Li Lulin, Nguyen Andy, Zhao Brian, Vest Ryan, Yerra Lakshmi, Sun Bryan, Luo Jian
Palo Alto Veterans Institute for Research, VA Palo Alto Health Care System, Palo Alto, California, USA.
Department of Chemical Engineering, Stanford University, Stanford, California, USA.
Neurotrauma Rep. 2024 Oct 22;5(1):1016-1026. doi: 10.1089/neur.2024.0060. eCollection 2024.
Traumatic brain injury (TBI) remains a significant public health concern, with no effective therapeutic interventions to ameliorate the enduring consequences. The prevailing understanding of TBI pathophysiology indicates a central role for vascular dysfunction. Transforming growth factor-β (TGF-β) is a multifunctional cytokine crucial for vascular development. Aberrant TGF-β signaling is implicated in vascular pathologies associated with various neurological conditions. We recently developed a novel small molecule drug, C381, a TGF-β activator with the ability to restore lysosomal function. Here we used a mouse model of repetitive mild TBI (mTBI) to examine whether C381 would attenuate vascular injury. We first employed RNA-seq analysis to investigate the gene expression patterns associated with mTBI and evaluated the therapeutic potential of C381 in mitigating these changes. Our results demonstrate distinct mTBI-related gene expression signatures, prominently implicating pathways related to vascular integrity and endothelial function. Notably, treatment with C381 reversed these mTBI-induced gene expression changes. Immunohistochemical analysis further corroborated these findings, revealing that C381 treatment attenuated vascular damage in mTBI-affected brain tissue. These findings strongly support the potential clinical usefulness of C381 as a novel therapeutic intervention for mTBI.
创伤性脑损伤(TBI)仍然是一个重大的公共卫生问题,目前尚无有效的治疗干预措施来改善其长期后果。目前对TBI病理生理学的普遍认识表明血管功能障碍起着核心作用。转化生长因子-β(TGF-β)是一种对血管发育至关重要的多功能细胞因子。异常的TGF-β信号传导与各种神经系统疾病相关的血管病变有关。我们最近开发了一种新型小分子药物C381,它是一种能够恢复溶酶体功能的TGF-β激活剂。在此,我们使用重复性轻度TBI(mTBI)小鼠模型来研究C381是否能减轻血管损伤。我们首先采用RNA测序分析来研究与mTBI相关的基因表达模式,并评估C381减轻这些变化的治疗潜力。我们的结果显示了与mTBI相关的独特基因表达特征,显著涉及与血管完整性和内皮功能相关的通路。值得注意的是,C381治疗逆转了这些mTBI诱导的基因表达变化。免疫组织化学分析进一步证实了这些发现,表明C381治疗减轻了mTBI影响的脑组织中的血管损伤。这些发现有力地支持了C381作为mTBI新型治疗干预措施的潜在临床应用价值。