Student or educator? Sign up with your school email and get 6 months of Pro free.
Cited by 860

The DOI matches its Crossref record; 34 of the 34 references it cites were found in a registry or an index.

Neurovascular mechanisms and blood–brain barrier disorder in Alzheimer’s disease

Open access
Bell, Robert D., Zlokovic, Berislav V.·2009·Acta Neuropathologica

Abstract

Vascular dysfunction has a critical role in Alzheimer’s disease (AD). Recent data from brain imaging studies in humans and animal models suggest that cerebrovascular dysfunction may precede cognitive decline and onset of neurodegenerative changes in AD and AD models. Cerebral hypoperfusion and impaired amyloid β-peptide (Aβ) clearance across the blood–brain barrier (BBB) may contribute to the onset and progression of dementia AD type. Decreased cerebral blood flow (CBF) negatively affects the synthesis of proteins required for memory and learning, and may eventually lead to neuritic injury and neuronal death. Impaired clearance of Aβ from the brain by the cells of the neurovascular unit may lead to its accumulation on blood vessels and in brain parenchyma. The accumulation of Aβ on the cerebral blood vessels, known as cerebral amyloid angiopathy (CAA), is associated with cognitive decline and is one of the hallmarks of AD pathology. CAA can severely disrupt the integrity of the blood vessel wall resulting in micro or macro intracerebral bleedings that exacerbates neurodegenerative process and inflammatory response and may lead to hemorrhagic stroke, respectively. Here, we review the role of the neurovascular unit and molecular mechanisms in vascular cells behind AD and CAA pathogenesis. First, we discuss apparent vascular changes, including the cerebral hypoperfusion and vascular degeneration that contribute to different stages of the disease process in AD individuals. We next discuss the role of the low-density lipoprotein receptor related protein-1 (LRP), a key Aβ clearance receptor at the BBB and along the cerebrovascular system, whose expression is suppressed early in AD. We also discuss how brain-derived apolipoprotein E isoforms may influence Aβ clearance across the BBB. We then review the role of two interacting transcription factors, myocardin and serum response factor, in cerebral vascular cells in controlling CBF responses and LRP-mediated Aβ clearance. Finally, we discuss the role of microglia and perivascular macrophages in Aβ clearance from the brain. The data reviewed here support an essential role of neurovascular and BBB mechanisms in contributing to both, onset and progression of AD.

