Corpora amylacea in human hippocampal brain tissue are intracellular bodies that exhibit a homogeneous distribution of neo-epitopes

被引:27
作者
Auge, Elisabet [1 ,2 ]
Bechmann, Ingo [3 ]
Llor, Nuria [4 ]
Vilaplana, Jordi [1 ,2 ,5 ]
Krueger, Martin [3 ]
Pelegri, Carme [1 ,2 ,5 ]
机构
[1] Univ Barcelona, Dept Bioquim & Fisiol, Secc Fisiol, Barcelona, Spain
[2] Univ Barcelona, Inst Neurociencies, Barcelona, Spain
[3] Univ Leipzig, Inst Anat, Leipzig, Germany
[4] Univ Barcelona, Dept Farmacol Toxicol & Quim Terapeut, Secc Quim Terapeut, Barcelona, Spain
[5] Ctr Biomed Red Enfermedades Neurodegenerativas CI, Barcelona, Spain
关键词
APOLIPOPROTEIN-E-DEFICIENT; SCHIFF-POSITIVE GRANULES; AGED MICE; FIBRILLAR MATERIAL; INCLUSIONS; DEPOSITION; GLIA;
D O I
10.1038/s41598-018-38010-7
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Corpora amylacea are spherical bodies of unknown origin and function, which accumulate in the human brain during the aging process and neurodegenerative disorders. In recent work, we reported that they contain some neo-epitopes that are recognized by natural IgMs, revealing a possible link between them and the natural immune system. Here, we performed an ultrastructural study complemented with confocal microscopy in order to shed light on the formation of corpora amylacea and to precisely localize the neo-epitopes. We show that immature corpora amylacea are intracellular astrocytic structures formed by profuse cellular debris and membranous blebs entrapped in a scattered mass of randomly oriented short linear fibers. In mature corpora amylacea, the structure becomes compacted and fibrillary material constitutes the principal component. We also determined that the neo-epitopes were uniformly localized throughout the whole structure. All these observations reinforce the idea that corpora amylacea of human brain are equivalent to another type of polyglucosan bodies named PAS granules, present in mouse brain and originated from degenerative processes. All those findings support the hypothesis that corpora amylacea are involved in the entrapment of damaged materials and non-degradable products and have a role in protective or cleaning mechanisms.
引用
收藏
页数:9
相关论文
共 27 条
  • [1] INTRANEURITIC CORPORA AMYLACEA - DEMONSTRATION IN ORBITAL CORTEX OF ELDERLY SUBJECTS BY MEANS OF EARLY POSTMORTEM BRAIN SAMPLING AND ELECTRON-MICROSCOPY
    ANZIL, AP
    HERRLINGER, H
    BLINZINGER, K
    KRONSKI, D
    [J]. VIRCHOWS ARCHIV ABTEILUNG A PATHOLOGISCHE ANATOMIE, 1974, 364 (04): : 297 - 301
  • [2] Exploring the elusive composition of corpora amylacea of human brain
    Auge, Elisabet
    Duran, Jordi
    Guinovart, Joan J.
    Pelegri, Carme
    Vilaplana, Jordi
    [J]. SCIENTIFIC REPORTS, 2018, 8
  • [3] New perspectives on corpora amylacea in the human brain
    Auge, Elisabet
    Cabezon, Itsaso
    Pelegri, Carme
    Vilaplana, Jordi
    [J]. SCIENTIFIC REPORTS, 2017, 7
  • [4] Corpora-amylacea and the family of polyglucosan diseases
    Cavanagh, JB
    [J]. BRAIN RESEARCH REVIEWS, 1999, 29 (2-3) : 265 - 295
  • [5] JUCKER M, 1992, SCIENCE, V255, P1443, DOI 10.1126/science.1542796
  • [6] AGE-RELATED DEPOSITION OF GLIA-ASSOCIATED FIBRILLAR MATERIAL IN BRAINS OF C57BL/6 MICE
    JUCKER, M
    WALKER, LC
    SCHWARB, P
    HENGEMIHLE, J
    KUO, H
    SNOW, AD
    BAMERT, F
    INGRAM, DK
    [J]. NEUROSCIENCE, 1994, 60 (04) : 875 - 889
  • [7] AGE-RELATED FIBRILLAR DEPOSITS IN BRAINS OF C57BL/6 MICE - A REVIEW OF LOCALIZATION, STAINING CHARACTERISTICS, AND STRAIN SPECIFICITY
    JUCKER, M
    WALKER, LC
    KUO, H
    TIAN, M
    INGRAM, DK
    [J]. MOLECULAR NEUROBIOLOGY, 1994, 9 (1-3) : 125 - 133
  • [8] AGE-RELATED FIBRILLAR MATERIAL IN MOUSE-BRAIN - ASSESSING ITS POTENTIAL AS A BIOMARKER OF AGING AND AS A MODEL OF HUMAN NEURODEGENERATIVE DISEASE
    JUCKER, M
    INGRAM, DK
    [J]. AGING CLOCK: THE PINEAL GLAND AND OTHER PACEMAKERS IN THE PROGRESSION OF AGING AND CARCINOGENESIS, 1994, 719 : 238 - 247
  • [9] Similarities in the age-related hippocampal deposition of periodic acid-Schiff-positive granules in the senescence-accelerated mouse P8 and C57BL/6 mouse strains
    Kuo, H
    Ingram, DK
    Walker, LC
    Tian, M
    Hengemihle, JM
    Jucker, M
    [J]. NEUROSCIENCE, 1996, 74 (03) : 733 - 740
  • [10] Leel-Ossy Lorant, 2001, Pathology and Oncology Research, V7, P145