Abstract

The blood-brain barrier (BBB) is a fundamental component of the central nervous system (CNS). Its functional and structural integrity is vital to maintain the homeostasis of the brain microenvironment by controlling the passage of substances and regulating the trafficking of immune cells between the blood and the brain. The BBB is primarily composed of highly specialized microvascular endothelial cells. These cells’ special features and physiological properties are acquired and maintained through the concerted effort of hemodynamic and cellular cues from the surrounding environment. This complex multicellular system, comprising endothelial cells, astrocytes, pericytes, and neurons, is known as the neurovascular unit (NVU). The BBB strictly controls the transport of nutrients and metabolites into brain parenchyma through a tightly regulated transport system while limiting the access of potentially harmful substances via efflux transcytosis and metabolic mechanisms. Not surprisingly, a disruption of the BBB has been associated with the onset and/or progression of major neurological disorders. Although the association between disease and BBB disruption is clear, its nature is not always evident, specifically with regard to whether an impaired BBB function results from the pathological condition or whether the BBB damage is the primary pathogenic factor prodromal to the onset of the disease. In either case, repairing the barrier could be a viable option for treating and/or reducing the effects of CNS disorders. In this review, we describe the fundamental structure and function of the BBB in both healthy and altered/diseased conditions. Additionally, we provide an overview of the potential therapeutic targets that could be leveraged to restore the integrity of the BBB concomitant to the treatment of these brain disorders.

Highlights

  • Biological barriers perform a significant role in maintaining the integrity and function of many vertebrate organs

  • In vivo studies have shown that the blood-brain barrier (BBB) is already experiencing development before the astrocytes envelop the brain capillaries; it has been concluded that while astrocytes may not perform a significant role in the initial setting of BBB development, they enact a crucial role in the modulation and maintenance of BBB integrity post-formation [27,66]

  • Natalizumab, a humanized monoclonal antibody against the cell adhesion molecule α4-integrin, has been able to inhibit BBB endothelial inflammation by blocking the interaction between α4 integrin on white blood cells that are involved in inflammation and the vascular cell adhesion molecule-1 (VCAM-1) expressed on the vascular endothelium, thereby preventing white blood cells from entering the brain and spinal cord tissue [112,113]

Read more

Summary

Introduction

Biological barriers perform a significant role in maintaining the integrity and function of many vertebrate organs. The. CNS is protected from the external environment by three biological barriers at three interfaces. CNS is protected from the external environment by three biological barriers at three interfaces These are the blood-brain barrier (BBB), the blood–CSF barrier (BCB), and the arachnoid barrier [2]. The arachnoid barriers are formed by epithelium positioned between the blood and subarachnoid CSF. Pharmaceutics 2021, 13, 1779 its fluid spaces Among these CNS barriers, the BBB exerts the tightest control over the surrounding brain microenvironment. Different efflux transporters provide the second barrier, with a wide range of affinity for lipophilic substances. These include a P-glycoprotein (P-gp), breast cancer resistant protein (BCRP), and multidrug resistance-associated proteins (MRPs) [2]. This review highlights the pathological conditions associated with dysfunction of the BBB and the therapeutic targets currently exploited to promote BBB restoration

The Function of the BBB
Structure of the Blood-Brain Barrier
The Basement Membrane
Astrocytes
Mural Cells and Pericytes
Immune Cells
Adrenergic System and BBB
BBB Dysfunction in CNS Disorders
Stroke
Brain Tumor
Septic Encephalopathy
5.11. HIV Encephalitis
5.12. Epilepsy
5.13. Schizophrenia
5.14. Meningitis
Biological Targets for Restoring BBB Viability
Matrix Metalloproteinases
Endothelins
Adherens Junctions
Tight Junctions
Endothelium
Cytokines
Oxidative Stress
Actin-Myosin Cytoskeleton
Findings
Conclusions
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call