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Lipid Transport and Metabolism at the Blood-Brain Interface: Implications in Health and Disease
Abstract
Many prospective studies have shown that a diet enriched in omega-3 polyunsaturated fatty acids (n-3 PUFAs) can improve cognitive function during normal aging and prevent the development of neurocognitive diseases. However, researchers have not elucidated how n-3 PUFAs are transferred from the blood to the brain or how they relate to cognitive scores. Transport into and out of the central nervous system depends on two main sets of barriers: the blood-brain barrier (BBB) between peripheral blood and brain tissue and the blood-cerebrospinal fluid (CSF) barrier (BCSFB) between the blood and the CSF. In this review, the current knowledge of how lipids cross these barriers to reach the CNS is presented and discussed. Implications of these processes in health and disease, particularly during aging and neurodegenerative diseases, are also addressed. An assessment provided here is that the current knowledge of how lipids cross these barriers in humans is limited, which hence potentially restrains our capacity to intervene in and prevent neurodegenerative diseases.
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Transcytosis across the blood-brain barrier occurs as an efflux mechanism to eliminate cholesterol excess.
“Transcytosis across the blood-brain barrier (BBB) occurs as an efflux mechanism to eliminate cholesterol excess.21”
From Canonical Wnt pathway and the LDL receptor superfamily in neuronal cholesterol homeostasis and function (2024) · cites this paper as [21]
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Ngandu, T., Lehtisalo, J., Solomon, A., Levälahti, E., Ahtiluoto, S., Antikainen, R., Bäckman, L., Hänninen, T., Jula, A., Laatikainen, T., et al. (2015) · The Lancet · doi:10.1016/s0140-6736(15)60461-5 · Cited by 3,689
Neurovascular pathways to neurodegeneration in Alzheimer’s disease and other disorders
Zlokovic, B. V. (2011) · Nature Reviews Neuroscience · doi:10.1038/nrn3114 · Cited by 2,969
Cerebrospinal fluid secretion by the choroid plexus
Damkier, H. H., Brown, P. D., & Praetorius, J. (2013) · Physiological Reviews · doi:10.1152/physrev.00004.2013 · Cited by 606
Age-Dependent Niche Signals from the Choroid Plexus Regulate Adult Neural Stem Cells
Silva-Vargas, V., Maldonado-Soto, A. R., Mizrak, D., Codega, P., & Doetsch, F. (2016) · Cell stem cell · doi:10.1016/j.stem.2016.06.013 · Cited by 306
Dehouck, B., Dehouck, M. P., Fruchart, J. C., & Cecchelli, R. (1994) · The Journal of cell biology · doi:10.1083/jcb.126.2.465 · Cited by 240
Svennerholm, L., Boström, K., & Jungbjer, B. (1997) · Acta Neuropathologica · doi:10.1007/s004010050717 · Cited by 232
Circulating metabolites and general cognitive ability and dementia: evidence from 11 cohort studies
van der Lee, S. J., Teunissen, C. E., Pool, R., Shipley, M. J., Teumer, A., Chouraki, V., Melo van Lent, D., Tynkkynen, J., Fischer, K., Hernesniemi, J., et al. (2018) · Alzheimer's & Dementia · doi:10.1016/j.jalz.2017.11.012 · Cited by 197
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Research works printed but not linked: 82
- Alberghina, 1994, Differential transport of docosahexaenoate and palmitate through the blood-retina and blood-brain barrier of the rat., Neurosci. Lett., 171, 133, 10.1016/0304-3940(94)90623-8 · DOI
- Alberghina, 1993, Palmitate transport through the blood-retina and blood-brain barrier of rat visual system during aging., Neurosci. Lett., 150, 17, 10.1016/0304-3940(93)90097-5 · DOI
