Solár Peter, Klusáková Ilona, Jančálek Radim, Dubový Petr, Joukal Marek
Department of Anatomy, Cellular and Molecular Neurobiology Research Group, Faculty of Medicine, Masaryk University, Brno, Czechia.
Department of Neurosurgery, Faculty of Medicine, Masaryk University and St. Anne's University Hospital Brno, Brno, Czechia.
Front Cell Neurosci. 2020 Feb 11;14:18. doi: 10.3389/fncel.2020.00018. eCollection 2020.
Subarachnoid hemorrhage (SAH) is a specific form of hemorrhagic stroke that frequently causes intracranial hypertension. The choroid plexus (CP) of the brain ventricles is responsible for producing cerebrospinal fluid and forms the blood - cerebrospinal fluid barrier. The aim of the current study was to determine whether SAH induces an immune cell reaction in the CP and whether the resulting increase in intracranial pressure (ICP) itself can lead to cellular changes in the CP. SAH was induced by injecting non-heparinized autologous blood to the cisterna magna. Artificial cerebrospinal fluid (ACSF) instead of blood was used to assess influence of increased ICP alone. SAH and ACSF animals were left to survive for 1, 3, and 7 days. SAH induced significantly increased numbers of M1 (ED1+, CCR7+) and M2 (ED2+, CD206+) macrophages as well as MHC-II+ antigen presenting cells (APC) compared to naïve and ACSF animals. Increased numbers of ED1+ macrophages and APC were found in the CP only 3 and 7 days after ACSF injection, while ED2+ macrophage number did not increase. CD3+ T cells were not found in any of the animals. Following SAH, proliferation activity in the CP gradually increased over time while ACSF application induced higher cellular proliferation only 1 and 3 days after injection. Our results show that SAH induces an immune reaction in the CP resulting in an increase in the number of several macrophage types in the epiplexus position. Moreover, we also found that increased ICP due to ACSF application induced both an immune reaction and increased proliferation of epiplexus cells in the CP. These findings indicate that increased ICP, and not just blood, contributes to cellular changes in the CP following SAH.
蛛网膜下腔出血(SAH)是出血性卒中的一种特殊形式,常导致颅内高压。脑室脉络丛(CP)负责产生脑脊液,并形成血-脑脊液屏障。本研究的目的是确定SAH是否会在CP中引发免疫细胞反应,以及由此导致的颅内压(ICP)升高本身是否会导致CP中的细胞变化。通过向枕大池注射未肝素化的自体血来诱导SAH。使用人工脑脊液(ACSF)代替血液来单独评估ICP升高的影响。SAH和ACSF组动物分别存活1天、3天和7天。与未处理组和ACSF组动物相比,SAH组诱导出显著增多的M1(ED1+、CCR7+)和M2(ED2+、CD206+)巨噬细胞以及MHC-II+抗原呈递细胞(APC)。仅在注射ACSF后3天和7天,在CP中发现ED1+巨噬细胞和APC数量增加,而ED2+巨噬细胞数量未增加。在任何动物中均未发现CD3+ T细胞。SAH后,CP中的增殖活性随时间逐渐增加,而注射ACSF仅在注射后1天和3天诱导更高的细胞增殖。我们的结果表明,SAH在CP中诱导免疫反应,导致丛间位置几种巨噬细胞类型数量增加。此外,我们还发现,ACSF导致的ICP升高诱导了CP中的免疫反应以及丛间细胞增殖增加。这些发现表明,SAH后导致CP细胞变化的原因不仅是血液,ICP升高也起了作用。