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...
Autores principales: | , , , , , , , |
---|---|
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 |