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Updated: Oct 1, 2026

Rat Mesentery Angiogenesis Assay
Published on: June 18, 2011
Leukocyte function-associated antigen-1-dependent adhesion of rat ascites hepatoma AH66F to mesentery-derived
M Nomura1, H Yamamoto, N Sugiura
1Research Laboratory for Development of Medicine, Faculty of Pharmaceutical Sciences, Hokuriku University.
Abstract:
Rat ascites hepatoma AH66F cells adhered better than AH130 cells to mesentery-derived mesothelial cells (M-cells), though both cells secreted Mr 92,000 matrix metalloproteinase on a gelatin zymogram with similar activity. AH66F cells expressed leukocyte function-associated antigen-1 (LFA-1) and intercellular adhesion molecule-1 (ICAM-1), a ligand of LFA-1, on the cell surface, while AH130 cells had ICAM-1 alone. The adhesion of M-cells of AH66F cells was inhibited to the adhesion level of AH130 cells by anti-rat LFA-1 alpha -and/or beta-chain monoclonal antibody (mAb) and also by anti-rat ICAM-1 mAb. This is the first report to show the LFA-1-dependent adhesion of cells other than leukocytes, because AH66F cells did not express CD45, T cell-alpha beta receptor or Cd11b/c (Mac-1/p150,95). These results indicate that a part of the adhesion of AH66F cells to M-cells is due to LFA-1/ICAM-1 interaction, and we suggest that this characteristic feature of AH66F cells may be related to the malignant properties.
Insights
Rat hepatoma cells show distinct adhesion properties. AH66F cells, expressing leukocyte function-associated antigen-1 (LFA-1) and intercellular adhesion molecule-1 (ICAM-1), adhere more strongly to mesothelial cells than AH130 cells, which express only ICAM-1.
Area of Science:
- Cell Biology
- Oncology
- Immunology
Background:
- Mesothelial cells form a crucial barrier in the peritoneum.
- Cancer cell adhesion plays a role in metastasis.
- Leukocyte adhesion molecules are typically found on immune cells.
Purpose of the Study:
- To investigate the adhesion mechanisms of rat ascites hepatoma cells (AH66F and AH130) to mesentery-derived mesothelial cells (M-cells).
- To determine the role of specific adhesion molecules, including leukocyte function-associated antigen-1 (LFA-1) and intercellular adhesion molecule-1 (ICAM-1), in this interaction.
- To identify novel adhesion pathways in non-leukocyte cancer cells.
Main Methods:
- Comparing the adhesion of AH66F and AH130 cells to M-cells in vitro.
- Analyzing the expression of LFA-1 and ICAM-1 on hepatoma cells using cell surface markers.
- Utilizing monoclonal antibodies (mAbs) against LFA-1 and ICAM-1 to block adhesion.
- Assessing the expression of typical leukocyte markers (CD45, T cell receptor, CD11b/c) on hepatoma cells.
Main Results:
- AH66F cells exhibited significantly higher adhesion to M-cells compared to AH130 cells.
- AH66F cells expressed both LFA-1 and ICAM-1, while AH130 cells expressed only ICAM-1.
- Blocking LFA-1 and/or ICAM-1 with mAbs reduced AH66F cell adhesion to levels similar to AH130 cells.
- AH66F cells did not express standard leukocyte markers, indicating a non-leukocyte LFA-1-dependent adhesion.
Conclusions:
- A portion of AH66F cell adhesion to M-cells is mediated by the LFA-1/ICAM-1 pathway.
- This study demonstrates LFA-1-dependent adhesion in non-leukocyte cancer cells for the first time.
- The unique adhesion characteristics of AH66F cells may contribute to their malignant properties and potential for peritoneal spread.
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