Liposomes were prepared from an extract of all human stratum corneum l
ipids (hSCL) and characterised in terms of temperature and the presenc
e of Ca2+ by different physicochemical methods, Vesicle aggregation an
d lateral phase separation were induced by divalent cations with Ca2being more efficient than Mg2+. At 24.1 degrees C, i.e. well below phy
siological temperatures the suspensions consisted of a lamellar phase
and crystalline cholesterol, At and above 37 degrees C, this cholester
ol surplus was dissolved in the hSCL. membranes. However, melting of t
he hSCL was not completed up to 60 degrees C. The presence of Ca2+ (gr
eater than or equal to 9 mM) induced lateral phase separation and fusi
on of vesicles into extended multilamellar lipid sheets (MLLS) at and
above 32.5 degrees C. Upon a subsequent cooling cycle recrystallisatio
n of cholesterol occurred within the MLLS. Finally, membrane mixing of
hSCL liposomes with vesicles made of synthetic lipids was investigate
d. No mixing was observed between either of DPPE/oleic acid, DPPC/DPPE
, DPPC/lyso-PC and hSCL liposomes, Mixtures of DPPC/cholesterol hemisu
ccinate showed a temperature-dependent membrane mixing behaviour, whil
st hSCL liposomes and phosphatidylserine liposomes fused temperature-i
ndependently with hSCL liposomes. (C) 1998 Elsevier Science Ireland Lt
d. All rights reserved.