{"id":2397,"date":"2012-10-19T00:00:00","date_gmt":"2012-10-19T07:00:00","guid":{"rendered":"https:\/\/vermont.salk.edu\/news-release\/salk-scientists-pinpoint-key-player-in-parkinsons-disease-neuron-loss\/"},"modified":"2012-10-19T00:00:00","modified_gmt":"2012-10-19T07:00:00","slug":"salk-scientists-pinpoint-key-player-in-parkinsons-disease-neuron-loss","status":"publish","type":"disclosure","link":"https:\/\/www.salk.edu\/es\/news-release\/salk-scientists-pinpoint-key-player-in-parkinsons-disease-neuron-loss\/","title":{"rendered":"Salk scientists pinpoint key player in Parkinson’s disease neuron loss"},"content":{"rendered":"

LA JOLLA, CA\u2014By reprogramming skin cells from Parkinson’s disease patients with a known genetic mutation, researchers at the Salk Institute for Biological Studies have identified damage to neural stem cells as a powerful player in the disease. The findings, reported online October 17, 2013 in Naturaleza<\/em>, may lead to new ways to diagnose and treat the disease.\n <\/p>\n

\nThe scientists found that a common mutation to a gene that produce the enzyme LRRK2, which is responsible for both familial and sporadic cases of Parkinson’s disease<\/a>, deforms the membrane surrounding the nucleus of a neural stem cell. Damaging the nuclear architecture leads to destruction of these powerful cells, as well as their decreased ability to spawn functional neurons, such as the ones that respond to dopamine.\n <\/p>\n

\"genetic<\/p>\n

\nThe Salk researchers found that a common genetic mutation involved in Parkinson’s disease deforms the membranes (green) surrounding the nuclei (blue) of neural stem cells. The discovery may lead to new ways to diagnose and treat the disease.\n<\/p>\n

Imagen: Cortes\u00eda del Instituto Salk de Estudios Biol\u00f3gicos<\/p>\n<\/div>\n

\nThe researchers checked their laboratory findings with brain samples from Parkinson’s disease patients and found the same nuclear envelope impairment.\n <\/p>\n

\n“This discovery helps explain how Parkinson’s disease, which has been traditionally associated with loss of neurons that produce dopamine and subsequent motor impairment, could lead to locomotor dysfunction and other common non-motor manifestations, such as depression and anxiety,” says Juan Carlos Izpisua Belmonte<\/a>, profesor del Instituto Salk Laboratorio de Expresi\u00f3n G\u00e9nica<\/a>, who led the research team. “Similarly, current clinical trials explore the possibility of neural stem cell transplantation to compensate for dopamine deficits. Our work provides the platform for similar trials by using patient-specific corrected cells. It identifies degeneration of the nucleus as a previously unknown player in Parkinson’s.”\n <\/p>\n

\nAlthough the researchers say that they don’t yet know whether these nuclear aberrations cause Parkinson’s disease or are a consequence of it, they say the discovery could offer clues about potential new therapeutic approaches.\n <\/p>\n

\nFor example, they were able to use targeted gene-editing technologies to correct the mutation in patient’s nuclear stem cells. This genetic correction repaired the disorganization of the nuclear envelope, and improved overall survival and functioning of the neural stem cells.\n <\/p>\n

\nThey were also able to chemically inhibit damage to the nucleus, producing the same results seen with genetic correction. “This opens the door for drug treatment of Parkinson’s disease patients who have this genetic mutation,” says Belmonte.\n <\/p>\n

\nThe new finding may also help clinicians better diagnose this form of Parkinson’s disease, he adds. “Due to the striking appearance in patient samples, nuclear deformation parameters could add to the pool of diagnostic features for Parkinson’s disease,” he says.\n <\/p>\n

\nThe research team, which included scientists from China, Spain, and the Universidad de California, San Diego<\/a>, and Scripps Research Institute<\/a>, made their discoveries using human induced pluripotent stem cells (iPSCs). These cells are similar to natural stem cells, such as embryonic stem cells, except that they are derived from adult cells. While generation of these cells has raised expectations within the biomedical community due to their transplant potential\u2014the idea that they could morph into tissue that needs to be replaced\u2014they also provide exceptional research opportunities, says Belmonte.\n <\/p>\n

\n“We can model disease using these cells in ways that are not possible using traditional research methods, such as established cell lines, primary cultures and animal models,” he says.\n <\/p>\n

\"Research<\/p>\n

\nFrom left: Research associate Guanghui Liu, Professor Juan Carols Izpisua Belmonte, and Keiichiro Suzuki, research associate.\n<\/p>\n

Imagen: Cortes\u00eda del Instituto Salk de Estudios Biol\u00f3gicos<\/p>\n<\/div>\n

