ArticleMicromachines2025
Development of an Easy-to-Fabricate Microdevice for Three-Dimensional Culture and Its Application to Glomerular Endothelial Cell Culture.
Article in Micromachines, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
1 citing paper in PubMed.
- Article
Corrections and comments
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Authors and funding
3 authors.
Funding
Abstract
The development of an organ-on-a-chip to reproduce organ functions requires the incorporation of a vascular network within the tissue to transport the necessary nutrients. Tissues thicker than 200 µm cannot survive without a capillary network, necessitating the construction of a vascular network exceeding that thickness. Therefore, we focused on the development of an inexpensive and easy-to-fabricate device for thick three-dimensional(3D)-cultured tissues. This device does not have a conventional pillar array structure, and the nutrient supply to the cells from adjacent media channels is not obstructed. Additionally, this device does not require expensive soft lithography equipment or a high-precision 3D printer to fabricate the mold. Human glomerular endothelial cells and human dermal fibroblasts were co-cultured using this device, and a 3D network of vascular endothelial cells (200 µm thick) was successfully constructed. The results of this study are expected to contribute not only to the study of angiogenesis, but also to the development of 3D tissue models that require the incorporation of capillary networks as well as the development of vascularized organ-on-a-chip and disease models for drug screening.
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Registered trials
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