Characterization exploration of endothelial progenitor cells from bovine bone marrow

Objective: This research is designed to explore the methods of isolation and culture for endothelial progenitor cells from bovine bone marrow, characteristic, induced differentiative capacity in vitro. Material and methods: Main experimental reagents contain DMEM/F12, fetal bovine serum, percoll ly...

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Main Authors: Mingming Ning, Chunyu Bai, Yujiao Sun, Xiuxia Li, Weijun Guan
Format: Article
Language:English
Published: Network for the Veterinarians of Bangladesh 2017-03-01
Series:Journal of Advanced Veterinary and Animal Research
Subjects:
Online Access:http://www.ejmanager.com/fulltextpdf.php?mno=256929
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spelling doaj-bcd7d0b4df174f60a05b5ac42ee8fcb12020-11-25T01:02:25ZengNetwork for the Veterinarians of BangladeshJournal of Advanced Veterinary and Animal Research2311-77102017-03-0141889610.5455/javar.2017.d196256929Characterization exploration of endothelial progenitor cells from bovine bone marrowMingming Ning0Chunyu Bai1Yujiao Sun2Xiuxia Li3Weijun Guan4Institute of Animal Sciences, Chinese Academy of Agricultural Sciences, Beijing 100193, China Institute of Animal Sciences, Chinese Academy of Agricultural Sciences, Beijing 100193, China Institute of Animal Sciences, Chinese Academy of Agricultural Sciences, Beijing 100193, China College of Life Science, Jiamusi University, Jiamusi 154007, China Institute of Animal Sciences, Chinese Academy of Agricultural Sciences, Beijing 100193, ChinaObjective: This research is designed to explore the methods of isolation and culture for endothelial progenitor cells from bovine bone marrow, characteristic, induced differentiative capacity in vitro. Material and methods: Main experimental reagents contain DMEM/F12, fetal bovine serum, percoll lymphocyte separating, Trypsin 1: 250, VEGF, bFGF, GF-1, EDTA and so on. Cultivation system is DMEM/F12 with 10% FBS and VEGF 10 ng/mL, cultured under 37°C, 5% CO2, saturated humidity. Cell viability is measured by trypan blue solution exclusion test. Immunofluorescent detection is used to detected cell surface markers and double swallows, while bovine chromosome is analyzed by karyotyping. Results: We find that the majority of bovine endothelial progenitor cells (EPCs) are fibrous shaped. Frozen survival of bovine EPCs before and after cryopreservation is 95.2±0.14% and 80.9±0.30% respectively; cryopreservation affects little on the viability of bovine EPCs. Immunofluorescent detection of the cell surface markers CD34, CD133 and flk present positive, which can confirm that the cell cultured in vitro are EPCs. Then Dil-ac-LDL and FITC-UAE-1 uptake assays are carried out. Eventually, bovine EPCs are induced to differentiate into endothelial cells and smooth muscle cells respectively, demonstrating the multi-lineage differentiation potential of bovine EPCs in vitro. Conclusion: EPCs can be got with proper culture system. The little cell cryopreservation effect and stronger induced differentiation potential in vitro imply that EPCs can be applied in genetic resources conservation and reuse. [J Adv Vet Anim Res 2017; 4(1.000): 88-96]http://www.ejmanager.com/fulltextpdf.php?mno=256929Bovine; Bone marrow; EPCs; Culture
collection DOAJ
language English
format Article
sources DOAJ
author Mingming Ning
Chunyu Bai
Yujiao Sun
Xiuxia Li
Weijun Guan
spellingShingle Mingming Ning
Chunyu Bai
Yujiao Sun
Xiuxia Li
Weijun Guan
Characterization exploration of endothelial progenitor cells from bovine bone marrow
Journal of Advanced Veterinary and Animal Research
Bovine; Bone marrow; EPCs; Culture
author_facet Mingming Ning
Chunyu Bai
Yujiao Sun
Xiuxia Li
Weijun Guan
author_sort Mingming Ning
title Characterization exploration of endothelial progenitor cells from bovine bone marrow
title_short Characterization exploration of endothelial progenitor cells from bovine bone marrow
title_full Characterization exploration of endothelial progenitor cells from bovine bone marrow
title_fullStr Characterization exploration of endothelial progenitor cells from bovine bone marrow
title_full_unstemmed Characterization exploration of endothelial progenitor cells from bovine bone marrow
title_sort characterization exploration of endothelial progenitor cells from bovine bone marrow
publisher Network for the Veterinarians of Bangladesh
series Journal of Advanced Veterinary and Animal Research
issn 2311-7710
publishDate 2017-03-01
description Objective: This research is designed to explore the methods of isolation and culture for endothelial progenitor cells from bovine bone marrow, characteristic, induced differentiative capacity in vitro. Material and methods: Main experimental reagents contain DMEM/F12, fetal bovine serum, percoll lymphocyte separating, Trypsin 1: 250, VEGF, bFGF, GF-1, EDTA and so on. Cultivation system is DMEM/F12 with 10% FBS and VEGF 10 ng/mL, cultured under 37°C, 5% CO2, saturated humidity. Cell viability is measured by trypan blue solution exclusion test. Immunofluorescent detection is used to detected cell surface markers and double swallows, while bovine chromosome is analyzed by karyotyping. Results: We find that the majority of bovine endothelial progenitor cells (EPCs) are fibrous shaped. Frozen survival of bovine EPCs before and after cryopreservation is 95.2±0.14% and 80.9±0.30% respectively; cryopreservation affects little on the viability of bovine EPCs. Immunofluorescent detection of the cell surface markers CD34, CD133 and flk present positive, which can confirm that the cell cultured in vitro are EPCs. Then Dil-ac-LDL and FITC-UAE-1 uptake assays are carried out. Eventually, bovine EPCs are induced to differentiate into endothelial cells and smooth muscle cells respectively, demonstrating the multi-lineage differentiation potential of bovine EPCs in vitro. Conclusion: EPCs can be got with proper culture system. The little cell cryopreservation effect and stronger induced differentiation potential in vitro imply that EPCs can be applied in genetic resources conservation and reuse. [J Adv Vet Anim Res 2017; 4(1.000): 88-96]
topic Bovine; Bone marrow; EPCs; Culture
url http://www.ejmanager.com/fulltextpdf.php?mno=256929
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