Andrew Bacyinski1
Wei Wang
Jiani Hu- 1School of Medicine, Wayne State University, Detroit, MI, United States
- 2Department of Radiology, The First Affiliated Hospital of Zhejiang Chinese Medical University, Hangzhou, China
- 3Department of Radiology, Wayne State University, Detroit, MI, United States
The paravascular pathway, also known as the “glymphatic” pathway, is a recently described system for waste clearance in the brain. According to this model, cerebrospinal fluid (CSF) enters the paravascular spaces surrounding penetrating arteries of the brain, mixes with interstitial fluid (ISF) and solutes in the parenchyma, and exits along paravascular spaces of draining veins. Studies have shown that metabolic waste products and solutes, including proteins involved in the pathogenesis of neurodegenerative diseases such as amyloid-beta, may be cleared by this pathway. Consequently, a growing body of research has begun to explore the association between glymphatic dysfunction and various disease states. However, significant controversy exists in the literature regarding both the direction of waste clearance as well as the anatomical space in which the waste-fluid mixture is contained. Some studies have found no evidence of interstitial solute clearance along the paravascular space of veins. Rather, they demonstrate a perivascular pathway in which waste is cleared from the brain along an anatomically distinct perivascular space in a direction opposite to that of paravascular flow. Although possible explanations have been offered, none have been able to fully reconcile the discrepancies in the literature, and many questions remain. Given the therapeutic potential that a comprehensive understanding of brain waste clearance pathways might offer, further research and clarification is highly warranted.
Introduction
In peripheral tissues, the lymphatic system functions to clear proteins solutes and metabolic wastes from the interstitial spaces between cells (Ellis, 2006). The brain parenchyma lacks a typical, histologically identifiable lymphatic system, which is curious given the brain’s high metabolic rate and sensitivity to alterations in its extracellular space (Abbott, 2004). For decades, it was generally understood that waste substances in the central nervous system (CNS) were cleared to cerebrospinal fluid (CSF) by convective bulk flow of interstitial fluid (ISF) coursing diffusely through brain parenchyma (Cserr et al., 1981; Abbott, 2004; Sykova and Nicholson, 2008), draining into peripheral lymphatics of the neck to ultimately reach systemic circulation (Bradbury et al., 1981; Bradbury and Westrop, 1983). However, some early studies argued that, rather than a diffuse process, solute transport occurred via an anatomically and functionally discrete space surrounding the blood vessels of the brain (Földi et al., 1968; Rennels et al., 1985, 1990). This space, termed the paravascular space, was later identified as a possible route for the clearance of glucose, lactate and amyloid beta (Ball et al., 2010).
Recently, a team of researchers headed by Iliff and Nedergaard fully characterized the paravascular space as a pathway for the clearance of interstitial solutes. By tracking the movement of small fluorescent tracers, they showed that CSF enters the brain parenchyma along para-arterial spaces, mixes with ISF and solutes, and follows para-venous spaces to ultimately be removed from the brain. This paravascular pathway was termed the “glymphatic” system due to its dependence on glial cells and functional similarity to the peripheral lymphatic system (Iliff et al., 2012).
Since its discovery, significant research has been conducted on the paravascular pathway, further elucidating its physiological function and possible role in disease. However, disagreement still exists in the literature regarding the structures involved in interstitial waste clearance and the direction of fluid flow. This brief review article will examine the anatomy, function and clinical significance of the paravascular pathway, as well as the controversy associated with it. An examination of what is currently known and what remains to be clarified may provide inspiration for future research on this clinically important topic.
Anatomy of the Spaces Surrounding the Cerebral Vasculature
The brain is vascularized by the anterior and posterior cerebral circulation (Prince and Ahn, 2013). At the surface of the cortex, cerebral arteries form pial arteries, which extend through the subarachnoid and subpial spaces. Leptomeningeal cells forming a pial sheath are reflected from the surface of the brain to coat these arteries and veins in the CSF-containing subarachnoid space (Weller, 2005; Bakker et al., 2016). As pial arteries enter the brain parenchyma, they transition into penetrating arterioles with a surrounding paravascular space, known as the Virchow-Robin space (Zhang et al., 1990). This donut-shaped space surrounding the vasculature contains CSF and is bounded by a pial sheath internally and the basement membrane of astrocytic endfeet, known as the glia limitans, externally (Figure 1; Weller et al., 2009; Jessen et al., 2015; Bakker et al., 2016). Recent evidence suggests that, in rodent models, no pial sheath is found at the internal boundary of the paravascular space (Bedussi et al., 2017), and this space forms a continuous fluid compartment with the subarachnoid space (Bedussi et al., 2015). However, as reviewed by Brinker et al. (2014) there may be structural differences between rodents and humans regarding the continuity of the paravascular and subarachnoid spaces.
