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Ataxia telangiectasia alters the ApoB and reelin pathway.
- Source :
-
Neurogenetics [Neurogenetics] 2018 Dec; Vol. 19 (4), pp. 237-255. Date of Electronic Publication: 2018 Oct 21. - Publication Year :
- 2018
-
Abstract
- Autosomal recessive ataxia telangiectasia (A-T) is characterized by radiosensitivity, immunodeficiency, and cerebellar neurodegeneration. A-T is caused by inactivating mutations in the ataxia telangiectasiamutated (ATM) gene, a serine-threonine protein kinase involved in DNA damage response and excitatory neurotransmission. The selective vulnerability of cerebellar Purkinje neurons (PN) to A-T is not well understood. Employing global proteomic profiling of cerebrospinal fluid from patients at ages around 15 years, we detected reduced calbindin, reelin, cerebellin-1, cerebellin-3, protocadherin fat 2, sempahorin 7A, and increased apolipoprotein B and J peptides. Bioinformatic enrichment was observed for pathways of lipoproteins, endocytosis, extracellular matrix receptor interaction, peptidase activity, adhesion, calcium binding, and complement immunity. This seemed important since secretion of reelin from glutamatergic afferent axons is crucial for PN lipoprotein receptor endocytosis and lipid signaling. Reelin expression is downregulated by irradiation and reelin/ApoB mutations are known causes of ataxia. Validation efforts in 2-month-old Atm-/- mice before onset of motor deficits confirmed cerebellar transcript reductions for reelin receptors Apoer2/Vldlr with increases for their ligands Apoe/Apoh and cholesterol 24-hydroxylase Cyp46a1. Concomitant dysregulations were found for Vglut2/Sema7a as climbing fiber markers, glutamate receptors like Grin2b, and calcium homeostasis factors (Atp2b2, Calb1, Itpr1), while factors involved in DNA damage, oxidative stress, neuroinflammation, and cell adhesion were normal at this stage. Quantitative immunoblots confirmed ApoB and ApoJ increases and VLDLR reduction in cerebellar tissue at the age of 2 months. These findings show that ApoB excess and reelin signaling deficits reflect the neurodegeneration in A-T in a sensitive and specific way. As extracellular factors, apolipoproteins and their cargo such as vitamin E may be useful for neuroprotective interventions.
- Subjects :
- Adolescent
Animals
Ataxia Telangiectasia pathology
Ataxia Telangiectasia Mutated Proteins genetics
Case-Control Studies
Child
Child, Preschool
Disease Models, Animal
Female
Humans
Infant
Infant, Newborn
Male
Mice
Mice, Knockout
Reelin Protein
Signal Transduction genetics
Apolipoproteins B genetics
Apolipoproteins B metabolism
Ataxia Telangiectasia genetics
Ataxia Telangiectasia metabolism
Cell Adhesion Molecules, Neuronal genetics
Cell Adhesion Molecules, Neuronal metabolism
Extracellular Matrix Proteins genetics
Extracellular Matrix Proteins metabolism
Nerve Tissue Proteins genetics
Nerve Tissue Proteins metabolism
Serine Endopeptidases genetics
Serine Endopeptidases metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1364-6753
- Volume :
- 19
- Issue :
- 4
- Database :
- MEDLINE
- Journal :
- Neurogenetics
- Publication Type :
- Academic Journal
- Accession number :
- 30343341
- Full Text :
- https://doi.org/10.1007/s10048-018-0557-5