损伤的水平降低,但 YTHDF3-/- 小鼠则没有。
我们的结果表明,YTHDF1 的缺失而非 YTHDF3 的缺失可减轻 TBI 后脑和肠道的损伤。