Figure 1. Anatomy of the paravascular and perivascular spaces. The arterial paravascular space is bounded internally by the pial sheath (4) and externally by the basement membrane of glia limitans (5). The venous paravascular space is bounded internally by the vein wall (6) and externally by the glia limitans. The perivascular space is found within the middle layers of the basement membrane of arterial smooth muscle cells (3). No perivascular space is present in venous vasculature. In each space, the direction of fluid flow and waste clearance, such as amyloid beta (Aβ), is depicted with arrows. Reprinted with permission © Bakker et al. (2016).
Another space exists within the arterial tunica media, between the middle layers of the basement membrane of arterial smooth muscle cells (Figure 1). This structure, known as the perivascular space, is also a conduit for fluid flow. Multiple studies have demonstrated its involvement in ISF and solute flux from the brain parenchyma to the cervical lymphatic system in a direction opposite to that of blood flow (Carare et al., 2008; Weller et al., 2009; Abbott, 2013; Hawkes et al., 2014; Bakker et al., 2016; Morris et al., 2016; Ueno et al., 2016). Retrograde fluid flow through this space forms the crux of the controversy surrounding the paravascular pathway and will be discussed later.
As penetrating arterioles dive deeper into the parenchyma and narrow to form capillaries, the smooth muscle layer and pial sheath are abolished, and both the paravascular and perivascular spaces become continuous with the endothelial basal lamina (Morris et al., 2016). This structure is a thin matrix derived from endothelial and astrocytic elements (Bakker et al., 2016; Morris et al., 2016). As capillaries continue to form venules and veins, this fluid-filled space expands and becomes bounded by the venous wall internally and the glia limitans externally (Figure 1). Thus, the paravascular space is a continuous compartment from arteries to capillaries to veins.
Proposed Model for Glymphatic Fluid Flow
With a working anatomical understanding of the compartments surrounding the cerebral vasculature, we can now turn our attention to the model of paravascular fluid flow. As described, the glymphatic system is composed of a unidirectional current of fluid flowing through the paravascular space of penetrating arteries and arterioles to that of large caliber parenchymal draining veins (Iliff et al., 2012). The schematic, seen in Figure 2, shows CSF entering the brain along the Virchow-Robins space and flowing centrally into brain parenchyma within the para-arterial compartment and capillary basal lamina. Due to the loose composition of the basal lamina, there is little resistance to CSF influx (Jessen et al., 2015). Large solutes (>100 kDa) present in CSF that lack a specific molecular transport pathway are unable to pass through the 20–50 nm clefts that separate astrocytic endfeet of the glia limitans and are constrained to this space, flowing along the capillary basal lamina as it becomes continuous with the perivenous space (Iliff et al., 2013; Jessen et al., 2015). CSF water, ions, and small solutes (<100 kDa) may enter the interstitial space through aquaporin-4 (AQP4) channels, ion transporters or channels, and astrocytic endfeet clefts, respectively (Iliff et al., 2012, 2013; Hubbard et al., 2015; Jessen et al., 2015). After mixing with ISF and interstitial solutes, this fluid re-enters the paravascular space of draining veins by similar mechanisms. From this space, waste may ultimately be cleared from the brain by draining into cervical lymphatics, dispersing into the subarachnoid CSF, or crossing the vasculature to enter the bloodstream (Iliff et al., 2012; Tarasoff-Conway et al., 2015; Louveau et al., 2016). Additionally, lymphatic vessels lining the dural sinuses have recently been identified (Louveau et al., 2015). These meningeal vessels may play an important role in draining glymphatic fluid and solutes to deep cervical lymph nodes and other peripheral structures.
Figure 2. Schematic of glymphatic and perivascular waste clearance routes. According to the glymphatic model, cerebrospinal fluid (CSF) flows along para-arterial spaces (1), mixes with interstitial fluid (ISF) and solutes (2), and is cleared from the brain along para-venous spaces (3). Efficient glymphatic clearance of waste and solutes is dependent on fluid movement across aquaporin-4 (AQP4) channels located on astrocytic endfeet surrounding the parenchymal vasculature. In contrast, perivascular drainage of ISF and solutes occurs along the middle layers of the basement membrane of arterial smooth muscle cells and, as indicated by arrows, flows in a direction opposite to that of glymphatic clearance. Reprinted with permission from Macmillan Publishers Ltd: © Tarasoff-Conway et al. (2015).
Consistent with previous observations (Cserr et al., 1981; Geer and Grossman, 1997; Abbott, 2004), it was postulated by Iliff and Nedergaard that the transport of CSF and solutes through the glymphatic pathway was driven by convective bulk flow, which is characterized by the concomitant movement of water and solutes due to changes in pressure gradients (Iliff et al., 2012). They hypothesized that high pressure arterial pulsations, combined with low pressure paravenous spaces and increased expression of AQP4 in paravenous astrocytic endfeet, may create an arteriovenous hydrostatic gradient that drives paravascular CSF bulk flow and ISF clearance (Iliff et al., 2012). Further evidence suggests that respiration, vasomotor wave fluctuations, and body posture may also contribute to this mechanism (Lee et al., 2015; Kiviniemi et al., 2016). Recently, however, the bulk flow hypothesis has been challenged (Hladky and Barrand, 2014; Asgari et al., 2016). Future studies investigating the forces driving fluid flow through the paravascular pathway are expected.
