Vascular Biology Program, Boston Children's Hospital and Harvard Medical School, Boston, MA, 02115, USA.
Department of Surgery, Boston Children's Hospital and Harvard Medical School, Boston, MA, 02115, USA.
Acta Neuropathol Commun. 2024 Mar 26;12(1):47. doi: 10.1186/s40478-024-01757-4.
Sturge-Weber syndrome (SWS), a neurocutaneous disorder, is characterized by capillary malformations (CM) in the skin, brain, and eyes. Patients may suffer from seizures, strokes, and glaucoma, and only symptomatic treatment is available. CM are comprised of enlarged vessels with endothelial cells (ECs) and disorganized mural cells. Our recent finding indicated that the R183Q mutation in ECs leads to heightened signaling through phospholipase Cβ3 and protein kinase C, leading to increased angiopoietin-2 (ANGPT2). Furthermore, knockdown of ANGPT2, a crucial mediator of pro-angiogenic signaling, inflammation, and vascular remodeling, in EC-R183Q rescued the enlarged vessel phenotype in vivo. This prompted us to look closer at the microenvironment in CM-affected vascular beds. We analyzed multiple brain histological sections from patients with GNAQ-R183Q CM and found enlarged vessels devoid of mural cells along with increased macrophage-like cells co-expressing MRC1 (CD206, a mannose receptor), CD163 (a scavenger receptor and marker of the monocyte/macrophage lineage), CD68 (a pan macrophage marker), and LYVE1 (a lymphatic marker expressed by some macrophages). These macrophages were not found in non-SWS control brain sections. To investigate the mechanism of increased macrophages in the perivascular environment, we examined THP1 (monocytic/macrophage cell line) cell adhesion to EC-R183Q versus EC-WT under static and laminar flow conditions. First, we observed increased THP1 cell adhesion to EC-R183Q compared to EC-WT under static conditions. Next, using live cell imaging, we found THP1 cell adhesion to EC-R183Q was dramatically increased under laminar flow conditions and could be inhibited by anti-ICAM1. ICAM1, an endothelial cell adhesion molecule required for leukocyte adhesion, was strongly expressed in the endothelium in SWS brain histological sections, suggesting a mechanism for recruitment of macrophages. In conclusion, our findings demonstrate that macrophages are an important component of the perivascular environment in CM suggesting they may contribute to the CM formation and SWS disease progression.
斯特奇-韦伯综合征(SWS)是一种神经皮肤疾病,其特征是皮肤、大脑和眼睛中有毛细血管畸形(CM)。患者可能会出现癫痫发作、中风和青光眼,目前仅能进行对症治疗。CM 由内皮细胞(EC)和排列紊乱的壁细胞组成的增大的血管组成。我们最近的发现表明,EC 中的 R183Q 突变导致通过磷脂酶 Cβ3 和蛋白激酶 C 的信号转导增强,从而导致血管生成素-2(ANGPT2)增加。此外,在 EC-R183Q 中敲低关键的促血管生成信号、炎症和血管重塑介质 ANGPT2,可挽救体内增大的血管表型。这促使我们更深入地研究 CM 影响的血管床的微环境。我们分析了来自具有 GNAQ-R183Q CM 的患者的多个大脑组织切片,发现没有壁细胞的增大血管,同时伴有表达 MRC1(CD206,甘露糖受体)、CD163(单核细胞/巨噬细胞谱系的清道夫受体和标志物)、CD68(一种泛巨噬细胞标志物)和 LYVE1(一些巨噬细胞表达的淋巴标记物)的巨噬细胞样细胞增加。这些巨噬细胞未在非 SWS 对照大脑切片中发现。为了研究血管周围环境中巨噬细胞增加的机制,我们在静态和层流条件下检查了 THP1(单核细胞/巨噬细胞细胞系)细胞与 EC-R183Q 与 EC-WT 的粘附。首先,我们观察到与 EC-WT 相比,THP1 细胞在静态条件下与 EC-R183Q 的粘附增加。接下来,通过活细胞成像,我们发现 THP1 细胞与 EC-R183Q 的粘附在层流条件下显著增加,并且可以通过抗 ICAM1 抑制。ICAM1 是白细胞粘附所需的内皮细胞粘附分子,在 SWS 大脑组织切片中在内皮细胞中强烈表达,提示存在招募巨噬细胞的机制。总之,我们的研究结果表明,巨噬细胞是 CM 血管周围环境的重要组成部分,这表明它们可能有助于 CM 的形成和 SWS 疾病的进展。