3D血脑屏障模型芯片,SynBBB,SynBBB 3D Model 

SynBBB 3D血脑屏障模型芯片，SynBBB 3D Blood Brain Barrier Model,SynBBB 3D Model – Assay Kits,SynBBB 3D Model Assay Kit SynBBB 3D Model Chip,SynBBB 3D Model Starter Kit

SynBBB 3D Blood Brain Barrier Model – Real-time visualization of cellular and barrier functionality

SynVivo的SynBBB 3D血脑屏障模型通过模拟与跨血脑屏障（BBB）的内皮细胞通讯的脑组织细胞的组织切片来重建体内微环境。剪切诱导的内皮细胞紧密连接在Transwell®模型中无法实现，而在SynBBB模型中使用生理性流体流很容易实现。紧密变化的形成可以使用SynVivo细胞阻抗分析仪通过生化或电气分析（评估电阻变化）进行测量。脑组织细胞与内皮细胞之间的相互作用在SynBBB分析中很容易观察到。 Transwell模型不允许实时显示这些细胞相互作用，这对于了解BBB微环境至关重要。

SynBBB是wei一可以实现以下功能的体外BBB模型：

准确的体内血液动力学切应力
实时可视化细胞和屏障功能
大大减少了成本和时间
稳健易用的协议

BBB模型的示意图。顶腔（外通道）用于培养血管（内皮细胞），而基底外侧腔（中央腔）用于培养脑组织细胞（星形细胞，周细胞，神经元）。多孔结构使血管细胞与组织细胞之间可以进行通讯。

SynBBB系统是一个高度通用的平台，可用于调查：

紧密连接蛋白：确定紧密连接蛋白的水平，即调节BBB的小带闭合蛋白，claudins和occludins。
转运蛋白：分析正常和功能异常的血脑屏障中转运蛋白的功能（例如Pgp）。
药物渗透性：评估治疗剂和小分子穿过BBB内皮细胞的实时渗透性。
炎症：了解炎症反应对血脑屏障调节的潜在机制。
细胞迁移：可视化并量化免疫细胞在BBB中的实时迁移。
渗透性变化：对正常和功能异常的血脑屏障进行基因组，蛋白质组和代谢分析。
神经毒性：分析化学，生物和物理试剂对血脑屏障细胞的毒性作用。
神经肿瘤学：研究肿瘤细胞对血脑屏障的影响。
根据您的研究需求，您可以从“基本” SynBBB模型或“ TEER兼容” SynBBB配置中进行选择。

SynBBB 3D模型套件组件
可以以试剂盒形式购买运行SynBBB分析所需的所有基本组件。 根据个人研究需求，您可以从SynBBB芯片的“基本”或“ TEER兼容”配置中进行选择。 包括所有附件，包括管子，夹子，针头和注射器。 入门工具包还将包括气动启动装置（运行SynBBB分析所需）和细胞阻抗分析仪（收集SynBBB TEER测量值所需）。

套件内容和说明
 

SynVivo used to create the first neonatal BBB model on a chip

Researchers at Temple University used the SynVivo® SynBBB^TM cell-based in vitro assay platform to model the attributes and functions of the neonatal stage blood-brain barrier (BBB) [1]. The SynBBB model closely mimics the in vivo microenvironment including three-dimensional morphology, cellular interactions and flow characteristics on a microfluidic chip. This work marks the first dynamic in vitro neonatal BBB model that offers real time visualization and analysis and is suitable for studies of BBB function as well as screening of novel therapeutics.

“The work is important because studies of neonatal neuropathologies and development of appropriate therapeutics are hampered by a lack of relevant in vitro models of the neonatal blood-brain barrier,” said Dr. Sudhir Deosarkar, the lead author of this paper.

In the SynBBB assay, which includes a tissue compartment and vascular channels placed side-by-side and separated by an engineered porous barrier, the researchers were able to co-culture neonatal rat brain endothelial cells and rat astrocytes under physiological conditions observed in vivo. The endothelial cells formed a full lumen and exhibited tight junction formation which increased under co-culture with astrocytes. The permeability of small molecules in the developed model was found to in excellent agreement with in vivo observations.

“The real-time visualization capabilities of the SynBBB co-culture platform allowed, for the first time, visualization of astrocyte end-feet and endothelial cell interactions in anin vitro model,” said Prof. Mohammad Kiani who is the senior author of the paper. “This is a unique capability and will help us to understand and develop therapeutics for several developmental disorders and diseases of the brain.”

