Matrix metalloproteinase-9 regulates TNF-α and FasL expression in neuronal, glial cells and its absence extends life in a transgenic mouse model of amyotrophic lateral sclerosis

التفاصيل البيبلوغرافية
العنوان: Matrix metalloproteinase-9 regulates TNF-α and FasL expression in neuronal, glial cells and its absence extends life in a transgenic mouse model of amyotrophic lateral sclerosis
المؤلفون: M. Flint Beal, Noel Y. Calingasan, Junyu Chen, Stefan Lorenzl, Shahin Rafii, Mahmoud Kiaei, Elizabeth Wille, Beate Heissig, Khatuna Kipiani
المصدر: Experimental Neurology. 205:74-81
بيانات النشر: Elsevier BV, 2007.
سنة النشر: 2007
مصطلحات موضوعية: Male, Genetically modified mouse, Programmed cell death, Fas Ligand Protein, Longevity, SOD1, Central nervous system, Glycine, Mice, Inbred Strains, Mice, Transgenic, ADAM17 Protein, Matrix metalloproteinase, Nervous System, Pathogenesis, Mice, Superoxide Dismutase-1, Developmental Neuroscience, Animals, Humans, Medicine, Amyotrophic lateral sclerosis, Neurons, Alanine, Staining and Labeling, Superoxide Dismutase, Tumor Necrosis Factor-alpha, business.industry, Amyotrophic Lateral Sclerosis, medicine.disease, ADAM Proteins, medicine.anatomical_structure, Matrix Metalloproteinase 9, Neurology, Mutation, Immunologic Techniques, Cancer research, Neuroglia, business, Neuroscience
الوصف: Whether increased levels of matrix metalloproteinases (MMPs) correspond to a role in the pathogenesis of amyotrophic lateral sclerosis (ALS) needs to be determined and it is actively being pursued. Here we present evidence suggesting that MMP-9 contributes to the motor neuron cell death in ALS. We examined the role of MMP-9 in a mouse model of familial ALS and found that lack of MMP-9 increased survival (31%) in G93A SOD1 mice. Also, MMP-9 deficiency in G93A mice significantly attenuated neuronal loss, and reduced neuronal TNF-alpha and FasL immunoreactivities in the lumbar spinal cord. These findings suggest that MMP-9 is an important player in the pathogenesis of ALS. Our data suggest that the mechanism for MMP-9 neurotoxicity in ALS may be by upregulating neuronal TNF-alpha and FasL expression and activation. This study provides new mechanism and suggests that MMP inhibitors may offer a new therapeutic strategy for ALS.
تدمد: 0014-4886
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::74abf382a118e5da00cf183d481ca5eaTest
https://doi.org/10.1016/j.expneurol.2007.01.036Test
حقوق: CLOSED
رقم الانضمام: edsair.doi.dedup.....74abf382a118e5da00cf183d481ca5ea
قاعدة البيانات: OpenAIRE