Abstract

The blood-brain barrier (BBB) is a specialized brain endothelial barrier structure that regulates the highly selective transport of molecules under continuous blood flow. Recently, various types of BBB-on-chip models have been developed to mimic the microenvironmental cues that regulate the human BBB drug transport. However, technical difficulties in complex microfluidic systems limit their accessibility. Here, we propose a simple and easy-to-handle microfluidic device integrated with a cell culture insert to investigate the functional regulation of the human BBB endothelium in response to fluid shear stress (FSS). Using currently established immortalized human brain microvascular endothelial cells (HBMEC/ci18), we formed a BBB endothelial barrier without the substantial loss of barrier tightness under the relatively low range of FSS (0.1–1 dyn/cm2). Expression levels of key BBB transporters and receptors in the HBMEC/ci18 cells were dynamically changed in response to the FSS, and the effect of FSS reached a plateau around 1 dyn/cm2. Similar responses were observed in the primary HBMECs. Taking advantage of the detachable cell culture insert from the device, the drug efflux activity of P-glycoprotein (P-gp) was analyzed by the bidirectional permeability assay after the perfusion culture of cells. The data revealed that the FSS-stimulated BBB endothelium exhibited the 1.9-fold higher P-gp activity than that of the static culture control. Our microfluidic system coupling with the transwell model provides a functional human BBB endothelium with secured transporter activity, which is useful to investigate the bidirectional transport of drugs and its regulation by FSS.

Highlights

  • The blood-brain barrier (BBB) is a highly selective endothelial barrier, which ensures the separation of circulating blood from the brain parenchyma.[1,2] Brain microvascular endothelial cells (BMECs) lining the cerebral capillaries express several tight junctions, adherence junctions, and key transporters/receptors, including zonula occludins-1 (ZO-1), claudin-5, CD31, vascular endothelial-cadherin (VE-cadherin), P-glycoprotein (P-gp), breast cancer resistant protein (BCRP), glucose transporter-1 (GLUT-1), and transferrin receptor (TfR)

  • By culturing recently established immortalized human brain microvascular endothelial cells (HBMEC/ci[18] cells), which has been shown to have broad dynamic range of the compound permeability profiles,[17] in the microfluidic device, we demonstrate that our device provides the functional human BBB endothelium model with higher activity of P-gp drug efflux pump even in the absence of BBB-associated cells

  • This study demonstrated the utility of a microfluidic device to apply fluid shear stress (FSS) on the BBB endothelium grown on the cell culture insert, which is designed to be detachable from the device after the perfusion culture of cells

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Summary

Introduction

The blood-brain barrier (BBB) is a highly selective endothelial barrier, which ensures the separation of circulating blood from the brain parenchyma.[1,2] Brain microvascular endothelial cells (BMECs) lining the cerebral capillaries express several tight junctions, adherence junctions, and key transporters/receptors, including zonula occludins-1 (ZO-1), claudin-5, CD31, vascular endothelial-cadherin (VE-cadherin), P-glycoprotein (P-gp), breast cancer resistant protein (BCRP), glucose transporter-1 (GLUT-1), and transferrin receptor (TfR). Brain microvascular endothelial cells (BMECs) lining the cerebral capillaries express several tight junctions, adherence junctions, and key transporters/receptors, including zonula occludins-1 (ZO-1), claudin-5, CD31, vascular endothelial-cadherin (VE-cadherin), P-glycoprotein (P-gp), breast cancer resistant protein (BCRP), glucose transporter-1 (GLUT-1), and transferrin receptor (TfR). These BBBrelated proteins govern the barrier tightness and the controlled transport of nutrients, metabolites, and drugs between blood and the brain.[3]. BMECs are cocultured with astrocytes and pericytes in the basolateral compartment to recapitulate the paracrine or cell–cell contact communication in the APL Bioeng.

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