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Transmission of α-synuclein-containing erythrocyte-derived extracellular vesicles across the blood-brain barrier via adsorptive mediated transcytosis: another mechanism for initiation and progression of Parkinson’s disease?

Matsumoto, Junichi, Stewart, Tessandra, Sheng, Lifu, Li, Na, Bullock, Kristin, Song, Ning, Shi, Min, Banks, William A, Zhang, Jing·2017·Acta Neuropathologica Communications

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Crossref · 10.1186/s40478-017-0470-4

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  • sEVs can cross the blood-brain barrier and deliver cargo with crucial roles in many neurological disorders.

    “sEVs can cross the blood–brain barrier and deliver cargo with crucial roles in many neurological disorders [17–23].”

    From Differential RNA packaging into small extracellular vesicles by neurons and astrocytes (2021) · cites this paper as [22]

    The Introduction says EVs carry cargo and are considered important in a variety of neurodegenerative diseases. The Results and Discussion show that erythrocyte-derived EV components can cross the blood–brain barrier, particularly under LPS-induced inflammation, but the Discussion says the tested EVs likely included both exosomes and microvesicles and does not establish that intact vesicles crossed. The paper therefore does not establish the claim specifically for sEVs or without that condition. (LLM, conf=0.86)

    Experimental — accuracy not yet measured
  • RBC-EVs are enriched in the liver, spleen, and kidney.

    “(3) RBC-EVs are enriched in the liver, spleen, and kidney (Matsumoto et al., 2017), and RBC miRNAs are possibly involved in kidney-related diseases (Abraham et al., 2017; Fang et al., 2018).”

    From Red Blood Cells as Potential Repositories of MicroRNAs in the Circulatory System (2020) · cites this paper as Matsumoto et al., 2017

  • Erythrocyte-derived EVs containing α-synuclein may be another mechanism for the initiation and progression of Parkinson's disease.

    “Investigations have revealed that erythrocyte-derived EVs containing α-synuclein move across the blood–brain barrier through adsorptive-mediated transcytosis, which may be another mechanism for the initiation and progression of Parkinson’s disease (Matsumoto et al., 2017).”

    From Red Blood Cells as Potential Repositories of MicroRNAs in the Circulatory System (2020) · cites this paper as Matsumoto et al., 2017

  • Erythrocyte-derived EVs containing α-synuclein move across the blood-brain barrier through adsorptive-mediated transcytosis.

    “Investigations have revealed that erythrocyte-derived EVs containing α-synuclein move across the blood–brain barrier through adsorptive-mediated transcytosis, which may be another mechanism for the initiation and progression of Parkinson’s disease (Matsumoto et al., 2017).”

    From Red Blood Cells as Potential Repositories of MicroRNAs in the Circulatory System (2020) · cites this paper as Matsumoto et al., 2017

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Research works printed but not linked: 53

