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Data on the expression and role of TREM-1 in the development of in-stent restenosis

The data presented in this article are related to the research article entitled “Increased serum TREM-1 level is associated with in-stent restenosis, and activation of TREM-1 promotes inflammation, proliferation and migration in vascular smooth muscle cells” (Wang et al., 2017) [1], which demonstrat...

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Autores principales: Wang, Fang, Li, Chang, Ding, Feng Hua, Shen, Ying, Gao, Jie, Liu, Zhu Hui, Chen, Jia Wei, Zhang, Rui Yan, Shen, Wei Feng, Wang, Xiao Qun, Lu, Lin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5726749/
https://www.ncbi.nlm.nih.gov/pubmed/29264376
http://dx.doi.org/10.1016/j.dib.2017.11.065
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author Wang, Fang
Li, Chang
Ding, Feng Hua
Shen, Ying
Gao, Jie
Liu, Zhu Hui
Chen, Jia Wei
Zhang, Rui Yan
Shen, Wei Feng
Wang, Xiao Qun
Lu, Lin
author_facet Wang, Fang
Li, Chang
Ding, Feng Hua
Shen, Ying
Gao, Jie
Liu, Zhu Hui
Chen, Jia Wei
Zhang, Rui Yan
Shen, Wei Feng
Wang, Xiao Qun
Lu, Lin
author_sort Wang, Fang
collection PubMed
description The data presented in this article are related to the research article entitled “Increased serum TREM-1 level is associated with in-stent restenosis, and activation of TREM-1 promotes inflammation, proliferation and migration in vascular smooth muscle cells” (Wang et al., 2017) [1], which demonstrated that TREM-1 is expressed on vascular smooth cells (VSMCs) and promotes inflammation, proliferation and migration in cultured VSMCs. In this dataset, the expression of TREM-1 in leukocytes and endothelial cells of carotid artery after ligation was evaluated. The effect of TREM-1 on stenosis was analyzed in cultured human saphenous veins (HSVs) that spontaneously undergo remodeling which involves VSMC proliferation and migration.
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spelling pubmed-57267492017-12-20 Data on the expression and role of TREM-1 in the development of in-stent restenosis Wang, Fang Li, Chang Ding, Feng Hua Shen, Ying Gao, Jie Liu, Zhu Hui Chen, Jia Wei Zhang, Rui Yan Shen, Wei Feng Wang, Xiao Qun Lu, Lin Data Brief Medicine and Dentistry The data presented in this article are related to the research article entitled “Increased serum TREM-1 level is associated with in-stent restenosis, and activation of TREM-1 promotes inflammation, proliferation and migration in vascular smooth muscle cells” (Wang et al., 2017) [1], which demonstrated that TREM-1 is expressed on vascular smooth cells (VSMCs) and promotes inflammation, proliferation and migration in cultured VSMCs. In this dataset, the expression of TREM-1 in leukocytes and endothelial cells of carotid artery after ligation was evaluated. The effect of TREM-1 on stenosis was analyzed in cultured human saphenous veins (HSVs) that spontaneously undergo remodeling which involves VSMC proliferation and migration. Elsevier 2017-11-22 /pmc/articles/PMC5726749/ /pubmed/29264376 http://dx.doi.org/10.1016/j.dib.2017.11.065 Text en © 2017 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Medicine and Dentistry
Wang, Fang
Li, Chang
Ding, Feng Hua
Shen, Ying
Gao, Jie
Liu, Zhu Hui
Chen, Jia Wei
Zhang, Rui Yan
Shen, Wei Feng
Wang, Xiao Qun
Lu, Lin
Data on the expression and role of TREM-1 in the development of in-stent restenosis
title Data on the expression and role of TREM-1 in the development of in-stent restenosis
title_full Data on the expression and role of TREM-1 in the development of in-stent restenosis
title_fullStr Data on the expression and role of TREM-1 in the development of in-stent restenosis
title_full_unstemmed Data on the expression and role of TREM-1 in the development of in-stent restenosis
title_short Data on the expression and role of TREM-1 in the development of in-stent restenosis
title_sort data on the expression and role of trem-1 in the development of in-stent restenosis
topic Medicine and Dentistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5726749/
https://www.ncbi.nlm.nih.gov/pubmed/29264376
http://dx.doi.org/10.1016/j.dib.2017.11.065
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