Glial fibrillary acidic protein isoform expression in plaque related astrogliosis in Alzheimer's disease

NEUROBIOLOGY OF AGING

卷:35

Article

Kamphuis, Willem¹  Middeldorp, Jinte^1,2  Kooijman, Lieneke¹  Sluijs, Jacqueline A.¹  Kooi, Evert-Jan^1,3  Moeton, Martina¹  Freriks, Michel¹  Mizee, Mark R.^1,4  Hol, Elly M.^1,5,6 

[1] Inst Royal Netherlands Acad Arts & Sci KNAW, Netherlands Inst Neurosci, Dept Astrocyte Bology & Neurodegenerat, Amsterdam, Netherlands

[2] Stanford Univ, Sch Med, Dept Neurol & Neurol Sci, Stanford, CA 94305 USA

[3] Vrije Univ Amsterdam, Med Ctr, Sect Clin Neurosci, Dept Anat & Neurosci, Amsterdam, Netherlands

[4] Vrije Univ Amsterdam, Med Ctr, Dept Mol Cell Biol & Immunol, Blood Brain Barrier Res Grp, Amsterdam, Netherlands

[5] Univ Amsterdam, Ctr Neurosci, Swammerdam Inst Life Sci, Amsterdam, Netherlands

[6] Rudolf Magnus,Univ, Med Ctr Utrecht, Brain Ctr, Dept Translat Neurosci, Utrecht, Netherlands

关键词: Glial fibrillary acidic protein;    GFAP;    Alzheimer's disease;    Gliosis;    Astrocytes;    Hippocampus;    Intermediate filaments;    Vimentin;    Nestin;    Synemin;    Isoforms;    Plaques;   

DOI  :  10.1016/j.neurobiolaging.2013.09.035

来源: Elsevier

【 摘 要 】

In Alzheimer's disease (AD), amyloid plaques are surrounded by reactive astrocytes with an increased expression of intermediate filaments including glial fibrillary acidic protein (GFAP). Different GFAP isoforms have been identified that are differentially expressed by specific subpopulations of astrocytes and that impose different properties to the intermediate filament network. We studied transcript levels and protein expression patterns of all known GFAP isoforms in human hippocampal AD tissue at different stages of the disease. Ten different transcripts for GFAP isoforms were detected at different abundancies. Transcript levels of most isoforms increased with AD progression. GFAP delta-immunopositive astrocytes were observed in subgranular zone, hilus, and stratum-lacunosum-moleculare. GFAP delta-positive cells also stained for GFAP alpha. In AD donors, astrocytes near plaques displayed increased staining of both GFAP alpha and GFAP delta. The reading-frame-shifted isoform, GFAP(+1), staining was confined to a subset of astrocytes with long processes, and their number increased in the course of AD. In conclusion, the various GFAP isoforms show differential transcript levels and are upregulated in a concerted manner in AD. The GFAP(+1) isoform defines a unique subset of astrocytes, with numbers increasing with AD progression. These data indicate the need for future exploration of underlying mechanisms concerning the functions of GFAP delta and GFAP(+1) isoforms in astrocytes and their possible role in AD pathology. (C) 2014 Elsevier Inc. All rights reserved.

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