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Related Concept Videos

iChip01:24

iChip

The cultivation of environmental microorganisms has long been hindered by the inability to replicate complex native conditions in vitro. The isolation chip (iChip) addresses this limitation by facilitating the growth of previously uncultivable microorganisms through in situ incubation. Designed for high-throughput microbial cultivation, the iChip comprises hundreds of microchambers, each capable of housing a single microbial cell. These microchambers are loaded with a mixture of molten agar and...

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Generation of a Human iPSC-Based Blood-Brain Barrier Chip
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An Easy-to-Use Arrayed Brain-Heart Chip.

Xiyao Peng1,2, Lei Wu1,2, Qiushi Li1

  • 1State Key Laboratory of Transducer Technology, Shanghai Institute of Microsystem and Information Technology, Chinese Academy of Sciences, Shanghai 200050, China.

Biosensors
|November 26, 2024
PubMed
Summary
This summary is machine-generated.

Researchers developed an arrayed brain-heart chip using endothelial barriers to enable organoid crosstalk. This multi-organ system successfully co-cultured brain and heart organoids, demonstrating potential for complex physiological modeling.

Keywords:
brain–heart chipcardiac organoidcerebral organoidendothelial barrierfibrin

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Area of Science:

  • Biomedical Engineering
  • Organ-on-a-chip Technology
  • Tissue Engineering

Background:

  • Multi-organ chips are crucial for emulating human physiology and inter-organ interactions.
  • Existing models often lack the complexity to replicate dynamic tissue crosstalk effectively.

Purpose of the Study:

  • To develop and validate an arrayed brain-heart chip with endothelial barriers for studying inter-organ communication.
  • To assess the stability and functionality of co-cultured cerebral and cardiac organoids within the chip.

Main Methods:

  • An arrayed chip design featuring open culture chambers and closed vascular channels separated by a fibrin-based endothelial barrier.
  • Co-culture of cerebral organoids, cardiac organoids, and endothelial cells for at least one week.
  • Numerical simulations to optimize fibrin barrier construction and experimental parameters.
  • Analysis of material transport, crosstalk, and cellular infiltration of the barrier.

Main Results:

  • Stable co-culture of cerebral organoids, cardiac organoids, and endothelial cells was achieved for over a week.
  • The endothelial barrier facilitated crosstalk, evidenced by cardiac troponin I detection in cerebral organoid chambers.
  • Cerebral organoids and endothelial cells infiltrated the fibrin matrix, indicating successful integration.
  • Numerical simulations accurately predicted experimental outcomes for barrier construction.

Conclusions:

  • The arrayed brain-heart chip effectively models inter-organ crosstalk between brain and heart organoids.
  • The endothelial barrier design is crucial for enabling controlled communication and material transport.
  • The chip's ease of use and compatibility with automation suggest significant potential for drug screening and disease modeling.