Overview

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.1007/s00401-009-0522-3

Cites

34 of 34 references verified0 citation errors · 0 not checkable

Statistics

Verification

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Citations

Cites

Research works printed but not linked: 71

  1. Alonzo NC, Hyman BT, Rebeck GW, Greenberg SM (1998) Progression of cerebral amyloid angiopathy: accumulation of amyloid-beta40 in affected vessels. J Neuropathol Exp Neurol 57:353–359. doi: 10.1097/00005072-199804000-00008 · DOI · Paper page
  2. Asahina M, Yoshiyama Y, Hattori T (2001) Expression of matrix metalloproteinase-9 and urinary-type plasminogen activator in Alzheimer’s disease brain. Clin Neuropathol 20:60–63
  3. Attems J, Jellinger KA, Lintner F (2005) Alzheimer’s disease pathology influences severity and topographical distribution of cerebral amyloid angiopathy. Acta Neuropathol 110:222–231. doi: 10.1007/s00401-005-1064-y · DOI · Paper page
  4. Attems J, Quass M, Jellinger KA, Lintner F (2007) Topographical distribution of cerebral amyloid angiopathy and its effect on cognitive decline are influenced by Alzheimer disease pathology. J Neurol Sci 257:49–55. doi: 10.1016/j.jns.2007.01.013 · DOI
  5. Beach TG, Wilson JR, Sue LI et al (2007) Circle of Willis atherosclerosis: association with Alzheimer’s disease, neuritic plaques and neurofibrillary tangles. Acta Neuropathol 113:13–21. doi: 10.1007/s00401-006-0136-y · DOI
  6. Begley DJ, Brightman MW (2003) Structural and functional aspects of the blood–brain barrier. Prog Drug Res 61:39–78
  7. Berzin TM, Zipser BD, Rafii MS et al (2000) Agrin and microvascular damage in Alzheimer’s disease. Neurobiol Aging 21:349–355. doi: 10.1016/S0197-4580(00)00121-4 · DOI
  8. Bradbury M (1979) Cerebral arterial supply. In: Bradbury M (ed) The concept of a blood–brain barrier. Wiley, New York, pp 18–19
  9. Chen J, Kitchen CM, Streb JW, Miano JM (2002) Myocardin: a component of a molecular switch for smooth muscle differentiation. J Mol Cell Cardiol 34:1345–1356. doi: 10.1006/jmcc.2002.2086 · DOI
  10. Cheng T, Petraglia AL, Li Z et al (2006) Activated protein C inhibits tissue plasminogen activator-induced brain hemorrhage. Nat Med 12:1278–1285. doi: 10.1038/nm1498 · DOI
  11. Clifford PM, Zarrabi S, Siu G et al (2007) Abeta peptides can enter the brain through a defective blood–brain barrier and bind selectively to neurons. Brain Res 1142:223–236. doi: 10.1016/j.brainres.2007.01.070 · DOI
  12. de la Torre JC (2004) Is Alzheimer’s disease a neurodegenerative or a vascular disorder? Data, dogma, and dialectics. Lancet Neurol 3:184–190. doi: 10.1016/S1474-4422(04)00683-0 · DOI · Paper page
  13. Deane R, Bell RD, Sagare A, Zlokovic BZ (2009) Clearance of amyloid-beta peptide across the blood–brain barrier: implications for therapies in Alzhiemer’s disease. CNS Neurol Disord Drug Targets 8. doi: 10.2174/187152709787601867 (in press) · DOI · Paper page
  14. Deane R, Wu Z, Sagare A et al (2004) LRP/amyloid beta-peptide interaction mediates differential brain efflux of Abeta isoforms. Neuron 43:333–344. doi: 10.1016/j.neuron.2004.07.017 · DOI · Paper page
  15. Drzezga A, Lautenschlager N, Siebner H et al (2003) Cerebral metabolic changes accompanying conversion of mild cognitive impairment into Alzheimer’s disease: a PET follow-up study. Eur J Nucl Med Mol Imaging 30:1104–1113. doi: 10.1007/s00259-003-1194-1 · DOI · Paper page
  16. Ervin JF, Pannell C, Szymanski M, Welsh-Bohmer K, Schmechel DE, Hulette CM (2004) Vascular smooth muscle actin is reduced in Alzheimer disease brain: a quantitative analysis. J Neuropathol Exp Neurol 63:735–741 · DOI
  17. Fiala M, Lin J, Ringman J et al (2005) Ineffective phagocytosis of amyloid-beta by macrophages of Alzheimer’s disease patients. J Alzheimers Dis 7:221–232 discussion 55–62 · DOI · Paper page
  18. Fukuda S, Fini CA, Mabuchi T, Koziol JA, Eggleston LL Jr, del Zoppo GJ (2004) Focal cerebral ischemia induces active proteases that degrade microvascular matrix. Stroke 35:998–1004. doi: 10.1161/01.STR.0000119383.76447.05 · DOI · Paper page
