Single-cell RNA-Seq resolves cellular complexity in sensory organs from the neonatal inner ear.
Single-cell RNA-Seq resolves cellular complexity in sensory organs from the neonatal inner ear.
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DOI:
10.1038/ncomms9557
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发表时间:
2015-10-15
影响因子:
16.6
通讯作者:
Kelley MW
中科院分区:
文献类型:
--
作者:
Burns JC;Kelly MC;Hoa M;Morell RJ;Kelley MW
In the inner ear, cochlear and vestibular sensory epithelia utilize grossly similar cell types to transduce different stimuli: sound and acceleration. Each individual sensory epithelium is composed of highly heterogeneous populations of cells based on physiological and anatomical criteria. However, limited numbers of each cell type have impeded transcriptional characterization. Here we generated transcriptomes for 301 single cells from the utricular and cochlear sensory epithelia of newborn mice to circumvent this challenge. Cluster analysis indicates distinct profiles for each of the major sensory epithelial cell types, as well as less-distinct sub-populations. Asynchrony within utricles allows reconstruction of the temporal progression of cell-type-specific differentiation and suggests possible plasticity among cells at the sensory–nonsensory boundary. Comparisons of cell types from utricles and cochleae demonstrate divergence between auditory and vestibular cells, despite a common origin. These results provide significant insights into the developmental processes that form unique inner ear cell types. Heterogeneous sensory epithelia of the inner ear are difficult to study owing to the few cells that can be isolated. Here the authors provide insight into the developmental processes underlying the formation of these cells by single-cell RNA-Seq.