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A new look at cerebrospinal fluid circulation
Open accessAbstract
According to the traditional understanding of cerebrospinal fluid (CSF) physiology, the majority of CSF is produced by the choroid plexus, circulates through the ventricles, the cisterns, and the subarachnoid space to be absorbed into the blood by the arachnoid villi. This review surveys key developments leading to the traditional concept. Challenging this concept are novel insights utilizing molecular and cellular biology as well as neuroimaging, which indicate that CSF physiology may be much more complex than previously believed. The CSF circulation comprises not only a directed flow of CSF, but in addition a pulsatile to and fro movement throughout the entire brain with local fluid exchange between blood, interstitial fluid, and CSF. Astrocytes, aquaporins, and other membrane transporters are key elements in brain water and CSF homeostasis. A continuous bidirectional fluid exchange at the blood brain barrier produces flow rates, which exceed the choroidal CSF production rate by far. The CSF circulation around blood vessels penetrating from the subarachnoid space into the Virchow Robin spaces provides both a drainage pathway for the clearance of waste molecules from the brain and a site for the interaction of the systemic immune system with that of the brain. Important physiological functions, for example the regeneration of the brain during sleep, may depend on CSF circulation.
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“Uptake into arachnoid villi, as proposed more than one hundred years ago, seems to be of minor importance in humans, as reviewed by Brinker et al. (50) and as indicated in our recent study (13).”
From Brain-wide glymphatic enhancement and clearance in humans assessed with MRI. (2018) · cites this paper as [50]
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Iliff, J. J., Wang, M., Liao, Y., Plogg, B. A., Peng, W., Gundersen, G. A., Benveniste, H., Vates, G. E., Deane, R., Goldman, S. A., et al. (2012) · Science Translational Medicine · doi:10.1126/scitranslmed.3003748 · Cited by 5,824
Sleep Drives Metabolite Clearance from the Adult Brain
Xie, L., Kang, H., Xu, Q., Chen, M. J., Liao, Y., Thiyagarajan, M., O’Donnell, J., Christensen, D. J., Nicholson, C., Iliff, J. J., et al. (2013) · Science · doi:10.1126/science.1241224 · Cited by 5,411
Structure and function of the blood–brain barrier
Abbott, N. J., Patabendige, A. A. K., Dolman, D. E. M., Yusof, S. R., & Begley, D. J. (2010) · Neurobiology of Disease · doi:10.1016/j.nbd.2009.07.030 · Cited by 5,185
Daneman, R., & Prat, A. (2015) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a020412 · Cited by 3,437
Aquaporin-4 deletion in mice reduces brain edema after acute water intoxication and ischemic stroke
Manley, G. T., Fujimura, M., Ma, T., Noshita, N., Filiz, F., Bollen, A. W., Chan, P. H., & Verkman, A. S. (2000) · Nature Medicine · doi:10.1038/72256 · Cited by 1,501
Diffusion in Brain Extracellular Space
Syková, E., & Nicholson, C. (2008) · Physiological Reviews · doi:10.1152/physrev.00027.2007 · Cited by 1,481
Nielsen, S. M., Nagelhus, E. A., Amiry-Moghaddam, M. R., Bourque, C. W., Agre, P. C., & Ottersen, O. P. (1997) · Journal of Neuroscience · doi:10.1523/jneurosci.17-01-00171.1997 · Cited by 1,440
Brain-wide pathway for waste clearance captured by contrast-enhanced MRI
Iliff, J. J., Lee, H., Yu, M., Feng, T., Logan, J., Nedergaard, M., & Benveniste, H. (2013) · Journal of Clinical Investigation · doi:10.1172/jci67677 · Cited by 1,148
