Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2013
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
_version_ 1782286879244156928
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
work_keys_str_mv AT xutianjiao anoveldimericthymosinbeta4withenhancedactivitiesacceleratestherateofwoundhealing
AT wangqi anoveldimericthymosinbeta4withenhancedactivitiesacceleratestherateofwoundhealing
AT maxiaowen anoveldimericthymosinbeta4withenhancedactivitiesacceleratestherateofwoundhealing
AT zhangzhen anoveldimericthymosinbeta4withenhancedactivitiesacceleratestherateofwoundhealing
AT zhangwei anoveldimericthymosinbeta4withenhancedactivitiesacceleratestherateofwoundhealing
AT xuexiaochang anoveldimericthymosinbeta4withenhancedactivitiesacceleratestherateofwoundhealing
AT zhangcun anoveldimericthymosinbeta4withenhancedactivitiesacceleratestherateofwoundhealing
AT haoqiang anoveldimericthymosinbeta4withenhancedactivitiesacceleratestherateofwoundhealing
AT liweina anoveldimericthymosinbeta4withenhancedactivitiesacceleratestherateofwoundhealing
AT zhangyingqi anoveldimericthymosinbeta4withenhancedactivitiesacceleratestherateofwoundhealing
AT limeng anoveldimericthymosinbeta4withenhancedactivitiesacceleratestherateofwoundhealing
AT xutianjiao noveldimericthymosinbeta4withenhancedactivitiesacceleratestherateofwoundhealing
AT wangqi noveldimericthymosinbeta4withenhancedactivitiesacceleratestherateofwoundhealing
AT maxiaowen noveldimericthymosinbeta4withenhancedactivitiesacceleratestherateofwoundhealing
AT zhangzhen noveldimericthymosinbeta4withenhancedactivitiesacceleratestherateofwoundhealing
AT zhangwei noveldimericthymosinbeta4withenhancedactivitiesacceleratestherateofwoundhealing
AT xuexiaochang noveldimericthymosinbeta4withenhancedactivitiesacceleratestherateofwoundhealing
AT zhangcun noveldimericthymosinbeta4withenhancedactivitiesacceleratestherateofwoundhealing
AT haoqiang noveldimericthymosinbeta4withenhancedactivitiesacceleratestherateofwoundhealing
AT liweina noveldimericthymosinbeta4withenhancedactivitiesacceleratestherateofwoundhealing
AT zhangyingqi noveldimericthymosinbeta4withenhancedactivitiesacceleratestherateofwoundhealing
AT limeng noveldimericthymosinbeta4withenhancedactivitiesacceleratestherateofwoundhealing