Cell Death and Learning Impairment in Mice Caused by in Vitro Modified Pro-NGF Can Be Related to Its Increased Oxidative Modifications in Alzheimer Disease

التفاصيل البيبلوغرافية
العنوان: Cell Death and Learning Impairment in Mice Caused by in Vitro Modified Pro-NGF Can Be Related to Its Increased Oxidative Modifications in Alzheimer Disease
المؤلفون: Gerard Piñol-Ripoll, Petar Podlesniy, Manuel Portero-Otin, Anton Kichev, Carme Espinet, Reinald Pamplona, Ekaterina V. Ilieva, Isidro Ferrer
بيانات النشر: American Society for Investigative Pathology, 2009.
سنة النشر: 2009
مصطلحات موضوعية: Adult, Glycation End Products, Advanced, Male, Programmed cell death, Blotting, Western, Hippocampus, Apoptosis, Pharmacology, Biology, In Vitro Techniques, medicine.disease_cause, PC12 Cells, Receptor, Nerve Growth Factor, Pathology and Forensic Medicine, Mice, Glycation, Alzheimer Disease, Nerve Growth Factor, medicine, Low-affinity nerve growth factor receptor, Animals, Humans, Immunoprecipitation, Protein Precursors, Aged, Aged, 80 and over, Learning Disabilities, Human brain, Middle Aged, medicine.disease, Rats, Oxidative Stress, medicine.anatomical_structure, Nerve growth factor, nervous system, Immunology, Female, Alzheimer's disease, Oxidative stress, Regular Articles
الوصف: Pro-nerve growth factor (pro-NGF) is expressed at increased levels in Alzheimer's disease (AD)-affected brains and is able to induce cell death in cultures; however, the reasons for these phenomena remain elusive. Here we show that pro-NGF in human AD-affected hippocampus and entorhinal cortex is modified by advanced glycation and lipoxidation end-products in a stage-dependent manner. These modifications block pro-NGF processing to mature NGF, thus making the proneurotrophin especially effective in inducing apoptosis of PC12 cells in culture through the p75 neurotrophin receptor. The processing of advanced glycation and lipoxidation end-products in vitro modified recombinant human pro-NGF is severely impaired, as evidenced by Western blot and by examining its physiological functionality in cell cultures. We also report that modified recombinant human pro-NGF, as well as pro-NGF isolated from human brain affected by AD, cause impairment of learning tasks when administered intracerebroventricularly in mice, which correlates with AD-associated learning impairment. Taken together, the data we present here offer a novel pathway of ethiopathogenesis in AD caused by advanced glycation and lipoxidation end-products modification of pro-NGF.
اللغة: English
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bc1f243e2e850deabeb2791373fd4f42Test
https://europepmc.org/articles/PMC2789641Test/
حقوق: OPEN
رقم الانضمام: edsair.doi.dedup.....bc1f243e2e850deabeb2791373fd4f42
قاعدة البيانات: OpenAIRE