Skip to main content
Log in

Ultrastructural studies of the cells forming amyloid in the cortical vessel wall in Alzheimer's disease

  • Regular Papers
  • Published:
Acta Neuropathologica Aims and scope Submit manuscript

Summary

Ultrastructural studies of serial sections of the vessels with amyloid deposits in the brain cortex of patients with Alzheimer's disease showed that cells in the position of pericytes — perivascular cells - and perivascular microglial cells are producers of amyloid fibrils in the vascular wall. Three types of changes from normal are distinguishable in the vessel wall: (1) semicircular or circular thickening of vascular wall containing a large amount of amorphous material and various number of amyloid fibrils, (2) tuberous amyloid deposits containing both amorphous material and amyloid fibrils, some of the fibrils being arranged in strata and others arranged radially, and (3) amyloid star composed of a predominantly radial arrangement of bundles of amyloid fibrils and a less prominent amorphous component. A mixture of amorphous material and amyloid fibrils is present in cell membrane envaginations of perivascular cells, and occasionally perivascular microglial cells. Bundles of amyloid fibrils are found in altered cisternae of the endoplasmic reticulum and in the channels confluent with the infoldings of the plasma membrane of perivascular microglial cells. The amyloid deposition in the wall of the vessel causes degeneration of endothelial cells and the reduction of, and in some vessels obliteration of, the vessel lumen. In areas affected by amyloid angiopathy, extensive degeneration both of the neuropil and of neurons was observed. These changes were accompanied by astrogliosis. This study demonstrates similarities in amyloid formation in amyloid angiopathy and in β-amyloid plaques in the neuropil and suggests that cells of the mononuclear phagocyte system of the brain (perivascular cells and perivascular microglia) are engaged in amyloid fibril formation.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Institutional subscriptions

Similar content being viewed by others

References

  1. Bartlett PF (1982) Pluripotential hemopoietic stem cells in adult mouse brain. Proc Natl Acad Sci USA 79:2722–2725

    Google Scholar 

  2. Castano EM, Frangione B (1988) Biology of disease. Human amyloidosis, Alzheimer disease and related disorders. Lab Invest 58:122–132

    Google Scholar 

  3. Cork LC, Masters C, Beyreuther K, Price DL (1990) Development of senile plaques. Relationships of neuronal abnormalities and amyloid deposits. Am J Pathol 137:1383–1392

    Google Scholar 

  4. Friede RL, Magee KR (1962) Alzheimer's disease: presentation of a case with pathologic and enzymatic-histochemical observations. Neurology 12:213–222

    Google Scholar 

  5. Fujita S, Tsuchihashi Y, Kitamura T (1981) Origin, morphology and function of the microglia. In: Glial and Neuronal Cell Biology. Eleventh International Congress of Anatomy. Alan R. Liss, New York, pp 141–169

    Google Scholar 

  6. Glenner GG, (1979) Congophilic microangiopathy in the pathogenesis of Alzheimer's syndrome (presenile dementia). Med Hypotheses 5:1231–1236

    Google Scholar 

  7. Glenner GG (1980) Amyloid deposits and amyloidosis. The β-fibrilloses. N Engl J Med 302:1283–1292, 1333–1343

    Google Scholar 

  8. Glenner GG, Wong CW (1984) Alzheimer's disease: initial report of the purification and characterization of novel cerebrovascular amyloid protein. Biochem Biophys Res Commun 120:885–890

    Google Scholar 

  9. Glenner GG, Wong CW (1984) Alzheimer's disease and Down's syndrome: sharing of a unique cerebrovascular amyloid fibril protein. Biochem Biophys Res Commun 122:1131–1135

    Google Scholar 

  10. Glenner GG, Wong CW (1986) The significance of cerebrovascular amyloid in Alzheimer's disease. International symposium on dementia and amyloid. Neuropathology [Suppl] 3:67–78

    Google Scholar 

  11. Goldgaber D, Lerman MI, McBride OW, Saffiotti U, Gajdusek CD (1987) Characterization and chromosomal localization of a cDNA encoding brain amyloid of Alzheimer disease. Science 235:877–880

    Google Scholar 

  12. Graeber MB, Streit WJ (1990) Perivascular microglia defined. Trends Neurosci 13:66

    Google Scholar 

  13. Graeber MB, Streit WJ, Kreutzberg GW, (1989) Identity of ED2-positive perivascular cells in rat brain. J Neurosci Res 22:103–106

