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Updated: Sep 20, 2026

Isolation of Group 2 Innate Lymphoid Cells from Mouse Nasal Mucosa to Detect the Expression of CD226
Published on: May 10, 2022
The expression, regulation and adhesion function of a novel CD molecule, CD226, on human endothelial cells
Lihua Chen1, Xin Xie, Xinhai Zhang
1Department of Immunology, the Fourth Military Medical University, Xi'an 710032, People's Republic of China.
Insights
CD226 is a novel inducible adhesion molecule found on human endothelial cells. Its expression increases upon cell stimulation, playing a role in cell adhesion processes.
Area of Science:
- Immunology
- Cell Biology
- Molecular Biology
Background:
- CD226 is a transmembrane glycoprotein expressed on immune cells like T cells and NK cells.
- It plays a role in immune cell differentiation and platelet activation.
Purpose of the Study:
- To investigate the expression and function of CD226 on human endothelial cells.
- To determine if CD226 acts as an adhesion molecule in endothelial cells.
Main Methods:
- Studied CD226 protein and mRNA expression in resting and stimulated HUVEC and ECV304 cells.
- Utilized CD226/Ig fusion protein to block binding and adhesion assays.
Main Results:
- CD226 expression was low in resting endothelial cells but significantly increased upon stimulation.
- CD226/Ig fusion protein partially blocked the binding of activated endothelial cells to Jurkat cells.
- CD226/Ig also partially inhibited the adhesion of activated endothelial cells to leukocytes and colo205 cells.
Conclusions:
- Activated human endothelial cells express high levels of CD226.
- CD226 functions as an inducible adhesion molecule on endothelial cells, mediating interactions with other cells.
Abstract:
CD226 is a 67 kDa type I transmembrane glycoprotein mainly expressed on activated T cells, NK cells and platelets, and involved in the differentiation of cytotoxic T lymphocytes (CTL) and NK, as well as platelet activation and aggregation. Here we found that the expression of CD226 protein and CD226mRNA were very weak in resting HUVEC and ECV304 cells, whereas high level expression could be observed when these cells were stimulated. The binding activities between activated endothelial cells and activated Jurkat cells could be partly blocked by CD226/Ig fusion protein. Similarly, CD226/Ig could also partly block the adhesion between activated endothelial cells and some leukocytes or colo205 cells. These data provided the evidence that activated endothelial cells could express high level of CD226, and CD226 was involved in the endothelial cells' adhesion. The above findings suggested that CD226 is a novel inducible adhesion molecule on human endothelial cells.
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