<p>Panels A,B: In cytomix-stimulated PMN/PMVEC co-cultures, PMVEC permeability and PMN migration were measured in the presence vs absence of A549 cells (non-contact co-culture model). Septic PMN-dependent PMVEC hyper-permeability and trans-PMVEC PMN migration were inhibited in the presence of A549 cells. Panels C,D: Similarly, A549-CM inhibited both septic PMN-dependent PMVEC hyper-permeability and trans-PMVEC PMN migration. *: P<0.05 and **: P<0.01 vs respective control; #: P<0.05 and ##: P<0.01 vs PMVEC alone (panels A,B) or EGM-treated (panels C,D).</p
A. Transmigration of PMNs into the lumen of HIOs was quantified using flow cytometry. HIOs were micr...
<p>(A) MPCs were seeded in the upper chamber of chemotactic inserts with or without MP-conditioned m...
<p>(A) MPM cells were either untreated (Control) or treated with indicated dose of respective CFMs, ...
<p>(A) A549 cell-conditioned medium (CM) was generated by culturing A549 cells alone in Endothelial ...
<p>Conditioned medium was obtained by prior incubation of A549 cells in EGM with or without concurre...
<p>Panel A: The protective effect of A549-CM against cytomix-stimulated septic PMVEC hyper-permeabil...
<p>(A) PMVEC monolayers on the apical aspect of inserts were co-cultured with A549 cells on the unde...
<p>PMVEC on the apical aspect of inserts were stimulated with cytomix (10 ng/mL), LPS (1 µg/mL), or ...
<p>(A) PMVEC on the apical aspect of inserts were cultured for 8-hours with 20% FBS control, 20% pla...
<p>MKN45 (5x10<sup>3</sup>-1x10<sup>5</sup>) were cultured in 6-well culture plates with or without ...
<p>HUVECd were stimulated with CM-Control, CM−LPS, CM−Stx1 or CM−LPS+Stx1 for 24 h. Then, PMN were s...
<p><b>(A-D)</b> iHIOs microinjected with saline or 10<sup>3</sup> commensal bacteria or O157:H7 in t...
<p>(A, C, E) Co-culture with MCM enhanced the cell migration of LNCaP, DU145 and PC-3 cells. SmsDX s...
<p>HUVEC cells were treated with 2 µM rMASP-1, or left untreated for 30 minutes. Then, the medium wa...
<p>(A) Media alone or <i>S</i>. <i>pneumoniae-</i>containing media was added to the lower chamber of...
A. Transmigration of PMNs into the lumen of HIOs was quantified using flow cytometry. HIOs were micr...
<p>(A) MPCs were seeded in the upper chamber of chemotactic inserts with or without MP-conditioned m...
<p>(A) MPM cells were either untreated (Control) or treated with indicated dose of respective CFMs, ...
<p>(A) A549 cell-conditioned medium (CM) was generated by culturing A549 cells alone in Endothelial ...
<p>Conditioned medium was obtained by prior incubation of A549 cells in EGM with or without concurre...
<p>Panel A: The protective effect of A549-CM against cytomix-stimulated septic PMVEC hyper-permeabil...
<p>(A) PMVEC monolayers on the apical aspect of inserts were co-cultured with A549 cells on the unde...
<p>PMVEC on the apical aspect of inserts were stimulated with cytomix (10 ng/mL), LPS (1 µg/mL), or ...
<p>(A) PMVEC on the apical aspect of inserts were cultured for 8-hours with 20% FBS control, 20% pla...
<p>MKN45 (5x10<sup>3</sup>-1x10<sup>5</sup>) were cultured in 6-well culture plates with or without ...
<p>HUVECd were stimulated with CM-Control, CM−LPS, CM−Stx1 or CM−LPS+Stx1 for 24 h. Then, PMN were s...
<p><b>(A-D)</b> iHIOs microinjected with saline or 10<sup>3</sup> commensal bacteria or O157:H7 in t...
<p>(A, C, E) Co-culture with MCM enhanced the cell migration of LNCaP, DU145 and PC-3 cells. SmsDX s...
<p>HUVEC cells were treated with 2 µM rMASP-1, or left untreated for 30 minutes. Then, the medium wa...
<p>(A) Media alone or <i>S</i>. <i>pneumoniae-</i>containing media was added to the lower chamber of...
A. Transmigration of PMNs into the lumen of HIOs was quantified using flow cytometry. HIOs were micr...
<p>(A) MPCs were seeded in the upper chamber of chemotactic inserts with or without MP-conditioned m...
<p>(A) MPM cells were either untreated (Control) or treated with indicated dose of respective CFMs, ...