Function and Significance of the Paravascular Pathway
The glymphatic system allows for intimate exchange between CSF and ISF, and is involved in the delivery of nutrients to brain parenchyma and interstitial waste clearance (Matsumae et al., 2016). Recent studies have demonstrated that apolipoprotein E, small lipid molecules and signaling molecules may be delivered from CSF to the brain parenchyma via the glymphatic pathway (Rangroo Thrane et al., 2013; Achariyar et al., 2016). ApoE, a compound highly expressed by the choroid plexus and the predominant apolipoprotein in CSF, is a major carrier of cholesterol and is essential for neuron function and plasticity. Although this lipoprotein is locally produced by astrocytes, glymphatic transport of CSF-derived ApoE may facilitate a wider distribution in the brain parenchyma. It is likely that the glymphatic pathway also contributes to the distribution of other growth factors, neuromodulators, carrier proteins, and nutrients (Kress et al., 2014). Additionally, the paravascular system might serve as a useful pathway for drug delivery to the brain (Hadaczek et al., 2006).
It is well established that the glymphatic system participates in the removal of amyloid beta (Aβ), a pathological hallmark of Alzheimer disease, from the brain (Tarasoff-Conway et al., 2015; Simon and Iliff, 2016). Iliff and Nedergaard originally demonstrated that the clearance of radiolabeled Aβ injected into brain parenchyma was cleared via paravascular routes. Moreover, they found that this process was dependent on AQP4, as AQP4-knockout mice showed a 55% reduction in Aβ clearance compared to controls (Iliff et al., 2012). A later study explored Aβ clearance in the aging brain and found a 40% reduction in old mice compared to young, accompanied by decreased arterial pulsatility and AQP4 expression (Kress et al., 2014). Other studies have found decreased glymphatic Aβ clearance in various disease state models, including sleep deprivation (Xie et al., 2013), depression (Xia et al., 2017) and obstructive sleep apnea (Ju et al., 2016). In contrast, exercise (He et al., 2017) and omega-3 fatty acids (Ren et al., 2017) have been associated with improved glymphatic Aβ removal. Not surprisingly, dysfunction of the paravascular pathway may serve as an early biomarker of Alzheimer disease (Peng et al., 2016), and novel methods of evaluating glymphatic function are currently being developed (Yang et al., 2013; Eide and Ringstad, 2015; Huffman et al., 2016; Kiviniemi et al., 2016; Ramirez et al., 2016; Rivera-Rivera et al., 2016; Taoka et al., 2017).
In addition to Aβ clearance, the glymphatic system may be involved in the removal of other interstitial solutes and metabolites. By measuring the lactate concentration in the brains and cervical lymph nodes of awake and sleeping mice, Lundgaard et al. (2017) demonstrated that lactate can exit the CNS via the paravascular pathway. Their analysis took advantage of the substantiated hypothesis that glymphatic function is promoted during sleep (Xie et al., 2013; Lee et al., 2015; Liu et al., 2017). In another study, Iliff et al. (2014) showed that tau, a protein implicated in progressive neurodegenerative diseases, is also cleared by this pathway. Moreover, they demonstrated that glymphatic function is impaired after traumatic brain injury, which is clinically relevant given that common biomarkers for this insult are transported to the peripheral blood via the paravascular pathway (Plog et al., 2015). There is also evidence that alpha-synuclein, a protein involved in neurodegenerative diseases such as Parkinson’s disease, may also be cleared, and possibly spread, by this pathway (Valdinocci et al., 2017).
As dysfunction of the glymphatic system has been implicated in many disease states, including neurodegenerative disease (Iliff et al., 2012, 2014), microinfarcts (Venkat et al., 2017; Wang et al., 2017), migraines (Schain et al., 2017), diabetes (Jiang et al., 2017) and glaucoma (Wostyn et al., 2017), further research on this pathway is highly anticipated. However, the literature suggests that the glymphatic system may not be the only route for waste clearance in the brain. Multiple studies have shown that a perivascular pathway plays an important role in the drainage of ISF and solutes to peripheral structures.
Controversy: the Perivascular Pathway
Evidence for a periarterial pathway for brain waste clearance was demonstrated as early as 1984. Szentistványi et al. (1984) discovered that when tracer was injected into the brain parenchyma of mice, it subsequently was found in the periarterial space of major cerebral arteries supplying the tissue. Interestingly, the measured concentration of tracer was much higher within the periarterial space than the surrounding CSF, and no tracer was found along draining veins. In 2008, similar results were demonstrated by Carare et al. (2008), who used confocal microscopy to visualize tracer in the basement membrane of capillaries and within the tunica media of penetrating arteries following injection into the gray matter of the caudate and putamen in mice. These results have been verified and expounded upon in more recent experiments (Arbel-Ornath et al., 2013; Morris et al., 2016), further lending evidence to the perivascular hypothesis.
