Clearance of erythrocytes from the subarachnoid space through cribriform plate lymphatics in female mice.

IF 9.7 1区 医学 Q1 MEDICINE, RESEARCH & EXPERIMENTAL EBioMedicine Pub Date : 2024-09-01 Epub Date: 2024-08-22 DOI:10.1016/j.ebiom.2024.105295
Adrian Madarasz, Li Xin, Steven T Proulx
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引用次数: 0

Abstract

Background: Atraumatic subarachnoid haemorrhage (SAH) is associated with high morbidity and mortality. Proposed mechanisms for red blood cell (RBC) clearance from the subarachnoid space (SAS) are erythrolysis, erythrophagocytosis or through efflux along cerebrospinal fluid (CSF) drainage routes. We aimed to elucidate the mechanisms of RBC clearance from the SAS to identify targetable efflux pathways.

Methods: Autologous fluorescently-labelled RBCs along with PEGylated 40 kDa near-infrared tracer (P40D800) were infused via the cisterna magna (i.c.m.) in female reporter mice for lymphatics or for resident phagocytes. Drainage pathways for RBCs to extracranial lymphatics were evaluated by in vivo and in situ near-infrared imaging and by immunofluorescent staining on decalcified cranial tissue or dural whole-mounts.

Findings: RBCs drained to the deep cervical lymph nodes 15 min post i.c.m. infusion, showing similar dynamics as P40D800 tracer. Postmortem in situ imaging and histology showed perineural accumulations of RBCs around the optic and olfactory nerves. Numerous RBCs cleared through the lymphatics of the cribriform plate, whilst histology showed no relevant fast RBC clearance through dorsal dural lymphatics or by tissue-resident macrophage-mediated phagocytosis.

Interpretation: This study provides evidence for rapid RBC drainage through the cribriform plate lymphatic vessels, whilst neither fast RBC clearance through dorsal dural lymphatics nor through spinal CSF efflux or phagocytosis was observed. Similar dynamics of P40D800 and RBCs imply open pathways for clearance that do not impose a barrier for RBCs. This finding suggests further evaluation of the cribriform plate lymphatic function and potential pharmacological targeting in models of SAH.

Funding: Swiss National Science Foundation (310030_189226), SwissHeart (FF191155).

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雌性小鼠通过楔形板淋巴管清除蛛网膜下腔的红细胞
背景:创伤性蛛网膜下腔出血(SAH)与高发病率和高死亡率有关。红细胞(RBC)从蛛网膜下腔(SAS)清除的拟议机制包括溶红细胞、红细胞吞噬或沿脑脊液(CSF)引流途径外流。我们旨在阐明 RBC 从 SAS 清除的机制,以确定可靶向的外流途径:方法:将自体荧光标记的 RBC 与 PEG 化 40 kDa 近红外示踪剂(P40D800)一起通过雌性报告小鼠的蝶窦(i.c.m.)注入淋巴管或常驻吞噬细胞。通过体内和原位近红外成像以及对脱钙颅骨组织或硬脑膜全切片进行免疫荧光染色,评估了 RBC 向颅外淋巴管的排泄途径:结果:红细胞在静注后15分钟排至颈深淋巴结,显示出与P40D800示踪剂相似的动态。死后原位成像和组织学检查显示,RBC在视神经和嗅神经周围的神经周围聚集。大量 RBC 通过楔形板的淋巴管清除,而组织学显示,没有相关的 RBC 通过硬膜背淋巴管或组织驻留的巨噬细胞介导的吞噬作用快速清除:这项研究提供了通过楔形板淋巴管快速排出 RBC 的证据,同时既没有观察到通过硬膜背淋巴管快速清除 RBC,也没有观察到通过脊髓 CSF 外流或吞噬作用快速清除 RBC。P40D800 和 RBC 的相似动态意味着清除途径是开放的,不会对 RBC 造成障碍。这一发现建议进一步评估楔形板的淋巴功能以及在 SAH 模型中的潜在药理靶点:瑞士国家科学基金会(310030_189226)、瑞士心脏中心(FF191155)。
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来源期刊
EBioMedicine
EBioMedicine Biochemistry, Genetics and Molecular Biology-General Biochemistry,Genetics and Molecular Biology
CiteScore
17.70
自引率
0.90%
发文量
579
审稿时长
5 weeks
期刊介绍: eBioMedicine is a comprehensive biomedical research journal that covers a wide range of studies that are relevant to human health. Our focus is on original research that explores the fundamental factors influencing human health and disease, including the discovery of new therapeutic targets and treatments, the identification of biomarkers and diagnostic tools, and the investigation and modification of disease pathways and mechanisms. We welcome studies from any biomedical discipline that contribute to our understanding of disease and aim to improve human health.
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