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A novel dimeric thymosin beta 4 with enhanced activities accelerates the rate of wound healing
OBJECTIVE: Thymosin beta 4 (Tβ4) is a peptide with 43 amino acids that is critical for repair and remodeling tissues on the skin, eye, heart, and neural system following injury. To fully realize its utility as a treatment for disease caused by injury, the authors constructed a cost-effective novel T...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3792846/ https://www.ncbi.nlm.nih.gov/pubmed/24109178 http://dx.doi.org/10.2147/DDDT.S50183 |
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author | Xu, Tian-Jiao Wang, Qi Ma, Xiao-Wen Zhang, Zhen Zhang, Wei Xue, Xiao-Chang Zhang, Cun Hao, Qiang Li, Wei-Na Zhang, Ying-Qi Li, Meng |
author_facet | Xu, Tian-Jiao Wang, Qi Ma, Xiao-Wen Zhang, Zhen Zhang, Wei Xue, Xiao-Chang Zhang, Cun Hao, Qiang Li, Wei-Na Zhang, Ying-Qi Li, Meng |
author_sort | Xu, Tian-Jiao |
collection | PubMed |
description | OBJECTIVE: Thymosin beta 4 (Tβ4) is a peptide with 43 amino acids that is critical for repair and remodeling tissues on the skin, eye, heart, and neural system following injury. To fully realize its utility as a treatment for disease caused by injury, the authors constructed a cost-effective novel Tβ4 dimer and demonstrated that it was better able to accelerate tissue repair than native Tβ4. METHODS: A prokaryotic vector harboring two complete Tβ4 genes with a short linker was constructed and expressed in Escherichia coli. A pilot-scale fermentation (10 L) was performed to produce engineered bacteria and the Tβ4 dimer was purified by one-step hydrophobic interaction chromatography. The activities of the Tβ4 dimer to promote endothelial cell proliferation, migration, and sprouting were assessed by tetramethylbenzidine (methylthiazol tetrazolium), trans-well, scratch, and tube formation assays. The ability to accelerate dermal healing was assessed on rats. RESULTS: After fermentation, the Tβ4 dimer accounted for about 30% of all the bacteria proteins. The purity of the Tβ4 dimer reached 98% after hydrophobic interaction chromatography purification. An average of 562.4 mg/L Tβ4 dimer was acquired using a 10 L fermenter. In each assay, the dimeric Tβ4 exhibited enhanced activities compared with native Tβ4. Notably, the ability of the dimeric Tβ4 to promote cell migration was almost two times higher than that of Tβ4. The rate of dermal healing in the dimeric Tβ4-treated rats was approximately 1 day faster than with native Tβ4-treated rats. CONCLUSION: The dimeric Tβ4 exhibited enhanced activity on wound healing than native Tβ4, and the purification process was simple and cost-effective. This data could be of significant benefit for the high pain and morbidity associated with chronic wounds disease. A better strategy to develop Tβ4 as a treatment for other diseases caused by injuries such as heart attack, neurotrophic keratitis, and multiple sclerosis was also described. |
format | Online Article Text |
id | pubmed-3792846 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-37928462013-10-09 A novel dimeric thymosin beta 4 with enhanced activities accelerates the rate of wound healing Xu, Tian-Jiao Wang, Qi Ma, Xiao-Wen Zhang, Zhen Zhang, Wei Xue, Xiao-Chang Zhang, Cun Hao, Qiang Li, Wei-Na Zhang, Ying-Qi Li, Meng Drug Des Devel Ther Original Research OBJECTIVE: Thymosin beta 4 (Tβ4) is a peptide with 43 amino acids that is critical for repair and remodeling tissues on the skin, eye, heart, and neural system following injury. To fully realize its utility as a treatment for disease caused by injury, the authors constructed a cost-effective novel Tβ4 dimer and demonstrated that it was better able to accelerate tissue repair than native Tβ4. METHODS: A prokaryotic vector harboring two complete Tβ4 genes with a short linker was constructed and expressed in Escherichia coli. A pilot-scale fermentation (10 L) was performed to produce engineered bacteria and the Tβ4 dimer was purified by one-step hydrophobic interaction chromatography. The activities of the Tβ4 dimer to promote endothelial cell proliferation, migration, and sprouting were assessed by tetramethylbenzidine (methylthiazol tetrazolium), trans-well, scratch, and tube formation assays. The ability to accelerate dermal healing was assessed on rats. RESULTS: After fermentation, the Tβ4 dimer accounted for about 30% of all the bacteria proteins. The purity of the Tβ4 dimer reached 98% after hydrophobic interaction chromatography purification. An average of 562.4 mg/L Tβ4 dimer was acquired using a 10 L fermenter. In each assay, the dimeric Tβ4 exhibited enhanced activities compared with native Tβ4. Notably, the ability of the dimeric Tβ4 to promote cell migration was almost two times higher than that of Tβ4. The rate of dermal healing in the dimeric Tβ4-treated rats was approximately 1 day faster than with native Tβ4-treated rats. CONCLUSION: The dimeric Tβ4 exhibited enhanced activity on wound healing than native Tβ4, and the purification process was simple and cost-effective. This data could be of significant benefit for the high pain and morbidity associated with chronic wounds disease. A better strategy to develop Tβ4 as a treatment for other diseases caused by injuries such as heart attack, neurotrophic keratitis, and multiple sclerosis was also described. Dove Medical Press 2013-10-01 /pmc/articles/PMC3792846/ /pubmed/24109178 http://dx.doi.org/10.2147/DDDT.S50183 Text en © 2013 Xu 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 Xu, Tian-Jiao Wang, Qi Ma, Xiao-Wen Zhang, Zhen Zhang, Wei Xue, Xiao-Chang Zhang, Cun Hao, Qiang Li, Wei-Na Zhang, Ying-Qi Li, Meng A novel dimeric thymosin beta 4 with enhanced activities accelerates the rate of wound healing |
title | A novel dimeric thymosin beta 4 with enhanced activities accelerates the rate of wound healing |
title_full | A novel dimeric thymosin beta 4 with enhanced activities accelerates the rate of wound healing |
title_fullStr | A novel dimeric thymosin beta 4 with enhanced activities accelerates the rate of wound healing |
title_full_unstemmed | A novel dimeric thymosin beta 4 with enhanced activities accelerates the rate of wound healing |
title_short | A novel dimeric thymosin beta 4 with enhanced activities accelerates the rate of wound healing |
title_sort | novel dimeric thymosin beta 4 with enhanced activities accelerates the rate of wound healing |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3792846/ https://www.ncbi.nlm.nih.gov/pubmed/24109178 http://dx.doi.org/10.2147/DDDT.S50183 |
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