Department of Neurosurgery, The Affiliated Guangdong Second Provincial General Hospital of Jinan University, Guangdong Second Provincial General Hospital, Guangzhou, Guangdong 510317, China.
School of Medicine, Southern University of Science and Technology, Shenzhen, Guangdong, China.
Int J Med Sci. 2024 Aug 13;21(11):2189-2200. doi: 10.7150/ijms.100127. eCollection 2024.
In the realm of this study, obtaining a comprehensive understanding of ischemic brain injury and its molecular foundations is of paramount importance. Our study delved into single-cell data analysis, with a specific focus on sub-celltypes and differentially expressed genes in the aftermath of ischemic injury. Notably, we observed a significant enrichment of the "ATP METABOLIC PROCESS" and "ATP HYDROLYSIS ACTIVITY" pathways, featuring pivotal genes such as Pbx3, Dguok, and Kif21b. A remarkable finding was the consistent upregulation of genes like Fabp7 and Bcl11a within the MCAO group, highlighting their crucial roles in regulating the pathway of mitochondrial ATP synthesis coupled proton transport. Furthermore, our network analysis unveiled pathways like "Neuron differentiation" and "T cell differentiation" as central in the regulatory processes of sub-celltypes. These findings provide valuable insights into the intricate molecular responses and regulatory mechanisms that govern brain injury. The shared differentially expressed genes among sub-celltypes emphasize their significance in orchestrating responses post-ischemic injury. Our research, viewed from the perspective of a medical researcher, contributes to the evolving understanding of the molecular landscape underlying ischemic brain injury, potentially paving the way for targeted therapeutic strategies and improved patient outcomes.
在本研究领域中,全面理解缺血性脑损伤及其分子基础至关重要。我们的研究深入探讨了单细胞数据分析,特别关注缺血损伤后的亚细胞类型和差异表达基因。值得注意的是,我们观察到“ATP 代谢过程”和“ATP 水解活性”途径显著富集,其中关键基因包括 Pbx3、Dguok 和 Kif21b。一个显著的发现是,在 MCAO 组中 Fabp7 和 Bcl11a 等基因的一致上调,突出了它们在调节线粒体 ATP 合成偶联质子转运途径中的关键作用。此外,我们的网络分析揭示了“神经元分化”和“T 细胞分化”等途径在亚细胞类型的调控过程中处于核心地位。这些发现为调控缺血性脑损伤的复杂分子反应和调控机制提供了有价值的见解。亚细胞类型之间共享的差异表达基因强调了它们在协调缺血后反应中的重要性。从医学研究人员的角度来看,我们的研究有助于深入了解缺血性脑损伤的分子基础,为靶向治疗策略和改善患者预后铺平道路。