18
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Differential Co-Expression between α-Synuclein and IFN-γ Signaling Genes across Development and in Parkinson’s Disease

      research-article
      1 , 2 , *
      PLoS ONE
      Public Library of Science

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Expression patterns of the alpha-synuclein gene (SNCA) were studied across anatomy, development, and disease to better characterize its role in the brain. In this postmortem study, negative spatial co-expression between SNCA and 73 interferon-γ (IFN-γ) signaling genes was observed across many brain regions. Recent animal studies have demonstrated that IFN-γ induces loss of dopamine neurons and nigrostriatal degeneration. This opposing pattern between SNCA and IFN-γ signaling genes increases with age (rho = −0.78). In contrast, a meta-analysis of four microarray experiments representing 126 substantia nigra samples reveals a switch to positive co-expression in Parkinson’s disease (p<0.005). Use of genome-wide testing demonstrates this relationship is specific to SNCA (p<0.002). This change in co-expression suggests an immunomodulatory role of SNCA that may provide insight into neurodegeneration. Genes showing similar co-expression patterns have been previously linked to Alzheimer’s (ANK1) and Parkinson’s disease (UBE2E2, PCMT1, HPRT1 and RIT2).

          Related collections

          Most cited references29

          • Record: found
          • Abstract: found
          • Article: not found

          Alpha-synuclein acts in the nucleus to inhibit histone acetylation and promote neurotoxicity.

          Alpha-synuclein is a neuronal protein implicated genetically in Parkinson's disease. alpha-synuclein localizes to the nucleus and presynaptic nerve terminals. Here we show that alpha-synuclein mediates neurotoxicity in the nucleus. Targeting of alpha-synuclein to the nucleus promotes toxicity, whereas cytoplasmic sequestration is protective in both cell culture and transgenic Drosophila. Toxicity of alpha-synuclein can be rescued by administration of histone deacetylase inhibitors in both cell culture and transgenic flies. Alpha-synuclein binds directly to histones, reduces the level of acetylated histone H3 in cultured cells and inhibits acetylation in histone acetyltransferase assays. Alpha-synuclein mutations that cause familial Parkinson's disease, A30P and A53T, exhibit increased nuclear targeting in cell culture. These findings implicate nuclear alpha-synuclein in promoting nigrostriatal degeneration in Parkinson's disease and encourage exploration of histone deacetylase inhibitors as potential therapies for the disorder.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            LRRK2 is involved in the IFN-gamma response and host response to pathogens.

            LRRK2 was previously identified as a defective gene in Parkinson's disease, and it is also located in a risk region for Crohn's disease. In this study, we aim to determine whether LRRK2 could be involved in immune responses. We show that LRRK2 expression is enriched in human immune cells. LRRK2 is an IFN-γ target gene, and its expression increased in intestinal tissues upon Crohn's disease inflammation. In inflamed intestinal tissues, LRRK2 is detected in the lamina propria macrophages, B-lymphocytes, and CD103-positive dendritic cells. Furthermore, LRRK2 expression enhances NF-κB-dependent transcription, suggesting its role in immune response signaling. Endogenous LRRK2 rapidly translocates near bacterial membranes, and knockdown of LRRK2 interferes with reactive oxygen species production during phagocytosis and bacterial killing. These observations indicate that LRRK2 is an IFN-γ target gene, and it might be involved in signaling pathways relevant to Crohn's disease pathogenesis.
              Bookmark
              • Record: found
              • Abstract: not found
              • Article: not found

              Guilt-by-association goes global.

              S. Oliver (2000)
                Bookmark

                Author and article information

                Contributors
                Role: Editor
                Journal
                PLoS One
                PLoS ONE
                plos
                plosone
                PLoS ONE
                Public Library of Science (San Francisco, USA )
                1932-6203
                2014
                10 December 2014
                : 9
                : 12
                : e115029
                Affiliations
                [1 ]The Leslie and Susan Gonda Multidisciplinary Brain Research Center, Bar Ilan University, Ramat Gan, Israel
                [2 ]Rotman Research Institute, Baycrest Hospital, Toronto, Ontario, Canada
                Hertie Institute for Clinical Brain Research and German Center for Neurodegenerative Diseases, Germany
                Author notes

                Competing Interests: The authors have declared that no competing interests exist.

                Conceived and designed the experiments: NL LF. Performed the experiments: NL LF. Analyzed the data: NL LF. Contributed reagents/materials/analysis tools: NL LF. Contributed to the writing of the manuscript: NL LF.

                Article
                PONE-D-14-46807
                10.1371/journal.pone.0115029
                4262449
                25493648
                43d59db2-9597-4d46-b2c7-a104ee93654a
                Copyright @ 2014

                This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

                History
                : 17 October 2014
                : 17 November 2014
                Page count
                Pages: 13
                Funding
                A National Sciences and Engineering Research Council of Canada Postdoctoral fellowship award supports LF. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
                Categories
                Research Article
                Biology and Life Sciences
                Veterinary Science
                Veterinary Anatomy
                Medicine and Health Sciences
                Anatomy
                Brain
                Neurology
                Neurodegenerative Diseases
                Movement Disorders
                Parkinson Disease
                Brain Diseases
                Physical Sciences
                Chemistry
                Organic Chemistry
                Organic Compounds
                Amines
                Catecholamines
                Dopamine
                Research and Analysis Methods
                Animal Studies
                Bioassays and Physiological Analysis
                Microarrays
                Mathematical and Statistical Techniques
                Statistical Methods
                Meta-Analysis
                Custom metadata
                The authors confirm that all data underlying the findings are fully available without restriction. All relevant data are within the paper, its Supporting Information files and public databases. Expression atlases from the Allen Institute Brain Atlas are available at http://www.brain-map.org. Microarray data from gene expression studies were obtained from the Gene Expression Omnibus database (accession numbers: GSE6613, GSE7621, GSE8397, GSE20295 and GSE20159).

                Uncategorized
                Uncategorized

                Comments

                Comment on this article