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On the mechanism of hepatic transendothelial passage of large liposomes
Author(s) -
Romero Eder L.,
Morilla Maria-José,
Regts Joke,
Koning Gerben A.,
Scherphof Gerrit L.
Publication year - 1999
Publication title -
febs letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.593
H-Index - 257
eISSN - 1873-3468
pISSN - 0014-5793
DOI - 10.1016/s0014-5793(99)00364-6
Subject(s) - liposome , phosphatidylserine , chemistry , phosphatidylglycerol , in vivo , endothelium , biophysics , biochemistry , phosphatidylcholine , phospholipid , biology , endocrinology , membrane , microbiology and biotechnology
Liposomes of 400 nm in diameter can cross the 100‐nm fenestrations in the endothelium of the hepatic sinusoid, provided they contain phosphatidylserine (PS) but not phosphatidylglycerol (PG) [Daemen et al. (1997) Hepatology 26, 416]. We present evidence indicating that (i) the PS effect does not involve a pharmacological action of this lipid on the size of the fenestrations, (ii) fluid‐type but not solid‐type PS liposomes have access to the hepatocytes and (iii) the lack of uptake of PG liposomes by hepatocytes is not due to a lack of affinity of the hepatocytes for PG surfaces. We conclude that the mechanism responsible for the uptake of large PS‐containing liposomes by hepatocytes in vivo involves a mechanical deformation of these liposomes during their passage across the endothelial fenestrations.