  19. Giri R, Shen Y, Stins M et al (2000) Beta-amyloid-induced migration of monocytes across human brain endothelial cells involves RAGE and PECAM-1. Am J Physiol Cell Physiol 279:C1772–C1781 · DOI · Paper page
  20. Girouard H, Iadecola C (2006) Neurovascular coupling in the normal brain and in hypertension, stroke, and Alzheimer disease. J Appl Physiol 100:328–335. doi: 10.1152/japplphysiol.00966.2005 · DOI · Paper page
  21. Grammas P, Yamada M, Zlokovic B (2002) The cerebromicrovasculature: a key player in the pathogenesis of Alzheimer’s disease. J Alzheimers Dis 4:217–223 · DOI
  22. Greenberg SM, Gurol ME, Rosand J, Smith EE (2004) Amyloid angiopathy-related vascular cognitive impairment. Stroke 35:2616–2619. doi: 10.1161/01.STR.0000143224.36527.44 · DOI · Paper page
  23. Griffin JH, Zlokovic B, Fernandez JA (2002) Activated protein C: potential therapy for severe sepsis, thrombosis, and stroke. Semin Hematol 39:197–205. doi: 10.1053/shem.2002.34093 · DOI
  24. Hendriks L, van Duijn CM, Cras P et al (1992) Presenile dementia and cerebral haemorrhage linked to a mutation at codon 692 of the beta-amyloid precursor protein gene. Nat Genet 1:218–221. doi: 10.1038/ng0692-218 · DOI · Paper page
  25. Hirao K, Ohnishi T, Hirata Y et al (2005) The prediction of rapid conversion to Alzheimer’s disease in mild cognitive impairment using regional cerebral blood flow SPECT. Neuroimage 28:1014–1021. doi: 10.1016/j.neuroimage.2005.06.066 · DOI · Paper page
  26. Hofman A, Ott A, Breteler MM et al (1997) Atherosclerosis, apolipoprotein E, and prevalence of dementia and Alzheimer’s disease in the Rotterdam Study. Lancet 349:151–154. doi: 10.1016/S0140-6736(96)09328-2 · DOI · Paper page
  27. Honig LS, Kukull W, Mayeux R (2005) Atherosclerosis and AD: analysis of data from the US National Alzheimer’s Coordinating Center. Neurology 64:494–500 · DOI · Paper page
  28. Itoh Y, Yamada M, Hayakawa M, Otomo E, Miyatake T (1993) Cerebral amyloid angiopathy: a significant cause of cerebellar as well as lobar cerebral hemorrhage in the elderly. J Neurol Sci 116:135–141. doi: 10.1016/0022-510X(93)90317-R · DOI · Paper page
  29. Johnson NA, Jahng GH, Weiner MW et al (2005) Pattern of cerebral hypoperfusion in Alzheimer disease and mild cognitive impairment measured with arterial spin-labeling MR imaging: initial experience. Radiology 234:851–859. doi: 10.1148/radiol.2343040197 · DOI · Paper page
  30. Jung SS, Zhang W, Van Nostrand WE (2003) Pathogenic A beta induces the expression and activation of matrix metalloproteinase-2 in human cerebrovascular smooth muscle cells. J Neurochem 85:1208–1215. doi: 10.1046/j.1471-4159.2003.01745.x · DOI
  31. Kalaria RN, Hedera P (1995) Differential degeneration of the cerebral microvasculature in Alzheimer’s disease. Neuroreport 6:477–480. doi: 10.1097/00001756-199502000-00018 · DOI
  32. Kalaria RN, Pax AB (1995) Increased collagen content of cerebral microvessels in Alzheimer’s disease. Brain Res 705:349–352. doi: 10.1016/0006-8993(95)01250-8 · DOI
  33. Kalback W, Esh C, Castano EM et al (2004) Atherosclerosis, vascular amyloidosis and brain hypoperfusion in the pathogenesis of sporadic Alzheimer’s disease. Neurol Res 26:525–539. doi: 10.1179/016164104225017668 · DOI
  34. Kawai M, Kalaria RN, Cras P et al (1993) Degeneration of vascular muscle cells in cerebral amyloid angiopathy of Alzheimer disease. Brain Res 623:142–146. doi: 10.1016/0006-8993(93)90021-E · DOI
  35. Kim HC, Yamada K, Nitta A et al (2003) Immunocytochemical evidence that amyloid beta (1–42) impairs endogenous antioxidant systems in vivo. Neuroscience 119:399–419. doi: 10.1016/S0306-4522(02)00993-4 · DOI
  36. Li S, Wang DZ, Wang Z, Richardson JA, Olson EN (2003) The serum response factor coactivator myocardin is required for vascular smooth muscle development. Proc Natl Acad Sci USA 100:9366–9370. doi: 10.1073/pnas.1233635100 · DOI · Paper page
