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Glycocalyx Remodeling with Proteoglycan Mimetics Promotes Neural Specification in Embryonic Stem Cells
[Image: see text] Growth factor (GF) signaling is a key determinant of stem cell fate. Interactions of GFs with their receptors are often mediated by heparan sulfate proteoglycans (HSPGs). Here, we report a cell surface engineering strategy that exploits the function of HSPGs to promote differentiat...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2014
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4121001/ https://www.ncbi.nlm.nih.gov/pubmed/25019314 http://dx.doi.org/10.1021/ja505012a |
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author | Huang, Mia L. Smith, Raymond A. A. Trieger, Greg W. Godula, Kamil |
author_facet | Huang, Mia L. Smith, Raymond A. A. Trieger, Greg W. Godula, Kamil |
author_sort | Huang, Mia L. |
collection | PubMed |
description | [Image: see text] Growth factor (GF) signaling is a key determinant of stem cell fate. Interactions of GFs with their receptors are often mediated by heparan sulfate proteoglycans (HSPGs). Here, we report a cell surface engineering strategy that exploits the function of HSPGs to promote differentiation in embryonic stem cells (ESCs). We have generated synthetic neoproteoglycans (neoPGs) with affinity for the fibroblast growth factor 2 (FGF2) and introduced them into plasma membranes of ESCs deficient in HS biosynthesis. There, the neoPGs assumed the function of native HSPGs, rescued FGF2-mediated kinase activity, and promoted neural specification. This glycocalyx remodeling strategy is versatile and may be applicable to other types of differentiation. |
format | Online Article Text |
id | pubmed-4121001 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-41210012015-07-14 Glycocalyx Remodeling with Proteoglycan Mimetics Promotes Neural Specification in Embryonic Stem Cells Huang, Mia L. Smith, Raymond A. A. Trieger, Greg W. Godula, Kamil J Am Chem Soc [Image: see text] Growth factor (GF) signaling is a key determinant of stem cell fate. Interactions of GFs with their receptors are often mediated by heparan sulfate proteoglycans (HSPGs). Here, we report a cell surface engineering strategy that exploits the function of HSPGs to promote differentiation in embryonic stem cells (ESCs). We have generated synthetic neoproteoglycans (neoPGs) with affinity for the fibroblast growth factor 2 (FGF2) and introduced them into plasma membranes of ESCs deficient in HS biosynthesis. There, the neoPGs assumed the function of native HSPGs, rescued FGF2-mediated kinase activity, and promoted neural specification. This glycocalyx remodeling strategy is versatile and may be applicable to other types of differentiation. American Chemical Society 2014-07-14 2014-07-30 /pmc/articles/PMC4121001/ /pubmed/25019314 http://dx.doi.org/10.1021/ja505012a Text en Copyright © 2014 American Chemical Society Terms of Use (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) |
spellingShingle | Huang, Mia L. Smith, Raymond A. A. Trieger, Greg W. Godula, Kamil Glycocalyx Remodeling with Proteoglycan Mimetics Promotes Neural Specification in Embryonic Stem Cells |
title | Glycocalyx
Remodeling with Proteoglycan Mimetics Promotes
Neural Specification in Embryonic Stem Cells |
title_full | Glycocalyx
Remodeling with Proteoglycan Mimetics Promotes
Neural Specification in Embryonic Stem Cells |
title_fullStr | Glycocalyx
Remodeling with Proteoglycan Mimetics Promotes
Neural Specification in Embryonic Stem Cells |
title_full_unstemmed | Glycocalyx
Remodeling with Proteoglycan Mimetics Promotes
Neural Specification in Embryonic Stem Cells |
title_short | Glycocalyx
Remodeling with Proteoglycan Mimetics Promotes
Neural Specification in Embryonic Stem Cells |
title_sort | glycocalyx
remodeling with proteoglycan mimetics promotes
neural specification in embryonic stem cells |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4121001/ https://www.ncbi.nlm.nih.gov/pubmed/25019314 http://dx.doi.org/10.1021/ja505012a |
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