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Three-dimensional (3D) in vitro cell culture models have revolutionized biomedical research by mimicking the complex 3D in vivo environment in the human body. Different types of 3D models have been established, including heterotypic systems such as, organ-on-a-chips which have been further developed into multiorgan-on-chip systems that simulate or mimic the mutual and multiplex physiological communication between (distant) organs that may not be physically connected with each other known as multiorgan crosstalk/interactions. These multiorgan interactions have been shown to be mediated by various factors including cells, soluble mediators (growth factors, cytokines etc.,) and cellular vesicles and are responsible for regulating metabolic, inflammatory, and tissue repair processes in the body. Different multiorgan-on-chip systems have been developed to mimic and study these interactions and their role in various molecular and toxicological processes. Of these, the TissUse HUMIMIC Starter and Chip microphysiological system is a commercially available multiorgan model that has been used to study inter-organ crosstalk between organs such as the gut and liver, liver and brain, liver and kidney, among others and applied in cellular, molecular and toxicology studies to among other things aid in the reduction of animals in drug and toxicological research. In this review, we provide a brief overview of multiorgan systems and summarize studies that have specifically used the TissUse system to investigate multiorgan crosstalk in the human body to deliver an update in the field of multiorgan microphysiological systems.
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http://dx.doi.org/10.1002/bit.70031 | DOI Listing |
Biotechnol Bioeng
July 2025
Department of Biology, University of British Columbia, Kelowna, BC, Canada.
Three-dimensional (3D) in vitro cell culture models have revolutionized biomedical research by mimicking the complex 3D in vivo environment in the human body. Different types of 3D models have been established, including heterotypic systems such as, organ-on-a-chips which have been further developed into multiorgan-on-chip systems that simulate or mimic the mutual and multiplex physiological communication between (distant) organs that may not be physically connected with each other known as multiorgan crosstalk/interactions. These multiorgan interactions have been shown to be mediated by various factors including cells, soluble mediators (growth factors, cytokines etc.
View Article and Find Full Text PDFSci Rep
April 2024
Department of Urology, University Medicine Greifswald, DZ7 J05.15, Fleischmannstraße 8, 17475, Greifswald, Germany.
The advent of micro-physiological systems (MPS) in biomedical research has enabled the introduction of more complex and relevant physiological into in vitro models. The recreation of complex morphological features in three-dimensional environments can recapitulate otherwise absent dynamic interactions in conventional models. In this study we developed an advanced in vitro Renal Cell Carcinoma (RCC) that mimics the interplay between healthy and malignant renal tissue.
View Article and Find Full Text PDFJ Appl Toxicol
March 2024
TissUse GmbH, Oudenarder Str. 16, D-13347, Berlin, Germany.
The HUMIMIC skin-liver Chip2 microphysiological systems model using the epidermal model, EpiDerm™, was reported previously to mimic application route-dependent metabolism of the hair dye, 4-amino-2-hydroxytoluene (AHT). Therefore, we evaluated the use of alternative skin models-SkinEthic™, EpiDermFT™ and PhenionFT™-for the same purpose. In static incubations, AHT permeation was similar using SkinEthic™ and EpiDerm™ models.
View Article and Find Full Text PDFFront Pharmacol
February 2023
Cosmetics Europe, Auderghem, Belgium.
All cosmetic ingredients registered in Europe must be evaluated for their safety using non-animal methods. Microphysiological systems (MPS) offer a more complex higher tier model to evaluate chemicals. Having established a skin and liver HUMIMIC Chip2 model demonstrating how dosing scenarios impact the kinetics of chemicals, we investigated whether thyroid follicles could be incorporated to evaluate the potential of topically applied chemicals to cause endocrine disruption.
View Article and Find Full Text PDFFront Toxicol
February 2022
Department of Molecular Cell Biology and Immunology, Amsterdam University Medical Centre, Amsterdam Infection and Immunity Institute, Vrije Universiteit Amsterdam, Amsterdam, Netherlands.
Investigating systemic toxicity is still a huge challenge. Here, a multi-organ-on-chip approach is presented as a typical case of topical exposure of oral mucosa to metals, which are known to activate the immune system and in turn may result in skin inflammation. Reconstructed human gingiva (RHG) and reconstructed human skin containing MUTZ-3-derived Langerhans cells (MUTZ-LC) in the epidermis (RHS-LC) were incorporated into a HUMIMIC Chip3plus, connected by dynamic flow and cultured for a total period of 72 h.
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