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Comment
. 2022 Aug 20;13(1):431.
doi: 10.1186/s13287-022-03130-5.

Towards establishing human body-on-a-chip systems

Affiliations
Comment

Towards establishing human body-on-a-chip systems

Zhong Alan Li et al. Stem Cell Res Ther. .

Abstract

Body-on-a-chip (BoC) platforms are established from multiple organs-on-chips (OoCs) to recapitulate the interactions between different tissues. Recently, Vunjak-Novakovic and colleagues reported the creation of a BoC system comprising four fluidically linked OoCs. Herein, the major innovations in their BoC system are discussed, followed by our future perspectives on enhancing the physiological relevance and scalability of BoCs for applications in studying disease mechanisms, testing potential therapeutics, and developing personalized medicine.

Keywords: Body-on-a-chip; Disease modelling; Drug testing; Microfluidic device; Organ-on-a-chip; Patient-on-a-chip; Precision medicine; Stem cell.

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Conflict of interest statement

RST is an Editor-in-Chief of Stem Cell Research and Therapy and was not involved in the peer-review or editorial handling of the manuscript. The authors have no other competing interests to disclose.

Figures

Fig. 1
Fig. 1
Representative BoC systems and future perspectives. (A) The BoC system created by Vunjak-Novakovic and colleagues: schematic of tissue components (left), the cell types utilized (middle), and validation and applications of the chip (right) [1]. NHDF: normal human dermal fibroblast; MSC: mesenchymal stromal cell; HUVEC: human umbilical venous endothelial cell. (B) A modular design approach to creating a representative six-organ BoC characterized by the sharing of a common “blood substitute”. The vascular channel is separated from the organ mimics by an endothelial barrier. (C) The application of iPSCs to generate patient-specific BoCs for personalized drug screening. By complementing the traditional drug development pipeline (conventional in vitro assays not shown) with personalized BoCs (from route ➀ route ➁), the ineffective and/or unsafe drugs for specific patients can “fail fast and fail early”, thus improving treatment outcomes at reduced costs. (D) Key considerations and technical challenges in establishing BoC systems

Comment on

  • A multi-organ chip with matured tissue niches linked by vascular flow.
    Ronaldson-Bouchard K, Teles D, Yeager K, Tavakol DN, Zhao Y, Chramiec A, Tagore S, Summers M, Stylianos S, Tamargo M, Lee BM, Halligan SP, Abaci EH, Guo Z, Jacków J, Pappalardo A, Shih J, Soni RK, Sonar S, German C, Christiano AM, Califano A, Hirschi KK, Chen CS, Przekwas A, Vunjak-Novakovic G. Ronaldson-Bouchard K, et al. Nat Biomed Eng. 2022 Apr;6(4):351-371. doi: 10.1038/s41551-022-00882-6. Epub 2022 Apr 27. Nat Biomed Eng. 2022. PMID: 35478225 Free PMC article.

References

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