Cell-Based Therapy Restores Olfactory Function in an Inducible Model of Hyposmia

被引:39
作者
Kurtenbach, Sarah [1 ,2 ]
Goss, Garrett M. [1 ,2 ]
Goncalves, Stefania [2 ]
Choi, Rhea [3 ,4 ]
Hare, Joshua M. [1 ,5 ]
Chaudhari, Nirupa [2 ,4 ,6 ]
Goldstein, Bradley J. [1 ,2 ,4 ]
机构
[1] Univ Miami, Miller Sch Med, Interdisciplinary Stem Cell Inst, 1501 NW 10th Ave,Biomed Res Bldg,Room 809, Miami, FL 33136 USA
[2] Univ Miami, Miller Sch Med, Dept Otolaryngol, Miami, FL 33136 USA
[3] Univ Miami, Miller Sch Med, Med Scientist Training Program, Miami, FL 33136 USA
[4] Univ Miami, Miller Sch Med, Grad Program Neurosci, Miami, FL 33136 USA
[5] Univ Miami, Miller Sch Med, Div Cardiol, Dept Med, Miami, FL 33136 USA
[6] Univ Miami, Miller Sch Med, Dept Physiol & Biophys, Miami, FL 33136 USA
来源
STEM CELL REPORTS | 2019年 / 12卷 / 06期
基金
美国国家卫生研究院;
关键词
GLOBOSE BASAL-CELLS; TYROSINE-HYDROXYLASE EXPRESSION; STEM-CELLS; PROGENITOR CELLS; MULTIPOTENT PROGENITORS; GENE-EXPRESSION; SELF-RENEWAL; MOUSE; EPITHELIUM; NEURONS;
D O I
10.1016/j.stemcr.2019.05.001
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Stem cell-based therapies have been proposed as a strategy to replace damaged tissues, especially in the nervous system. A primary sensory modality, olfaction, is impaired in 12% of the US population, but lacks treatment options. We report here the development of a novel mouse model of inducible hyposmia and demonstrate that purified tissue-specific stem cells delivered intranasally engraft to produce olfactory neurons, achieving recovery of function. Adult mice were rendered hyposmic by conditional deletion of the ciliopathy-related IFT88 gene in the olfactory sensory neuron lineage and following experimentally induced olfactory injury, received either vehicle or stem cell infusion intranasally. Engraftment-derived olfactory neurons were identified histologically, and functional improvements were measured via electrophysiology and behavioral assay. We further explored mechanisms in culture that promote expansion of engraftment-competent adult olfactory basal progenitor cells. These findings provide a basis for translational research on propagating adult tissue-specific sensory progenitor cells and testing their therapeutic potential.
引用
收藏
页码:1354 / 1365
页数:12
相关论文
共 65 条
[1]  
BAKER H, 1983, J NEUROSCI, V3, P69
[2]   UNILATERAL, NEONATAL OLFACTORY DEPRIVATION ALTERS TYROSINE-HYDROXYLASE EXPRESSION BUT NOT AROMATIC AMINO-ACID DECARBOXYLASE OR GABA IMMUNOREACTIVITY [J].
BAKER, H .
NEUROSCIENCE, 1990, 36 (03) :761-771
[3]   Olfactory ensheathing cells (OECs) and the treatment of CNS injury: advantages and possible caveats [J].
Barnett, SC ;
Riddell, JS .
JOURNAL OF ANATOMY, 2004, 204 (01) :57-67
[4]   Differential effects of olfactory toxicants on olfactory regeneration [J].
Bergman, U ;
Östergren, A ;
Gustafson, AL ;
Brittebo, EB .
ARCHIVES OF TOXICOLOGY, 2002, 76 (02) :104-112
[5]   Regenerative Medicine for the Special Senses: Restoring the Inputs [J].
Bermingham-McDonogh, Olivia ;
Corwin, Jeffrey T. ;
Hauswirth, William W. ;
Heller, Stefan ;
Reed, Randall ;
Reh, Thomas A. .
JOURNAL OF NEUROSCIENCE, 2012, 32 (41) :14053-14057
[6]   General anosmia caused by a targeted disruption of the mouse olfactory cyclic nucleotide-gated cation channel [J].
Brunet, LJ ;
Gold, GH ;
Ngai, J .
NEURON, 1996, 17 (04) :681-693
[7]   A NOVEL MULTIGENE FAMILY MAY ENCODE ODORANT RECEPTORS - A MOLECULAR-BASIS FOR ODOR RECOGNITION [J].
BUCK, L ;
AXEL, R .
CELL, 1991, 65 (01) :175-187
[8]   Progenitor cells of the olfactory receptor neuron lineage [J].
Calof, AL ;
Bonnin, A ;
Crocker, C ;
Kawauchi, S ;
Murray, RC ;
Shou, JY ;
Wu, HH .
MICROSCOPY RESEARCH AND TECHNIQUE, 2002, 58 (03) :176-188
[9]   THE DYNAMICS OF CELL-DEATH IN THE OLFACTORY EPITHELIUM [J].
CARR, VM ;
FARBMAN, AI .
EXPERIMENTAL NEUROLOGY, 1993, 124 (02) :308-314
[10]   Wnt-Responsive Lgr5+ Globose Basal Cells Function as Multipotent Olfactory Epithelium Progenitor Cells [J].
Chen, Mengfei ;
Tian, Shenghe ;
Yang, Xiaoling ;
Lane, Andrew P. ;
Reed, Randall R. ;
Liu, Hongjun .
JOURNAL OF NEUROSCIENCE, 2014, 34 (24) :8268-8276