  1. Alvarez-Erviti L, Seow Y, Schapira AH, Gardiner C, Sargent IL, Wood MJ, Cooper JM (2011) Lysosomal dysfunction increases exosome-mediated alpha-synuclein release and transmission. Neurobiol Dis 42:360–367. doi: 10.1016/j.nbd.2011.01.029 · DOI
  2. Banks WA, Gray AM, Erickson MA, Salameh TS, Damodarasamy M, Sheibani N, Meabon JS, Wing EE, Morofuji Y, Cook DG, Reed MJ (2015) Lipopolysaccharide-induced blood-brain barrier disruption: roles of cyclooxygenase, oxidative stress, neuroinflammation, and elements of the neurovascular unit. J Neuroinflammation 12:223. doi: 10.1186/s12974-015-0434-1 · DOI · Paper page
  3. Banks WA, Kastin AJ, Akerstrom V (1997) HIV-1 protein gp120 crosses the blood-brain barrier: role of adsorptive endocytosis. Life Sci 61: Pl119-25, · DOI
  4. Banks WA, Kastin AJ, Brennan JM, Vallance KL (1999) Adsorptive endocytosis of HIV-1gp120 by blood-brain barrier is enhanced by lipopolysaccharide. Exp Neurol 156:165–171. doi: 10.1006/exnr.1998.7011 · DOI
  5. Banks WA, Robinson SM, Diaz-Espinoza R, Urayama A, Soto C (2009) Transport of prion protein across the blood-brain barrier. Exp Neurol 218:162–167. doi: 10.1016/j.expneurol.2009.04.025 · DOI
  6. Barbour R, Kling K, Anderson JP, Banducci K, Cole T, Diep L, Fox M, Goldstein JM, Soriano F, Seubert P, Chilcote TJ (2008) Red blood cells are the major source of alpha-synuclein in blood. Neurodegener Dis 5:55–59. doi: 10.1159/000112832 · DOI
  7. Blasberg RG, Fenstermacher JD, Patlak CS (1983) Transport of alpha-aminoisobutyric acid across brain capillary and cellular membranes. J Cereb Blood Flow Metab 3:8–32. doi: 10.1038/jcbfm.1983.2 · DOI
  8. Bliederhaeuser C, Grozdanov V, Speidel A, Zondler L, Ruf WP, Bayer H, Kiechle M, Feiler MS, Freischmidt A, Brenner D, Witting A, Hengerer B, Fandrich M, Ludolph AC, Weishaupt JH, Gillardon F, Danzer KM (2016) Age-dependent defects of alpha-synuclein oligomer uptake in microglia and monocytes. Acta Neuropathol 131:379–391. doi: 10.1007/s00401-015-1504-2 · DOI
  9. Boing AN, van der Pol E, Grootemaat AE, Coumans FA, Sturk A, Nieuwland R (2014) Single-step isolation of extracellular vesicles by size-exclusion chromatography. J Extracell Vesicles. 3. doi: 10.3402/jev.v3.23430 · DOI
  10. Braak H, de Vos RA, Bohl J, Del Tredici K (2006) Gastric alpha-synuclein immunoreactive inclusions in Meissner's and Auerbach's plexuses in cases staged for Parkinson's disease-related brain pathology. Neurosci Lett 396:67–72. doi: 10.1016/j.neulet.2005.11.012 · DOI · Paper page
  11. Chen CC, Liu L, Ma F, Wong CW, Guo XE, Chacko JV, Farhoodi HP, Zhang SX, Zimak J, Ségaliny A, Riazifar M, Pham V, Digman MA, Pone EJ, Zhao W (2016) Elucidation of Exosome Migration Across the Blood-Brain Barrier Model In Vitro. Cell Mol Bioeng 9:509–529. doi: 10.1007/s12195-016-0458-3 · DOI · Paper page
  12. Chen L, Brigstock DR (2016) Integrins and heparan sulfate proteoglycans on hepatic stellate cells (HSC) are novel receptors for HSC-derived exosomes. FEBS Lett 590:4263–4274. doi: 10.1002/1873-3468.12448 · DOI
  13. Chen Y, Liu L (2012) Modern methods for delivery of drugs across the blood-brain barrier. Adv Drug Deliv Rev 64:640–665. doi: 10.1016/j.addr.2011.11.010 · DOI
  14. Christianson HC, Svensson KJ, van Kuppevelt TH, Li JP, Belting M (2013) Cancer cell exosomes depend on cell-surface heparan sulfate proteoglycans for their internalization and functional activity. Proc Natl Acad Sci U S A 110:17380–17385. doi: 10.1073/pnas.1304266110 · DOI · Paper page
