| Autor: |
An SM; Department of Chemistry, The University of British Columbia; Biochemistry and Molecular Biology, The University of British Columbia., Kim SH; Department of Chemistry, The University of British Columbia., White VJ; Department of Chemistry, The University of British Columbia; Biochemistry and Molecular Biology, The University of British Columbia., Yasunaga AB; Department of Chemistry, The University of British Columbia; Biochemistry and Molecular Biology, The University of British Columbia., McMahon KM; Biochemistry and Molecular Biology, The University of British Columbia., Murad Y; Department of Chemistry, The University of British Columbia; Faculty of Medicine, The University of British Columbia., Li ITS; Department of Chemistry, The University of British Columbia; Biochemistry and Molecular Biology, The University of British Columbia; isaac.li@ubc.ca. |
| Jazyk: |
angličtina |
| Zdroj: |
Journal of visualized experiments : JoVE [J Vis Exp] 2021 Sep 27 (175). Date of Electronic Publication: 2021 Sep 27. |
| DOI: |
10.3791/63013 |
| Abstrakt: |
Rolling adhesion, facilitated by selectin-mediated interactions, is a highly dynamic, passive motility in recruiting leukocytes to the site of inflammation. This phenomenon occurs in postcapillary venules, where blood flow pushes leukocytes in a rolling motion on the endothelial cells. Stable rolling requires a delicate balance between adhesion bond formation and their mechanically-driven dissociation, allowing the cell to remain attached to the surface while rolling in the direction of flow. Unlike other adhesion processes occurring in relatively static environments, rolling adhesion is highly dynamic as the rolling cells travel over thousands of microns at tens of microns per second. Consequently, conventional mechanobiology methods such as traction force microscopy are unsuitable for measuring the individual adhesion events and the associated molecular forces due to the short timescale and high sensitivity required. Here, we describe our latest implementation of the adhesion footprint assay to image the P-selectin: PSGL-1 interactions in rolling adhesion at the molecular level. This method utilizes irreversible DNA-based tension gauge tethers to produce a permanent history of molecular adhesion events in the form of fluorescence tracks. These tracks can be imaged in two ways: (1) stitching together thousands of diffraction-limited images to produce a large field of view, enabling the extraction of adhesion footprint of each rolling cell over thousands of microns in length, (2) performing DNA-PAINT to reconstruct super-resolution images of the fluorescence tracks within a small field of view. In this study, the adhesion footprint assay was used to study HL-60 cells rolling at different shear stresses. In doing so, we were able to image the spatial distribution of the P-selectin: PSGL-1 interaction and gain insight into their molecular forces through fluorescence intensity. Thus, this method provides the groundwork for the quantitative investigation of the various cell-surface interactions involved in rolling adhesion at the molecular level. |
| Databáze: |
MEDLINE |
| Externí odkaz: |
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