- Andreone, 2017, Blood-Brain barrier permeability is regulated by lipid transport-dependent suppression of caveolae-mediated transcytosis., Neuron, 94, 581, 10.1016/j.neuron.2017.03.043 · DOI · Paper page
- Balusu, 2016, The choroid plexus-cerebrospinal fluid interface in Alzheimer’s disease: more than just a barrier., Neural Regen. Res., 11, 534, 10.4103/1673-5374.180372 · DOI
- Banks, 2016, From blood–brain barrier to blood–brain interface: new opportunities for CNS drug delivery., Nat. Rev. Drug Discov., 15, 275, 10.1038/nrd.2015.21 · DOI · Paper page
- Benistant, 1995, Fatty acid composition of brain capillary endothelial cells: effect of the coculture with astrocytes., J. Lipid Res., 36, 2311, 10.1016/S0022-2275(20)39712-1 · DOI
- Ben-Zvi, 2014, Mfsd2a is critical for the formation and function of the blood-brain barrier., Nature, 509, 507, 10.1038/nature13324 · DOI · Paper page
- Bernoud, 1998, Astrocytes are mainly responsible for the polyunsaturated fatty acid enrichment in blood-brain barrier endothelial cells in vitro., J. Lipid Res., 39, 1816, 10.1016/S0022-2275(20)32169-6 · DOI
- Björkhem, 2004, Brain cholesterol: long secret life behind a barrier., Arterioscler. Thromb. Vasc. Biol., 24, 806, 10.1161/01.ATV.0000120374.59826.1b · DOI · Paper page
- Bourre, 1991, Protection contre les peroxidations radicalaires au cours du vieillissement cerebral dans les capillaires et microvaisseaux cérébraux., C.R. Seances Soc. Biol. Fil., 185, 5
- Bourre, 2006, Effects of nutrients (in food) on the structure and function of the nervous system: update on dietary requirements for brain. Part 2: macronutrients., J. Nutr. Health Aging, 10, 386
- Bourre, 1997, Possible role of the choroid plexus in the supply of brain tissue with polyunsaturated fatty acids., Neurosci. Lett., 224, 1, 10.1016/S0304-3940(97)13440-1 · DOI
- Brossard, 1997, Human plasma albumin transports [13C]docosahexaenoic acid in two lipid forms to blood cells., J. Lipid Res., 38, 1571, 10.1016/S0022-2275(20)37175-3 · DOI
- Calon, 2011, Omega-3 polyunsaturated fatty acids in Alzheimer’s disease: key questions and partial answers., Curr. Alzheimer Res., 8, 470, 10.2174/156720511796391881 · DOI
- Chouinard-Watkins, 2018, Mechanisms regulating brain docosahexaenoic acid uptake: what is the recent evidence?, Curr. Opin. Clin. Nutr. Metab. Care, 21, 71, 10.1097/MCO.0000000000000440 · DOI
- Cunnane, 2012, Plasma and brain fatty acid profiles in mild cognitive impairment and Alzheimer’s disease., J. Alzheimers Dis., 29, 691, 10.3233/JAD-2012-110629 · DOI
- Dehouck, 1997, A new function for the LDL receptor: transcytosis of LDL across the blood-brain barrier., J. Cell Biol., 138, 877, 10.1083/jcb.138.4.877 · DOI · Paper page
- Delton-Vandenbroucke, 1997, Polyunsaturated fatty acid metabolism in retinal and cerebral microvascular endothelial cells., J. Lipid Res., 38, 147, 10.1016/S0022-2275(20)37284-9 · DOI
- Dhopeshwarkar, 1973, Uptake and transport of fatty acids into the brain and the role of the blood-brain barrier system., Adv. Lipid Res., 11, 109, 10.1016/b978-0-12-024911-4.50010-6 · DOI
- Dias, 2019, Molecular sciences structure and junctional complexes of endothelial, epithelial and glial brain barriers., Int. J. Mol. Sci., 20, 10.3390/ijms20215372 · DOI
- Dietschy, 2001, Cholesterol metabolism in the brain., Curr. Opin. Lipidol., 12, 105, 10.1097/00041433-200104000-00003 · DOI · Paper page
- Do, 2011, Direct evidence of abca1-mediated efflux of cholesterol at the mouse blood-brain barrier., Mol. Cell. Biochem, 357, 397, 10.1007/s11010-011-0910-6 · DOI · Paper page
