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An Increase in Endothelial Intracellular Calcium and F‐Actin Precedes the Extravasation of Interleukin‐2‐Activated Lymphocytes
Author(s) -
EHRINGER WILLIAM D.,
EDWARDS MICHAEL J.,
WINTERGERST KUPPER A.,
COX ABIGAIL,
MILLER FREDERICK N.
Publication year - 1998
Publication title -
microcirculation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.793
H-Index - 83
eISSN - 1549-8719
pISSN - 1073-9688
DOI - 10.1111/j.1549-8719.1998.tb00054.x
Subject(s) - extravasation , lymph , calcium in biology , albumin , evans blue , vascular permeability , calcium , lymphocyte , intracellular , chemistry , medicine , immunology , endocrinology , pathology , biochemistry
Objective : Interleukin‐2 (IL‐2) induces protein leakage from the microcirculation and activates lymphocytes; yet it is unclear how it alters endothelial barrier function. Here, we report of a new continuous monitoring system that allows for the continuous measurement and correlation of endothelial calcium, permeability to albumin, and extravasation of lymphocytes. Methods : IL‐2 activated lymphocytes (IL‐2 LYMPH) or unstimulated lymphocytes (LYMPH) were co‐incubated with human microvascular endothelial cells (HMVEC). Endothelial albumin permeability, lymphocyte extravasation, intracellular calcium mobilization, and f‐actin distribution were examined using a new continuous monitoring system. Results : The clearance rate of fluorescein isothiocyanate‐labeled‐human serum albumin (FITC‐HSA) in the presence of IL‐2 LYMPH peaked at 20 minutes, whereas the clearance rate of LYMPH peaked at 40 minutes. Approximately 40 minutes after the peak in the clearance rate to albumin, extravasation of carboxyfluorescein‐labeled lymphocytes was detected. Peak clearance rates for the extravasation of IL‐2 LYMPH occurred at approximately 40 minutes after the addition of the lymphocytes to the HMVEC, whereas the peak clearance rate for the LYMPH occurred at 60 minutes after their addition. Both FITC‐HSA and lymphocyte extravasation were measured concurrent to endothelial intracellular calcium mobilization by FURA‐2. There was an increase in calcium activation after the addition of IL‐2 stimulated lymphocytes (71 ± 5.1 nmol/L to 185 ± 18.9 nmol/L) compared with unstimulated lymphocytes (71 ± 5.1 nmol/L to 110 ± 12.2 nmol/L). The addition of IL‐2 had little or no effect on endothelial actin, whereas the unstimulated lymphocytes and, to a greater extent, IL‐2 LYMPH increased the presence of transversing stress fibers and decreased peripheral actin. Conclusions : The findings reported here suggest that the permeability and extravasation events that occur upon addition of lymphocytes proceeds by a calcium‐ and actin‐dependent mechanism and that incubation of lymphocytes with IL‐2 enhances normal lymphocyte mechanisms of extravasation.