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Lipopolysaccharide activation of pericyte’s Toll-like receptor-4 regulates co-culture permeability

Abstract Background Pericytes (PCs) have a synergistic relationship with endothelial cells (MVEC) in regulating capillary permeability. PCs express Toll-like receptor-4 (TLR-4). We hypothesize one mechanism of MVEC/PC co-culture permeability is regulated through lipopolysaccharide (LPS) activation o...

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Published in:The American journal of surgery 2007-06, Vol.193 (6), p.730-735
Main Authors: Edelman, David A., M.D, Jiang, Yang, M.D, Tyburski, James G., M.D, Wilson, Robert F., M.D, Steffes, Christopher P., M.D
Format: Article
Language:English
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Summary:Abstract Background Pericytes (PCs) have a synergistic relationship with endothelial cells (MVEC) in regulating capillary permeability. PCs express Toll-like receptor-4 (TLR-4). We hypothesize one mechanism of MVEC/PC co-culture permeability is regulated through lipopolysaccharide (LPS) activation of pericyte TLR-4. Methods Rat PCs were harvested and cultured. PCs were transfected with siRNA targeted to TLR-4. Western blotting was used to confirm gene silencing of TLR-4. A previously described co-culture permeability assay was performed after LPS treatment. Results Western blot confirmed successful silencing of TLR-4 in PCs, which was sustained for 7 days. A dose- and time-dependent effect of LPS on albumin clearance was seen in MVEC/PC co-cultures. Co-cultures with TLR-4 silenced in PCs eliminated the LPS dose-dependent increase in albumin clearance. Conclusions TLR-4 regulates pericyte mediated capillary leak seen with LPS exposure. Our TLR-4 silencing model can be used to further investigate TLR-4’s role in pericyte mediated capillary leak.
ISSN:0002-9610
1879-1883
DOI:10.1016/j.amjsurg.2006.08.086