Neuroinflammation refers to the inflammation of the nervous tissue, and is an immune response often initiated against a variety of harmful stimuli such as pathogens or trauma. Neuroinflammation is a complex biological response involving many signaling proteins, receptors, and cell types. Neuroinflammation stems from a combination of responses from resident glial cells in the central nervous system (CNS), which include microglia, oligodendrocytes, astrocytes, and non-glial resident myeloid cells (macrophages and dendritic cells) and peripheral leukocytes.


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The blood-brain barrier (BBB) is a unique vasculature structure at the interface between the blood circulation and the central nervous system (CNS). This barrier is formed at the level of CNS microvessels, capillaries and post-capillary venules, and tightly regulates the passage of molecules and peripheral immune cells into the CNS. This selective BBB permeability renders the CNS parenchymal tissue an immunologically privileged site.

The BBB is composed of highly specialized endothelial cells (ECs) that establish continuous intercellular tight junctions (TJs) sealing the paracellular space. ECs demonstrate low pinocytotic activity, which coupled with TJs, limits the diffusion of molecules between and across the EC layer. In addition, ECs express low levels of leukocyte adhesion molecules preventing peripheral immune cell infiltration into the healthy CNS. ECs also create an endothelial basement membrane where pericytes can be embedded. Pericytes ensheath the outer surface of the microvessels and contribute to BBB integrity and function by regulating vessel stability, diameter and blood flow. This barrier is further reinforced by the glia limitans, which is a thin barrier composed of astrocytes and astrocytic endfeet associated with the parenchymal basement membrane. At the CNS capillaries, the endothelial and parenchymal basement membranes fuse to create one basement membrane. At the post-capillary venules, these membranes remain separate and create the inner and outer limits of cerebrospinal fluid (CSF)-filled perivascular space where antigen presenting cells can be found.



  1. Engelhardt B & Ransohoff RM. 2012. Trends Immunol. 33:579. Pubmed
  2. Obermeier et al. 2013. Nat Med. 19:1584. Pubmed

Peripheral Immune Cell Infiltration into the Brain Parenchyma

The entry and infiltration of immune cells into the brain parenchyma involves migration across the BBB, followed by progression across the glia limitans into the parenchyma. Inflammation-induced disturbances in the BBB are partly due to activation of endothelial cells and are characterized by increased expression of: 1) cell adhesion molecules such as ICAM-1 and VCAM-1; 2) pro-inflammatory chemokines such as CCL2/MCP-1 and CXCL10/IP-10; and 3) cytokine receptors such as TNF-R and IL-17R. These factors affect the endothelial cell phenotype, and support extravasation and accumulation of infiltrating leukocytes (e.g. Th1 and Th17 effector T cells) in the perivascular space. To further gain access into the CNS, these cells secrete matrix metalloproteinases (MMPs) which help breakdown the astrocytic endfeet and the parenchymal basement membrane, and enter the parenchyma where they subsequently contribute to disease progression.

The CNS houses a number of glial and non-glial cell types that work cooperatively to counteract immune threats and maintain homeostasis. Innate immune responses in the CNS can be initiated locally through the function of these CNS resident cells. Sustained inflammation can lead to a hyperactive immune response, disruption of the BBB, and recruitment of peripheral immune cells. Depending on the nature and duration of the neurotoxic insult, these events can dampen or amplify the inflammatory signals leading to cell death or resolution of inflammation.

Check out our additional webpages below for more information on each of these CNS-related cells: 
Dendritic Cells



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