  15. Fitzner D, Schnaars M, van Rossum D, Krishnamoorthy G, Dibaj P, Bakhti M, Regen T, Hanisch UK, Simons M (2011) Selective transfer of exosomes from oligodendrocytes to microglia by macropinocytosis. J Cell Sci 124:447–458. doi: 10.1242/jcs.074088 · DOI · Paper page
  16. Glass CK, Saijo K, Winner B, Marchetto MC, Gage FH (2010) Mechanisms underlying inflammation in neurodegeneration. Cell 140:918–934. doi: 10.1016/j.cell.2010.02.016 · DOI · Paper page
  17. Haney MJ, Klyachko NL, Zhao Y, Gupta R, Plotnikova EG, He Z, Patel T, Piroyan A, Sokolsky M, Kabanov AV, Batrakova EV (2015) Exosomes as drug delivery vehicles for Parkinson's disease therapy. J Control Release 207:18–30. doi: 10.1016/j.jconrel.2015.03.033 · DOI · Paper page
  18. Hendrickx DAE, van Eden CG, Schuurman KG, Hamann J, Huitinga I (2017) Staining of HLA-DR, Iba1 and CD68 in human microglia reveals partially overlapping expression depending on cellular morphology and pathology. J Neuroimmunol 309:12–22. doi: 10.1016/j.jneuroim.2017.04.007 · DOI · Paper page
  19. Herve F, Ghinea N, Scherrmann JM (2008) CNS delivery via adsorptive transcytosis. AAPS J 10:455–472. doi: 10.1208/s12248-008-9055-2 · DOI · Paper page
  20. Hoheisel D, Nitz T, Franke H, Wegener J, Hakvoort A, Tilling T, Galla HJ (1998) Hydrocortisone reinforces the blood-brain properties in a serum free cell culture system. Biochem Biophys Res Commun 247:312–315 · DOI
  21. Hong Z, Shi M, Chung KA, Quinn JF, Peskind ER, Galasko D, Jankovic J, Zabetian CP, Leverenz JB, Baird G, Montine TJ, Hancock AM, Hwang H, Pan C, Bradner J, Kang UJ, Jensen PH, Zhang J (2010) DJ-1 and alpha-synuclein in human cerebrospinal fluid as biomarkers of Parkinson's disease. Brain 133:713–726. doi: 10.1093/brain/awq008 · DOI · Paper page
  22. Hunot S, Boissiere F, Faucheux B, Brugg B, Mouatt-Prigent A, Agid Y, Hirsch EC (1996) Nitric oxide synthase and neuronal vulnerability in Parkinson's disease. Neuroscience 72:355–363 · DOI · Paper page
  23. Hwang DW, Choi H, Jang SC, Yoo MY, Park JY, Choi NE, Oh HJ, Ha S, Lee YS, Jeong JM, Gho YS, Lee DS (2015) Noninvasive imaging of radiolabeled exosome-mimetic nanovesicle using (99m)Tc-HMPAO. Sci Rep 5:15636. doi: 10.1038/srep15636 · DOI
  24. Jang H, Boltz D, Sturm-Ramirez K, Shepherd KR, Jiao Y, Webster R, Smeyne RJ (2009) Highly pathogenic H5N1 influenza virus can enter the central nervous system and induce neuroinflammation and neurodegeneration. Proc Natl Acad Sci U S A 106:14063–14068. doi: 10.1073/pnas.0900096106 · DOI
  25. Lai CP, Breakefield XO (2012) Role of exosomes/microvesicles in the nervous system and use in emerging therapies. Front Physiol 3:228. doi: 10.3389/fphys.2012.00228 · DOI
  26. Lai CP, Mardini O, Ericsson M, Prabhakar S, Maguire CA, Chen JW, Tannous BA, Breakefield XO (2014) Dynamic biodistribution of extracellular vesicles in vivo using a multimodal imaging reporter. ACS Nano 8:483–494. doi: 10.1021/nn404945r · DOI
  27. Maries E, Dass B, Collier TJ, Kordower JH, Steece-Collier K (2003) The role of alpha-synuclein in Parkinson's disease: insights from animal models. Nat Rev Neurosci 4:727–738. doi: 10.1038/nrn1199 · DOI
  28. Mulcahy LA, Pink RC, Carter DR (2014) Routes and mechanisms of extracellular vesicle uptake. J Extracell Vesicles 3. 10.3402/jev.v3.24641 · DOI · Paper page
