Solutes, but not cells, drain from the brain parenchyma along basement membranes of capillaries and arteries: significance for cerebral amyloid angiopathy and neuroimmunology

Elimination of interstitial fluid and solutes plays a role in homeostasis in the brain, but the pathways are unclear. Previous work suggests that interstitial fluid drains along the walls of arteries. Aims: to define the pathways within the walls of capillaries and arteries for drainage of fluid and solutes out of the brain. Methods: Fluorescent soluble tracers, dextran (3 kDa) and ovalbumin (40 kDa), and particulate fluospheres (0.02 μm and 1.0 μm in diameter) were injected into the corpus striatum of mice. Brains were examined from 5 min to 7 days by immunocytochemistry and confocal microscopy. Results: soluble tracers initially spread diffusely through brain parenchyma and then drain out of the brain along basement membranes of capillaries and arteries. Some tracer is taken up by vascular smooth muscle cells and by perivascular macrophages. No perivascular drainage was observed when dextran was injected into mouse brains following cardiac arrest. Fluospheres expand perivascular spaces between vessel walls and surrounding brain, are ingested by perivascular macrophages but do not appear to leave the brain even following an inflammatory challenge with lipopolysaccharide or kainate. Conclusions: capillary and artery basement membranes act as ‘lymphatics of the brain’ for drainage of fluid and solutes; such drainage appears to require continued cardiac output as it ceases following cardiac arrest. This drainage pathway does not permit migration of cells from brain parenchyma to the periphery. Amyloid‐β is deposited in basement membrane drainage pathways in cerebral amyloid angiopathy, and may impede elimination of amyloid‐β and interstitial fluid from the brain in Alzheimer's disease. Soluble antigens, but not cells, drain from the brain by perivascular pathways. This atypical pattern of drainage may contribute to partial immune privilege of the brain and play a role in neuroimmunological diseases such as multiple sclerosis.

[1]  Mathias Jucker,et al.  Mechanism of cerebral beta-amyloid angiopathy: murine and cellular models. , 2006, Brain pathology.

[2]  R O Weller,et al.  Perivascular spaces in the basal ganglia of the human brain: their relationship to lacunes , 1997, Journal of anatomy.

[3]  R. Weller Microscopic morphology and histology of the human meninges. , 2005, Morphologie : bulletin de l'Association des anatomistes.

[4]  J. Wegiel,et al.  Beta-amyloid formation by myocytes of leptomeningeal vessels. , 1994, Acta neuropathologica.

[5]  N. Joan Abbott,et al.  Evidence for bulk flow of brain interstitial fluid: significance for physiology and pathology , 2004, Neurochemistry International.

[6]  Thermodynamics of beta-amyloid fibril formation. , 2004, The Journal of chemical physics.

[7]  S. D. Preston,et al.  Capillary and arterial cerebral amyloid angiopathy in Alzheimer's disease: defining the perivascular route for the elimination of amyloid β from the human brain , 2003, Neuropathology and applied neurobiology.

[8]  M. Bergsneider,et al.  Evolving concepts of cerebrospinal fluid physiology. , 2001, Neurosurgery clinics of North America.

[9]  Mims Ca Intracerebral Injections and the Growth of Viruses in the Mouse Brain. , 1960 .

[10]  V. Perry,et al.  The kinetics and morphological characteristics of the macrophage-microglial response to kainic acid-induced neuronal degeneration , 1991, Neuroscience.

[11]  J. Rosenbaum,et al.  APCs in the Anterior Uveal Tract Do Not Migrate to Draining Lymph Nodes1 , 2004, The Journal of Immunology.

[12]  Brian J Bacskai,et al.  Progression of Cerebral Amyloid Angiopathy in Transgenic Mouse Models of Alzheimer Disease , 2005, Journal of neuropathology and experimental neurology.

[13]  T. Beach,et al.  Cortical and Leptomeningeal Cerebrovascular Amyloid and White Matter Pathology in Alzheimer’s Disease , 2003, Molecular medicine.

[14]  J. Frackowiak,et al.  Secretion and Accumulation of Aβ by Brain Vascular Smooth Muscle Cells from AβPP‐Swedish Transgenic Mice , 2003 .

[15]  R O Weller,et al.  Cerebral amyloid angiopathy: amyloid beta accumulates in putative interstitial fluid drainage pathways in Alzheimer's disease. , 1998, The American journal of pathology.

[16]  Seokmann Hong,et al.  Immune Privilege , 1999, The Journal of experimental medicine.

[17]  R. Weller,et al.  Lymphocyte targeting of the brain in adoptive transfer cryolesion‐EAE , 1999, The Journal of pathology.

[18]  V. Perry,et al.  Differential Blood–Brain Barrier Breakdown and Leucocyte Recruitment Following Excitotoxic Lesions in Juvenile and Adult Rats , 1998, Experimental Neurology.

[19]  C. Patlak,et al.  Drainage of interstitial fluid from different regions of rat brain. , 1984, The American journal of physiology.

[20]  R. Weller,et al.  Role of cervical lymph nodes in autoimmune encephalomyelitis in the Lewis rat , 1997, The Journal of pathology.

