Literature DB >> 10978635

Lectin-histochemical detection of degenerative glycoconjugate deposits in human brain.

A Nishimura1, S Sawada, I Ushiyama, Y Yamamoto, T Nakagawa, A Tanegashima, K Nishi.   

Abstract

Several lectins were used to study the localization of glycoconjugates in brain of elderly people and patients with Alzheimer type dementia (ATD) and Down's syndrome (DS). Five kinds of degenerated or deposited materials stained clearly by lectins specific to GalNAC, Gal, Fuc, and/or Man were recognized much in ATD and DS, less in elderly peoples, in addition to the binding of the lectins to neurons. (i) Round shape deposits called corpora amylacea (CA) which consisted of various sizes of round material, existed mainly on the surface of cerebral cortex and some in white matter of the brain. They were colored by Alcian blue (AB), Aldehyde fucsin (AF) and periodic acid shiff (PAS) and weakly by Hematoxylin (H), but not by Eosin (B). They showed clear reactivity with lectins specific to GalNAC, Gal, Fuc and Gal-GalNAC. (ii) Amorphous and variform amyloid deposits existed around blood vessels in the white matter were stained by thioflavin and lectins specific to GalNAC, Gal and Fuc, but not with Man specific lectins and PAS, AB, AF and HE. (iii) Another kind of amyloid deposits which showed a similar characteristic to the previous one and were recognized mainly in white matter and independent blood vessels. These deposits were stained by thioflavin but not by PAS, AB, AF and HE and showed good reactivity with lectins specific to GalNAC, Gal, Fuc, Gal-GalNAC, Gal-GIcNAc and Man. The reactivity with lectins specific to Gal, Fuc, and Man was seen in senile plaques (iv) and neurofibrillary tangles (v). Although at present we are unable to explain the origin of these deposits, it is clear from this study that the glycoconjugates form an integral part of the degeneration in the brain. The lectin staining with GS-I is useful in the forensic pathology to diagnose brain disorders at postmortem examination, since these lectin were able to detect five types of degeneration changes and/or deposits.

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Year:  2000        PMID: 10978635     DOI: 10.1016/s0379-0738(00)00228-0

Source DB:  PubMed          Journal:  Forensic Sci Int        ISSN: 0379-0738            Impact factor:   2.395


  7 in total

1.  The carbohydrate deposits detected by histochemical methods in the molecular layer of the dentate gyrus in the hippocampal formation of patients with schizophrenia, Down's syndrome and dementia, and aged person.

Authors:  A Nishimura; K Ikemoto; K Satoh; Y Yamamoto; S Rand; B Brinkmann; K Nishi
Journal:  Glycoconj J       Date:  2000-11       Impact factor: 2.916

Review 2.  Carbohydrate structural units in glycosphingolipids as receptors for Gal and GalNAc reactive lectins.

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Journal:  Neurochem Res       Date:  2002-08       Impact factor: 3.996

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Journal:  Curr Alzheimer Res       Date:  2016       Impact factor: 3.498

4.  Alzheimer's Disease in Down Syndrome.

Authors:  Elizabeth Head; David Powell; Brian T Gold; Frederick A Schmitt
Journal:  Eur J Neurodegener Dis       Date:  2012-12

5.  Brain glycogen serves as a critical glucosamine cache required for protein glycosylation.

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Journal:  Cell Metab       Date:  2021-05-26       Impact factor: 31.373

Review 6.  Research advances and prospects of legume lectins.

Authors:  Rajan Katoch; Ankur Tripathi
Journal:  J Biosci       Date:  2021       Impact factor: 1.826

7.  Distribution of microglial phenotypes as a function of age and Alzheimer's disease neuropathology in the brains of people with Down syndrome.

Authors:  Alessandra C Martini; Alex M Helman; Katie L McCarty; Ira T Lott; Eric Doran; Frederick A Schmitt; Elizabeth Head
Journal:  Alzheimers Dement (Amst)       Date:  2020-10-14
  7 in total

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