Generation of inner ear hair cells by direct lineage conversion of primary somatic cells.


Journal

eLife
ISSN: 2050-084X
Titre abrégé: Elife
Pays: England
ID NLM: 101579614

Informations de publication

Date de publication:
30 06 2020
Historique:
received: 17 01 2020
accepted: 27 05 2020
entrez: 1 7 2020
pubmed: 1 7 2020
medline: 17 2 2021
Statut: epublish

Résumé

The mechanoreceptive sensory hair cells in the inner ear are selectively vulnerable to numerous genetic and environmental insults. In mammals, hair cells lack regenerative capacity, and their death leads to permanent hearing loss and vestibular dysfunction. Their paucity and inaccessibility has limited the search for otoprotective and regenerative strategies. Growing hair cells in vitro would provide a route to overcome this experimental bottleneck. We report a combination of four transcription factors ( Worldwide, hearing loss is the most common loss of sensation. Most cases of hearing loss are due to the death of specialized hair cells found deep inside the ear. These hair cells convert sounds into nerve impulses which can be understood by the brain. Hair cells naturally degrade as part of aging and can be damaged by other factors including loud noises, and otherwise therapeutic drugs, such as those used in chemotherapy for cancer. In humans and other mammals, once hair cells are lost they cannot be replaced. Hair cells have often been studied using mice, but the small number of hair cells in their ears, and their location deep inside the skull, makes it particularly difficult to study them in this way. Scientists are seeking ways to grow hair cells in the laboratory to make it easier to understand how they work and the factors that contribute to their damage and loss. Different cell types in the body are formed in response to specific combinations of biological signals. Currently, scientists do not have an efficient way to grow hair cells in the laboratory, because the correct signals needed to create them are not known. Menendez et al. have now identified four proteins which, when activated, convert fibroblasts, a common type of cell, into hair cells similar to those in the ear. These proteins are called Six1, Atoh1, Pou4f3 and Gfi1. Menendez et al. termed the resulting cells induced hair cells, or iHCs for short, and analyzed these cells to identify those characteristics that are similar to normal hair cells, as well as their differences. Importantly, the iHCs were found to be damaged by the same chemicals that specifically harm normal hair cells, suggesting they are useful test subjects. The ability to create hair cells in the laboratory using more easily available cells has many uses. These cells can help to understand the normal function of hair cells and how they become damaged. They can also be used to test new drugs to assess their success in preventing or reversing hearing loss. These findings may also lead to genetic solutions to curing hearing loss.

Autres résumés

Type: plain-language-summary (eng)
Worldwide, hearing loss is the most common loss of sensation. Most cases of hearing loss are due to the death of specialized hair cells found deep inside the ear. These hair cells convert sounds into nerve impulses which can be understood by the brain. Hair cells naturally degrade as part of aging and can be damaged by other factors including loud noises, and otherwise therapeutic drugs, such as those used in chemotherapy for cancer. In humans and other mammals, once hair cells are lost they cannot be replaced. Hair cells have often been studied using mice, but the small number of hair cells in their ears, and their location deep inside the skull, makes it particularly difficult to study them in this way. Scientists are seeking ways to grow hair cells in the laboratory to make it easier to understand how they work and the factors that contribute to their damage and loss. Different cell types in the body are formed in response to specific combinations of biological signals. Currently, scientists do not have an efficient way to grow hair cells in the laboratory, because the correct signals needed to create them are not known. Menendez et al. have now identified four proteins which, when activated, convert fibroblasts, a common type of cell, into hair cells similar to those in the ear. These proteins are called Six1, Atoh1, Pou4f3 and Gfi1. Menendez et al. termed the resulting cells induced hair cells, or iHCs for short, and analyzed these cells to identify those characteristics that are similar to normal hair cells, as well as their differences. Importantly, the iHCs were found to be damaged by the same chemicals that specifically harm normal hair cells, suggesting they are useful test subjects. The ability to create hair cells in the laboratory using more easily available cells has many uses. These cells can help to understand the normal function of hair cells and how they become damaged. They can also be used to test new drugs to assess their success in preventing or reversing hearing loss. These findings may also lead to genetic solutions to curing hearing loss.

