Cargando…

Directed differentiation of human iPSCs into mesenchymal lineages by optogenetic control of TGF-β signaling

In tissue development and homeostasis, transforming growth factor (TGF)-β signaling is finely coordinated by latent forms and matrix sequestration. Optogenetics can offer precise and dynamic control of cell signaling. We report the development of an optogenetic human induced pluripotent stem cell sy...

Descripción completa

Detalles Bibliográficos
Autores principales: Wu, Josephine Y., Yeager, Keith, Tavakol, Daniel Naveed, Morsink, Margaretha, Wang, Bryan, Soni, Rajesh Kumar, Hung, Clark T., Vunjak-Novakovic, Gordana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10278972/
https://www.ncbi.nlm.nih.gov/pubmed/37178118
http://dx.doi.org/10.1016/j.celrep.2023.112509
_version_ 1785060579560390656
author Wu, Josephine Y.
Yeager, Keith
Tavakol, Daniel Naveed
Morsink, Margaretha
Wang, Bryan
Soni, Rajesh Kumar
Hung, Clark T.
Vunjak-Novakovic, Gordana
author_facet Wu, Josephine Y.
Yeager, Keith
Tavakol, Daniel Naveed
Morsink, Margaretha
Wang, Bryan
Soni, Rajesh Kumar
Hung, Clark T.
Vunjak-Novakovic, Gordana
author_sort Wu, Josephine Y.
collection PubMed
description In tissue development and homeostasis, transforming growth factor (TGF)-β signaling is finely coordinated by latent forms and matrix sequestration. Optogenetics can offer precise and dynamic control of cell signaling. We report the development of an optogenetic human induced pluripotent stem cell system for TGF-β signaling and demonstrate its utility in directing differentiation into the smooth muscle, tenogenic, and chondrogenic lineages. Light-activated TGF-β signaling resulted in expression of differentiation markers at levels close to those in soluble factor-treated cultures, with minimal phototoxicity. In a cartilage-bone model, light-patterned TGF-β gradients allowed the establishment of hyaline-like layer of cartilage tissue at the articular surface while attenuating with depth to enable hypertrophic induction at the osteochondral interface. By selectively activating TGF-β signaling in co-cultures of light-responsive and non-responsive cells, undifferentiated and differentiated cells were simultaneously maintained in a single culture with shared medium. This platform can enable patient-specific and spatiotemporally precise studies of cellular decision making.
format Online
Article
Text
id pubmed-10278972
institution National Center for Biotechnology Information
language English
publishDate 2023
record_format MEDLINE/PubMed
spelling pubmed-102789722023-06-19 Directed differentiation of human iPSCs into mesenchymal lineages by optogenetic control of TGF-β signaling Wu, Josephine Y. Yeager, Keith Tavakol, Daniel Naveed Morsink, Margaretha Wang, Bryan Soni, Rajesh Kumar Hung, Clark T. Vunjak-Novakovic, Gordana Cell Rep Article In tissue development and homeostasis, transforming growth factor (TGF)-β signaling is finely coordinated by latent forms and matrix sequestration. Optogenetics can offer precise and dynamic control of cell signaling. We report the development of an optogenetic human induced pluripotent stem cell system for TGF-β signaling and demonstrate its utility in directing differentiation into the smooth muscle, tenogenic, and chondrogenic lineages. Light-activated TGF-β signaling resulted in expression of differentiation markers at levels close to those in soluble factor-treated cultures, with minimal phototoxicity. In a cartilage-bone model, light-patterned TGF-β gradients allowed the establishment of hyaline-like layer of cartilage tissue at the articular surface while attenuating with depth to enable hypertrophic induction at the osteochondral interface. By selectively activating TGF-β signaling in co-cultures of light-responsive and non-responsive cells, undifferentiated and differentiated cells were simultaneously maintained in a single culture with shared medium. This platform can enable patient-specific and spatiotemporally precise studies of cellular decision making. 2023-05-30 2023-05-12 /pmc/articles/PMC10278972/ /pubmed/37178118 http://dx.doi.org/10.1016/j.celrep.2023.112509 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ).
spellingShingle Article
Wu, Josephine Y.
Yeager, Keith
Tavakol, Daniel Naveed
Morsink, Margaretha
Wang, Bryan
Soni, Rajesh Kumar
Hung, Clark T.
Vunjak-Novakovic, Gordana
Directed differentiation of human iPSCs into mesenchymal lineages by optogenetic control of TGF-β signaling
title Directed differentiation of human iPSCs into mesenchymal lineages by optogenetic control of TGF-β signaling
title_full Directed differentiation of human iPSCs into mesenchymal lineages by optogenetic control of TGF-β signaling
title_fullStr Directed differentiation of human iPSCs into mesenchymal lineages by optogenetic control of TGF-β signaling
title_full_unstemmed Directed differentiation of human iPSCs into mesenchymal lineages by optogenetic control of TGF-β signaling
title_short Directed differentiation of human iPSCs into mesenchymal lineages by optogenetic control of TGF-β signaling
title_sort directed differentiation of human ipscs into mesenchymal lineages by optogenetic control of tgf-β signaling
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10278972/
https://www.ncbi.nlm.nih.gov/pubmed/37178118
http://dx.doi.org/10.1016/j.celrep.2023.112509
work_keys_str_mv AT wujosephiney directeddifferentiationofhumanipscsintomesenchymallineagesbyoptogeneticcontroloftgfbsignaling
AT yeagerkeith directeddifferentiationofhumanipscsintomesenchymallineagesbyoptogeneticcontroloftgfbsignaling
AT tavakoldanielnaveed directeddifferentiationofhumanipscsintomesenchymallineagesbyoptogeneticcontroloftgfbsignaling
AT morsinkmargaretha directeddifferentiationofhumanipscsintomesenchymallineagesbyoptogeneticcontroloftgfbsignaling
AT wangbryan directeddifferentiationofhumanipscsintomesenchymallineagesbyoptogeneticcontroloftgfbsignaling
AT sonirajeshkumar directeddifferentiationofhumanipscsintomesenchymallineagesbyoptogeneticcontroloftgfbsignaling
AT hungclarkt directeddifferentiationofhumanipscsintomesenchymallineagesbyoptogeneticcontroloftgfbsignaling
AT vunjaknovakovicgordana directeddifferentiationofhumanipscsintomesenchymallineagesbyoptogeneticcontroloftgfbsignaling