Figure 5
Figure 5. Suppressed migration of α4-R/AGFFKR T lymphocytes on VCAM-1 and MAdCAM-1 substrates. Lateral migration of T lymphocytes on VCAM-1 and MAdCAM-1 in response to chemokine CXCL12 was studied using live-cell imaging. (A) Representative confocal and DIC images of migrating cells stained for actin (Alexa 488) and α4 integrin (Cy3) are shown. (B) Morphologic analysis showing the strong presence of α4 integrin–rich trailing edge “tethers” (arrows) in α4-R/AGFFKR cells, but not WT cells, migrating on VCAM-1 and MAdCAM-1 (not shown). (C) The number of tethers per cell. Data are expressed as the mean plus or minus SEM of at least 20 cells from randomly selected fields. *P < .01 versus WT.

Suppressed migration of α4-R/AGFFKR T lymphocytes on VCAM-1 and MAdCAM-1 substrates. Lateral migration of T lymphocytes on VCAM-1 and MAdCAM-1 in response to chemokine CXCL12 was studied using live-cell imaging. (A) Representative confocal and DIC images of migrating cells stained for actin (Alexa 488) and α4 integrin (Cy3) are shown. (B) Morphologic analysis showing the strong presence of α4 integrin–rich trailing edge “tethers” (arrows) in α4-R/AGFFKR cells, but not WT cells, migrating on VCAM-1 and MAdCAM-1 (not shown). (C) The number of tethers per cell. Data are expressed as the mean plus or minus SEM of at least 20 cells from randomly selected fields. *P < .01 versus WT.

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