{"id":14724,"date":"2017-09-14T10:31:25","date_gmt":"2017-09-14T17:31:25","guid":{"rendered":"https:\/\/vermont.salk.edu\/?post_type=disclosure&#038;p=14724"},"modified":"2024-01-30T15:29:35","modified_gmt":"2024-01-30T23:29:35","slug":"partnership-healthy-brain","status":"publish","type":"disclosure","link":"https:\/\/www.salk.edu\/de\/news-release\/partnership-healthy-brain\/","title":{"rendered":"Partnerschaft f\u00fcr ein gesundes Gehirn"},"content":{"rendered":"<p>LA JOLLA\u2014Salk Institute scientists have discovered that an interaction between two key proteins helps regulate and maintain the cells that produce neurons. The work, published in <a href=\"http:\/\/www.cell.com\/cell-stem-cell\/fulltext\/S1934-5909(17)30330-2\" target=\"_blank\" rel=\"noopener\"><em>Cell Stem Cell<\/em><\/a> on September 14, 2017, offers insight into why an imbalance between these precursor cells and neurons might contribute to mental illness or age-related brain disease.<\/p>\n<p>&#8220;Increasingly, we are learning that diseases like schizophrenia, depression and Alzheimer&#8217;s all have a cellular basis,&#8221; says <a href=\"https:\/\/www.salk.edu\/de\/scientist\/rusty-gage\/\">Rusty Gage<\/a>, a professor in Salk\u2019s Laboratory of Genetics and senior author of the new work. &#8220;So we are eager to understand how specific brain cells develop, what keeps them healthy and why advancing age or other factors can lead to disease.&#8221;<\/p>\n<figure id=\"attachment_14728\"  class=\"wp-caption alignright\"><img loading=\"lazy\" decoding=\"async\" width=\"331\" height=\"311\" class=\"img-responsive wp-image-14728 size-full\" src=\"https:\/\/www.salk.edu\/wp-content\/uploads\/2017\/09\/HCN-Nup153-Sox2-Press.jpg\" alt=\"A fluorescent microscopy image shows Nup153 (red) in pore complexes encircling and associating with Sox2 (green) in a precursor cell nucleus. \" srcset=\"https:\/\/www.salk.edu\/wp-content\/uploads\/2017\/09\/HCN-Nup153-Sox2-Press.jpg 331w, https:\/\/www.salk.edu\/wp-content\/uploads\/2017\/09\/HCN-Nup153-Sox2-Press-300x282.jpg 300w, https:\/\/www.salk.edu\/wp-content\/uploads\/2017\/09\/HCN-Nup153-Sox2-Press-147x138.jpg 147w\" sizes=\"auto, (max-width: 331px) 100vw, 331px\" \/><figcaption class=\"wp-caption-text\">A fluorescent microscopy image shows Nup153 (red) in pore complexes encircling and associating with Sox2 (green) in a precursor cell nucleus. <\/p>\n<p> <a href=\"https:\/\/www.salk.edu\/wp-content\/uploads\/2017\/09\/HCN-Nup153-Sox2-Press.jpg\">Klicken Sie hier<\/a> for a high-resolution image <\/p>\n<p> Credit: Salk Institute\/Waitt Center<\/figcaption><\/figure>\n<p>In 1998, Gage led a research team which discovered that adult brains do produce new neurons, contrary to decades of dogma saying we are born with all the neurons we will ever have. Since then, he has been elucidating various aspects of this neurogenesis as well as what goes wrong in various neurological disorders. (In 2015, for example, his lab <a href=\"https:\/\/www.salk.edu\/de\/news-release\/bipolar-patients-brain-cells-predict-response-lithium\/\">identified a cellular basis for bipolar disorder<\/a>.)<\/p>\n<p>The new work sought to understand how neural precursor cells maintain their own cellular identity as they divide and create neurons or astrocytes. Gage&#8217;s team already knew that the cell nucleus\u2014the ball-shaped membrane containing the genome\u2014looks very different in the three cell types, with different genes active in each. Another Salk professor and a coauthor on the paper, Martin Hetzer, previously found that <a href=\"https:\/\/www.salk.edu\/de\/news-release\/heart-disease-leukemia-linked-dysfunction-nucleus\/\">proteins in the nuclear membrane influence gene expression<\/a> in different kinds of cancer cells. The Gage team sought the expertise of the Hetzer lab to explore whether something similar was at play in brain cells.<\/p>\n<p>\u201cResearch from my lab has found that the nuclear membrane is a dynamic structure that plays a key role in developmental gene regulation,&#8221; says Hetzer, Salk&#8217;s chief science officer and holder of the Jesse and Caryl Philips Foundation Chair. &#8220;So we were very interested to see what the Gage lab, working with entirely different cell types, would uncover.\u201d<\/p>\n<p>Gage&#8217;s team conducted screens in cells from mice and rats to see which genes were being transcribed into proteins in precursor cells, immature neurons and astrocytes. In the precursors, they discovered high numbers of a protein called Nup153, which is part of a multiprotein complex that forms a gatekeeping pore in the nuclear membrane, controlling what goes in or out. Immature neurons had an intermediate level of Nup153, and astrocytes had the lowest level. Because all three cell types have roughly the same number of nuclear pores, the team concluded that Nup153 levels influence cell type and that a high level is necessary to maintain cells&#8217; precursor status. This was supported by the fact that disrupting Nup153&#8217;s function in the precursor cells triggered differentiation.