    Google Scholar 

  14. Hart MN, Merz P, Bennett-Gray J, Menezes AH, Goeken JA, Schelper RL, Wisniewski HM (1988) β-Amyloid protein of Alzheimer's disease is found in cerebral and spinal cord vascular malformations. Am J Pathol 132:167–172

    Google Scholar 

  15. Hickey WF, Kimura H (1988) Perivascular microglial cells of the CNS are bone marrow-derived and present antigen in vivo. Science 239:290–292

    Google Scholar 

  16. Ishihara T, Gondo T, Takahashi M, Uchino F, Ikeda S-I, Allsop D, Imai K (1991) Immunohistochemical and immunoelectron microscopical characterization of cerebrovascular and senile plaque amyloid in aged dog's brains. Brain Res 548:196–205

    Google Scholar 

  17. Ishii T (1958) Histochemistry of the senile changes of the brain of the senile dementia. Psychiatr Neurol Jpn 60:768–781

    Google Scholar 

  18. Ishii T (1969) Enzyme histochemical studies of senile plaques and the plaque-like degeneration of arteries and capillaries (Scholz). Acta neuropathol (Berl) 14:250–260

    Google Scholar 

  19. Kawai M, Kalaria RN, Harik SI, Perry G (1990) The relationship of amyloid plaques to cerebral capillaries in Alzheimer's disease. Am J Pathol 137:1435–1446

    Google Scholar 

  20. Mandybur TI (1975) The incidence of cerebral amyloid angiopathy in Alzheimer's disease. Neurology 25:120–126

    Google Scholar 

  21. Mandybur TI (1986) Cerebral amyloid angiopathy: the vascular pathology and complications. J Neuropathol Exp Neurol 45:79–90

    Google Scholar 

  22. Matsumoto Y, Kawai K, Fujiwara M (1989) In situ Ia expression on brain cells in the rat: autoimmune encephalomyelitis-resistant strain (BN) and susceptible strain (Lewis) compared. Immunology 66:621–627

    Google Scholar 

  23. Miyakawa T (1986) The relationship between amyloid fibrils around cerebral blood vessels and senile plaques, and ultrastructure of amyloid fibrils. International Symposium on Dementia and Amyloid. Neuropathology [Suppl] 3:37–48

    Google Scholar 

  24. Miyakawa T, Sumiyoshi S, Murayama E, Deshimaru M (1974) Ultrastructure of capillary plaque-like degeneration in senile dementia. Acta Neuropathol (Berl), 29:229–236

    Google Scholar 

  25. Miyakawa T, Shimoji A, Kumamoto R, Higuchi Y (1982) The relationship between senile plaques and cerebral blood vessels in Alzheimer's disease and senile dementia. Morphological mechanism of senile plaque production. Virchows Arch [B] 40:121–129

    Google Scholar 

  26. Morel F, Wildi E (1954) General and cellular pathochemistry of senile and presenile alterations of the brain. Proceedings of the 1st International Congress on Neuropathology, Rome, September 1952. Rosenberg and Sellier, Torino, pp 347–374

    Google Scholar 

  27. Morimatsu M, Hirai S, Muramatsu A, Yoshikawa M (1975) Senile degenerative brain lesions and dementia. J Am Geriatr Soc 23:390–406

    Google Scholar 

  28. Mountjoy CQ, Tomlinson BE, Gibson RH (1982) Amyloid and senile plaques and cerebral blood vessels. A semi-quantitative investigation of a possible relationship. J Neurol Sci 57:89–103

    Google Scholar 

  29. Osetowska E (1966) Etude anatomopatologique sur le cerveau de chiens senile. In: Luthy F, Bischoff A (eds) Proceedings of the Fifth International Congress of Neuropathology. Excerpta Medica, Amsterdam, pp 497–502

    Google Scholar 

  30. Peterson EW, Schulz DM, (1961) Amyloid in vessels of vascular malformations in brain. Arch Pathol 72:480–483

    Google Scholar 

  31. Robakis NK, Ramakrishna N, Wolfe G, Wisniewski HM, (1987) Molecular cloning and characterization of a cDNA encoding the cerebrovascular and the neuritic plaques amyloid peptides. Proc Natl Acad Sci USA 84:4190–4194

    Google Scholar 

  32. Scholz W (1938) Studien zur Pathologie der Hirngefäße. II. Die drusige Entartung der Hirnarterien und Capillaren (eine Form seniler Gefäßerkrankung). Z Gesamte Neurol Psychiatr 162:694–715