  37. Llorente-Cortes V, Costales P, Bernues J, Camino-Lopez S, Badimon L (2006) Sterol regulatory element-binding protein-2 negatively regulates low density lipoprotein receptor-related protein transcription. J Mol Biol 359:950–960. doi: 10.1016/j.jmb.2006.04.008 · DOI
  38. McComb JG, Zlokovic BV (1994) Cerebrospinal fluid and the blood–brain interface. In: Cheek WR (ed) Pediatric neurosurgery: surgery of the developing nervous system, 3rd edn. Saunders, Philladelphia, pp 180–198
  39. Monro OR, Mackic JB, Yamada S et al (2002) Substitution at codon 22 reduces clearance of Alzheimer’s amyloid-beta peptide from the cerebrospinal fluid and prevents its transport from the central nervous system into blood. Neurobiol Aging 23:405–412. doi: 10.1016/S0197-4580(01)00317-7 · DOI · Paper page
  40. Mosconi L, Sorbi S, de Leon MJ et al (2006) Hypometabolism exceeds atrophy in presymptomatic early-onset familial Alzheimer’s disease. J Nucl Med 47:1778–1786
  41. Park L, Anrather J, Forster C, Kazama K, Carlson GA, Iadecola C (2004) Abeta-induced vascular oxidative stress and attenuation of functional hyperemia in mouse somatosensory cortex. J Cereb Blood Flow Metab 24:334–342. doi: 10.1097/01.WCB.0000105800.49957.1E · DOI
  42. Parks JK, Smith TS, Trimmer PA, Bennett JP Jr, Parker WD Jr (2001) Neurotoxic Abeta peptides increase oxidative stress in vivo through NMDA-receptor and nitric-oxide-synthase mechanisms, and inhibit complex IV activity and induce a mitochondrial permeability transition in vitro. J Neurochem 76:1050–1056. doi: 10.1046/j.1471-4159.2001.00112.x · DOI
  43. Peppiatt CM, Howarth C, Mobbs P, Attwell D (2006) Bidirectional control of CNS capillary diameter by pericytes. Nature 443:700–704. doi: 10.1038/nature05193 · DOI · Paper page
  44. Pettersen JA, Sathiyamoorthy G, Gao FQ et al (2008) Microbleed topography, leukoaraiosis, and cognition in probable Alzheimer disease from the Sunnybrook dementia study. Arch Neurol 65:790–795. doi: 10.1001/archneur.65.6.790 · DOI · Paper page
  45. Preston SD, Steart PV, Wilkinson A, Nicoll JA, Weller RO (2003) Capillary and arterial cerebral amyloid angiopathy in Alzheimer’s disease: defining the perivascular route for the elimination of amyloid beta from the human brain. Neuropathol Appl Neurobiol 29:106–117. doi: 10.1046/j.1365-2990.2003.00424.x · DOI
  46. Quinn KA, Grimsley PG, Dai YP, Tapner M, Chesterman CN, Owensby DA (1997) Soluble low density lipoprotein receptor-related protein (LRP) circulates in human plasma. J Biol Chem 272:23946–23951. doi: 10.1074/jbc.272.38.23946 · DOI
  47. Reynolds PR, Mucenski ML, Le Cras TD, Nichols WC, Whitsett JA (2004) Midkine is regulated by hypoxia and causes pulmonary vascular remodeling. J Biol Chem 279:37124–37132. doi: 10.1074/jbc.M405254200 · DOI
  48. Rombouts SA, Goekoop R, Stam CJ, Barkhof F, Scheltens P (2005) Delayed rather than decreased BOLD response as a marker for early Alzheimer’s disease. Neuroimage 26:1078–1085. doi: 10.1016/j.neuroimage.2005.03.022 · DOI
  49. Sagare A, Deane R, Bell RD et al (2007) Clearance of amyloid-beta by circulating lipoprotein receptors. Nat Med 13:1029–1031. doi: 10.1038/nm1635 · DOI · Paper page
  50. Saido TC, Iwata N (2006) Metabolism of amyloid beta peptide and pathogenesis of Alzheimer’s disease. Towards presymptomatic diagnosis, prevention and therapy. Neurosci Res 54:235–253. doi: 10.1016/j.neures.2005.12.015 · DOI
  51. Santpere G, Puig B, Ferrer I (2007) Oxidative damage of 14-3-3 zeta and gamma isoforms in Alzheimer’s disease and cerebral amyloid angiopathy. Neuroscience 146:1640–1651. doi: 10.1016/j.neuroscience.2007.03.013 · DOI
  52. Scheibel AB, Duong TH, Jacobs R (1989) Alzheimer’s disease as a capillary dementia. Ann Med 21:103–107. doi: 10.3109/07853898909149194 · DOI
  53. Segal MB, Preston JE, Collis CS, Zlokovic BV (1990) Kinetics and Na independence of amino acid uptake by blood side of perfused sheep choroid plexus. Am J Physiol 258:F1288–F1294
