McLean Will J, Yin Xiaolei, Lu Lin, Lenz Danielle R, McLean Dalton, Langer Robert, Karp Jeffrey M, Edge Albert S B
Department of Otology and Laryngology, Harvard Medical School, Boston, MA 02115, USA; Eaton-Peabody Laboratory, Massachusetts Eye and Ear Infirmary, Boston, MA 02114, USA; Program in Speech and Hearing Bioscience and Technology, Harvard-MIT Division of Health Sciences and Technology, Cambridge, MA 02139, USA.
Koch Institute for Integrative Cancer Research at MIT, Cambridge, MA 02142, USA; Division of Engineering in Medicine, Department of Medicine, Brigham and Women's Hospital, Boston, MA 02115, USA; Department of Medicine, Harvard Medical School, Boston, MA 02115, USA; Harvard Stem Cell Institute, Cambridge, MA 02138, USA; Harvard-MIT Division of Health Sciences and Technology, Cambridge, MA 02139, USA.
Cell Rep. 2017 Feb 21;18(8):1917-1929. doi: 10.1016/j.celrep.2017.01.066.
Death of cochlear hair cells, which do not regenerate, is a cause of hearing loss in a high percentage of the population. Currently, no approach exists to obtain large numbers of cochlear hair cells. Here, using a small-molecule approach, we show significant expansion (>2,000-fold) of cochlear supporting cells expressing and maintaining Lgr5, an epithelial stem cell marker, in response to stimulation of Wnt signaling by a GSK3β inhibitor and transcriptional activation by a histone deacetylase inhibitor. The Lgr5-expressing cells differentiate into hair cells in high yield. From a single mouse cochlea, we obtained over 11,500 hair cells, compared to less than 200 in the absence of induction. The newly generated hair cells have bundles and molecular machinery for transduction, synapse formation, and specialized hair cell activity. Targeting supporting cells capable of proliferation and cochlear hair cell replacement could lead to the discovery of hearing loss treatments.
不能再生的耳蜗毛细胞死亡是导致很大一部分人听力丧失的原因。目前,尚无获得大量耳蜗毛细胞的方法。在此,我们采用小分子方法,发现通过GSK3β抑制剂刺激Wnt信号通路以及通过组蛋白脱乙酰酶抑制剂进行转录激活,可使表达并维持上皮干细胞标志物Lgr5的耳蜗支持细胞显著扩增(超过2000倍)。表达Lgr5的细胞可高效分化为毛细胞。从单只小鼠耳蜗中,我们获得了超过11500个毛细胞,而在未诱导的情况下少于200个。新生成的毛细胞具有用于转导、突触形成和特殊毛细胞活动的束状结构和分子机制。靶向能够增殖的支持细胞和进行耳蜗毛细胞替代可能会带来听力丧失治疗方法的发现。