<\/p>\n<figure id=\"attachment_14731\"  class=\"wp-caption alignleft\"><img loading=\"lazy\" decoding=\"async\" width=\"458\" height=\"305\" class=\"img-responsive wp-image-14731 size-col-md-5\" src=\"https:\/\/www.salk.edu\/wp-content\/uploads\/2017\/09\/Tomohisa-Toda-and-Rusty-Gage_e_MG_9993-458x305.jpg\" alt=\"Tomohisa Toda and Rusty Gage\" srcset=\"https:\/\/www.salk.edu\/wp-content\/uploads\/2017\/09\/Tomohisa-Toda-and-Rusty-Gage_e_MG_9993-458x305.jpg 458w, https:\/\/www.salk.edu\/wp-content\/uploads\/2017\/09\/Tomohisa-Toda-and-Rusty-Gage_e_MG_9993-300x200.jpg 300w, https:\/\/www.salk.edu\/wp-content\/uploads\/2017\/09\/Tomohisa-Toda-and-Rusty-Gage_e_MG_9993-768x512.jpg 768w, https:\/\/www.salk.edu\/wp-content\/uploads\/2017\/09\/Tomohisa-Toda-and-Rusty-Gage_e_MG_9993-1024x682.jpg 1024w, https:\/\/www.salk.edu\/wp-content\/uploads\/2017\/09\/Tomohisa-Toda-and-Rusty-Gage_e_MG_9993-147x98.jpg 147w, https:\/\/www.salk.edu\/wp-content\/uploads\/2017\/09\/Tomohisa-Toda-and-Rusty-Gage_e_MG_9993-585x390.jpg 585w, https:\/\/www.salk.edu\/wp-content\/uploads\/2017\/09\/Tomohisa-Toda-and-Rusty-Gage_e_MG_9993-553x369.jpg 553w, https:\/\/www.salk.edu\/wp-content\/uploads\/2017\/09\/Tomohisa-Toda-and-Rusty-Gage_e_MG_9993-750x500.jpg 750w, https:\/\/www.salk.edu\/wp-content\/uploads\/2017\/09\/Tomohisa-Toda-and-Rusty-Gage_e_MG_9993-945x630.jpg 945w, https:\/\/www.salk.edu\/wp-content\/uploads\/2017\/09\/Tomohisa-Toda-and-Rusty-Gage_e_MG_9993.jpg 2000w\" sizes=\"auto, (max-width: 458px) 100vw, 458px\" \/><figcaption class=\"wp-caption-text\">Tomohisa Toda and Rusty Gage<\/p>\n<p> <a href=\"https:\/\/www.salk.edu\/wp-content\/uploads\/2017\/09\/Tomohisa-Toda-and-Rusty-Gage_e_MG_9993.jpg\">Klicken Sie hier<\/a> for a high-resolution image<\/p>\n<p> Kredit: Salk Institut<\/figcaption><\/figure>\n<p>Interestingly, Nup153 levels are also known to be high in cells with elevated levels of a mobile protein called Sox2, a transcription factor that floats around the nucleus and binds to genes and turns them on or off. By fluorescently tagging Nup153 and Sox2 in the different cells types, they observed that Nup153 was interacting with Sox2.<\/p>\n<p>&#8220;The fact that we were able to connect transcription factors, which are mobile switches, to the pore complex, which is a very stable structure, offers a clue as to how cells maintain their identity through regulated gene expression,&#8221; says Tomohisa Toda, a Salk research associate and first author of the paper.<\/p>\n<p>Next, the team wants to explore how the interaction of the pore complex with other transcription factors affects neuronal function, which could yield insights into the underlying causes of certain neurological disorders.<\/p>\n<p>Other authors included: Jonathan Y. Hsu, Sara B. Linker, Lauren Hu, Simon T. Schafer, Jerome Mertens, Felipe V. Jacinto and Martin Hetzer.<\/p>\n<p>The work was funded by: the Japan Society for the Promotion of Science, the Kanae Foundation for the Promotion of Medical Science, the Paul G. Allen Family Foundation, The JPB Foundation, The Dolby Foundation, The Leona M. and Harry B. Helmsley Charitable Trust, the National Institutes of Health\u2013National Cancer Institute, the Chapman Foundation, the Waitt Foundation, and the National Institute of Neurological Disorders and Stroke Neuroscience Center.<\/p>","protected":false},"featured_media":14726,"template":"","faculty":[86,76],"disease-research":[171,124,167],"class_list":["post-14724","disclosure","type-disclosure","status-publish","has-post-thumbnail","hentry","faculty-martin-hetzer","faculty-rusty-gage","disease-research-bipolar-disorder","disease-research-neuroscience-and-neurological-disorders","disease-research-schizophrenia"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.3 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Partnership for a healthy brain - Salk Institute for Biological Studies<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/www.salk.edu\/de\/news-release\/partnership-healthy-brain\/\" \/>\n<meta property=\"og:locale\" content=\"de_DE\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Partnership for a healthy brain - Salk Institute for Biological Studies\" \/>\n<meta property=\"og:description\" content=\"LA JOLLA\u2014Salk Institute scientists have discovered that an interaction between two key proteins helps regulate and maintain the cells that produce neurons. 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