中文摘要：
腦血管中β淀粉樣蛋白（β-β）的積累會損害腦淀粉樣血管病（CAA）中的血腦屏障（BBB）完整性。巨噬細胞譜系細胞清除 Aβ 并產生疾病緩解介質。在此，我們報告了Aβ40誘導的巨噬細胞衍生的遷移體粘在CAA患者的皮膚活檢樣本和CAA小鼠模型（Tg-SwDI/B和5xFAD小鼠）的腦組織上的血管上。我們表明，CD5L 被包裝在遷移體中并對接到血管中，并且 CD5L 的富集會損害對補體激活的抵抗力。血液中巨噬細胞和膜攻擊復合物 （MAC） 的遷移體產生能力增加與患者和 Tg-SwDI/B 小鼠的疾病嚴重程度相關。值得注意的是，補體抑制治療可防止 Tg-SwDI/B 小鼠遷移體介導的血腦屏障損傷。因此，我們提出巨噬細胞衍生的遷移體和隨之而來的補體激活是 CAA 中潛在的生物標志物和治療靶點。
英文摘要：
Accumulation of amyloid beta protein (Aβ) in brain vessels damages blood brain barrier (BBB) integrity in cerebral amyloid angiopathy (CAA). Macrophage lineage cells scavenge Aβ and produce disease-modifying mediators. Herein, we report that Aβ40-induced macrophage-derived migrasomes are sticky to blood vessels in skin biopsy samples from CAA patients and brain tissue from CAA mouse models (Tg-SwDI/B and 5xFAD mice). We show that CD5L is packed in migrasomes and docked to blood vessels, and that enrichment of CD5L impairs the resistance to complement activation. Increased migrasome-producing capacity of macrophages and membrane attack complex (MAC) in blood are associated with disease severity in both patients and Tg-SwDI/B mice. Of note, complement inhibitory treatment protects against migrasomes-mediated blood-brain barrier injury in Tg-SwDI/B mice. We thus propose that macrophage-derived migrasomes and the consequent complement activation are potential biomarkers and therapeutic targets in CAA.
論文信息：
論文題目：Macrophage-induced reduction of bacteriophage density limits the efficacy of in vivo pulmonary phage therapy
期刊名稱：Nature Communications
時間期卷：14, Article number: 3945 (2023)
在線時間：2023年7月4日
DOI：doi.org/10.1038/s41467-023-39693-x
產品信息：
貨號：CP-005-005
規(guī)格：5ml+5ml
品牌：Liposoma
產地：荷蘭
名稱：Clodronate Liposomes and Control Liposomes
辦事處：Target Technology(靶點科技)
Clodronate Liposomes氯膦酸鹽脂質體清除血管周圍巨噬細胞（Perivascular macrophages，PVMs
Liposoma巨噬細胞清除劑Clodronate Liposomes氯膦酸二鈉脂質體的材料和方法：
Peripheral blood monocyte depletion was carried out according to published procedure. Clodronate liposomes (Liposoma, 10?ml/kg, i.p.) was administered to 12-week-old Tg-SwDI/B mice every 3 days to deplete peripheral monocytes/macrophages prior to sacrifice at day 7. Depletion efficacy was confirmed with flow cytometric analysis.
For microglia depletion, PLX5622 was supplied to 12-week-old Tg-SwDI/B mice in the diet at 1200 PPM (1200?mg/kg of chow), starting 7 days prior to sacrifice. Depletion efficacy of was confirmed with immunostaining.
Perivascular macrophage depletion was carried out according to published procedure. 12-week-old Tg-SwDI/B mice were anesthetized with isoflurane and stereotaxically injected with 10?μL of clodronate-containing liposomes into the left lateral ventricle (coordinates from Bregma: anteroposterior, 0.2?mm; mediolateral, 1.2?mm; dorsoventral, 2.3?mm). Animals were sacrificed 7 days later and brains were processed for further analysis. Depletion efficacy of was confirmed with immunostaining.
材料和方法文獻截圖：