- Edmond, 2001, Essential polyunsaturated fatty acids and the barrier to the brain: the components of a model for transport., J. Mol. Neurosci., 16, 181, 10.1385/JMN:16:2-3:181 · DOI
- Edwards, 2002, BAREing it all: the adoption of LXR and FXR and their roles in lipid homeostasis., J. Lipid Res., 43, 2, 10.1016/S0022-2275(20)30180-2 · DOI
- Erdö, 2017, Age-associated physiological and pathological changes at the blood-brain barrier: a review., J. Cereb. Blood Flow Metab., 37, 4, 10.1177/0271678X16679420 · DOI · Paper page
- Etschmaier, 2011, Adipose triglyceride lipase affects triacylglycerol metabolism at brain barriers., J. Neurochem., 119, 1016, 10.1111/j.1471-4159.2011.07498.x · DOI
- Fujiyoshi, 2007, 24S-hydroxycholesterol induces cholesterol release from choroid plexus epithelial cells in an apical- and apoE isoform-dependent manner concomitantly with the induction of ABCA1 and ABCG1 expression., J. Neurochem., 100, 968, 10.1111/j.1471-4159.2006.04240.x · DOI · Paper page
- Galea, 2018, The blood-brain interface: a culture change., Brain Behav. Immun., 68, 11, 10.1016/j.bbi.2017.10.014 · DOI
- Gomez-Zepeda, 2020, ABC transporters at the blood–brain interfaces, their study models, and drug delivery implications in gliomas., Pharmaceutics, 12, 10.3390/pharmaceutics12010020 · DOI
- Hamilton, 2007, A model for fatty acid transport into the brain., J. Mol. Neurosci., 33, 12, 10.1007/s12031-007-0050-3 · DOI
- Helmy, 1963, Histochemical and lipid studies on human choroid plexus., Proc. Soc. Exp. Biol. Med., 114, 361, 10.3181/00379727-114-28677 · DOI
- Hirsch-Reinshagen, 2004, Deficiency of ABCA1 impairs apolipoprotein E metabolism in brain., J. Biol. Chem., 279, 41197, 10.1074/jbc.M407962200 · DOI · Paper page
- Holman, 2010, Cerebrospinal fluid dynamics in the human cranial subarachnoid space: an overlooked mediator of cerebral disease. II. In vitro arachnoid outflow model., J. R. Soc. Interface, 7, 1205, 10.1098/rsif.2010.0032 · DOI
- Homayoun, 1988, Alteration in fatty acid composition of adult rat brain capillaries and choroid plexus induced by a diet deficient in n-3 fatty acids: slow recovery after substitution with a nondeficient diet., J. Neurochem., 51, 45, 10.1111/j.1471-4159.1988.tb04833.x · DOI
- Iadecola, 2017, The neurovascular unit coming of age: a journey through neurovascular coupling in health and disease., Neuron, 96, 17, 10.1016/j.neuron.2017.07.030 · DOI · Paper page
- Igarashi, 2007, Docosahexaenoic acid synthesis from α-linolenic acid by rat brain is unaffected by dietary n-3 PUFA deprivation., J. Lipid Res., 48, 1150, 10.1194/jlr.M600549-JLR200 · DOI
- Kamp, 2006, How fatty acids of different chain length enter and leave cells by free diffusion., Prostaglandins Leukot. Essent. Fatty Acids, 75, 149, 10.1016/j.plefa.2006.05.003 · DOI
- Karasinska, 2009, Specific loss of brain ABCA1 increases brain cholesterol uptake and influences neuronal structure and function., J. Neurosci., 29, 3579, 10.1523/JNEUROSCI.4741-08.2009 · DOI · Paper page
- Keaney, 2015, The dynamic blood-brain barrier., FEBS J., 282, 4067, 10.1111/febs.13412 · DOI · Paper page
- Kim, 1996, Human apolipoprotein E receptor 2: a novel lipoprotein receptor of the low density lipoprotein receptor family predominantly expressed in brain., J. Biol. Chem., 271, 8373, 10.1074/jbc.271.14.8373 · DOI · Paper page
- Kirchhausen, 2005, Single-molecule live-cell imaging of clathrin-based endocytosis., Biochem. Soc. Symp., 72, 71, 10.1042/bss0720071 · DOI
- Kounnas, 1994, Immunological localization of glycoprotein 330, low density lipoprotein receptor related protein and 39 kDa receptor associated protein in embryonic mouse tissues., In Vivo (Brooklyn), 8, 343
