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Transmembrane stem cell factor protein therapeutics enhance revascularization in ischemia without mast cell activation

Stem cell factor (SCF) is a cytokine that regulates hematopoiesis and other biological processes. While clinical treatments using SCF would be highly beneficial, these have been limited by toxicity related to mast cell activation. Transmembrane SCF (tmSCF) has differential activity from soluble SCF...

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Autores principales: Takematsu, Eri, Massidda, Miles, Auster, Jeff, Chen, Po-Chih, Im, ByungGee, Srinath, Sanjana, Canga, Sophia, Singh, Aditya, Majid, Marjan, Sherman, Michael, Dunn, Andrew, Graham, Annette, Martin, Patricia, Baker, Aaron B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9076913/
https://www.ncbi.nlm.nih.gov/pubmed/35523773
http://dx.doi.org/10.1038/s41467-022-30103-2
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author Takematsu, Eri
Massidda, Miles
Auster, Jeff
Chen, Po-Chih
Im, ByungGee
Srinath, Sanjana
Canga, Sophia
Singh, Aditya
Majid, Marjan
Sherman, Michael
Dunn, Andrew
Graham, Annette
Martin, Patricia
Baker, Aaron B.
author_facet Takematsu, Eri
Massidda, Miles
Auster, Jeff
Chen, Po-Chih
Im, ByungGee
Srinath, Sanjana
Canga, Sophia
Singh, Aditya
Majid, Marjan
Sherman, Michael
Dunn, Andrew
Graham, Annette
Martin, Patricia
Baker, Aaron B.
author_sort Takematsu, Eri
collection PubMed
description Stem cell factor (SCF) is a cytokine that regulates hematopoiesis and other biological processes. While clinical treatments using SCF would be highly beneficial, these have been limited by toxicity related to mast cell activation. Transmembrane SCF (tmSCF) has differential activity from soluble SCF and has not been explored as a therapeutic agent. We created novel therapeutics using tmSCF embedded in proteoliposomes or lipid nanodiscs. Mouse models of anaphylaxis and ischemia revealed the tmSCF-based therapies did not activate mast cells and improved the revascularization in the ischemic hind limb. Proteoliposomal tmSCF preferentially acted on endothelial cells to induce angiogenesis while tmSCF nanodiscs had greater activity in inducing stem cell mobilization and recruitment to the site of injury. The type of lipid nanocarrier used altered the relative cellular uptake pathways and signaling in a cell type dependent manner. Overall, we found that tmSCF-based therapies can provide therapeutic benefits without off target effects.
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spelling pubmed-90769132022-05-08 Transmembrane stem cell factor protein therapeutics enhance revascularization in ischemia without mast cell activation Takematsu, Eri Massidda, Miles Auster, Jeff Chen, Po-Chih Im, ByungGee Srinath, Sanjana Canga, Sophia Singh, Aditya Majid, Marjan Sherman, Michael Dunn, Andrew Graham, Annette Martin, Patricia Baker, Aaron B. Nat Commun Article Stem cell factor (SCF) is a cytokine that regulates hematopoiesis and other biological processes. While clinical treatments using SCF would be highly beneficial, these have been limited by toxicity related to mast cell activation. Transmembrane SCF (tmSCF) has differential activity from soluble SCF and has not been explored as a therapeutic agent. We created novel therapeutics using tmSCF embedded in proteoliposomes or lipid nanodiscs. Mouse models of anaphylaxis and ischemia revealed the tmSCF-based therapies did not activate mast cells and improved the revascularization in the ischemic hind limb. Proteoliposomal tmSCF preferentially acted on endothelial cells to induce angiogenesis while tmSCF nanodiscs had greater activity in inducing stem cell mobilization and recruitment to the site of injury. The type of lipid nanocarrier used altered the relative cellular uptake pathways and signaling in a cell type dependent manner. Overall, we found that tmSCF-based therapies can provide therapeutic benefits without off target effects. Nature Publishing Group UK 2022-05-06 /pmc/articles/PMC9076913/ /pubmed/35523773 http://dx.doi.org/10.1038/s41467-022-30103-2 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Takematsu, Eri
Massidda, Miles
Auster, Jeff
Chen, Po-Chih
Im, ByungGee
Srinath, Sanjana
Canga, Sophia
Singh, Aditya
Majid, Marjan
Sherman, Michael
Dunn, Andrew
Graham, Annette
Martin, Patricia
Baker, Aaron B.
Transmembrane stem cell factor protein therapeutics enhance revascularization in ischemia without mast cell activation
title Transmembrane stem cell factor protein therapeutics enhance revascularization in ischemia without mast cell activation
title_full Transmembrane stem cell factor protein therapeutics enhance revascularization in ischemia without mast cell activation
title_fullStr Transmembrane stem cell factor protein therapeutics enhance revascularization in ischemia without mast cell activation
title_full_unstemmed Transmembrane stem cell factor protein therapeutics enhance revascularization in ischemia without mast cell activation
title_short Transmembrane stem cell factor protein therapeutics enhance revascularization in ischemia without mast cell activation
title_sort transmembrane stem cell factor protein therapeutics enhance revascularization in ischemia without mast cell activation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9076913/
https://www.ncbi.nlm.nih.gov/pubmed/35523773
http://dx.doi.org/10.1038/s41467-022-30103-2
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