\nIn this study, the researchers used skin fibroblast cells taken from Parkinson’s disease patients who have the LRRK2 mutation, and they reprogrammed them to iPSC stem cells and developed them into neural stem cells.\n <\/p>\n

\nThen, by using an approach to model what happens when these neural stem cells aged, they found that older Parkinson disease neural stem cells increasingly displayed deformed nuclear envelopes and nuclear architecture. “This means that, over time, the LRRK2 mutation affects the nucleus of neural stem cells, hampering both their survival and their ability to produce neurons,” Belmonte says.\n <\/p>\n

\n“It is the first time to our knowledge that human neural stem cells have been shown to be affected during Parkinson’s pathology due to aberrant LRRK2,” he says. “Before development of these reprogramming technologies, studies on human neural stem cells were elusive because they needed to be isolated directly from the brain.”\n <\/p>\n

\nBelmonte speculates that the dysfunctional neural stem cell pools that result from the LRRK2 mutation might contribute to other health issues associated with this form of Parkinson’s disease, such as depression, anxiety and the inability to detect smells.\n <\/p>\n

\nFinally, the study shows that these reprogramming technologies are very useful for modeling disease as well as dysfunction caused by aging, Belmonte says.\n <\/p>\n

\nOther researchers on the study were: Guang-Hui Liu, Jing Qu, Keiichiro Suzuki, Emmanuel Nivet, Mo Li, Nuria Montserrat, Fei Yi. Xiuling Xu, Sergio Ruiz, Weiqi Zhang, Bing Ren, Ulrich Wagner, Audrey Kim, Ying Li, April Goebl, Jessica Kim, Rupa Devi Soligalla, Ilir Dubova, James Thompson, John Yates III, Concepcion Rodriguez Esteban, and Ignacio Sancho-Martinez.\n <\/p>\n

\nThe research was supported by Glenn Foundation for Medical Research<\/a>, G. Harold and Leila Y. Mathers Charitable Foundation<\/a>, Sanofi<\/a>, The California Institute of Regenerative Medicine<\/a>, Ellison Medical Foundation<\/a> y Fundaci\u00f3n Ben\u00e9fica Leona M. y Harry B. Helmsley<\/a>, MINECO and Fundacion Cellex.\n<\/p>\n


\nAcerca del Instituto Salk de Estudios Biol\u00f3gicos:<\/strong>
\nEl Instituto Salk de Estudios Biol\u00f3gicos es una de las instituciones de investigaci\u00f3n b\u00e1sica m\u00e1s destacadas del mundo, donde un cuerpo docente de prestigio internacional investiga cuestiones fundamentales de las ciencias de la vida en un entorno \u00fanico, colaborativo y creativo. Centrados tanto en el descubrimiento como en la formaci\u00f3n de las futuras generaciones de investigadores, los cient\u00edficos del Salk realizan contribuciones revolucionarias a nuestra comprensi\u00f3n del c\u00e1ncer, el envejecimiento, el Alzheimer, la diabetes y las enfermedades infecciosas mediante el estudio de la neurociencia, la gen\u00e9tica, la biolog\u00eda celular y vegetal, y otras disciplinas relacionadas.\n<\/p>\n

\nLos logros del cuerpo docente han sido reconocidos con numerosos galardones, entre los que se incluyen premios Nobel y la pertenencia a la Academia Nacional de Ciencias. Fundado en 1960 por el Dr. Jonas Salk, pionero en la vacuna contra la poliomielitis, el Instituto es una organizaci\u00f3n independiente sin fines de lucro y un hito arquitect\u00f3nico.<\/p>","protected":false},"featured_media":0,"template":"","faculty":[],"disease-research":[161,146,124,162],"class_list":["post-2397","disclosure","type-disclosure","status-publish","hentry","disease-research-depression","disease-research-aging-and-regenerative-medicine","disease-research-neuroscience-and-neurological-disorders","disease-research-parkinsons-disease"],"acf":[],"yoast_head":"\nSalk scientists pinpoint key player in Parkinson's disease neuron loss - 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\/es\/news-release\/salk-scientists-pinpoint-key-player-in-parkinsons-disease-neuron-loss\/\" \/>\n<meta property=\"og:locale\" content=\"es_MX\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Salk scientists pinpoint key player in Parkinson's disease neuron loss - Salk Institute for Biological Studies\" \/>\n<meta property=\"og:description\" content=\"LA JOLLA, CA\u2014By reprogramming skin cells from Parkinson’s disease patients with a known genetic mutation, researchers at the Salk Institute for Biological Studies have identified damage to neural stem cells as a powerful player in the disease. 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