  29. Pardridge WM, Eisenberg J, Yang J (1987) Human blood-brain barrier transferrin receptor. Metab Clin Exp 36:892–895 · DOI
  30. Patlak CS, Blasberg RG, Fenstermacher JD (1983) Graphical evaluation of blood-to-brain transfer constants from multiple-time uptake data. J Cereb Blood Flow Metab 3:1–7. 10.1038/jcbfm.1983.1 · DOI
  31. Phillips RJ, Walter GC, Wilder SL, Baronowsky EA, Powley TL (2008) Alpha-synuclein-immunopositive myenteric neurons and vagal preganglionic terminals: autonomic pathway implicated in Parkinson's disease? Neuroscience 153:733–750. doi: 10.1016/j.neuroscience.2008.02.074 · DOI
  32. Pretorius E, Swanepoel AC, Buys AV, Vermeulen N, Duim W, Kell DB (2014) Eryptosis as a marker of Parkinson's disease. Aging 6:788–819. doi: 10.18632/aging.100695 · DOI
  33. Qian L, Flood PM (2008) Microglial cells and Parkinson's disease. Immunol Res 41:155–164. doi: 10.1007/s12026-008-8018-0 · DOI
  34. Qian L, Gao X, Pei Z, Wu X, Block M, Wilson B, Hong JS, Flood PM (2007) NADPH oxidase inhibitor DPI is neuroprotective at femtomolar concentrations through inhibition of microglia over-activation. Parkinsonism Relat Disord 13(Suppl 3):S316–S320. doi: 10.1016/s1353-8020(08)70023-3 · DOI
  35. Qin XY, Zhang SP, Cao C, Loh YP, Cheng Y (2016) Aberrations in Peripheral Inflammatory Cytokine Levels in Parkinson Disease: A Systematic Review and Meta-analysis. JAMA Neurol 73:1316–1324. doi: 10.1001/jamaneurol.2016.2742 · DOI
  36. Ren B, Zhang YX, Zhou HX, Sun FW, Zhang ZF, Wei Z, Zhang CY, Si DW (2015) Tanshinone IIA prevents the loss of nigrostriatal dopaminergic neurons by inhibiting NADPH oxidase and iNOS in the MPTP model of Parkinson's disease. J Neurol Sci 348:142–152. doi: 10.1016/j.jns.2014.11.026 · DOI
  37. Rey NL, Petit GH, Bousset L, Melki R, Brundin P (2013) Transfer of human alpha-synuclein from the olfactory bulb to interconnected brain regions in mice. Acta Neuropathol 126:555–573. doi: 10.1007/s00401-013-1160-3 · DOI
  38. Sacino AN, Brooks M, Thomas MA, McKinney AB, Lee S, Regenhardt RW, McGarvey NH, Ayers JI, Notterpek L, Borchelt DR, Golde TE, Giasson BI (2014) Intramuscular injection of alpha-synuclein induces CNS alpha-synuclein pathology and a rapid-onset motor phenotype in transgenic mice. Proc Natl Acad Sci U S A 111:10732–10737. doi: 10.1073/pnas.1321785111 · DOI
  39. Sampson TR, Debelius JW, Thron T, Janssen S, Shastri GG, Ilhan ZE, Challis C, Schretter CE, Rocha S, Gradinaru V, Chesselet MF, Keshavarzian A, Shannon KM, Krajmalnik-Brown R, Wittung-Stafshede P, Knight R, Mazmanian SK (2016) Gut Microbiota Regulate Motor Deficits and Neuroinflammation in a Model of Parkinson's Disease. Cell 167:1469–1480. e12. doi: 10.1016/j.cell.2016.11.018 · DOI · Paper page
  40. Schmalbach B, Lepsveridze E, Djogo N, Papashvili G, Kuang F, Leshchyns'ka I, Sytnyk V, Nikonenko AG, Dityatev A, Jakovcevski I, Schachner M (2015) Age-dependent loss of parvalbumin-expressing hippocampal interneurons in mice deficient in CHL1, a mental retardation and schizophrenia susceptibility gene. J Neurochem 135:830–844. doi: 10.1111/jnc.13284 · DOI
  41. Shi M, Liu C, Cook TJ, Bullock KM, Zhao Y, Ginghina C, Li Y, Aro P, Dator R, He C, Hipp MJ, Zabetian CP, Peskind ER, Hu SC, Quinn JF, Galasko DR, Banks WA, Zhang J (2014) Plasma exosomal alpha-synuclein is likely CNS-derived and increased in Parkinson's disease. Acta Neuropathol 128:639–650 · DOI · Paper page