Blood–brain barrier structure and function and the challenges for CNS drug delivery
Abbott, N. J. (2013) · Journal of Inherited Metabolic Disease · doi:10.1007/s10545-013-9608-0 · Cited by 951
Mathiisen, T. M., Lehre, K. P., Danbolt, N. C., & Ottersen, O. (2010) · Glia · doi:10.1002/glia.20990 · Cited by 893
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Horie, T., Kajihara, N., Matsumae, M., Obara, M., Hayashi, N., Hirayama, A., Takizawa, K., Takahara, T., Yatsushiro, S., & Kuroda, K. (2016) · World Neurosurgery · doi:10.1016/j.wneu.2016.07.062 · Cited by 41
Schön, M., Kovaničová, Z., Košutzká, Z., Nemec, M., Tomková, M., Jacková, L., Máderová, D., Slobodová, L., Valkovič, P., Ukropec, J., et al. (2019) · Scientific Reports · doi:10.1038/s41598-018-38201-2 · Cited by 40
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Kompaníková, P., & Bryja, V. (2022) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-022-04314-1 · Cited by 42
Chen, J. C., Luu, A. R., Wise, N., Angelis, R. D., Agrawal, V., Mangini, L., Vincelette, J., Handyside, B., Sterling, H. J., Lo, M. J., et al. (2019) · Journal of Biological Chemistry · doi:10.1074/jbc.ra119.009811 · Cited by 41
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Teunissen, C. E., Verheul, C., & Willemse, E. A. J. (2017) · Handbook of clinical neurology · doi:10.1016/b978-0-12-804279-3.00001-0 · Cited by 40
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Hale, A. T., Bastarache, L. A., Morales, D. M., Wellons, J. C., Limbrick, D. D., & Gamazon, E. R. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.109085 · Cited by 39
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Gholampour, S., Bahmani, M., & Shariati, A. (2018) · Basic and Clinical Neuroscience Journal · doi:10.32598/bcn.9.10.285 · Cited by 38
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Ma, S., Björninen, T., Sydanheimo, L. T., Voutilainen, M. H., & Ukkonen, L. (2020) · IEEE Transactions on Antennas and Propagation · doi:10.1109/tap.2020.3016459 · Cited by 37
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Wilson, R., Osborne, C., & Halsey, C. (2018) · Pediatric Drugs · doi:10.1007/s40272-018-0298-9 · Cited by 35
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Rasmussen, J. C., Kwon, S., Pinal, A., Bareis, A., Velasquez, F. C., Janssen, C. F., Morrow, J. R., Fife, C. E., Karni, R. J., & Sevick-Muraca, E. M. (2020) · Physiological Reports · doi:10.14814/phy2.14375 · Cited by 36
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Knirsch, W., Heye, K., Scheer, I., Tuura, R., Schranz, D., Hahn, A., Wetterling, K., Beck, I., Latal, B., & Reich, B. (2016) · European Journal of Cardio-Thoracic Surgery · doi:10.1093/ejcts/ezw399 · Cited by 35
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Tuță, S. (2022) · Life · doi:10.3390/life12060854 · Cited by 29
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Faraji, A. H., Jaquins‐Gerstl, A., Valenta, A. C., Ou, Y., & Weber, S. G. (2020) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.0c00037 · Cited by 25
Hydrocephalus: An update on latest progress in pathophysiological and therapeutic research
Anwar, F., Zhang, K., Sun, C., Pang, M., Zhou, W., Li, H., He, R., Liu, X., & Ming, D. (2024) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2024.117702 · Cited by 24
Simats, A., García‐Berrocoso, T., Ramiro, L., Giralt, D., Gill, N., Peñalba, A., Bustamante, A., Rosell, A., & Montaner, J. (2018) · Scientific Reports · doi:10.1038/s41598-018-26237-3 · Cited by 24
