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Standardizing designed and emergent quantitative features in microphysiological systems

delete2024-08-26
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PRE
AI
D
Dennis M. Nahon
R
Renée Moerkens
H
Hande Aydoğmuş
B
Bas Lendemeijer
A
Adriana Martínez-Silgado
J
Jeroen M. Stein
M
Milica Dostanić
J
Jean‐Philippe Frimat
C
Cristina Gontan
M
Mees N. S. de Graaf
M
Michel Hu
D
Dhanesh G. Kasi
L
Lena Sophie Koch
K
Kieu T. T. Le
S
Sangho Lim
H
Heleen Middelkamp
J
Joram Mooiweer
P
Paul Motreuil-Ragot
E
Eva Niggl
C
Cayetano Pleguezuelos‐Manzano
J
Jens Puschhof
N
Nele Revyn
J
José M. Rivera‐Arbeláez
J
Jelle Slager
L
Laura M. Windt
M
Mariia Zakharova
B
Berend J. van Meer
V
Valeria V. Orlova
F
Femke M.S. de Vrij
S
Sebo Withoff
M
Massimo Mastrangeli
A
Andries D. van der Meer
C
Christine L. Mummery *
DOI:10.1038/s41551-024-01236-0delete
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摘要

摘要

En 中文
Microphysiological systems (MPSs) are cellular models that replicate aspects of organ and tissue functions in vitro. In contrast with conventional cell cultures, MPSs often provide physiological mechanical cues to cells, include fluid flow and can be interlinked (hence, they are often referred to as microfluidic tissue chips or organs-on-chips). Here, by means of examples of MPSs of the vascular system, intestine, brain and heart, we advocate for the development of standards that allow for comparisons of quantitative physiological features in MPSs and humans. Such standards should ensure that the in vivo relevance and predictive value of MPSs can be properly assessed as fit-for-purpose in specific applications, such as the assessment of drug toxicity, the identification of therapeutics or the understanding of human physiology or disease. Specifically, we distinguish designed features, which can be controlled via the design of the MPS, from emergent features, which describe cellular function, and propose methods for improving MPSs with readouts and sensors for the quantitative monitoring of complex physiology towards enabling wider end-user adoption and regulatory acceptance. This Perspective discusses the need for standards that allow for comparisons of quantitative physiological features in microphysiological systems and humans.
Keyword:
ON-A-CHIP
BLOOD-BRAIN-BARRIER
IN-VITRO
IMPEDANCE SPECTROSCOPY
MICROFLUIDIC PLATFORM
THERMOPLASTIC ELASTOMER
INTESTINAL VILLI
HIGH-THROUGHPUT
CELL-MIGRATION
MODEL

期刊

Nature Biomedical Engineering 封面图
Nature Biomedical Engineering
IF:
26.6
论文数:
1.7K
被引数:
2.0W

机构

D
Delft University of Technology
学者数:
2.6W
论文数: 2.5W
被引数: 3.8W
L
leiden university - excl lumc
学者数:
3.5W
论文数: 2.9W
被引数: 46
L
leiden university medical center (lumc)
学者数:
1.9W
论文数: 1.5W
被引数: 12
U
University of Groningen
学者数:
4.4W
论文数: 4.3W
被引数: 5.9W
L
Leiden University
学者数:
4.0W
论文数: 3.3W
被引数: 3.8W
E
Erasmus MC
学者数:
2.9W
论文数: 2.5W
被引数: 3.4W
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