The current model for the perivascular pathway depicts ISF and solutes entering the basement membrane of capillaries and following the tunica media of penetrating arteries within the basal lamina of smooth muscle cells. Curiously, solute clearance via the perivascular pathway is in a direction opposite to that of paravascular flow and blood flow (Figure 2). From the peri-arterial space, solute may ultimately be cleared from the brain by dispersing in CSF (Zhang et al., 1992; Kida et al., 1993; Carare et al., 2008) or directly emptying into peripheral lymphatic tissue surrounding the large arteries of the neck (Szentistványi et al., 1984; Shinkai et al., 1995; Weller, 2005).
The direction of fluid flow described by the perivascular and paravascular models seems to be the foundation of the controversy in the literature, and may be partially explained by methodological differences between studies. Bakker et al. (2016) note that, historically, most studies in which tracer was injected into CSF resulted in paravascular flow, while studies in which tracer was injected into brain parenchyma resulted in perivascular flow. Pressure and volume disturbances from injected tracer (Hladky and Barrand, 2014), compounded with dispersion forces caused by arterial pulsations (Asgari et al., 2016), may account for these differences. In their 2012 study, Iliff and Nedergaard maintained that the small amount of tracer Aβ observed in the periarterial space surrounding the parenchymal injection site was an artifact and did not reflect the natural pathway for solute efflux. In contrast to other studies, they showed that most of the labeled Aβ was localized around capillaries and draining veins following parenchymal injection, demonstrating paravascular flow (Iliff et al., 2012). However, other studies have demonstrated that both labeled and native Aβ is predominantly distributed in the walls of arteries, not veins (Hawkes et al., 2011, 2014). Is there a different explanation?
Another possibility that may account for the discrepancies noted in various studies is that the pathways are in fact two distinct systems functioning simultaneously (Morris et al., 2016). At the level of the penetrating arterioles the paravascular and perivascular spaces are separate, and fluid flow through one space does not necessarily preclude flow through the other. A comprehensive and recent review by Hladky and Barrand (2014) argues that the two pathways are not mutually exclusive, and both may contribute to interstitial solute clearance depending on the conditions and local environment within the brain. However, other authors have been critical of this idea, suggesting that the concomitant existence of the two pathways would make little sense physiologically, given the opposing directions of fluid flow, especially at the level of the capillary where only one compartment is present (Bakker et al., 2016). Furthermore, a recent study found no pial sheath separating the perivascular and paravascular spaces in mice (Bedussi et al., 2017), suggesting that the two spaces may be functionally continuous. If this is true in humans, it is unlikely that both pathways would function simultaneously under physiological conditions.
Obviously, many questions concerning the two pathways require further elucidation. Are they distinct compartments in humans or anatomically and functionally continuous? Does normal interstitial solute clearance follow a periarterial route, a paravenous route, or both? Does this process change with disease? What are the driving forces behind these pathways? Further research and clarification is highly anticipated.
Summary
In conclusion, the paravascular pathway is a recently characterized system for waste clearance in the brain. Since its discovery, a growing body of evidence has demonstrated the importance of this discrete system in metabolite and protein removal and, to a lesser extent, nutrient delivery. However, discrepancies in the literature suggest that there may be other mechanisms and complexities by which waste products are cleared to peripheral tissues. A comprehensive understanding of the routes by which brain-derived pathologic proteins and wastes are transported may give insight into the pathophysiology and treatment of neurodegenerative disease. While no explanation to date has been able to fully account for the inconsistencies noted in the literature, the studies reviewed in this article lay a solid foundation for future inquiry and discussion.
Author Contributions
All the authors contributed substantially to the work, including the concept, literature review, manuscript drafting and final review.
Funding
This work was supported in part by the National Institutes of Health (NIH) through Grant No. R21 CA184682 and RF1 AG057494. Its contents are solely the responsibility of the authors and do not necessarily represent the official views of the NIH. The views, opinions and/or findings contained in this report are those of the author(s) and should not be construed as an official government position, policy or decision unless so designated by other documentation.
Conflict of Interest Statement
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
The reviewer MS and handling Editor declared their shared affiliation.
