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Review
. 2016 Jan;131(1):87-102.
doi: 10.1007/s00401-015-1509-x. Epub 2015 Dec 10.

Aging-related tau astrogliopathy (ARTAG): harmonized evaluation strategy

Gabor G Kovacs  1 Isidro Ferrer  2 Lea T Grinberg  3   4 Irina Alafuzoff  5 Johannes Attems  6 Herbert Budka  7 Nigel J Cairns  8 John F Crary  9   10 Charles Duyckaerts  11 Bernardino Ghetti  12 Glenda M Halliday  13 James W Ironside  14 Seth Love  15 Ian R Mackenzie  16 David G Munoz  17 Melissa E Murray  18 Peter T Nelson  19 Hitoshi Takahashi  20 John Q Trojanowski  21 Olaf Ansorge  22 Thomas Arzberger  23 Atik Baborie  24 Thomas G Beach  25 Kevin F Bieniek  18 Eileen H Bigio  26 Istvan Bodi  27 Brittany N Dugger  25   28 Mel Feany  29 Ellen Gelpi  30 Stephen M Gentleman  31 Giorgio Giaccone  32 Kimmo J Hatanpaa  33 Richard Heale  6 Patrick R Hof  10 Monika Hofer  22 Tibor Hortobágyi  34 Kurt Jellinger  35 Gregory A Jicha  36 Paul Ince  37 Julia Kofler  38 Enikö Kövari  39 Jillian J Kril  40 David M Mann  41 Radoslav Matej  42 Ann C McKee  43 Catriona McLean  44 Ivan Milenkovic  45   46 Thomas J Montine  47 Shigeo Murayama  48 Edward B Lee  21 Jasmin Rahimi  45 Roberta D Rodriguez  49 Annemieke Rozemüller  50 Julie A Schneider  51   52 Christian Schultz  53 William Seeley  3 Danielle Seilhean  11 Colin Smith  14 Fabrizio Tagliavini  32 Masaki Takao  54 Dietmar Rudolf Thal  55   56 Jon B Toledo  21 Markus Tolnay  57 Juan C Troncoso  58 Harry V Vinters  59   60 Serge Weis  61 Stephen B Wharton  37 Charles L White 3rd  33 Thomas Wisniewski  62   63   64 John M Woulfe  65 Masahito Yamada  66 Dennis W Dickson  67
Affiliations
Review

Aging-related tau astrogliopathy (ARTAG): harmonized evaluation strategy

Gabor G Kovacs et al. Acta Neuropathol. 2016 Jan.

Abstract

Pathological accumulation of abnormally phosphorylated tau protein in astrocytes is a frequent, but poorly characterized feature of the aging brain. Its etiology is uncertain, but its presence is sufficiently ubiquitous to merit further characterization and classification, which may stimulate clinicopathological studies and research into its pathobiology. This paper aims to harmonize evaluation and nomenclature of aging-related tau astrogliopathy (ARTAG), a term that refers to a morphological spectrum of astroglial pathology detected by tau immunohistochemistry, especially with phosphorylation-dependent and 4R isoform-specific antibodies. ARTAG occurs mainly, but not exclusively, in individuals over 60 years of age. Tau-immunoreactive astrocytes in ARTAG include thorn-shaped astrocytes at the glia limitans and in white matter, as well as solitary or clustered astrocytes with perinuclear cytoplasmic tau immunoreactivity that extends into the astroglial processes as fine fibrillar or granular immunopositivity, typically in gray matter. Various forms of ARTAG may coexist in the same brain and might reflect different pathogenic processes. Based on morphology and anatomical distribution, ARTAG can be distinguished from primary tauopathies, but may be concurrent with primary tauopathies or other disorders. We recommend four steps for evaluation of ARTAG: (1) identification of five types based on the location of either morphologies of tau astrogliopathy: subpial, subependymal, perivascular, white matter, gray matter; (2) documentation of the regional involvement: medial temporal lobe, lobar (frontal, parietal, occipital, lateral temporal), subcortical, brainstem; (3) documentation of the severity of tau astrogliopathy; and (4) description of subregional involvement. Some types of ARTAG may underlie neurological symptoms; however, the clinical significance of ARTAG is currently uncertain and awaits further studies. The goal of this proposal is to raise awareness of astroglial tau pathology in the aged brain, facilitating communication among neuropathologists and researchers, and informing interpretation of clinical biomarkers and imaging studies that focus on tau-related indicators.