- Lacombe, 2018, Brain docosahexaenoic acid uptake and metabolism., Mol. Aspects Med., 64, 109, 10.1016/j.mam.2017.12.004 · DOI
- Lun, Spatially heterogeneous choroid plexus transcriptomes encode positional identity and contribute to regional CSF production., J. Neurosci., 35, 4903, 10.1523/JNEUROSCI.3081-14.2015 · DOI
- Lun, Development and functions of the choroid plexus-cerebrospinal fluid system., Nat. Rev. Neurosci., 16, 445, 10.1038/nrn3921 · DOI
- Mahley, 2016, Central nervous system lipoproteins: ApoE and regulation of cholesterol metabolism., Arterioscler. Thromb. Vasc. Biol., 36, 1305, 10.1161/ATVBAHA.116.307023 · DOI · Paper page
- Marinetti, 1971, Lipid metabolism in the rabbit choroid plexus., J. Neurochem., 18, 2003, 10.1111/j.1471-4159.1971.tb09606.x · DOI
- Marques, 2013, Blood-brain-barriers in aging and in Alzheimer’s disease., Mol. Neurodegener., 8, 10.1186/1750-1326-8-38 · DOI
- Mauch, 2001, CNS synaptogenesis promoted by glia-derived cholesterol., Science, 294, 1354, 10.1126/science.294.5545.1354 · DOI · Paper page
- Mitchell, 2011, Fatty acid transport protein expression in human brain and potential role in fatty acid transport across human brain microvessel endothelial cells., J. Neurochem., 117, 735, 10.1111/j.1471-4159.2011.07245.x · DOI · Paper page
- Mooradian, 1988, Effect of aging on the blood-brain barrier., Neurobiol. Aging, 9, 31, 10.1016/S0197-4580(88)80013-7 · DOI
- Mooradian, 1992, The effect of age on lipid composition and order of rat cerebral microvessels., Neurochem. Res, 17, 233, 10.1007/BF00966664 · DOI
- Moore, 2001, Polyunsaturated fatty acid synthesis and release by brain-derived cells in vitro., J. Mol. Neurosci., 16, 195, 10.1385/JMN:16:2-3:195 · DOI
- Nguyen, 2014, Mfsd2a is a transporter for the essential omega-3 fatty acid docosahexaenoic acid., Nature, 509, 503, 10.1038/nature13241 · DOI · Paper page
- Ouellet, 2009, Diffusion of docosahexaenoic and eicosapentaenoic acids through the blood-brain barrier: an in situ cerebral perfusion study., Neurochem. Int, 55, 476, 10.1016/j.neuint.2009.04.018 · DOI
- Pifferi, 2005, (n-3) polyunsaturated fatty acid deficiency reduces the expression of both isoforms of the brain glucose transporter GLUT1 in rats., J. Nutr., 135, 2241, 10.1093/jn/135.9.2241 · DOI
- Plourde, 2007, Extremely limited synthesis of long chain polyunsaturates in adults: implications for their dietary essentiality and use as supplements., Appl. Physiol. Nutr. Metab., 32, 619, 10.1139/H07-034 · DOI
- Qi, 2002, Long-chain polyunsaturated fatty acid accretion in brain., Curr. Opin. Clin. Nutr. Metab. Care, 5, 133, 10.1097/00075197-200203000-00003 · DOI
- Razmara, 2020, Novel neuroclinical findings of autosomal recessive primary microcephaly 15 in a consanguineous Iranian family., Eur. J. Med. Genet., 63, 10.1016/j.ejmg.2020.104096 · DOI
- Robinet, 2006, Dynamin is involved in endolysosomal cholesterol delivery to the endoplasmic reticulum: role in cholesterol homeostasis., Traffic, 7, 811, 10.1111/j.1600-0854.2006.00435.x · DOI
- Rosenberg, 2018, Multidomain lifestyle intervention benefits a large elderly population at risk for cognitive decline and dementia regardless of baseline characteristics: the FINGER trial., Alzheimers Dement., 14, 263, 10.1016/j.jalz.2017.09.006 · DOI · Paper page
- Rothberg, 1992, Caveolin, a protein component of caveolae membrane coats., Cell, 68, 673, 10.1016/0092-8674(92)90143-Z · DOI
- Saeed, 2014, Effects of a disrupted blood-brain barrier on cholesterol homeostasis in the brain., J. Biol. Chem., 289, 23712, 10.1074/jbc.M114.556159 · DOI