References
Abbott, N. J. (2004). Evidence for bulk flow of brain interstitial fluid: significance for physiology and pathology. Neurochem. Int. 45, 545–552. doi: 10.1016/j.neuint.2003.11.006
Abbott, N. J. (2013). Blood-brain barrier structure and function and the challenges for CNS drug delivery. J. Inherit. Metab. Dis. 36, 437–449. doi: 10.1007/s10545-013-9608-0
Achariyar, T. M., Li, B., Peng, W., Verghese, P. B., Shi, Y., McConnell, E., et al. (2016). Glymphatic distribution of CSF-derived apoE into brain is isoform specific and suppressed during sleep deprivation. Mol. Neurodegener. 11:74. doi: 10.1186/s13024-016-0138-8
Arbel-Ornath, M., Hudry, E., Eikermann-Haerter, K., Hou, S., Gregory, J. L., Zhao, L., et al. (2013). Interstitial fluid drainage is impaired in ischemic stroke and Alzheimer’s disease mouse models. Acta Neuropathol. 126, 353–364. doi: 10.1007/s00401-013-1145-2
Asgari, M., de Zélicourt, D., and Kurtcuoglu, V. (2016). Glymphatic solute transport does not require bulk flow. Sci. Rep. 6:38635. doi: 10.1038/srep38635
Bakker, E. N., Bacskai, B. J., Arbel-Ornath, M., Aldea, R., Bedussi, B., Morris, A. W., et al. (2016). Lymphatic clearance of the brain: perivascular, paravascular and significance for neurodegenerative diseases. Cell. Mol. Neurobiol. 36, 181–194. doi: 10.1007/s10571-015-0273-8
Ball, K. K., Cruz, N. F., Mrak, R. E., and Dienel, G. A. (2010). Trafficking of glucose, lactate and amyloid-β from the inferior colliculus through perivascular routes. J. Cereb. Blood Flow Metab. 30, 162–176. doi: 10.1038/jcbfm.2009.206
Bedussi, B., van der Wel, N. N., de Vos, J., van Veen, H., Siebes, M., VanBavel, E., et al. (2017). Paravascular channels, cisterns, and the subarachnoid space in the rat brain: a single compartment with preferential pathways. J. Cereb. Blood Flow Metab. 37, 1374–1385. doi: 10.1177/0271678x16655550
Bedussi, B., van Lier, M. G., Bartstra, J. W., de Vos, J., Siebes, M., VanBavel, E., et al. (2015). Clearance from the mouse brain by convection of interstitial fluid towards the ventricular system. Fluids Barriers CNS 12:23. doi: 10.1186/s12987-015-0019-5
Bradbury, M. W., Cserr, H. F., and Westrop, R. J. (1981). Drainage of cerebral interstitial fluid into deep cervical lymph of the rabbit. Am. J. Physiol. 240, F329–F336.
Bradbury, M. W., and Westrop, R. J. (1983). Factors influencing exit of substances from cerebrospinal fluid into deep cervical lymph of the rabbit. J. Physiol. 339, 519–534. doi: 10.1113/jphysiol.1983.sp014731
Brinker, T., Stopa, E., Morrison, J., and Klinge, P. (2014). A new look at cerebrospinal fluid circulation. Fluids Barriers CNS 11:10. doi: 10.1186/2045-8118-11-10
Carare, R. O., Bernardes-Silva, M., Newman, T. A., Page, A. M., Nicoll, J. A., Perry, V. H., et al. (2008). Solutes, but not cells, drain from the brain parenchyma along basement membranes of capillaries and arteries: significance for cerebral amyloid angiopathy and neuroimmunology. Neuropathol. Appl. Neurobiol. 34, 131–144. doi: 10.1111/j.1365-2990.2007.00926.x
Cserr, H. F., Cooper, D. N., Suri, P. K., and Patlak, C. S. (1981). Efflux of radiolabeled polyethylene glycols and albumin from rat brain. Am. J. Physiol. 240, F319–F328.
Eide, P. K., and Ringstad, G. (2015). MRI with intrathecal MRI gadolinium contrast medium administration: a possible method to assess glymphatic function in human brain. Acta Radiol. Open 4:2058460115609635. doi: 10.1177/2058460115609635
Ellis, S. (2006). Structure and function of the lymphatic system: an overview. Br. J. Community Nurs. 11, S4–S6. doi: 10.12968/bjcn.2006.11.sup2.20841
Földi, M., Csillik, B., and Zoltán, O. T. (1968). Lymphatic drainage of the brain. Experientia 24, 1283–1287. doi: 10.1007/bf02146675
Geer, C. P., and Grossman, S. A. (1997). Interstitial fluid flow along white matter tracts: a potentially important mechanism for the dissemination of primary brain tumors. J. Neurooncol. 32, 193–201. doi: 10.1023/A:1005761031077
Hadaczek, P., Yamashita, Y., Mirek, H., Tamas, L., Bohn, M. C., Noble, C., et al. (2006). The “perivascular pump” driven by arterial pulsation is a powerful mechanism for the distribution of therapeutic molecules within the brain. Mol. Ther. 14, 69–78. doi: 10.1016/j.ymthe.2006.02.018