    Google Scholar 

  33. Streit WJ, Graeber MB, Kreutzberg GW, (1989) Expression of Ia antigen on perivascular and microglial cells after sublethal and lethal motor neuron injury. Exp Neurol 105:115–126

    Google Scholar 

  34. Tanzi RE, Gusella JF, Watkins PC, Bruns GA, St George-Hyslop P, VanKeuran ML, Patterson D, Pagan S, Kurnit DM, Neve RL (1987) Amyloid beta protein gene: cDNA, mRNA distribution, and genetic linkage near the Alzheimer locus. Science 235:880–884

    Google Scholar 

  35. Tomonaga M (1981) Cerebral amyloid angiopathy in the elderly. J Am Geriatr Soc 29:151–157

    Google Scholar 

  36. van Duinen SG, Castano EM, Prelli F, Bots GTAB, Luyendijk W, Frangione B (1987) Hereditary cerebral hemorrhage with amyloidosis in patients of Dutch origin is related to Alzheimer's disease. Proc Natl Acad Sci USA 84:5991–5994

    Google Scholar 

  37. Vinters HV, Gilbert JJ (1983) Cerebral amyloid angiopathy: incidence and complications in the aging brain. II. The distribution of amyloid vascular changes. Stroke 14:924–928

    Google Scholar 

  38. Vinters HV, Miller BL, Pardrige WM, (1988) Brain amyloid and Alzheimer disease. Ann Intern Med 109:41–54

    Google Scholar 

  39. von Braunmuhl A (1956) Kongophile Angiopathie und senile Plaques bei greisen Hunden. Arch Psychiatr Nervenkr 194:396–414

    Google Scholar 

  40. Walker LC, Masters C, Beyreuther K, Price DL (1990) Amyloid in the brains of aged squirrel monkeys. Acta Neuropathol 80:381–387

    Google Scholar 

  41. Wegiel J, Wisniewski HM (1990) The complex of microglial cells and amyloid star in three-dimensional reconstruction. Acta Neuropathol 81:116–124

    Google Scholar 

  42. Wisniewski HM, Terry RD (1973) Reexamination of the pathogenesis of the senile plaque. Prog Neuropathol 2:1–26

    Google Scholar 

  43. Wisniewski HM, Wegiel J (1991) Spatial relationships between astrocytes and classical plaque components. Neurobiol Aging 12:593–600

    Google Scholar 

  44. Wisniewski HM, Johnson AB, Raine CS, Kay WJ, Terry RD (1970) Senile plaques and cerebral amyloidosis in aged dogs. A histochemical and ultrastructural study. Lab Invest 23:287–296

    Google Scholar 

  45. Wisniewski HM, Wegiel J, Wang KC, Kujawa M, Lach B (1989) Ultrastructural studies of the cells forming amyloid fibers in clasical plaques. Can J Neurol Sci 16:535–542

    Google Scholar 

  46. Wisniewski HM, Wegiel J, Morys J, Bancher C, Soltysiak Z, Kim KS (1990) Aged dogs: an animal model to study beta-protein amyloidogenesis. In: Maurer K, Riederer P, Beckmann H (eds) Alzheimer's disease. Epidemiology, neuropathology, neurochemistry, and clinics (Key topics in brain research). Springer Verlag, Wien New York, pp 151–168

    Google Scholar 

  47. Wisniewski HM, Wegiel J, Strojny P, Wang K-C, Kim K-S, Burrage T (1991) Ultrastructural morphology and immunocytochemistry of beta amyloid classical, primitive and diffuse plaque. In: Ishii T, et al (eds) Frontiers of Alzheimer research. Elsevier, Amsterdam, pp 99–108

    Google Scholar 

  48. Wisniewski HM, Weigiel J, Vorbrodt AW, Barcikowska M, Burrage TG (1991) The cellular basis for β-amyloid fibril formation and removal. In: Iqbal K, McLachlan DRC, Winblad B,Wisniewski HM (eds) Alzheimer's disease: basic mechanisms, diagnosis and therapeutic strategies. John Wiley and Sons, Chichester, pp 333–339

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

Supported in part by funds from the New York State Office of Mental Retardation and Developmental Disabilities and a grant from the National Institutes of Health, National Institute of Aging No. PO1-AGO-4220

Rights and permissions

Reprints and permissions

About this article

Cite this article

Wisniewski, H.M., Wegiel, J., Wang, K.C. et al. Ultrastructural studies of the cells forming amyloid in the cortical vessel wall in Alzheimer's disease. Acta Neuropathol 84, 117–127 (1992). https://doi.org/10.1007/BF00311383

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00311383

Key words

Navigation