{"id":118820,"date":"2014-03-24T19:44:28","date_gmt":"2014-03-24T23:44:28","guid":{"rendered":"http:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/uncategorized\/from-mouse-ears-to-humans-gene-therapy-to-address-progressive-hearing-loss.php"},"modified":"2014-03-24T19:44:28","modified_gmt":"2014-03-24T23:44:28","slug":"from-mouse-ears-to-humans-gene-therapy-to-address-progressive-hearing-loss","status":"publish","type":"post","link":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/gene-therapy\/from-mouse-ears-to-humans-gene-therapy-to-address-progressive-hearing-loss.php","title":{"rendered":"From mouse ears to human&#39;s? Gene therapy to address progressive hearing loss"},"content":{"rendered":"<p><p>  One in a thousand children in the United States is deaf, and one  in three adults will experience significant hearing loss after  the age of 65. Whether the result of genetic or environmental  factors, hearing loss costs billions of dollars in healthcare  expenses every year, making the search for a cure critical.<\/p>\n<p>    Now a team of researchers led by Karen B. Avraham of the    Department of Human Molecular Genetics and Biochemistry at Tel    Aviv University's Sackler Faculty of Medicine and Yehoash    Raphael of the Department of Otolaryngology-Head and Neck    Surgery at University of Michigan's Kresge Hearing Research    Institute have discovered that using DNA as a drug -- commonly    called gene therapy -- in laboratory mice may protect the inner    ear nerve cells of humans suffering from certain types of    progressive hearing loss.  <\/p>\n<p>    In the study, doctoral student Shaked Shivatzki created a mouse    population possessing the gene that produces the most prevalent    form of hearing loss in humans: the mutated connexin 26 gene.    Some 30 percent of American children born deaf have this form    of the gene. Because of its prevalence and the inexpensive    tests available to identify it, there is a great desire to find    a cure or therapy to treat it.  <\/p>\n<p>    \"Regenerating\" neurons  <\/p>\n<p>    Prof. Avraham's team set out to prove that gene therapy could    be used to preserve the inner ear nerve cells of the mice. Mice    with the mutated connexin 26 gene exhibit deterioration of the    nerve cells that send a sound signal to the brain. The    researchers found that a protein growth factor used to protect    and maintain neurons, otherwise known as brain-derived    neurotrophic factor (BDNF), could be used to block this    degeneration. They then engineered a virus that could be    tolerated by the body without causing disease, and inserted the    growth factor into the virus. Finally, they surgically injected    the virus into the ears of the mice. This factor was able to    \"rescue\" the neurons in the inner ear by blocking their    degeneration.  <\/p>\n<p>    \"A wide spectrum of people are affected by hearing loss, and    the way each person deals with it is highly variable,\" said    Prof. Avraham. \"That said, there is an almost unanimous    interest in finding the genes responsible for hearing loss. We    tried to figure out why the mouse was losing cells that enable    it to hear. Why did it lose its hearing? The collaborative work    allowed us to provide gene therapy to reverse the loss of nerve    cells in the ears of these deaf mice.\"  <\/p>\n<p>    Although this approach is short of improving hearing in these    mice, it has important implications for the enhancement of    sound perception with a cochlear implant, used by many people    whose connexin 26 mutation has led to impaired hearing.  <\/p>\n<p>    Embryonic hearing?  <\/p>\n<p>    Inner ear nerve cells facilitate the optimal functioning of    cochlear implants. Prof. Avraham's research suggests a possible    new strategy for improving implant function, particularly in    people whose hearing loss gets progressively worse with time,    such as those with profound hearing loss as well as those with    the connexin gene mutation. Combining gene therapy with the    implant could help to protect vital nerve cells, thus    preserving and improving the performance of the implant.  <\/p>\n<p>    More research remains. \"Safety is the main question. And what    about timing? Although over 80 percent of human and mouse genes    are similar, which makes mice the perfect lab model for human    hearing, there's still a big difference. Humans start hearing    as embryos, but mice don't start to hear until two weeks after    birth. So we wondered, do we need to start the corrective    process in utero, in infants, or later in life?\" said Prof.    Avraham.  <\/p>\n<p><!-- Auto Generated --><\/p>\n<p>The rest is here: <\/p>\n<p><a target=\"_blank\" href=\"http:\/\/www.sciencedaily.com\/releases\/2014\/03\/140324111918.htm\/RS=^ADA2as6c3Vl7mORSDh06rN7ho9l5Fk-\" title=\"From mouse ears to human&#39;s? Gene therapy to address progressive hearing loss\">From mouse ears to human&#39;s? Gene therapy to address progressive hearing loss<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p> One in a thousand children in the United States is deaf, and one in three adults will experience significant hearing loss after the age of 65. Whether the result of genetic or environmental factors, hearing loss costs billions of dollars in healthcare expenses every year, making the search for a cure critical <a href=\"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/gene-therapy\/from-mouse-ears-to-humans-gene-therapy-to-address-progressive-hearing-loss.php\">Continue reading <span class=\"meta-nav\">&rarr;<\/span><\/a><\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"limit_modified_date":"","last_modified_date":"","_lmt_disableupdate":"","_lmt_disable":"","footnotes":""},"categories":[24],"tags":[],"class_list":["post-118820","post","type-post","status-publish","format-standard","hentry","category-gene-therapy"],"modified_by":null,"_links":{"self":[{"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/posts\/118820"}],"collection":[{"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/comments?post=118820"}],"version-history":[{"count":0,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/posts\/118820\/revisions"}],"wp:attachment":[{"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/media?parent=118820"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/categories?post=118820"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/tags?post=118820"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}