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血小板衍生生长因子受体α(PDGFRα)抑制可减少纤维化边缘区肌成纤维细胞的增殖,并促进缺血性中风后的恢复。

PDGFRα inhibition reduces myofibroblast expansion in the fibrotic rim and enhances recovery after ischemic stroke.

作者信息

Protzmann Jil, Zeitelhofer Manuel, Stefanitsch Christina, Torrente Daniel, Adzemovic Milena Z, Matjunins Kirils, Randel Stella Ji, Lewandowski Sebastian A, Muhl Lars, Eriksson Ulf, Nilsson Ingrid, Su Enming J, Lawrence Daniel A, Fredriksson Linda

机构信息

Department of Medical Biochemistry and Biophysics, Karolinska Institutet, Stockholm, Sweden.

Department of Internal Medicine, University of Michigan Medical School, Ann Arbor, Michigan, USA.

出版信息

J Clin Invest. 2025 Jan 14;135(5):e171077. doi: 10.1172/JCI171077.

Abstract

Ischemic stroke is a major cause of disability in adults. Early treatment with thrombolytics and/or thrombectomy can significantly improve outcomes; however, following these acute interventions, treatment is limited to rehabilitation therapies. Thus, identification of therapeutic strategies that can help restore brain function in the post-acute phase remains a major challenge. Here we report that genetic or pharmacologic inhibition of the PDGF-CC/PDGFRα pathway, which has previously been implicated in stroke pathology, significantly reduced myofibroblast expansion in the border of the fibrotic scar and improved outcome in a sensory-motor integration test after experimental ischemic stroke. This was supported by gene expression analyses of cerebrovascular fragments showing upregulation of profibrotic/proinflammatory genes, including genes of the TGF pathway, after ischemic stroke or intracerebroventricular injection of active PDGF-CC. Further, longitudinal intravital 2-photon imaging revealed that inhibition of PDGFRα dampened the biphasic pattern of stroke-induced vascular leakage and enhanced vascular perfusion in the ischemic lesion. Importantly, we found PDGFRα inhibition to be effective in enhancing functional recovery when initiated 24 hours after ischemic stroke. Our data implicate the PDGF-CC/PDGFRα pathway as a crucial mediator modulating post-stroke pathology and suggest a post-acute treatment opportunity for patients with ischemic stroke targeting myofibroblast expansion to foster long-term CNS repair.

摘要

缺血性中风是成年人残疾的主要原因。早期使用溶栓剂和/或血栓切除术进行治疗可显著改善预后;然而,在这些急性干预之后,治疗仅限于康复治疗。因此,确定能够帮助恢复急性期后大脑功能的治疗策略仍然是一项重大挑战。在此,我们报告称,对血小板衍生生长因子CC(PDGF-CC)/血小板衍生生长因子受体α(PDGFRα)通路进行基因或药物抑制,此前该通路已被认为与中风病理相关,这可显著减少纤维化瘢痕边缘的肌成纤维细胞增殖,并改善实验性缺血性中风后感觉运动整合测试中的结果。这得到了脑血管片段基因表达分析的支持,该分析显示,在缺血性中风或脑室内注射活性PDGF-CC后,包括转化生长因子(TGF)通路基因在内的促纤维化/促炎基因上调。此外,纵向活体双光子成像显示,抑制PDGFRα可抑制中风诱导的血管渗漏的双相模式,并增强缺血性病变中的血管灌注。重要的是,我们发现,在缺血性中风后24小时开始抑制PDGFRα可有效增强功能恢复。我们的数据表明,PDGF-CC/PDGFRα通路是调节中风后病理的关键介质,并为缺血性中风患者提供了一个急性期后治疗机会,即针对肌成纤维细胞增殖以促进长期中枢神经系统修复。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c5a3/11870733/f832aa39b598/jci-135-171077-g250.jpg

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