Skip to content
DraconiticResearch
Search Sources API
186,546 studies31 sourcesUpdated 14 min ago
PreprintCC BYChemRxiv

Parallel Production of Uniform Artificial Multicellular Models Using Vibration-Induced Local Microvortices

  1. 1Graduate School of Science and Engineering, Chuo University, 1-13-27 Kasuga, Bunkyo-ku, Tokyo, Japan, 112-8551
  2. 2Earth-Life Science Institute (ELSI, Institute of Science Tokyo, 2-12-1 Ookayama, Meguro-ku, Tokyo, Japan, 152-8550

Abstract

In this study, we propose a facile and efficient method for constructing artificial multicellular models via vibration-induced flow (VIF), a local fluid flow induced around vibrating microstructures. By applying circular vibration to a substrate with a cylindrical micropillar array, uniform micro-vortices were generated, into which giant unilamellar vesicles (GUVs), as artificial cells, rapidly accumulated at the center. We show that by modifying two GUV populations with complementary single-stranded DNAs, we can promote specific adhesion between GUVs, leading to uniform parallel aggregates. Furthermore, the pillar-array design controls the size of GUV aggregates. Finally, we embedded nanopore-forming α-hemolysin with Spytag and SpyCatcher system in GUV populations, allowing the lumens of assembled GUVs to channel with one another and enable close-proximity molecular communication. This technology will contribute to future research on fabricating artificial multicellular models with complex functions.

Related

  1. Toward transgenic multicellular parasites: CRISPR-Cas12a germline editing of Schistosoma mansoni eggs as key to success
    Max F. Moescheid, Prapakorn Wisitpongpun, Vanessa Gross +7
    Science AdvancesPeer-reviewedCC BYMolecular biology & gene regulationCrossref
  2. Integrated Spatial and Bulk Transcriptomic Analysis Identifies a Multicellular Ecosystem Involved in Progression of Young Breast Cancer.
    Xiaolin Chen, Zhuozhi Liang, Xinming Chen +5
    Cancer medicinePeer-reviewedCC BY-NC-NDFull textMolecular biology & gene regulationEurope PMCDOAJ
  3. A mechanical model of multicellular remodelling in epithelial monolayers
    James Osborne, Reuben van Ammers, Yohan Davit +2
    HALPreprintCC BY 4.0Full textBiophysicsGeneral biologyHALbioRxiv
  4. The transcription factor PRO44 and the histone chaperone ASF1 regulate distinct aspects of multicellular development in the filamentous fungus Sordaria macrospora.
    Schumacher Di, Lütkenhaus R, Altegoer F +3
    BMC GeneticsPeer-reviewedCC BYFull text19 citedMolecular biology & gene regulationHAL
  5. Controlled Assembly and In Situ Reconfiguration of Multiphase DNA Droplets in a Vibration-Induced Local Vortex Microfluidic Platform
    Zhitai Huang, Naoki Asai, Tomoya Maruyama +2
    ChemRxivPreprintCC BYFull textMolecular biology & gene regulationChemRxiv
BibTeX
@misc{miyashita2026parallel,
  title = {{Parallel Production of Uniform Artificial Multicellular Models Using Vibration-Induced Local Microvortices}},
  author = {Daiki Miyashita and Yui Katsumata and Xu Han and Zhitai Huang and Mamiko Tsugane and Tomoaki Matsuura and Hiroaki Suzuki},
  howpublished = {ChemRxiv},
  year = {2026},
  month = oct,
  doi = {10.26434/chemrxiv.15010019/v1},
  url = {https://chemrxiv.org/doi/full/10.26434/chemrxiv.15010019/v1},
  note = {CC BY},
}
RIS
TY  - UNPB
TI  - Parallel Production of Uniform Artificial Multicellular Models Using Vibration-Induced Local Microvortices
AU  - Daiki Miyashita
AU  - Yui Katsumata
AU  - Xu Han
AU  - Zhitai Huang
AU  - Mamiko Tsugane
AU  - Tomoaki Matsuura
AU  - Hiroaki Suzuki
PY  - 2026
DA  - 2026/10/07
PB  - ChemRxiv
DO  - 10.26434/chemrxiv.15010019/v1
UR  - https://chemrxiv.org/doi/full/10.26434/chemrxiv.15010019/v1
AB  - In this study, we propose a facile and efficient method for constructing artificial multicellular models via vibration-induced flow (VIF), a local fluid flow induced around vibrating microstructures. By applying circular vibration to a substrate with a cylindrical micropillar array, uniform micro-vortices were generated, into which giant unilamellar vesicles (GUVs), as artificial cells, rapidly accumulated at the center. We show that by modifying two GUV populations with complementary single-stranded DNAs, we can promote specific adhesion between GUVs, leading to uniform parallel aggregates. Furthermore, the pillar-array design controls the size of GUV aggregates. Finally, we embedded nanopore-forming α-hemolysin with Spytag and SpyCatcher system in GUV populations, allowing the lumens of assembled GUVs to channel with one another and enable close-proximity molecular communication. This technology will contribute to future research on fabricating artificial multicellular models with complex functions.
ER  -