Microphysiological Systems to Recapitulate the Gut–Kidney Axis

Laura Giordano, Silvia Maria Mihaila, Hossein Eslami Amirabadi, Rosalinde Masereeuw (Corresponding author)

Research output: Contribution to journalArticleAcademicpeer-review

49 Citations (Scopus)
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Abstract

Chronic kidney disease (CKD) typically appears alongside other comorbidities, highlighting an underlying complex pathophysiology that is thought to be vastly modulated by the bidirectional gut–kidney crosstalk. By combining advances in tissue engineering, biofabrication, microfluidics, and biosensors, microphysiological systems (MPSs) have emerged as promising approaches for emulating the in vitro interconnection of multiple organs, while addressing the limitations of animal models. Mimicking the (patho)physiological states of the gut–kidney axis in vitro requires an MPS that can simulate not only this direct bidirectional crosstalk but also the contributions of other physiological participants such as the liver and the immune system. We discuss recent developments in the field that could potentially lead to in vitro modeling of the gut–kidney axis in CKD.
Original languageEnglish
Pages (from-to)811-823
Number of pages13
JournalTrends in Biotechnology
Volume39
Issue number8
DOIs
Publication statusPublished - Aug 2021
Externally publishedYes

Funding

FundersFunder number
European Union's Horizon 2020 - Research and Innovation Framework Programme860329, STRATEGY-CKD H2020-2019-ETN
Marie Skłodowska‐Curie

    Keywords

    • chronic kidney disease
    • gut–kidney axis
    • microphysiological systems
    • remote signaling
    • uremic toxins

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