  42. Shi M, Zabetian CP, Hancock AM, Ginghina C, Hong Z, Yearout D, Chung KA, Quinn JF, Peskind ER, Galasko D, Jankovic J, Leverenz JB, Zhang J (2010) Significance and confounders of peripheral DJ-1 and alpha-synuclein in Parkinson's disease. Neurosci Lett 480:78–82. doi: 10.1016/j.neulet.2010.06.009 · DOI
  43. Shoji H, Watanabe M, Itoh S, Kuwahara H, Hattori F (1993) Japanese encephalitis and parkinsonism. J Neurol 240:59–60 · DOI
  44. Takahashi Y, Nishikawa M, Shinotsuka H, Matsui Y, Ohara S, Imai T, Takakura Y (2013) Visualization and in vivo tracking of the exosomes of murine melanoma B16-BL6 cells in mice after intravenous injection. J Biotechnol 165:77–84. doi: 10.1016/j.jbiotec.2013.03.013 · DOI
  45. Triantafilou M, Triantafilou K (2002) Lipopolysaccharide recognition: CD14, TLRs and the LPS-activation cluster. Trends Immunol 23:301–304 · DOI
  46. Ulusoy A, Di Monte DA (2013) alpha-Synuclein elevation in human neurodegenerative diseases: experimental, pathogenetic, and therapeutic implications. Mol Neurobiol 47:484–494. doi: 10.1007/s12035-012-8329-y · DOI
  47. Ulusoy A, Rusconi R, Perez-Revuelta BI, Musgrove RE, Helwig M, Winzen-Reichert B, Di Monte DA (2013) Caudo-rostral brain spreading of alpha-synuclein through vagal connections. EMBO Mol Med 5:1119–1127. doi: 10.1002/emmm.201302475 · DOI
  48. Varga Z, Gyurko I, Paloczi K, Buzas EI, Horvath I, Hegedus N, Mathe D, Szigeti K (2016) Radiolabeling of Extracellular Vesicles with (99m)Tc for Quantitative In Vivo Imaging Studies. Cancer Biother Radiopharm 31:168–173. doi: 10.1089/cbr.2016.2009 · DOI
  49. Vestad B, Llorente A, Neurauter A (2017) Size and concentration analyses of extracellular vesicles by nanoparticle tracking analysis: a variation study. J Extracell Vesicles 6:1344087. doi: 10.1080/20013078.2017.1344087 · DOI
  50. Villegas JC, Broadwell RD (1993) Transcytosis of protein through the mammalian cerebral epithelium and endothelium. II. Adsorptive transcytosis of WGA-HRP and the blood-brain and brain–blood barriers. J Neurocytol 22:67–80 · DOI
  51. Wang X, Yu S, Li F, Feng T (2015) Detection of alpha-synuclein oligomers in red blood cells as a potential biomarker of Parkinson's disease. Neurosci Lett 599:115–119. doi: 10.1016/j.neulet.2015.05.030 · DOI
  52. Zhang Y, Zhang L, Li Y, Sun S, Tan H (2014) Different contributions of clathrin- and caveolae-mediated endocytosis of vascular endothelial cadherin to lipopolysaccharide-induced vascular hyperpermeability. PLoS One 9:e106328. doi: 10.1371/journal.pone.0106328 · DOI
  53. Zheng T, Pu J, Chen Y, Mao Y, Guo Z, Pan H, Zhang L, Zhang H, Sun B, Zhang B (2017) Plasma Exosomes Spread and Cluster Around beta-Amyloid Plaques in an Animal Model of Alzheimer's Disease. Front Aging Neurosci 9:12. doi: 10.3389/fnagi.2017.00012 · DOI

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Metadata

Authors
Matsumoto, J., Stewart, T., Sheng, L., Li, N., Bullock, K., Song, N., Shi, M., Banks, W. A., & Zhang, J.
Venue
Acta Neuropathologica Communications
Published
2017-09-13
Volume
5
Issue
1
ISSN
2051-5960
Cited by
279
References
10
Language
en
Funders
National Institutes of Health (R01 ES016873, ES019277, U01 NS091272, U01 NS082137)

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