Department of Pathology and Laboratory Medicine, School of Medicine and Public Health, University of Wisconsin-Madison, Madison, Wisconsin, USA.
Institute of Biophysics, Biological Research Centre, Szeged, Hungary.
Curr Protoc Immunol. 2020 Sep;130(1):e101. doi: 10.1002/cpim.101.
In vitro culture models of the blood-brain barrier (BBB) provide a useful platform to test the mechanisms of cellular infiltration and pathogen dissemination into the central nervous system (CNS). We present an in vitro mouse model of the BBB to test Mycobacterium tuberculosis (Mtb) dissemination across brain endothelial cells. One-third of the global population is infected with Mtb, and in 1%-2% of cases bacteria invade the CNS through a largely unknown process. The "Trojan horse" theory supports the role of a cellular carrier that engulfs bacteria and carries them to the brain without being recognized. We present for the first time a protocol for an in vitro BBB-granuloma model that supports the Trojan horse mechanism of Mtb dissemination into the CNS. Handling of bacterial cultures, in vivo and in vitro infections, isolation of primary astroglial and endothelial cells, and assembly of the in vitro BBB model is presented. These techniques can be used to analyze the interaction of adaptive and innate immune system cells with brain endothelial cells, cellular transmigration, BBB morphological and functional changes, and methods of bacterial dissemination. © 2020 Wiley Periodicals LLC. Basic Protocol 1: Isolation of primary mouse brain astrocytes and endothelial cells Basic Protocol 2: Isolation of primary mouse bone marrow-derived dendritic cells Support Protocol 1: Validation of dendritic cell purity by flow cytometry Basic Protocol 3: Isolation of primary mouse peripheral blood mononuclear cells Support Protocol 2: Isolation of primary mouse spleen cells Support Protocol 3: Purification and validation of CD4+ T cells from PBMCs and spleen cells Basic Protocol 4: Isolation of liver granuloma supernatant and determination of organ load Support Protocol 4: In vivo and in vitro infection with mycobacteria Basic Protocol 5: Assembly of the BBB co-culture model Basic Protocol 6: Assembly of the combined in vitro granuloma and BBB model.
体外血脑屏障 (BBB) 培养模型为测试细胞浸润和病原体向中枢神经系统 (CNS) 传播的机制提供了有用的平台。我们提出了一种体外小鼠 BBB 模型,用于测试结核分枝杆菌 (Mtb) 穿过脑内皮细胞的传播。全球有三分之一的人口感染了 Mtb,在 1%-2%的情况下,细菌通过一个很大程度上未知的过程侵入中枢神经系统。“特洛伊木马”理论支持一种细胞载体的作用,该载体吞噬细菌并将其携带到大脑而不被识别。我们首次提出了一种体外 BBB-肉芽肿模型的方案,该方案支持 Mtb 向中枢神经系统传播的“特洛伊木马”机制。介绍了细菌培养物的处理、体内和体外感染、原代星形胶质细胞和内皮细胞的分离以及体外 BBB 模型的组装。这些技术可用于分析适应性和先天免疫系统细胞与脑内皮细胞的相互作用、细胞迁移、BBB 形态和功能变化以及细菌传播的方法。© 2020 Wiley Periodicals LLC. 基本方案 1:原代小鼠脑星形胶质细胞和内皮细胞的分离 基本方案 2:原代小鼠骨髓来源树突状细胞的分离 支持方案 1:流式细胞术验证树突状细胞纯度 基本方案 3:原代小鼠外周血单核细胞的分离 支持方案 2:原代小鼠脾脏细胞的分离 支持方案 3:从 PBMCs 和脾细胞中纯化和验证 CD4+T 细胞 基本方案 4:肝脏肉芽肿上清液的分离和器官负荷的测定 支持方案 4:体内和体外分枝杆菌感染 基本方案 5:BBB 共培养模型的组装 基本方案 6:体外肉芽肿和 BBB 模型的联合组装