Hawkes, C. A., Jayakody, N., Johnston, D. A., Bechmann, I., and Carare, R. O. (2014). Failure of perivascular drainage of β-amyloid in cerebral amyloid angiopathy. Brain Pathol. 24, 396–403. doi: 10.1111/bpa.12159
Hawkes, C. A., Härtig, W., Kacza, J., Schliebs, R., Weller, R. O., Nicoll, J. A., et al. (2011). Perivascular drainage of solutes is impaired in the ageing mouse brain and in the presence of cerebral amyloid angiopathy. Acta Neuropathol. 121, 431–443. doi: 10.1007/s00401-011-0801-7
He, X. F., Liu, D. X., Zhang, Q., Liang, F. Y., Dai, G. Y., Zeng, J. S., et al. (2017). Voluntary exercise promotes glymphatic clearance of amyloid β and reduces the activation of astrocytes and microglia in aged mice. Front. Mol. Neurosci. 10:144. doi: 10.3389/fnmol.2017.00144
Hladky, S. B., and Barrand, M. A. (2014). Mechanisms of fluid movement into, through and out of the brain: evaluation of the evidence. Fluids Barriers CNS 11:26. doi: 10.1186/2045-8118-11-26
Hubbard, J. A., Hsu, M. S., Seldin, M. M., and Binder, D. K. (2015). Expression of the astrocyte water channel aquaporin-4 in the mouse brain. ASN Neuro 7:1759091415605486. doi: 10.1177/1759091415605486
Huffman, J., Phillips, S., Taylor, G. T., and Paul, R. (2016). The emerging field of perivascular flow dynamics: biological relevance and clinical applications. Technol. Innov. 18, 63–74. doi: 10.21300/18.1.2016.63
Iliff, J. J., Chen, M. J., Plog, B. A., Zeppenfeld, D. M., Soltero, M., Yang, L., et al. (2014). Impairment of glymphatic pathway function promotes tau pathology after traumatic brain injury. J. Neurosci. 34, 16180–16193. doi: 10.1523/JNEUROSCI.3020-14.2014
Iliff, J. J., Lee, H., Yu, M., Feng, T., Logan, J., Nedergaard, M., et al. (2013). Brain-wide pathway for waste clearance captured by contrast-enhanced MRI. J. Clin. Invest. 123, 1299–1309. doi: 10.1172/JCI67677
Iliff, J. J., Wang, M., Liao, Y., Plogg, B. A., Peng, W., Gundersen, G. A., et al. (2012). A paravascular pathway facilitates CSF flow through the brain parenchyma and the clearance of interstitial solutes, including amyloid β. Sci. Transl. Med. 4:147ra111. doi: 10.1126/scitranslmed.3003748
Jessen, N. A., Munk, A. S., Lundgaard, I., and Nedergaard, M. (2015). The glymphatic system: a beginner’s guide. Neurochem. Res. 40, 2583–2599. doi: 10.1007/s11064-015-1581-6
Jiang, Q., Zhang, L., Ding, G., Davoodi-Bojd, E., Li, Q., Li, L., et al. (2017). Impairment of the glymphatic system after diabetes. J. Cereb. Blood Flow Metab. 37, 1326–1337. doi: 10.1177/0271678x16654702
Ju, Y. E., Finn, M. B., Sutphen, C. L., Herries, E. M., Jerome, G. M., Ladenson, J. H., et al. (2016). Obstructive sleep apnea decreases central nervous system-derived proteins in the cerebrospinal fluid. Ann. Neurol. 80, 154–159. doi: 10.1002/ana.24672
Kida, S., Pantazis, A., and Weller, R. O. (1993). CSF drains directly from the subarachnoid space into nasal lymphatics in the rat. Anatomy, histology and immunological significance. Neuropathol. Appl. Neurobiol. 19, 480–488. doi: 10.1111/j.1365-2990.1993.tb00476.x
Kiviniemi, V., Wang, X., Korhonen, V., Keinänen, T., Tuovinen, T., Autio, J., et al. (2016). Ultra-fast magnetic resonance encephalography of physiological brain activity—Glymphatic pulsation mechanisms? J. Cereb. Blood Flow Metab. 36, 1033–1045. doi: 10.1177/0271678X15622047
Kress, B. T., Iliff, J. J., Xia, M., Wang, M., Wei, H. S., Zeppenfeld, D., et al. (2014). Impairment of paravascular clearance pathways in the aging brain. Ann. Neurol. 76, 845–861. doi: 10.1002/ana.24271
Lee, H., Xie, L., Yu, M., Kang, H., Feng, T., Deane, R., et al. (2015). The effect of body posture on brain glymphatic transport. J. Neurosci. 35, 11034–11044. doi: 10.1523/JNEUROSCI.1625-15.2015
Liu, D. X., He, X., Wu, D., Zhang, Q., Yang, C., Liang, F. Y., et al. (2017). Continuous theta burst stimulation facilitates the clearance efficiency of the glymphatic pathway in a mouse model of sleep deprivation. Neurosci. Lett. 653, 189–194. doi: 10.1016/j.neulet.2017.05.064
Louveau, A., Da Mesquita, S., and Kipnis, J. (2016). Lymphatics in neurological disorders: a neuro-lympho-vascular component of multiple sclerosis and Alzheimer’s disease? Neuron 91, 957–973. doi: 10.1016/j.neuron.2016.08.027
