In vitro 3D co-culture model of human endothelial and smooth muscle cells to study pathological vascular remodeling

被引:0
作者
San Sebastian-Jaraba, Irene [1 ,2 ]
Fernandez-Gomez, Maria Jose [1 ]
Blazquez-Serra, Rafael [1 ,2 ]
Sanz-Andrea, Sandra [1 ]
Blanco-Colio, Luis Miguel [1 ,2 ]
Mendez-Barbero, Nerea [1 ,2 ,3 ]
机构
[1] IIS Fdn Jimenez Diaz, Lab Patol Vasc, Madrid, Spain
[2] CIBER Enfermedades Cardiovasc CIBERCV, Madrid, Spain
[3] Univ Alfonso X Sabio, Fac Med & Biomed, Madrid, Spain
来源
CLINICA E INVESTIGACION EN ARTERIOSCLEROSIS | 2024年 / 36卷 / 06期
关键词
Spheroids; Vascular remodeling; 3D; In vitro; Endothelial cells; Vascular smooth muscle cells; Cells communication;
D O I
10.1016/j.arteri.2024.03.007
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
Pathological vascular remodeling of the vessel wall refers to the structural and functional changes of the vessel wall that occur in response to injury that eventually leads to cardiovascular disease. The vessel wall is composed of two main types of cells, endothelial cells and vascular smooth muscle cells, whose communication is crucial in both the development of the vasculature and the homeostasis of mature vessels. Changes in the dialogue between endothelial cells and vascular smooth muscle cells are associated with various pathological states that triggers remodeling of the vascular wall. For many years, considerable efforts have been made to develop effective diagnoses and treatments for these pathologies by studying their mechanisms in both in vitro and in vivo models. Compared to animal models, in vitro models can provide great opportunities to obtain data in a more homogeneous, economical and massive way, providing an overview of the signaling pathways responsible for these pathologies. The implementation of three-dimensional in vitro co-culture models for the study of other pathologies has been postulated as a potentially applicable methodology, which determines the importance of its application in studies of cardiovascular diseases. In this article we present a method for culturing human endothelial cells and vascular smooth muscle cells, grown under non-adherent conditions, that generate three-dimensional spheroidal structures with greater physiological equivalence to in vivo conditions. This in vitro modeling could be used as a study tool to identify cellular and molecular mechanisms involved in the pathological processes underlying vascular remodeling. (c) 2024 The Author(s). Published by Elsevier Espana, S.L.U. on behalf of Sociedad Espanola de Arteriosclerosis. This is an open access article under the CC BY-NC-ND license (http:// creativecommons.org/licenses/by-nc-nd/4.0/).
引用
收藏
页码:356 / 363
页数:8
相关论文
共 22 条
[1]   Membrane-Tethered Metalloproteinase Expressed by Vascular Smooth Muscle Cells Limits the Progression of Proliferative Atherosclerotic Lesions [J].
Barnes, Richard H., II ;
Akama, Takeshi ;
Ohman, Miina K. ;
Woo, Moon-Sook ;
Bahr, Julian ;
Weiss, Stephen J. ;
Eitzman, Daniel T. ;
Chun, Tae-Hwa .
JOURNAL OF THE AMERICAN HEART ASSOCIATION, 2017, 6 (07)
[2]   Atherosclerosis: Recent developments [J].
Bjoerkegren, Johan L. M. ;
Lusis, Aldons J. .
CELL, 2022, 185 (10) :1630-1645
[3]   Recent Progress in in vitro Models for Atherosclerosis Studies [J].
Chen, Jun ;
Zhang, Xixi ;
Millican, Reid ;
Lynd, Tyler ;
Gangasani, Manas ;
Malhotra, Shubh ;
Sherwood, Jennifer ;
Hwang, Patrick Taejoon ;
Cho, Younghye ;
Brott, Brigitta C. ;
Qin, Gangjian ;
Jo, Hanjoong ;
Yoon, Young-sup ;
Jun, Ho-Wook .
FRONTIERS IN CARDIOVASCULAR MEDICINE, 2022, 8
[4]   Spheroid culture as a tool for creating 3D complex tissues [J].
Fennema, Eelco ;
Rivron, Nicolas ;
Rouwkema, Jeroen ;
van Blitterswijk, Clemens ;
de Boer, Jan .
TRENDS IN BIOTECHNOLOGY, 2013, 31 (02) :108-115
[5]   Extracellular Vesicles Mediate Communication between Endothelial and Vascular Smooth Muscle Cells [J].
Fontaine, Marie ;
Herkenne, Stephanie ;
Olivier, Ek ;
Paquot, Alicia ;
Boeckx, Amandine ;
Paques, Cecile ;
Nivelles, Olivier ;
Thiry, Marc ;
Struman, Ingrid .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2022, 23 (01)
[6]   Animal Models of Atherosclerosis [J].
Getz, Godfrey S. ;
Reardon, Catherine A. .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2012, 32 (05) :1104-+
[7]   Endothelial Cell Dysfunction and the Pathobiology of Atherosclerosis [J].
Gimbrone, Michael A., Jr. ;
Garcia-Cardena, Guillermo .
CIRCULATION RESEARCH, 2016, 118 (04) :620-636
[8]   Comparison of 2D-and 3D-culture models as drug-testing platforms in breast cancer [J].
Imamura, Yoshinori ;
Mukohara, Toru ;
Shimono, Yohei ;
Funakoshi, Yohei ;
Chayahara, Naoko ;
Toyoda, Masanori ;
Kiyota, Naomi ;
Takao, Shintaro ;
Kono, Seishi ;
Nakatsura, Tetsuya ;
Minami, Hironobu .
ONCOLOGY REPORTS, 2015, 33 (04) :1837-1843
[9]   Assembly of vascular smooth muscle cells in 3D aggregates provokes cellular quiescence [J].
Jaeger, Marius Andreas ;
De La Torre, Carolina ;
Arnold, Caroline ;
Kohlhaas, Johanna ;
Kappert, Lena ;
Hecker, Markus ;
Feldner, Anja ;
Korff, Thomas .
EXPERIMENTAL CELL RESEARCH, 2020, 388 (01)
[10]   Directed Flow of Micromotors through Alignment Interactions with Micropatterned Ratchets [J].
Katuri, Jaideep ;
Caballero, David ;
Voituriez, Raphael ;
Samitier, Josep ;
Sanchez, Samuel .
ACS NANO, 2018, 12 (07) :7282-7291