- Schultz, 2000, Role of LXRs in control of lipogenesis., Genes Dev., 14, 2831, 10.1101/gad.850400 · DOI · Paper page
- Scott, 1989, Membrane docosahexaenoate is supplied to the developing brain and retina by the liver., Proc. Natl. Acad. Sci. U.S.A., 86, 2903, 10.1073/pnas.86.8.2903 · DOI
- Selivonchick, 1977, Lipid and fatty acyl composition of rat brain capillary endothelia isolated by a new technique., Lipids, 12, 165, 10.1007/BF02533288 · DOI
- Serot, 2003, Choroid plexus, ageing of the brain, and Alzheimer’s disease., Front. Biosci., 8, s515, 10.2741/1085 · DOI
- Smith, 1998, Clathrin coats at 21 Å resolution: a cellular assembly designed to recycle multiple membrane receptors., EMBO J., 17, 4943, 10.1093/emboj/17.17.4943 · DOI
- Spector, 2001, Plasma free fatty acid and lipoproteins as sources of polyunsaturated fatty acid for the brain., J. Mol. Neurosci., 16, 159, 10.1385/JMN:16:2-3:159 · DOI
- Strazielle, 2013, Physiology of blood-brain interfaces in relation to brain disposition of small compounds and macromolecules., Mol. Pharm., 10, 1473, 10.1021/mp300518e · DOI
- Strosznajder, 1996, Arachidonate transport through the blood-retina and blood-brain barrier of the rat during aging., Neurosci. Lett., 209, 145, 10.1016/0304-3940(96)12624-0 · DOI
- Sturrock, 1988, An ultrastructural study of the choroid plexus of aged mice., Anat. Anz., 165, 379
- Tayarani, 1989, Antioxidant enzymes and related trace elements in aging brain capillaries and choroid plexus., J. Neurochem., 53, 817, 10.1111/j.1471-4159.1989.tb11778.x · DOI
- Thouvenot, 2006, The proteomic analysis of mouse choroid plexus secretome reveals a high protein secretion capacity of choroidal epithelial cells., Proteomics, 6, 5941, 10.1002/pmic.200600096 · DOI
- Vandal, 2014, Reduction in DHA transport to the brain of mice expressing human APOE4 compared to APOE2., J. Neurochem., 129, 516, 10.1111/jnc.12640 · DOI
- Wang, 2002, Liver X receptors in the central nervous system: from lipid homeostasis to neuronal degeneration., Proc. Natl. Acad. Sci. U.S.A., 99, 13878, 10.1073/pnas.172510899 · DOI
- Wang, 2004, ATP-binding cassette transporters G1 and G4 mediate cellular cholesterol efflux to high-density lipoproteins., Proc. Natl. Acad. Sci. U.S.A., 101, 9774, 10.1073/pnas.0403506101 · DOI
- Wang, 2000, Specific binding of ApoA-I, enhanced cholesterol efflux, and altered plasma membrane morphology in cells expressing ABC1., J. Biol. Chem., 275, 33053, 10.1074/jbc.M005438200 · DOI
- Wong, 2020, Mfsd2a: a physiologically important lysolipid transporter in the brain and eye, Lipid Transfer in Lipoprotein Metabolism and Cardiovascular Disease. Advances in Experimental Medicine and Biology, 223, 10.1007/978-981-15-6082-8_14 · DOI
- Yang, 2020, Deciphering the roles of caveolin in neurodegenerative diseases: the good, the bad and the importance of context., Ageing Res. Rev., 62, 10.1016/j.arr.2020.101116 · DOI
- Yassine, 2017, DHA brain uptake and APOE4 status: a PET study with [1-(11)C]-DHA., Alzheimers Res. Ther, 9, 10.1186/s13195-017-0250-1 · DOI
- Zhou, 2019, Zika virus degrades the ω-3 fatty acid transporter Mfsd2a in brain microvascular endothelial cells and impairs lipid homeostasis., Sci. Adv., 5, 10.1126/sciadv.aax7142 · DOI
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Metadata
- Authors
- Pifferi, F., Laurent, B., & Plourde, M.
- Venue
- Frontiers in Physiology
- Publisher
- Frontiers Media SA
- Published
- 2021-03-30
- Volume
- 12
- ISSN
- 1664-042X
- PMC
- PMC8044814
- Cited by
- 148
- References
- 7
- Funders
- Canadian Institutes of Health Research
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