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- W2124454060 abstract "This work uses a novel heart-perfusion technique to measure [ 3 H]-lipopolysaccharide ([ 3 H]-LPS) binding on capillary endothelium and myocyte cell membranes in Sprague-Dawley rats. Free or serum-containing Ringer-Lock buffer was infused at a rate of 1 ml/min and in the presence of 20 mM K + and [ 3 H]-LPS through an aortic cannula, and the effluent was collected through a catheter introduced into the right atrium cavity. The capillary endothelial lining was removed by CHAPS treatment to expose the cardiac myocyte surface. A physical model describing 1:1 binding stoichiometry of [ 3 H]-LPS with its receptors is proposed and the mathematical equations derived allow for the calculation of binding constants (k n ), reversal constants (k -n ), dissociation constants (k d ), and residency time constants (τ). The results showed that the presence of serum in the perfusate, slowed the binding of [ 3 H]-LPS with the endothelial lining and myocytes, but increased the residency time by 3- and 50-fold, respectively. Hence, the endothelium and myofiber may contain LPS receptors that can bind more strongly with the ligand in association with sCD14-like and LBP-like molecules in rat serum. Thus it is postulated that the affinity of LPS to its receptor subtypes is not strictly and specifically dependent on the CD14 binding profile." @default.
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- W2124454060 date "1997-02-01" @default.
- W2124454060 modified "2023-09-27" @default.
- W2124454060 title "Endotoxin binding on capillary endothelium and myocyte plasma membranes in perfused rat heart" @default.
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- W2124454060 doi "https://doi.org/10.1177/096805199700400106" @default.
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