Age‐dependent increase of perineuronal nets in the human hippocampus and precocious aging in epilepsy

Author:

Lehner Annika12ORCID,Hoffmann Lucas12,Rampp Stefan34ORCID,Coras Roland12,Paulsen Friedrich5,Frischknecht Renato6,Hamer Hajo7ORCID,Walther Katrin7ORCID,Brandner Sebastian48,Hofer Wiebke9,Pieper Tom10,Reisch Lea‐Marie11,Bien Christian G.11ORCID,Blumcke Ingmar12ORCID

Affiliation:

1. Department of Neuropathology Universitätsklinikum Erlangen and FAU Erlangen‐Nürnberg Erlangen Germany

2. Partner of the European Reference Network (ERN) EpiCARE Barcelona Spain

3. Department of Neuroradiology Universitätsklinikum Erlangen and FAU Erlangen‐Nürnberg Erlangen Germany

4. Department of Neurosurgery Universitätsklinikum Erlangen and FAU Erlangen‐Nürnberg Erlangen Germany

5. Institute of Functional and Clinical Anatomy, FAU Erlangen‐Nürnberg Erlangen Germany

6. Department of Biology, Animal Physiology Friedrich‐Alexander‐Universität Erlangen‐Nürnberg Erlangen Germany

7. Epilepsy Center, Department of Neurology Universitätsklinikum Erlangen and FAU Erlangen‐Nürnberg Erlangen Germany

8. Department of Neurosurgery Klinikum Fürth Germany

9. Department of Psychology/Neuropsychology, Center for Pediatric Neurology, Neurorehabilitation, and Epileptology Schön Klinik Vogtareuth Germany

10. Center for Pediatric Neurology, Neurorehabilitation, and Epileptology Schön Klinik Vogtareuth Germany

11. Department of Epileptology (Krankenhaus Mara), Medical School Bielefeld University Bielefeld Germany

Abstract

AbstractObjectivePerineuronal nets (PNN) are specialized extracellular matrix (ECM) components of the central nervous system, frequently accumulating at the surface of inhibitory GABAergic interneurons. While an altered distribution of PNN has been observed in neurological disorders including Alzheimer's disease, schizophrenia and epilepsy, their anatomical distribution also changes during physiological brain maturation and aging. Such an age‐dependent shift was experimentally associated also with hippocampal engram formation during brain maturation. Our aim was to histopathologically assess PNN in the hippocampus of adult and pediatric patients with temporal lobe epilepsy (TLE) compared to age‐matched post‐mortem control subjects and to compare PNN‐related changes with memory impairment observed in our patient cohort.MethodsSixty‐six formalin‐fixed and paraffin‐embedded tissue specimens of the human hippocampus were retrieved from the European Epilepsy Brain Bank. Twenty‐nine patients had histopathologically confirmed hippocampal sclerosis (HS), and eleven patients suffered from TLE without HS. PNN were immunohistochemically visualized using an antibody directed against aggrecan and manually counted from hippocampus subfields and the subiculum.ResultsPNN density increased with age in both human controls and TLE patients. However, their density was significantly higher in all HS patients compared to age‐matched controls. Intriguingly, TLE patients presented presurgically with better memory when their hippocampal PNN density was higher (p < 0.05).SignificanceOur results were compatible with age‐dependent ECM specialization in the human hippocampus and its precocious aging in the epileptic condition. These observations confirm recent experimental animal models and also support the notion that PNN play a role in memory formation in the human brain.Plain Language Summary“Perineuronal nets” (PNN) are a specialized compartment of the extracellular matrix (ECM), especially surrounding highly active neurons of the mammalian brain. There is evidence that PNN play a role in memory formation, brain maturation, and in some pathologies like Alzheimer's disease, schizophrenia or epilepsy. In this study, we investigated the role of PNN in patients suffering from drug‐resistant focal epilepsy compared to controls. We found that with increasing age, more neurons are surrounded by PNN. Similarly, all epilepsy patients but especially patients with better memory performance also had more PNN. This study raises further interest in studying ECM molecules in the human brain under physiological and pathophysiological conditions.

Funder

Deutsche Forschungsgemeinschaft

Publisher

Wiley

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