Summary
Abnormal filaments (PHF) accumulate in neurons in Alzheimer’s disease in target areas. They fill the pericaryon but are also found in dendrites and axons. Their presence is associated with a disappearance of microtubules and neurofilaments, and an accumulation of dense bodies, altered mitochondria and smooth endoplasmic reticulum. Their ultrastructure differs from normal cytoskeletal fibers but one of their main components are the tau proteins. Senile plaques are composed of a core of amyloid fibers surrounded by abnormal neurites containing PHF and accumulations of organelles, reactive astrocytes and microglia.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
Preview
Unable to display preview. Download preview PDF.
References
Alzheimer A (1907) Über eine eigenartige Erkrankung der Hirnrinde. Allgemeine Zeitschrift für Psychiatrie 64: 146–148
Blessed G, Tomlinson BE, Roth M (1968) The association between quantitative measurements of dementia and of senile changes in the cerebral gray matter of elderly subjects. J Psychiat 114: 797–805
Braak H, Braak E, Grundke-Iqbal I, Iqbal K (1986) Occurrence of neuropil threads in the senile human brain and in Alzheimer’s disease: a third location of paired helical filaments outside of neurofibrillary tangles and neuritic plaques. Neurosci Lett 65: 251–355
Brion JP, Couck AM, Flament-Durand J (1984) Ultrastructural study of enriched fractions of “tangles” from human patients with senile dementia of the Alzheimer type. Acta Neuropathol (Berl) 64: 148 – 152
Brion JP, Couck AM, Passareiro H, Flament-Durand J (1985 a) Neurofibrillary tangles of Alzheimer’s disease: an immunocytochemical study. J Submicrosc Cytol 17: 89–96
Brion JP, Passareiro H, Nunez J, Flament-Durand J (1985 b) Mise en évidence immunologique de la protéine tau au niveau des lésions de dégénérescence neurofibrillaire de la maladie d’Alzheimer. Arch Biol (Brux) 95: 229–235
Brion JP, Power D, Hue D, Couck AM, Anderton BH, Flament-Durand J (1989 a) Heterogeneity of ubiquitin immunoreactivity in neurofibrillary tangles of Alzheimer’s disease. Neurochem Int 14: 121–128
Brion JP, Couck AM, Cheetham ME, Hanger D, Anderton BH, FlamentDurand J ( 1989 b) A cDNA encodes epitopes shared between microtubuleassociated protein MAP2 and Alzheimer neurofibrillary tangles: in situ hybridization and immunocytochemistry. In: Christen Y (ed) Biological markers of Alzheimer’s disease. Research and perspectives in Alzheimer’s disease. Springer, Berlin Heidelberg New York Tokyo, pp 56–65
Chretien M, Patey G, Souyri F, Droz B (1981) “Acrylamide-induced” neuropathy and impairment of axonal proteins. II. Abnormal accumulations of smooth endoplasmic reticulum at sites of focal retention of fast transported proteins. Electron microscope radioautographic study. Brain Res 205: 15–28
Crowther RA, Wischik CM (1985) Image reconstruction of the Alzheimer paired helical filament. EMBO J 4: 3661–3665
Delacourte A, Defossez A (1986) Alzheimer’s disease: tau proteins, the promoting factors of microtubule assembly, are major components of paired helical filaments. J Neurol Sci 76: 173–186
De Mey J, Moeremans M, Geuens G, Nuydens R, De Brabander M (1981) High-resolution light and electron-microscopic localization of tubulin with the IGS (immunogold staining) method. Cell Biol Int Rep 5: 889–899
Dustin P, Flament-Durand J (1982) Disturbances of axoplasmic transport in Alzheimer’s disease. In: Weiss DG, Gorio A (eds) Axoplasmic transport in physiology and pathology. Springer, Berlin Heidelberg New York, pp 131–136
Delaere P, Duyckaerts C, Brion JP, Poulain V, Hauw JJ (1989) Tau, paired helical filaments and amyloid in the neocortex: a morphometric study of 15 cases with graded intellectual status in aging and senile dementia of Alzheimer type. Acta Neuropathol (Berl) 77: 645–653
Duyckaerts C, Brion JP, Hauw JJ, Flament-Durand J (1987) Comparison of immunocytochemistry with a specific antibody and Bodian’s protargol method. Quantitative assessment of the density of neurofibrillary tangles and senile plaques in senile dementia of the Alzheimer type. Acta Neuropathol (Berl) 73: 167–170
Fischer O (1907) Miliare Nekrosen mit drusigen Wucherungen der Neurofibrillen, eine regelmäßige Veränderung der Hirnrinde bei seniler Demenz. Monatsschrift für Psychiatric and Neurologic 22: 361–372
Flament-Durand J, Couck AM (1979) Spongiform alterations in brain biopsies of presenile dementia. Acta Neuropathol (Berl) 46: 159–162
Glenner GG, Wong CW (1984) Alzheimer’s disease and Down’s syndrome: sharing of a unique cerebrovascular amyloid fibril protein. Biochem Biophys Res Comm 122: 1131–1135
Goedert M, Wischik CM, Crowther RA, Walker JE, Klug A (1988) Cloning and sequencing of the cDNA encoding a core protein of the paired helical filament of Alzheimer’s disease: identification as the microtubule-associated protein tau. Proc Natl Acad Sci USA 85: 4051–4055
Gonatas NK, Anderson W, Evangelistica I (1967) The contribution of altered synapses in the senile plaque: an electron microscope study in Alzheimer’s dementia. J Neuropathol Exp Neurol 26: 25–39