The PLOS ONE paper shows that in contrast to transwell models, the SynBBB model exhibits significantly improved barrier characteristics similar to in vivo observations.

¹A Novel Dynamic Neonatal Blood-Brain Barrier on a Chip. S. Deosarkar, B. Prabhakarpandian, B. Wang, J.B. Sheffield, B. Krynska, M. Kiani. PLOS ONE, 2015, DOI: 10.1371/journal.pone.0142725

The SynBBB 3D model has been validated in various BBB Assays

Mono-Culture Assays

Shear-induced endothelial cell tight junctions, which cannot be achieved in the Transwell® model, are easily achieved in the SynBBB assay using fluid perfusion. Formation of tight changes can be measured using biochemical or electrical analysis (assessing changes in electrical resistance) with the SynVivo Cell Impedance Analyzer.

Primary endothelial cells are cultured in the vascular channel under physiological fluid flow. Cells are stained for tight junction markers highlighting the increase under fluid flow compared to static conditions. The Cell Impedance Analyzer system is used to measure increases in Ohmic resistance (TEER), associated with the formation of tight junctions.

Top Left Panel: Phase Contrast imaging of brain endothelial cells cultured in the SynBBB model. Bottom Left Panel: Calcein AM and Ethidium homodimer-1 labeled brain endothelial cells indicating a highly viable population of cells in the SynBBB model. Right Panel: Plot highlighting the importance of flow on brain endothelial cells with increased TEER.

Co-Culture with Tissue Cells

Interactions between brain tissue cells and endothelial cells are readily visualized in the SynBBB assay. Transwell models do not allow real-time visualization of these cellular interactions, which are critical for understanding of the physiological environment.

Endothelial cells are cultured under flow in the vascular channel, and the tissue chamber is cultured with primary brain cells, such as astrocytes. Increases in Ohmic resistance across the barrier, measured with the Cell Impedance Analyzer, are associated with tight junction formation across the BBB. Endothelial cells co-cultured with astrocytes form significantly tighter cell junctions compared to mono-cultured endothelial cells.

Left Panel: CD-31 (green) stained endothelial cells and GFAP (red) stained astrocytes. All nucleus are stained with DAPI (blue). Right Panel: Plot highlighting increased TEER with co-culture of endothelial cells and astrocytes.

Real-Time Permeability Assays

Unlike BBB models which are arranged in top to bottom architecture (i.e., Transwell), small molecule transport can be assessed and quantified in real-time across the SynBBB system due to its side-by-side architecture.

A fluorescently-labeled drug molecule of interest is perfused through the vascular channels at physiological  flow rate. Real-time videos are acquired and analyzed to calculate the rate of permeability into the tissue chamber. Different rates of permeability is observed across the BBB due to tight junctions of endothelial cells.

Time-lapse imaging of permeability of small molecules across a tightly formed BBB.

Time-lapse imaging of permeability of small molecules across a leaky BBB.

Real-Time Tight Junction Modulation

SynBBB can be used to model inflammation responses. A pro-inflammatory compound, such as TNF-α, is added to mono-cultured endothelial cells to modulate the tight junctions, followed by a period of recovery under perfusion flow. Electrical resistance measurements provide a non-invasive method for real-time monitoring of tight junctions.

Modulation of Inflammation responses in SynBBB model. TNF-alpha induced leakiness in the BBB measured by changes in the resistance across the endothelial cells. Removal of TNF-alpha followed by media perfusion under physiological flow conditions enables recovery of the tight junction leading to increased tight junction formation. Static cells maintain a constant resistance due to lack of tight junctions.

SynBBB 3D模型–入门套件
包括消耗品（10个芯片，百英尺管，25个滑动夹具，50个钝头针头和50个1毫升注射器）。 入门套件还将包括气动启动装置（接种细胞所需）和细胞阻抗分析仪（仅适用于TEER配置）。


货号：402002，SynBBB 3D模型入门套件（基本

货号：402004，SynBBB 3D模型入门套件（TEER

SynBBB 3D模型–检测套件
包括消耗品（10个芯片，百英尺管，25个滑动夹具，50个钝头针头和50个1毫升注射器）。
货号：402001 SynBBB 3D模型测定试剂盒（基本配置）

货号：402003 SynBBB 3D模型测定套件（TEER配置）

SynBBB 3D模型–芯片
货号：102005-SB SynBBB 3D模型芯片（基本配置）
货号：102015-SB SynBBB 3D模型芯片（TEER配置）