Pubfacts - Scientific Publication Data
  • Categories
  • |
  • Journals
  • |
  • Authors
  • Login
  • Categories
  • Journals

Search Our Scientific Publications & Authors

Publications
  • Publications
  • Authors
find publications by category +
Translate page:

Single-Cell Sequencing Applications in the Inner Ear.

Authors:
Mingxuan Wu Mingyu Xia Wenyan Li Huawei Li

Front Cell Dev Biol 2021 12;9:637779. Epub 2021 Feb 12.

ENT Institute and Department of Otorhinolaryngology, Eye and ENT Hospital, State Key Laboratory of Medical Neurobiology and MOE Frontiers Center for Brain Science, Fudan University, Shanghai, China.

Genomics studies face specific challenges in the inner ear due to the multiple types and limited amounts of inner ear cells that are arranged in a very delicate structure. However, advances in single-cell sequencing (SCS) technology have made it possible to analyze gene expression variations across different cell types as well as within specific cell groups that were previously considered to be homogeneous. In this review, we summarize recent advances in inner ear research brought about by the use of SCS that have delineated tissue heterogeneity, identified unknown cell subtypes, discovered novel cell markers, and revealed dynamic signaling pathways during development. SCS opens up new avenues for inner ear research, and the potential of the technology is only beginning to be explored.

Download full-text PDF

Source
http://dx.doi.org/10.3389/fcell.2021.637779DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7907461PMC
February 2021

Publication Analysis

Top Keywords

inner ear
20
single-cell sequencing
8
inner
5
ear
5
summarize advances
4
review summarize
4
homogeneous review
4
considered homogeneous
4
advances inner
4
ear brought
4
brought scs
4
groups considered
4
delineated tissue
4
scs delineated
4
types well
4
expression variations
4
gene expression
4
analyze gene
4
cell
4
variations cell
4

Keyword Occurance

Similar Publications

AAV-S: A versatile capsid variant for transduction of mouse and primate inner ear.

Authors:
Maryna V Ivanchenko Killian S Hanlon Daniel M Hathaway Alex J Klein Cole W Peters Yaqiao Li Panos I Tamvakologos Josette Nammour Casey A Maguire David P Corey

Mol Ther Methods Clin Dev 2021 Jun 29;21:382-398. Epub 2021 Mar 29.

Department of Neurobiology, Harvard Medical School, 220 Longwood Avenue, Boston, MA 02115, USA.

Gene therapy strategies using adeno-associated virus (AAV) vectors to treat hereditary deafnesses have shown remarkable efficacy in some mouse models of hearing loss. Even so, there are few AAV capsids that transduce both inner and outer hair cells-the cells that express most deafness genes-and fewer still shown to transduce hair cells efficiently in primates. AAV capsids with robust transduction of inner and outer hair cells in primate cochlea will be needed for most clinical trials. Read More

View Article and Full-Text PDF
June 2021
Similar Publications

Cochlear implantation versus auditory brainstem implantation in children with auditory nerve deficiencies.

Authors:
Medhat Yousef Tamer A Mesallam Ayna Almasaad Salman Alhabib Abdulrahman Hagr Farid Alzhrani

Eur Arch Otorhinolaryngol 2021 Apr 18. Epub 2021 Apr 18.

King Abdullah Ear Specialist Center (KAESC), College of Medicine, King Saud University, Riyadh, Saudi Arabia.

Background: Cochlear nerve deficiency is one of the known causes of congenital sensorineural hearing loss. Management of hearing loss in children with cochlear nerve deficiency poses a multidimensional challenge. The absent or hypoplastic cochlear nerve may prevent electrical stimulation from reaching the brainstem and the auditory cortex. Read More

View Article and Full-Text PDF
April 2021
Similar Publications

Correlation between magnetic resonance imaging classification of endolymphatic hydrops and clinical manifestations and audiovestibular test results in patients with definite Ménière's disease.

Authors:
Agnieszka Jasińska Magdalena Lachowska Emilia Wnuk Katarzyna Pierchała Olgierd Rowiński Kazimierz Niemczyk

Auris Nasus Larynx 2021 Apr 14. Epub 2021 Apr 14.

Department of Otorhinolaryngology, Head and Neck Surgery, Medical University of Warsaw, Poland.

Objectives: The purpose was to evaluate magnetic resonance imaging (MRI) classification of endolymphatic hydrops with clinical features, audiological and vestibular tests in patients with definite unilateral Ménière's disease (MD).

Methods: Thirty-eight patients were enrolled in this study. The severity of the main clinical symptoms, audiovestibular tests, and MRI, performed 4 hours after intravenous injection of gadobutrol to visualize inner ear compartments, were evaluated. Read More

View Article and Full-Text PDF
April 2021
Similar Publications

A de novo mutation of the SOX10 gene associated with inner ear malformation in a Guangxi family with Waardenburg syndrome type II.

Authors:
Zhijie Niu Yongjing Lai Songhua Tan Fen Tang Xianglong Tang Yupei Su Lei Liu Lihong Xie Qin Fang Mao Xie Anzhou Tang

Int J Pediatr Otorhinolaryngol 2021 Apr 14;145:110711. Epub 2021 Apr 14.

Department of Otolaryngology-Head and Neck Surgery, The First Affiliated Hospital of Guangxi Medical University, Nanning, 530021, China; Regional Key Laboratory of Early Prevention and Treatment of High-Rise Tumors, Nanning, 530021, China. Electronic address:

Objective: Waardenburg syndrome type 2 (WS2) is a rare neural-crest disorder, characterized by heterochromic irides or blue eyes and sensorineural hearing loss. The aim of this study was to analyze the clinical features and investigate the genetic cause of WS2 in a small family from Guangxi Zhuang Autonomous region.

Methods: Whole-exome sequencing and mutational analysis were used to identify disease-causing genes in this family. Read More

View Article and Full-Text PDF
April 2021
Similar Publications

Molecular mechanisms of hearing loss in Nager syndrome.

Authors:
Santosh Kumar Maharana Jean-Pierre Saint-Jeannet

Dev Biol 2021 Apr 14. Epub 2021 Apr 14.

Department of Molecular Pathobiology, New York University, College of Dentistry, New York, USA. Electronic address:

Nager syndrome is a rare human developmental disorder characterized by hypoplastic neural crest-derived craniofacial bones and limb defects. Mutations in SF3B4 gene, which encodes a component of the spliceosome, are a major cause for Nager. A review of the literature indicates that 45% of confirmed cases are also affected by conductive, sensorineural or mixed hearing loss. Read More

View Article and Full-Text PDF
April 2021
Similar Publications
© 2021 PubFacts.
  • About PubFacts
  • Privacy Policy
  • Sitemap