Identifiants

pubmed: 32602462
doi: 10.7554/eLife.55249
pii: 55249
pmc: PMC7326493
doi:
pii:

Substances chimiques

Transcription Factors 0

Banques de données

GEO
['GSE149260']

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : NIDCD NIH HHS
ID : R01 DC015530
Pays : United States
Organisme : NINDS NIH HHS
ID : R01 NS097850
Pays : United States
Organisme : NIDCD NIH HHS
ID : T32 DC009975
Pays : United States
Organisme : NINDS NIH HHS
ID : R00 NS077435
Pays : United States

Informations de copyright

© 2020, Menendez et al.

Déclaration de conflit d'intérêts

LM, TT, LT, AM, HY, XW, JL, RK, JI, NS No competing interests declared, SG Currently employed at a for-profit corporation, Allogene. This company has no competing technology, nor is it involved in this research. CH, JL Employed by a for-profit company that will benefit from the software development that they contributed to this project.

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Auteurs

Louise Menendez (L)

Department of Stem Cell and Regenerative Medicine, University of Southern California, Los Angeles, United States.
Eli and Edythe Broad Center, University of Southern California, Los Angeles, United States.
Zilkha Neurogenetic Institute, University of Southern California, Los Angeles, United States.

Talon Trecek (T)

Department of Stem Cell and Regenerative Medicine, University of Southern California, Los Angeles, United States.
Eli and Edythe Broad Center, University of Southern California, Los Angeles, United States.

Suhasni Gopalakrishnan (S)

Department of Stem Cell and Regenerative Medicine, University of Southern California, Los Angeles, United States.
Eli and Edythe Broad Center, University of Southern California, Los Angeles, United States.
Zilkha Neurogenetic Institute, University of Southern California, Los Angeles, United States.

Litao Tao (L)

Department of Stem Cell and Regenerative Medicine, University of Southern California, Los Angeles, United States.
Eli and Edythe Broad Center, University of Southern California, Los Angeles, United States.

Alexander L Markowitz (AL)

Zilkha Neurogenetic Institute, University of Southern California, Los Angeles, United States.
USC Caruso Department of Otolaryngology - Head and Neck Surgery, University of Southern California, Los Angeles, United States.

Haoze V Yu (HV)

Department of Stem Cell and Regenerative Medicine, University of Southern California, Los Angeles, United States.
Eli and Edythe Broad Center, University of Southern California, Los Angeles, United States.

Xizi Wang (X)

Department of Stem Cell and Regenerative Medicine, University of Southern California, Los Angeles, United States.
Eli and Edythe Broad Center, University of Southern California, Los Angeles, United States.

Juan Llamas (J)

Department of Stem Cell and Regenerative Medicine, University of Southern California, Los Angeles, United States.
Eli and Edythe Broad Center, University of Southern California, Los Angeles, United States.

Chichou Huang (C)

DRVision Technologies, Bellevue, United States.

James Lee (J)

DRVision Technologies, Bellevue, United States.

Radha Kalluri (R)

Zilkha Neurogenetic Institute, University of Southern California, Los Angeles, United States.
USC Caruso Department of Otolaryngology - Head and Neck Surgery, University of Southern California, Los Angeles, United States.

Justin Ichida (J)

Department of Stem Cell and Regenerative Medicine, University of Southern California, Los Angeles, United States.
Eli and Edythe Broad Center, University of Southern California, Los Angeles, United States.
Zilkha Neurogenetic Institute, University of Southern California, Los Angeles, United States.

Neil Segil (N)

Department of Stem Cell and Regenerative Medicine, University of Southern California, Los Angeles, United States.
Eli and Edythe Broad Center, University of Southern California, Los Angeles, United States.
USC Caruso Department of Otolaryngology - Head and Neck Surgery, University of Southern California, Los Angeles, United States.

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