  54. Sun Q, Chen G, Streb JW et al (2006) Defining the mammalian CArGome. Genome Res 16:197–207. doi: 10.1101/gr.4108706 · DOI · Paper page
  55. Tagliavini FRG, Padovani A, Magoni M, Andora G, Sgarzi M, Bizzi ASM, Carella F, Morbin M, Giaccone G, Bugiani O (1999) A new beta APP mutation related to hereditary cerebral haemorrhage. Alzheimers Rep 2:S28
  56. Tanzi RE, Bertram L (2005) Twenty years of the Alzheimer’s disease amyloid hypothesis: a genetic perspective. Cell 120:545–555. doi: 10.1016/j.cell.2005.02.008 · DOI · Paper page
  57. Trembath D, Ervin JF, Broom L et al (2007) The distribution of cerebrovascular amyloid in Alzheimer’s disease varies with ApoE genotype. Acta Neuropathol 113:23–31. doi: 10.1007/s00401-006-0162-9 · DOI · Paper page
  58. Urmoneit B, Prikulis I, Wihl G et al (1997) Cerebrovascular smooth muscle cells internalize Alzheimer amyloid beta protein via a lipoprotein pathway: implications for cerebral amyloid angiopathy. Lab Invest 77:157–166
  59. Van Broeckhoven C, Haan J, Bakker E et al (1990) Amyloid beta protein precursor gene and hereditary cerebral hemorrhage with amyloidosis (Dutch). Science 248:1120–1122. doi: 10.1126/science.1971458 · DOI · Paper page
  60. van Oijen M, de Jong FJ, Witteman JC, Hofman A, Koudstaal PJ, Breteler MM (2007) Atherosclerosis and risk for dementia. Ann Neurol 61:403–410. doi: 10.1002/ana.21073 · DOI · Paper page
  61. Verbeek MM, Otte-Holler I, van den Born J et al (1999) Agrin is a major heparan sulfate proteoglycan accumulating in Alzheimer’s disease brain. Am J Pathol 155:2115–2125 · DOI
  62. Verbeek MM, Van Nostrand WE, Otte-Holler I, Wesseling P, De Waal RM (2000) Amyloid-beta-induced degeneration of human brain pericytes is dependent on the apolipoprotein E genotype. Ann N Y Acad Sci 903:187–199. doi: 10.1111/j.1749-6632.2000.tb06368.x · DOI
  63. Vinters HV, Secor DL, Read SL et al (1994) Microvasculature in brain biopsy specimens from patients with Alzheimer’s disease: an immunohistochemical and ultrastructural study. Ultrastruct Pathol 18:333–348. doi: 10.3109/01913129409023202 · DOI
  64. von Tell D, Armulik A, Betsholtz C (2006) Pericytes and vascular stability. Exp Cell Res 312:623–629. doi: 10.1016/j.yexcr.2005.10.019 · DOI · Paper page
  65. Wang D, Chang PS, Wang Z et al (2001) Activation of cardiac gene expression by myocardin, a transcriptional cofactor for serum response factor. Cell 105:851–862. doi: 10.1016/S0092-8674(01)00404-4 · DOI · Paper page
  66. Wegiel J, Wisniewski HM (1990) The complex of microglial cells and amyloid star in three-dimensional reconstruction. Acta Neuropathol 81:116–124. doi: 10.1007/BF00334499 · DOI
  67. Wisniewski T, Frangione B (1992) Apolipoprotein E: a pathological chaperone protein in patients with cerebral and systemic amyloid. Neurosci Lett 135:235–238. doi: 10.1016/0304-3940(92)90444-C · DOI · Paper page
  68. Wu Z, Guo H, Chow N et al (2005) Role of the MEOX2 homeobox gene in neurovascular dysfunction in Alzheimer disease. Nat Med 11:959–965 · DOI · Paper page
  69. Zhang ET, Inman CB, Weller RO (1990) Interrelationships of the pia mater and the perivascular (Virchow-Robin) spaces in the human cerebrum. J Anat 170:111–123
  70. Zlokovic BV (1996) Cerebrovascular transport of Alzheimer’s amyloid beta and apolipoproteins J and E: possible anti-amyloidogenic role of the blood–brain barrier. Life Sci 59:1483–1497. doi: 10.1016/0024-3205(96)00310-4 · DOI
  71. Zlokovic BV (2005) Neurovascular mechanisms of Alzheimer’s neurodegeneration. Trends Neurosci 28:202–208. doi: 10.1016/j.tins.2005.02.001 · DOI · Paper page

Cited by

See all 860

Metadata

Authors
Bell, R. D., & Zlokovic, B. V.
Venue
Acta Neuropathologica
Published
2009-03-25
Volume
118
Issue
1
Pages
103-113
ISSN
  • 0001-6322 (ISSN-L)
  • 1432-0533
OpenAlex
W2037904566
Cited by
860
References
34
FWCI
35.17
Type
journal article
Language
en
Open access
green
Licence
www.springer.com/tdm (tdm)

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

Data sources

Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.