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Advancements in Bovine Organoid Technology Using Small and Large Intestinal Monolayer Interfaces
Published on: June 14, 2024
Unidirectional transport across cultured ovine amniotic epithelial cell monolayer
Cecilia Y Cheung1, Robert A Brace
1Division of Maternal-Fetal Medicine, Department of Obstetrics and Gynecology, Oregon Health and Science University, Portland, Oregon 97210, USA.
Insights
Ovine amniotic cells show specific unidirectional transport, with a 6.2:1 ratio for (14)C-inulin. This suggests passive diffusion and directional vesicular transport across the monolayer.
Area of Science:
- Reproductive biology
- Cell biology
- Physiology
Background:
- Ovine amniotic cells are crucial for placental function.
- Understanding transcellular transport mechanisms is vital for reproductive physiology.
Purpose of the Study:
- To investigate unidirectional transport in ovine amniotic cells cultured as monolayers.
- To compare in vitro transport with in vivo pathways.
Main Methods:
- Cultured ovine amniotic cells to confluence on cell culture inserts.
- Measured (14)C-inulin permeability in two directions across the cell monolayer.
- Compared permeability with chorionic cells and umbilical vein endothelial cells.
Main Results:
- Ovine amniotic cells exhibited significantly higher permeability in one direction (0.69 ± 0.17 μl/min/cm²) compared to the reverse (0.11 ± 0.02 μl/min/cm²).
- The transport ratio of 6.2:1 for (14)C-inulin was observed.
- Vascular endothelial growth factor did not affect permeability.
Conclusions:
- Transcellular transport across ovine amniotic monolayers is directionally specific.
- The observed transport ratio aligns with in vivo ovine intramembranous pathway ratios.
- Findings suggest a combination of passive diffusion and directional vesicular transport.
Objective:
To determine whether ovine amniotic cells in monolayer culture exhibit unidirectional transport.
Methods:
Permeability of (14)C-inulin was measured in two directions across ovine amniotic cells grown to confluence on cell culture inserts.
Results:
Permeability was 0.69 + 0.17 (SE) microl/min/cm(2) from the top of the insert where the cells were attached to the bottom and 0.11 + 0.02 microl/min/cm(2) in the reverse direction (P < 0.001). Permeability was similar in the two directions for chorionic cells and umbilical vein endothelial cells. Addition of vascular endothelial growth factor did not alter permeability.
Conclusions:
Transcellular transport in ovine amniotic monolayers is directionally specific. The transport ratio of 6.2:1 for (14)C-inulin is comparable to the in vivo ratio of 4.7:1 for the ovine intramembranous pathway and is consistent with passive diffusion in both directions and vesicular transport in one direction across the monolayer at 5.2 times the rate of passive diffusion.
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