Abstract
Organ-on-Chip (OoC) systems are advanced in vitro models containing compartments and microchannels
in which the in vivo characteristics of the microenvironment of human organs are emulated
to enhance physiological relevance. OoC models often include microchannel-based vessels and
ducts with rectangular cross-sections, and therefore these lack the geometry and morphology found
in tubular structures in vivo. Channels with round cross sections can better mimic the physiology
and cellular behavior of tubular structures, such as (micro)vessels and breast ducts, via providing
a more in vivo-like geometry and a uniform wall shear stress under physiological flow conditions.
Here, we utilize femtosecond laser machining to integrate tubular lumens in an Organ-on-Chip device;
our "Lumina-Chip" contains two tubular lumens, both connected to a central channel along
their entire length. This versatile fabrication technique enables us to obtain a medium-throughput
version of the device including nine Lumina-Chips. Compared with rectangular channels, culture of
endothelial cells in our tubular channels results in better cell coverage along the entire channel cross
section and therefore better integrity of the endothelium, as well as in different cell morphology and
alignment due to the channel curvature. Permeability analysis shows that the vessel wall in the
Lumina-Chip has good barrier functionality. We demonstrate the we can use the Lumina-Chip to
mimic and observe breast cancer invasion from a breast duct (formed in the first lumen, lined with
normal epithelial cells), into extracellular matrix (formed by collagen I in the central channel), and
subsequent intravasation into a vessel (formed in the second lumen, lined with endothelial cells).
Two types of cancer cells (invasive and non-invasive) show distinctly different behavior throughout
this process. We demonstrate our model with cancer metastasis, but it also can be useful for other
biological applications in which epithelial ducts and vessels are essential components.
Supplementary materials
Title
Supplementary Figure 1
Description
Gaps between cells and sharp edges in the channel with a rectangular cross-section. Combined fluorescent images of HUVECs stained for cell nuclei (cyan), CD31 (green) and F-actin (red), that were residing after six days of static culture in the bottom the rectangular channel. Arrows show F-actin stress fibers that appear more intensely in the cells around the gaps. Scale bars, 30 μm
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Supplementary Figure 2
Description
Invasion experiments conditions and their corresponding time window. a-d, different culture conditions for invasion
experiments, including, a, tumoroid invasion, b, tumoroid invasion in co-culture with a vessel, c, tumoroid invasion from an epithelial duct, and d, tumoroid invasion from an epithelial duct in co-culture with a vessel. e, Time windows for different culture conditions in the invasion experiments.
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Supplementary Figure 3
Description
MCF-7 tumoroid behavior in the ductal lumen, in co-culture with HUVECs. Phase contrast and fluorescent images
represent MCF-7 cells (red) in the ductal lumen, slightly pushing into the collagen I after filling in the channel (DCIS), while HUVECs line the the other lumen. a-b and c-d show examples of region of interest in two chips. Scale bars, 200 μm.
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Supplementary Figure 4
Description
Mesh configuration for the cross-section of the Lumina-Chip. A total of 250k unstructured tetrahedral grids were generated in the computational domain
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Supplementary video 1
Description
Time-lapse video of HUVECs at the bottom of channel with circular cross-section in static culture. HUVECs move in the circumferential direction.
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Supplementary video 2
Description
Time-lapse video of cancer cell intravasation. A single MDA-MB-231 cell, after invasion from an epithelial protrusion, intravasates into the vessel. Two HUVECs open
the way for the traverse of the cancer cell.
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Fig.5
Description
Caption of Figure 5 is not completely shown in the template. Here you find the complete caption.
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