Louveau, A., Smirnov, I., Keyes, T. J., Eccles, J. D., Rouhani, S. J., Peske, J. D., et al. (2015). Structural and functional features of central nervous system lymphatic vessels. Nature 523, 337–341. doi: 10.1038/nature14432
Lundgaard, I., Lu, M. L., Yang, E., Peng, W., Mestre, H., Hitomi, E., et al. (2017). Glymphatic clearance controls state-dependent changes in brain lactate concentration. J. Cereb. Blood Flow Metab. 37, 2112–2124. doi: 10.1177/0271678x16661202
Matsumae, M., Atsumi, H., Hirayama, A., Hayashi, N., Takizawa, K., Sano, F., et al. (2016). A new look at cerebrospinal fluid motion. No Shinkei Geka 44, 909–924. doi: 10.11477/mf.1436203402
Morris, A. W., Sharp, M. M., Albargothy, N. J., Fernandes, R., Hawkes, C. A., Verma, A., et al. (2016). Vascular basement membranes as pathways for the passage of fluid into and out of the brain. Acta Neuropathol. 131, 725–736. doi: 10.1007/s00401-016-1555-z
Peng, W., Achariyar, T. M., Li, B., Liao, Y., Mestre, H., Hitomi, E., et al. (2016). Suppression of glymphatic fluid transport in a mouse model of Alzheimer’s disease. Neurobiol. Dis. 93, 215–225. doi: 10.1016/j.nbd.2016.05.015
Plog, B. A., Dashnaw, M. L., Hitomi, E., Peng, W., Liao, Y., Lou, N., et al. (2015). Biomarkers of traumatic injury are transported from brain to blood via the glymphatic system. J. Neurosci. 35, 518–526. doi: 10.1523/JNEUROSCI.3742-14.2015
Prince, E. A., and Ahn, S. H. (2013). Basic vascular neuroanatomy of the brain and spine: what the general interventional radiologist needs to know. Semin. Intervent. Radiol. 30, 234–239. doi: 10.1055/s-0033-1353475
Ramirez, J., Berezuk, C., McNeely, A. A., Gao, F., McLaurin, J., and Black, S. E. (2016). Imaging the perivascular space as a potential biomarker of neurovascular and neurodegenerative diseases. Cell. Mol. Neurobiol. 36, 289–299. doi: 10.1007/s10571-016-0343-6
Rangroo Thrane, V., Thrane, A. S., Plog, B. A., Thiyagarajan, M., Iliff, J. J., Deane, R., et al. (2013). Paravascular microcirculation facilitates rapid lipid transport and astrocyte signaling in the brain. Sci. Rep. 3:2582. doi: 10.1038/srep02582
Ren, H., Luo, C., Feng, Y., Yao, X., Shi, Z., Liang, F., et al. (2017). Omega-3 polyunsaturated fatty acids promote amyloid-β clearance from the brain through mediating the function of the glymphatic system. FASEB J. 31, 282–293. doi: 10.1096/fj.201600896
Rennels, M. L., Blaumanis, O. R., and Grady, P. A. (1990). Rapid solute transport throughout the brain via paravascular fluid pathways. Adv. Neurol. 52, 431–439.
Rennels, M. L., Gregory, T. F., Blaumanis, O. R., Fujimoto, K., and Grady, P. A. (1985). Evidence for a ‘paravascular’ fluid circulation in the mammalian central nervous system, provided by the rapid distribution of tracer protein throughout the brain from the subarachnoid space. Brain Res. 326, 47–63. doi: 10.1016/0006-8993(85)91383-6
Rivera-Rivera, L. A., Turski, P., Johnson, K. M., Hoffman, C., Berman, S. E., Kilgas, P., et al. (2016). 4D flow MRI for intracranial hemodynamics assessment in Alzheimer’s disease. J. Cereb. Blood Flow Metab. 36, 1718–1730. doi: 10.1177/0271678x15617171
Schain, A. J., Melo-Carrillo, A., Strassman, A. M., and Burstein, R. (2017). Cortical spreading depression closes paravascular space and impairs glymphatic flow: implications for migraine headache. J. Neurosci. 37, 2904–2915. doi: 10.1523/JNEUROSCI.3390-16.2017
Shinkai, Y., Yoshimura, M., Ito, Y., Odaka, A., Suzuki, N., Yanagisawa, K., et al. (1995). Amyloid β-proteins 1–40 and 1-42(43) in the soluble fraction of extra- and intracranial blood vessels. Ann. Neurol. 38, 421–428. doi: 10.1002/ana.410380312
Simon, M. J., and Iliff, J. J. (2016). Regulation of cerebrospinal fluid (CSF) flow in neurodegenerative, neurovascular and neuroinflammatory disease. Biochim. Biophys. Acta 1862, 442–451. doi: 10.1016/j.bbadis.2015.10.014
Sykova, E., and Nicholson, C. (2008). Diffusion in brain extracellular space. Physiol. Rev. 88, 1277–1340. doi: 10.1152/physrev.00027.2007
Szentistványi, I., Patlak, C. S., Ellis, R. A., and Cserr, H. F. (1984). Drainage of interstitial fluid from different regions of rat brain. Am. J. Physiol. 246, F835–F844.