Gray EG, Paula-Barbosa M, Rober A (1987) Alzheimer’s disease: paired helical filaments and cytomembranes. Neuropathol Appl Neurobiol 13: 91–110
Hirano A, Dembitzer HM, Kurland LT (1968) The fine structure of some intraganglionic alterations. J Neuropathol Exp Neurol 27: 167–182
Ihara Y, Abraham C, Selkoe DJ (1983) Antibodies to paired helical filaments in Alzheimer’s disease do not recognize normal brain proteins. Nature 304: 727–730
Iqbal K, Grundke-Iqbal I, Zaidi T, Merz PA, Wen GY, Shaikh SS, Wisniewski HM (1986) Defective brain microtubule assembly in Alzheimer’s disease. Lancet is 421–426
Katzman R, Terry RD, De Teresa R, Brown T, Davies P, Fuld P, Renbing X, Peck A (1988) Clinical, pathological and neurochemical changes in dementia: a subgroup with preserved mental status and numerous neocortical plaques. Ann Neurol 23: 138–144
Kidd M (1963) Paired helical filaments in electron microscopy of Alzheimer’s disease. Nature 197: 192–193
Kosik KS, Duffy LK, Dowling MM, Abraham C, McCluskey A, Selkoe DJ (1984) Microtubule-associated protein 2: monoclonal antibodies demonstrate the selective incorporation of certain epitopes into Alzheimer neurofibrillary tangles. Proc Natl Acad Sci USA 81: 7941–7945
Kosik KS, Joachim CL, Selkoe DJ (1986) The microtubule-associated protein, tau, is a major antigenic component of paired helical filaments in Alzheimer’s disease. Proc Natl Acad Sci USA 83: 4044–4048
Kowall NW, Kosik KS (1987) Axonal disruption and aberrant localization of tau protein characterize the neuropil pathology of Alzheimer’s disease. Ann Neurol 22: 639–643
Mann DMA (1985) The neuropathology of Alzheimer’s disease: a review with pathogenetic, aetiological and therapeutic considerations. Mech Ageing Dev 31: 213–255
Masters CL, Simms G, Weinman NA, Multhaup G, McDonald BL, Beyreuther K (1985) Amyloid plaque core protein in Alzheimer disease and Down syndrome. Proc Natl Acad Sci USA 82: 4245–4249
Miller CCJ, Brion JP, Calvert R, Chin TK, Eagles PAM, Downes MJ, FlamentDurand J, Haugh M, Kahn J, Probst A, Ulrich J, Anderton BH (1986) Alzheimer’s paired helical filaments share epitopes with neurofilament side arms. EMBO J 5: 269–276
Miyakawa T, Shimuji A, Kuramoto R, Higuchi Y (1982) The relationship between senile plaques and cerebral blood vessel in Alzheimer’s disease and senile dementia. Virchows Arch (Cell Pathol) 40: 121–129
Monpetit V, Clapin DF, Guberman A (1985) Substructure of 20 nm filaments of progressive supranuclear palsy. Acta Neuropathol (Berl) 68: 311–318
Mori H, Kondo J, Ihara Y (1987) Ubiquitin is a component of paired helical filaments in Alzheimer’s disease. Science 325: 1641–1644
Perry G, Friedman R, Shaw G, Chau V (1987) Ubiquitin is detected in neurofibrillary tangles and senile plaque neurites of Alzheimer’s disease brains. Proc Natl Acad Sci USA 84: 3033–3036
Probst A, Basler V, Bron B, Ulrich J (1983) Neuritic plaques in senile dementia of the Alzheimer type: a Golgi analysis in the hippocampal region. Brain Res 268: 249–254
Probst A, Brunnschweiler H, Lautenschlager C, Ulrich J (1987) A special type of senile plaque, possibly an initial stage. Acta Neuropathol (Berl) 74: 133–141
Richard S, Brion JP, Couck AM, Flament-Durand J (1989) Accumulation of smooth endoplasmic reticulum in Alzheimer’s disease: new morphological evidence of axoplasmic flow disturbances. J Submicrosc Cytol 21: 461–467
Sternberger LA (1979) Immunocytochemistry. Wiley, New York
Terry RD (1963) The fine structure of neurofibrillary tangles in Alzheimer’s disease. J Neuropathol Exp Neurol 22: 629–642
Tomlinson BE, Irving D, Blessed G (1981) Cell loss in the locus caeruleus in senile dementia of Alzheimer type. J Neurol Sci 49: 419–428
Wilcock GK, Esiri MM (1982) Plaques, tangles and dementia. A quantitative study. J Neurol Sci 56: 343–356
Wischik CM, Crowther RA, Stewart M, Roth M (1985) Subunit structure of paired helical filaments in Alzheimer’s disease. J Cell Biol 100: 1905–1912
Wisniewski HM, Narang HK, Terry RD (1976) Neurofibrillary tangles of paired helical filaments. J Neurol Sci 27: 173–181
Wisniewski HM, Merz PA, Iqbal K (1984) Ultrastructure of paired helical filaments of Alzheimer’s neurofibrillary tangles. J Neuropathol Exp Neurol 43: 643–656
Author information
Authors and Affiliations
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 1990 Springer-Verlag Wien
About this chapter
Cite this chapter
Flament-Durand, J., Brion, J.P. (1990). Morphology of neurofibrillary tangles and senile plaques. In: Maurer, K., Riederer, P., Beckmann, H. (eds) Alzheimer’s Disease. Epidemiology, Neuropathology, Neurochemistry, and Clinics. Key Topics in Brain Research. Springer, Vienna. https://doi.org/10.1007/978-3-7091-3396-5_11
Download citation
DOI: https://doi.org/10.1007/978-3-7091-3396-5_11
Publisher Name: Springer, Vienna
Print ISBN: 978-3-211-82197-8
Online ISBN: 978-3-7091-3396-5
eBook Packages: Springer Book Archive