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Intracellular delivery of cell-penetrating peptide-transcriptional factor fusion protein and its role in selective osteogenesis
Protein-transduction technology has been attempted to deliver macromolecular materials, including protein, nucleic acids, and polymeric drugs, for either diagnosis or therapeutic purposes. Herein, fusion protein composed of an arginine-rich cell-penetrating peptide, termed low-molecular-weight prota...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3956484/ https://www.ncbi.nlm.nih.gov/pubmed/24648725 http://dx.doi.org/10.2147/IJN.S55433 |
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author | Suh, Jin Sook Lee, Jue Yeon Choi, Yoon Jung You, Hyung Keun Hong, Seong-Doo Chung, Chong Pyoung Park, Yoon Jeong |
author_facet | Suh, Jin Sook Lee, Jue Yeon Choi, Yoon Jung You, Hyung Keun Hong, Seong-Doo Chung, Chong Pyoung Park, Yoon Jeong |
author_sort | Suh, Jin Sook |
collection | PubMed |
description | Protein-transduction technology has been attempted to deliver macromolecular materials, including protein, nucleic acids, and polymeric drugs, for either diagnosis or therapeutic purposes. Herein, fusion protein composed of an arginine-rich cell-penetrating peptide, termed low-molecular-weight protamine (LMWP), and a transcriptional coactivator with a PDZ-binding motif (TAZ) protein was prepared and applied in combination with biomaterials to increase bone-forming capacity. TAZ has been recently identified as a specific osteogenic stimulating transcriptional coactivator in human mesenchymal stem cell (hMSC) differentiation, while simultaneously blocking adipogenic differentiation. However, TAZ by itself cannot penetrate the cells, and thus needs a transfection tool for translocalization. The LMWP-TAZ fusion proteins were efficiently translocalized into the cytosol of hMSCs. The hMSCs treated with cell-penetrating LMWP-TAZ exhibited increased expression of osteoblastic genes and protein, producing significantly higher quantities of mineralized matrix compared to free TAZ. In contrast, adipogenic differentiation of the hMSCs was blocked by treatment of LMWP-TAZ fusion protein, as reflected by reduced marker-protein expression, adipocyte fatty acid-binding protein 2, and peroxisome proliferator-activated receptor-γ messenger ribonucleic acid levels. LMWP-TAZ was applied in alginate gel for the purpose of localization and controlled release. The LMWP-TAZ fusion protein-loaded alginate gel matrix significantly increased bone formation in rabbit calvarial defects compared with alginate gel matrix mixed with free TAZ protein. The protein transduction of TAZ fused with cell-penetrating LMWP peptide was able selectively to stimulate osteogenesis in vitro and in vivo. Taken together, this fusion protein-transduction technology for osteogenic protein can thus be applied in combination with biomaterials for tissue regeneration and controlled release for tissue-engineering purposes. |
format | Online Article Text |
id | pubmed-3956484 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-39564842014-03-19 Intracellular delivery of cell-penetrating peptide-transcriptional factor fusion protein and its role in selective osteogenesis Suh, Jin Sook Lee, Jue Yeon Choi, Yoon Jung You, Hyung Keun Hong, Seong-Doo Chung, Chong Pyoung Park, Yoon Jeong Int J Nanomedicine Original Research Protein-transduction technology has been attempted to deliver macromolecular materials, including protein, nucleic acids, and polymeric drugs, for either diagnosis or therapeutic purposes. Herein, fusion protein composed of an arginine-rich cell-penetrating peptide, termed low-molecular-weight protamine (LMWP), and a transcriptional coactivator with a PDZ-binding motif (TAZ) protein was prepared and applied in combination with biomaterials to increase bone-forming capacity. TAZ has been recently identified as a specific osteogenic stimulating transcriptional coactivator in human mesenchymal stem cell (hMSC) differentiation, while simultaneously blocking adipogenic differentiation. However, TAZ by itself cannot penetrate the cells, and thus needs a transfection tool for translocalization. The LMWP-TAZ fusion proteins were efficiently translocalized into the cytosol of hMSCs. The hMSCs treated with cell-penetrating LMWP-TAZ exhibited increased expression of osteoblastic genes and protein, producing significantly higher quantities of mineralized matrix compared to free TAZ. In contrast, adipogenic differentiation of the hMSCs was blocked by treatment of LMWP-TAZ fusion protein, as reflected by reduced marker-protein expression, adipocyte fatty acid-binding protein 2, and peroxisome proliferator-activated receptor-γ messenger ribonucleic acid levels. LMWP-TAZ was applied in alginate gel for the purpose of localization and controlled release. The LMWP-TAZ fusion protein-loaded alginate gel matrix significantly increased bone formation in rabbit calvarial defects compared with alginate gel matrix mixed with free TAZ protein. The protein transduction of TAZ fused with cell-penetrating LMWP peptide was able selectively to stimulate osteogenesis in vitro and in vivo. Taken together, this fusion protein-transduction technology for osteogenic protein can thus be applied in combination with biomaterials for tissue regeneration and controlled release for tissue-engineering purposes. Dove Medical Press 2014-03-10 /pmc/articles/PMC3956484/ /pubmed/24648725 http://dx.doi.org/10.2147/IJN.S55433 Text en © 2014 Suh et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Suh, Jin Sook Lee, Jue Yeon Choi, Yoon Jung You, Hyung Keun Hong, Seong-Doo Chung, Chong Pyoung Park, Yoon Jeong Intracellular delivery of cell-penetrating peptide-transcriptional factor fusion protein and its role in selective osteogenesis |
title | Intracellular delivery of cell-penetrating peptide-transcriptional factor fusion protein and its role in selective osteogenesis |
title_full | Intracellular delivery of cell-penetrating peptide-transcriptional factor fusion protein and its role in selective osteogenesis |
title_fullStr | Intracellular delivery of cell-penetrating peptide-transcriptional factor fusion protein and its role in selective osteogenesis |
title_full_unstemmed | Intracellular delivery of cell-penetrating peptide-transcriptional factor fusion protein and its role in selective osteogenesis |
title_short | Intracellular delivery of cell-penetrating peptide-transcriptional factor fusion protein and its role in selective osteogenesis |
title_sort | intracellular delivery of cell-penetrating peptide-transcriptional factor fusion protein and its role in selective osteogenesis |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3956484/ https://www.ncbi.nlm.nih.gov/pubmed/24648725 http://dx.doi.org/10.2147/IJN.S55433 |
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