[21]  D. Dickson,et al.  Extracellular Deposits of Aβ Produced in Cultures of Alzheimer Disease Brain Vascular Smooth Muscle Cells , 2005 .

[22]  E. Zhang,et al.  Directional and compartmentalised drainage of interstitial fluid and cerebrospinal fluid from the rat brain , 2004, Acta Neuropathologica.

[23]  V. Perry,et al.  Central and Systemic Endotoxin Challenges Exacerbate the Local Inflammatory Response and Increase Neuronal Death during Chronic Neurodegeneration , 2005, The Journal of Neuroscience.

[24]  A. Osborn,et al.  Giant tumefactive perivascular spaces. , 2005, AJNR. American journal of neuroradiology.

[25]  P. Knopf,et al.  Cervical lymphatics, the blood-brain barrier and the immunoreactivity of the brain: a new view. , 1992, Immunology today.

[26]  V. Perry,et al.  What is immune privilege (not)? , 2007, Trends in immunology.

[27]  V. Perry,et al.  The acute inflammatory response to lipopolysaccharide in cns parenchyma differs from that in other body tissues , 1992, Neuroscience.

[28]  R O Weller,et al.  CSF drains directly from the subarachnoid space into nasal lymphatics in the rat. Anatomy, histology and immunological significance , 1993, Neuropathology and applied neurobiology.

[29]  Yu-Min Kuo,et al.  Cerebral amyloid angiopathy: amyloid beta accumulates in putative interstitial fluid drainage pathways in Alzheimer's disease. , 1998, The American journal of pathology.

[30]  R. Weller,et al.  Cerebral amyloid angiopathy: Pathogenesis and effects on the ageing and Alzheimer brain , 2003, Neurological research.

[31]  P. Stevenson,et al.  The immunogenicity of intracerebral virus infection depends on anatomical site , 1997, Journal of virology.

[32]  Y. Ihara,et al.  Amyloid β‐proteins 1—40 and 1—42(43) in the soluble fraction of extra‐ and intracranial blood vessels , 1995 .

[33]  E. Syková,et al.  Extrasynaptic volume transmission and diffusion parameters of the extracellular space , 2004, Neuroscience.

[34]  V. Perry,et al.  Demyelination in the central nervous system following a delayed-type hypersensitivity response to bacillus Calmette-Guérin , 1995, Neuroscience.

[35]  T. Mazel,et al.  Changes in extracellular space size and geometry in APP23 transgenic mice: a model of Alzheimer's disease. , 2005, Proceedings of the National Academy of Sciences of the United States of America.

[36]  J. Frackowiak,et al.  Secretion and accumulation of Abeta by brain vascular smooth muscle cells from AbetaPP-Swedish transgenic mice. , 2003, Journal of neuropathology and experimental neurology.

[37]  Mathias Jucker,et al.  Mechanism of Cerebral β‐Amyloid Angiopathy: Murine and Cellular Models , 2006 .

[38]  R. Weller,et al.  Cerebral amyloid angiopathy plays a direct role in the pathogenesis of Alzheimer’s disease Pro-CAA position statement , 2004, Neurobiology of Aging.

[39]  R. Weller Pathology of Cerebrospinal Fluid and Interstitial Fluid of the CNS: Significance for Alzheimer Disease, Prion Disorders and Multiple Sclerosis , 1998, Journal of neuropathology and experimental neurology.

[40]  D. Selkoe,et al.  Beta amyloid is focally deposited within the outer basement membrane in the amyloid angiopathy of Alzheimer's disease. An immunoelectron microscopic study. , 1992, The American journal of pathology.

[41]  G. Randolph,et al.  Factors and signals that govern the migration of dendritic cells via lymphatics: recent advances , 2004, Springer Seminars in Immunopathology.

[42]  M. Lagios,et al.  Cerebral amyloid angiopathy. , 1981, Human pathology.

[43]  V. Perry,et al.  Mechanisms to explain the reverse perivascular transport of solutes out of the brain. , 2006, Journal of theoretical biology.

[44]  R O Weller,et al.  Interrelationships of the pia mater and the perivascular (Virchow-Robin) spaces in the human cerebrum. , 1990, Journal of anatomy.

[45]  P. Knopf,et al.  Role of the cervical lymphatics in the Th2-type hierarchy of CNS immune regulation 1 This work was supported by National Institute of Health Grant (RO1 NS33070-03) and The Brain Tumor Society. 1 , 1999, Journal of Neuroimmunology.

[46]  M. Johnston,et al.  Evidence of connections between cerebrospinal fluid and nasal lymphatic vessels in humans, non-human primates and other mammalian species , 2004, Cerebrospinal Fluid Research.

[47]  D. Dickson,et al.  Extracellular deposits of A beta produced in cultures of Alzheimer disease brain vascular smooth muscle cells. , 2005, Journal of neuropathology and experimental neurology.

[48]  N. Davoust,et al.  How to drain without lymphatics? Dendritic cells migrate from the cerebrospinal fluid to the B-cell follicles of cervical lymph nodes. , 2006, Blood.