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Updated: Sep 21, 2025

Prediction and Validation of Gene Regulatory Elements Activated During Retinoic Acid Induced Embryonic Stem Cell Differentiation
Published on: June 21, 2016
RGDX1 X2 motif regulates integrin αvβ5 binding for pluripotent stem cell adhesion
Yuji Yamada1, Toru Onda1, Ayami Hagiuda1
1Department of Clinical Biochemistry, School of Pharmacy, Tokyo University of Pharmacy and Life Sciences, Hachioji, Japan.
Induced pluripotent stem cell (iPSC) adhesion requires specific RGDX1X2 sequences, not just RGD motifs. The X1X2 residues are crucial for binding to integrin αvβ5, influencing cell adhesion and potential applications.
Area of Science:
- Cell Biology
- Biochemistry
- Biomaterials Science
Background:
- The arginine-glycine-aspartic acid (RGD) motif is recognized for its role in cell adhesion by binding to integrins.
- While some RGD-containing peptides support embryonic stem cell and induced pluripotent stem cell (iPSC) adhesion, their activity is not universal.
Purpose of the Study:
- To investigate the influence of sequences neighboring the RGD motif on iPSC adhesion.
- To identify specific RGD-neighboring sequences essential for iPSC binding to integrins.
Main Methods:
- Utilized diverse synthetic peptides and recombinant proteins to test iPSC adhesion.
- Analyzed the role of specific RGDX1X2 sequences in binding to integrin subtypes αvβ5 and αvβ3.
Main Results:
- iPSC adhesion is dependent on RGDX1X2 sequences, such as RGDVF and RGDNY.
- The X1X2 residues are critical for adhesion mediated by integrin αvβ5, but not αvβ3.
- iPSCs express integrin αvβ5, explaining their requirement for these specific RGDX1X2 sequences.
Conclusions:
- iPSC adhesion necessitates RGDX1X2 sequences, highlighting the importance of adjacent residues for integrin binding specificity.
- The findings provide crucial insights into integrin αvβ5 ligand recognition, with potential applications in drug development, delivery, cell culture, and tissue engineering.
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