Characterization of Endothelial and Smooth Muscle Cells From Different Canine Vessels

被引:21
作者
Oosterhoff, Loes A. [1 ]
Kruitwagen, Hedwig S. [1 ]
van Wolferen, Monique E. [1 ]
van Balkom, Bas W. M. [2 ]
Mokry, Michal [3 ,4 ]
Lansu, Nico [3 ,4 ]
van den Dungen, Noortje A. M. [4 ,5 ]
Penning, Louis C. [1 ]
Spanjersberg, Talitha C. F. [1 ]
de Graaf, Johannes W. [1 ]
Veenendaal, Tomas [1 ]
Zomerdijk, Flin [1 ]
Fledderus, Joost O. [2 ]
Spee, Bart [1 ]
van Steenbeek, Frank G. [1 ]
机构
[1] Univ Utrecht, Fac Vet Med, Dept Clin Sci Compan Anim, Utrecht, Netherlands
[2] Univ Med Ctr Utrecht, Div Internal Med & Dermatol, Nephrol & Hypertens, Utrecht, Netherlands
[3] Univ Med Ctr Utrecht, Wilhelmina Childrens Hosp, Div Pediat, Utrecht, Netherlands
[4] Univ Med Ctr Utrecht, Epigen Facil, Utrecht, Netherlands
[5] Univ Med Ctr Utrecht, Div Heart & Lungs, Dept Cardiol, Utrecht, Netherlands
来源
FRONTIERS IN PHYSIOLOGY | 2019年 / 10卷
关键词
angiogenesis; cell model system; endothelial cells; vascular cell interaction; vascular smooth muscle cells; STEM-CELLS; DUCTUS-ARTERIOSUS; IN-VIVO; ANGIOGENESIS; EXPRESSION; COCULTURE; FIBROBLASTS; MODEL; TOOL; RNA;
D O I
10.3389/fphys.2019.00101
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Vasculature performs a critical function in tissue homeostasis, supply of oxygen and nutrients, and the removal of metabolic waste products. Vascular problems are implicated in a large variety of pathologies and accurate in vitro models resembling native vasculature are of great importance. Unfortunately, existing in vitro models do not sufficiently reflect their in vivo counterpart. The complexity of vasculature requires the examination of multiple cell types including endothelial cells (ECs) and vascular smooth muscle cells (VSMCs), as well as vessel location in the body from which they originate. The use of canine blood vessels provides a way to study vasculature with similar vessel size and physiology compared to human vasculature. We report an isolation procedure that provides the possibility to isolate both the endothelial and smooth muscle cells from the same vessels simultaneously, enabling new opportunities in investigating vasculature behavior. Canine primary ECs and VSMCs were isolated from the vena cava, vena porta and aorta. All tissue sources were derived from three donors for accurate comparison and to reduce inter-animal variation. The isolation and purification of the two distinct cell types was confirmed by morphology, gene- and protein-expression and function. As both cell types can be derived from the same vessel, this approach allows accurate modeling of vascular diseases and can also be used more widely, for example, in vascular bioreactors and tissue engineering designs. Additionally, we identified several new genes that were highly expressed in canine ECs, which may become candidate genes for novel EC markers. In addition, we observed transcriptional and functional differences between arterial- and venous-derived endothelium. Further exploration of the transcriptome and physiology of arteriovenous differentiation of primary cells may have important implications for a better understanding of the fundamental behavior of the vasculature and pathogenesis of vascular disease.
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页数:11
相关论文
共 51 条
  • [1] Phenotypic heterogeneity of the endothelium II. Representative vascular beds
    Aird, William C.
    [J]. CIRCULATION RESEARCH, 2007, 100 (02) : 174 - 190
  • [2] HTSeq-a Python']Python framework to work with high-throughput sequencing data
    Anders, Simon
    Pyl, Paul Theodor
    Huber, Wolfgang
    [J]. BIOINFORMATICS, 2015, 31 (02) : 166 - 169
  • [3] Unraveling a novel transcription factor code determining the human arterial-specific endothelial cell signature
    Aranguren, Xabier L.
    Agirre, Xabier
    Beerens, Manu
    Coppiello, Giulia
    Uriz, Maialen
    Vandersmissen, Ine
    Benkheil, Mohammed
    Panadero, Joaquin
    Aguado, Natalia
    Pascual-Montano, Alberto
    Segura, Victor
    Prosper, Felipe
    Luttun, Aernout
    [J]. BLOOD, 2013, 122 (24) : 3982 - 3992
  • [4] Gene Ontology: tool for the unification of biology
    Ashburner, M
    Ball, CA
    Blake, JA
    Botstein, D
    Butler, H
    Cherry, JM
    Davis, AP
    Dolinski, K
    Dwight, SS
    Eppig, JT
    Harris, MA
    Hill, DP
    Issel-Tarver, L
    Kasarskis, A
    Lewis, S
    Matese, JC
    Richardson, JE
    Ringwald, M
    Rubin, GM
    Sherlock, G
    [J]. NATURE GENETICS, 2000, 25 (01) : 25 - 29
  • [5] Isolation and comparative analysis of potential stem/progenitor cells from different regions of human umbilical cord
    Beeravolu, Naimisha
    Khan, Irfan
    McKee, Christina
    Dinda, Sumi
    Thibodeau, Bryan
    Wilson, George
    Perez-Cruet, Mick
    Bahado-Singh, Ray
    Chaudhry, G. Rasul
    [J]. STEM CELL RESEARCH, 2016, 16 (03) : 696 - 711
  • [6] ToppGene Suite for gene list enrichment analysis and candidate gene prioritization
    Chen, Jing
    Bardes, Eric E.
    Aronow, Bruce J.
    Jegga, Anil G.
    [J]. NUCLEIC ACIDS RESEARCH, 2009, 37 : W305 - W311
  • [7] Cheung JWC, 2015, TISSUE ENG PT A, V21, P1587, DOI [10.1089/ten.tea.2014.0548, 10.1089/ten.TEA.2014.0548]
  • [8] Epidemiology, presentation and population genetics of patent ductus arteriosus (PDA) in the Dutch Stabyhoun dog
    den Toom, Marjolein L.
    Meiling, Agnes E.
    Thomas, Rachel E.
    Leegwater, Peter A. J.
    Heuven, Henri C. M.
    [J]. BMC VETERINARY RESEARCH, 2016, 12
  • [9] STAR: ultrafast universal RNA-seq aligner
    Dobin, Alexander
    Davis, Carrie A.
    Schlesinger, Felix
    Drenkow, Jorg
    Zaleski, Chris
    Jha, Sonali
    Batut, Philippe
    Chaisson, Mark
    Gingeras, Thomas R.
    [J]. BIOINFORMATICS, 2013, 29 (01) : 15 - 21
  • [10] DOT1L promotes angiogenesis through cooperative regulation of VEGFR2 with ETS-1
    Duan, Yang
    Wu, Xue
    Zhao, Qiang
    Gao, Jie
    Huo, Dawei
    Liu, Xinhua
    Ye, Zheng
    Dong, Xu
    Fu, Zheng
    Shang, Yongfeng
    Xuan, Chenghao
    [J]. ONCOTARGET, 2016, 7 (43): : 69674 - 69687