Keywords: ARTAG; Aging; Tau; Tau astrogliopathy.

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Figures

Fig. 1
Fig. 1
Comparison of tau (using AT8 antibody) immunoreactivities seen in primary tauopathies with those observed in aging-related tau astrogliopathy (ARTAG)
Fig. 2
Fig. 2
Representative photomicrographs of ARTAG types. Plump cytoplasmic tau immunoreactivity of astrocytes and tau-positive lining in subpial (a) and subependymal (b) location. Perivascular type: tau-immunoreactive astrocytic processes arranged around vessels (c). White matter (WM)-type: astrocytes in the subcortical white matter with plump cytoplasmic immunoreactivity (d). Gray matter (GM)-type: single-appearing (e, f) or clusters (g, h) of astrocytes with fine granular tau immunoreactivity in the processes without (e) or with (f) plump perinuclear cytoplasmic tau immunoreactivity. The bar shown in “a” represents 30 μm for a, b, f; 50 μm for d, e, h; and 100 μm for c, g
Fig. 3
Fig. 3
Representative images of different anatomical regions showing ARTAG. a Temporal cortex and white matter (WM); b dentate gyrus (gray matter-type cluster enlarged in the right); c amygdala; d frontal cortex (gray matter-type single); e nucleus accumbens (gray matter-type clusters and single forms); f substantia nigra; g, h medulla oblongata (IO inferior olive; ML medial lemniscus; n. XII hypoglossal nucleus). The bar shown in a represents 150 μm for a, b; 100 μm for the right inset in b, and ch
Fig. 4
Fig. 4
Summary of the concept of ARTAG. Four distinct astroglial tau pathologies are seen in primary tauopathies: tufted astrocytes (TA), astrocytic plaques (AP), globular astroglial inclusions (GAI), and ramified astrocytes (RA). Rarely there may be slight overlap of these morphologies, but predominance of a type is significantly associated with one of the specific primary tauopathies. ARTAG is characterized by two different morphologies: thorn-shaped astrocytes (TSA) and fine granular immunoreactivity in astrocytic processes (granular/fuzzy astrocytes: GFA); these are seen in the subpial (SP), sub-ependymal (SE), perivascular (PV) areas, and in the white (WM) and gray matter (GM). TSA and GFA may be present in the same brain together. Other neurodegenerative diseases (NDDs) may coexist with ARTAG or with primary tauopathies

References

    1. Ahmed Z, Bigio EH, Budka H, Dickson DW, Ferrer I, Ghetti B, Giaccone G, Hatanpaa KJ, Holton JL, Josephs KA, et al. Globular glial tauopathies (GGT): consensus recommendations. Acta Neuropathol. 2013;126:537–544. - PMC - PubMed
    1. Alafuzoff I, Arzberger T, Al-Sarraj S, Bodi I, Bogdanovic N, Braak H, Bugiani O, Del-Tredici K, Ferrer I, Gelpi E, et al. Staging of neurofibrillary pathology in Alzheimer’s disease: a study of the BrainNet Europe Consortium. Brain Pathol. 2008;18:484–496. - PMC - PubMed
    1. Alafuzoff I, Ince PG, Arzberger T, Al-Sarraj S, Bell J, Bodi I, Bogdanovic N, Bugiani O, Ferrer I, Gelpi E, et al. Staging/typing of Lewy body related alpha-synuclein pathology: a study of the BrainNet Europe Consortium. Acta Neuropathol. 2009;117:635–652. - PubMed
    1. Alafuzoff I, Thal DR, Arzberger T, Bogdanovic N, Al-Sarraj S, Bodi I, Boluda S, Bugiani O, Duyckaerts C, Gelpi E, et al. Assessment of beta-amyloid deposits in human brain: a study of the BrainNet Europe Consortium. Acta Neuropathol. 2009;117:309–320. - PMC - PubMed
    1. Arima K, Izumiyama Y, Nakamura M, Nakayama H, Kimura M, Ando S, Ikeda K, Takahashi K. Argyrophilic tau-positive twisted and non-twisted tubules in astrocytic processes in brains of Alzheimer-type dementia: an electron microscopical study. Acta Neuropathol. 1998;95:28–39. - PubMed

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