Taoka, T., Masutani, Y., Kawai, H., Nakane, T., Matsuoka, K., Yasuno, F., et al. (2017). Evaluation of glymphatic system activity with the diffusion MR technique: diffusion tensor image analysis along the perivascular space (DTI-ALPS) in Alzheimer’s disease cases. Jpn. J. Radiol. 35, 172–178. doi: 10.1007/s11604-017-0617-z
Tarasoff-Conway, J. M., Carare, R. O., Osorio, R. S., Glodzik, L., Butler, T., Fieremans, E., et al. (2015). Clearance systems in the brain-implications for Alzheimer disease. Nat. Rev. Neurol. 11, 457–470. doi: 10.1038/nrneurol.2015.119
Ueno, M., Chiba, Y., Murakami, R., Matsumoto, K., Kawauchi, M., and Fujihara, R. (2016). Blood-brain barrier and blood-cerebrospinal fluid barrier in normal and pathological conditions. Brain Tumor Pathol. 33, 89–96. doi: 10.1007/s10014-016-0255-7
Valdinocci, D., Radford, R. A., Siow, S. M., Chung, R. S., and Pountney, D. L. (2017). Potential modes of intercellular α-synuclein transmission. Int. J. Mol. Sci. 18:E469. doi: 10.3390/ijms18020469
Venkat, P., Chopp, M., Zacharek, A., Cui, C., Zhang, L., Li, Q., et al. (2017). White matter damage and glymphatic dysfunction in a model of vascular dementia in rats with no prior vascular pathologies. Neurobiol. Aging 50, 96–106. doi: 10.1016/j.neurobiolaging.2016.11.002
Wang, M., Ding, F., Deng, S., Guo, X., Wang, W., Iliff, J. J., et al. (2017). Focal solute trapping and global glymphatic pathway impairment in a murine model of multiple microinfarcts. J. Neurosci. 37, 2870–2877. doi: 10.1523/JNEUROSCI.2112-16.2017
Weller, R. O. (2005). Microscopic morphology and histology of the human meninges. Morphologie 89, 22–34. doi: 10.1016/s1286-0115(05)83235-7
Weller, R. O., Djuanda, E., Yow, H. Y., and Carare, R. O. (2009). Lymphatic drainage of the brain and the pathophysiology of neurological disease. Acta Neuropathol. 117, 1–14. doi: 10.1007/s00401-008-0457-0
Wostyn, P., Killer, H. E., and De Deyn, P. P. (2017). Glymphatic stasis at the site of the lamina cribrosa as a potential mechanism underlying open-angle glaucoma. Clin. Exp. Ophthalmol. 45, 539–547. doi: 10.1111/ceo.12915
Xia, M., Yang, L., Sun, G., Qi, S., and Li, B. (2017). Mechanism of depression as a risk factor in the development of Alzheimer’s disease: the function of AQP4 and the glymphatic system. Psychopharmacology (Berl) 234, 365–379. doi: 10.1007/s00213-016-4473-9
Xie, L., Kang, H., Xu, Q., Chen, M. J., Liao, Y., Thiyagarajan, M., et al. (2013). Sleep drives metabolite clearance from the adult brain. Science 342, 373–377. doi: 10.1126/science.1241224
Yang, L., Kress, B. T., Weber, H. J., Thiyagarajan, M., Wang, B., Deane, R., et al. (2013). Evaluating glymphatic pathway function utilizing clinically relevant intrathecal infusion of CSF tracer. J. Transl. Med. 11:107. doi: 10.1186/1479-5876-11-107
Zhang, E. T., Inman, C. B., and Weller, R. O. (1990). Interrelationships of the pia mater and the perivascular (Virchow-Robin) spaces in the human cerebrum. J. Anat. 170, 111–123.
Keywords: paravascular pathway, glymphatic system, perivascular pathway, brain waste clearance, amyloid-beta
Citation: Bacyinski A, Xu M, Wang W and Hu J (2017) The Paravascular Pathway for Brain Waste Clearance: Current Understanding, Significance and Controversy. Front. Neuroanat. 11:101. doi: 10.3389/fnana.2017.00101
Received: 09 September 2017; Accepted: 24 October 2017;
Published: 07 November 2017.
Edited by:
Francesco Fornai, University of Pisa, ItalyReviewed by:
Marco Scarselli, University of Pisa, ItalyYu-Min Kuo, National Cheng Kung University, Taiwan
Copyright © 2017 Bacyinski, Xu, Wang and Hu. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Wei Wang, wangwei_hz@zcmu.edu.cn
Jiani Hu, jhu@med.wayne.edu