Cao, D., Kang, N., Pillai, J. J., Miao, X., Paez, A. G., Xu, X., Xu, J., Xu, L., Qin, Q., van Zijl, P. C. M., et al. (2020) · Magnetic Resonance in Medicine · doi:10.1002/mrm.28389 · Cited by 25
[Retracted] Glymphatic System: Emerging Therapeutic Target for Neurological Diseases
Xuan, X., Zhou, G., Chen, C., Shao, A., Zhou, Y., Li, X., & Zhou, J. (2022) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2022/6189170 · Cited by 25
RetractedAβ Clearance, “hub” of Multiple Deficiencies Leading to Alzheimer Disease
Gallina, P., Scollato, A., Conti, R., Lorenzo, N. D., & Porfirio, B. (2015) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2015.00200 · Cited by 25
Zhang, C., Lin, J., Wei, F., Song, J. H., Chen, W., Shan, L., Xue, R., Wang, G., Tao, J., Zhang, G., et al. (2018) · Life Sciences · doi:10.1016/j.lfs.2018.03.057 · Cited by 24
Joseph, C. R., Benhatzel, C. M., Stern, L. J., Hopper, O. M., & Lockwood, M. D. (2020) · Magnetic Resonance Materials in Physics Biology and Medicine · doi:10.1007/s10334-019-00818-3 · Cited by 24
Robert, S. M., Reeves, B. C., Marlier, A., Duy, P. Q., DeSpenza, T., Kundishora, A. J., Kiziltug, E., Singh, A. K., Allington, G., Alper, S. L., et al. (2021) · Child s Nervous System · doi:10.1007/s00381-021-05255-z · Cited by 24
Basic principles of neuroimmunology
Yoshida, T. M., Wang, A., & Hafler, D. A. (2022) · Seminars in Immunopathology · doi:10.1007/s00281-022-00951-7 · Cited by 27
Ellenbogen, Y., Brar, K., Yang, K., Lee, Y., & Ajani, O. (2020) · Journal of Neurosurgery Pediatrics · doi:10.3171/2020.4.peds19720 · Cited by 23
Decoupling Between Brain Activity and Cerebrospinal Fluid Movement in Neurological Disorders
Liu, X. (2023) · Journal of Magnetic Resonance Imaging · doi:10.1002/jmri.29148 · Cited by 23
The role of astrocytes in the glymphatic network: a narrative review
Das, N., Dhamija, R., & Sarkar, S. (2023) · Metabolic Brain Disease · doi:10.1007/s11011-023-01327-y · Cited by 23
Immunological Barriers to Stem Cell Therapy in the Central Nervous System
Tullis, G. E., Spears, K., & Kirk, M. D. (2014) · Stem Cells International · doi:10.1155/2014/507905 · Cited by 23
Szpecht, D., Gadzinowski, J., Seremak‐Mrozikiewicz, A., Kurzawińska, G., & Szymankiewicz, M. (2017) · Scientific Reports · doi:10.1038/srep42541 · Cited by 23
Metadata
- Authors
- Brinker, T., Stopa, E., Morrison, J., & Klinge, P.
- Affiliations
- Brown University (US)
- Corresponding author
- Brinker, Thomas
- ORCID
- Klinge, Petra
- Venue
- Fluids and Barriers of the CNS
- Published
- 2014
- Volume
- 11
- Issue
- 1
- Pages
- 10
- ISSN
- 2045-8118 (ISSN-L)
- PMC
- PMC4016637
- OpenAlex
- W2157256907
- Cited by
- 819
- References
- 167
- Citations by year
- 2026: 32 · 2025: 63 · 2024: 66 · 2023: 72 · 2022: 105 · 2021: 72 · 2020: 70 · 2019: 91 · 2018: 74 · 2017: 68 · 2016: 48 · 2015: 42 · 2014: 13
- FWCI
- 6.51
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- cc-by
- Locations
- Fluids and Barriers of the CNS (publishedVersion, cc-by)
- Europe PMC (PubMed Central) (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Clinical Neurology › Cerebrospinal fluid and hydrocephalus
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Ion Transport and Channel Regulation
- Life Sciences › Neuroscience › Neurology › Barrier Structure and Function Studies
- Keywords
- cerebrospinal fluid flow, choroid plexus, arachnoid villi, CSF absorption, interstitial fluid, blood-CSF barrier, astrocytes, aquaporins, brain water homeostasis, perivascular spaces, cerebrospinal fluid drainage
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