Cardiovascular Organoids/3D Models Review Series: an Introduction.
Cardiovascular Organoids/3D Models Review Series: an Introduction.
复制标题
心血管类器官/3D 模型评论系列:简介。
DOI:
10.1161/circresaha.123.322561
复制
发表时间:
2023
影响因子:
20.1
通讯作者:
StHilaire,Cynthia
中科院分区:
文献类型:
--
作者:
StHilaire,Cynthia
Even with the vast amount of research focused on uncovering the etiology and molecular mechanisms that drive the progression of cardiovascular disease, along with concerted public health efforts to mitigate environmental contributors, and the groundbreaking drug discoveries made in recent years, heart disease is still the leading cause of death in the United States. 1 This year marks the Centennial anniversary of the founding of the American Heart Association, as well as the platinum anniversary of the publication of Circulation Research, and looking back to our first issue we see that the topics of 70 years ago are just as relevant today. The manuscripts in that first issue covered studies that investigated the differences in vasoreactivity of the vascular beds, 2 the impact of estrogen in atherosclerosis, 3 the importance of ATP in cardiac contraction, 4 and contractility of what we now know to be vascular smooth muscle cells. 5 Scrolling through these seminal studies, it is striking to see the variety of models utilized—humans, dogs, cats, and chickens—while not a single study used rodents, and the methods to culture vascular cells in vitro had not been established yet. While larger mammals more fully recapitulate human biology there are many reasons why research has moved away from them. Studies utilizing mice began in earnest in the early 1900s, but they did not become the primary in vivo system of study until the early 1990s; their advantages owing in part to the advances in genetic engineering, the relative speed of their reproduction, and lower cost and smaller footprint to house these smaller mammals. 6 Mice are still less costly and easier to house and care for than larger mammals, but they are by no means inexpensive. And in many cases, such as with monogenetic disease and age-related vascular remodeling, mice do not naturally recapitulate the pathogenesis and time course of the human maladies, 7, 8 and these differences contribute to the high failure rate of novel therapies that move from the laboratory to the clinic. 9 While animal models are indeed useful and essential tools, how can we fill in the gaps of their limitations? One answer lies in our ability to coax cells to self-assemble into 3 dimensional structures that can recapitulate human biology and physiology, which can serve as a cheaper and more efficient means for modelling vascular disease and for things like drug testing. In this review series we cover the current state of knowledge in the field of cardiovascular organoids and 3D cell culture models.
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DOI:
10.1161/atvbaha.118.311579
发表时间:
2019-03-01
影响因子:
8.7
作者:
Joolharzadeh, Pouya;St Hilaire, Cynthia
通讯作者:
St Hilaire, Cynthia
影响因子:
20.1
作者:
J. Stamler;R. Pick;L. Katz
通讯作者:
L. Katz
DOI:
--
发表时间:
2013
期刊:
Missouri medicine
影响因子:
--
作者:
Ericsson,AaronC;Crim,MarcusJ;Franklin,CraigL
通讯作者:
Franklin,CraigL
影响因子:
20.1
作者:
P. Khairallah;W. Mommaerts
通讯作者:
W. Mommaerts
影响因子:
20.1
作者:
P. Gaskell;A. C. Burton
通讯作者:
A. C. Burton