Docosahexaenoic acid (DHA) alters the phospholipid molecular species composition of membranous vesicles exfoliated from the surface of a murine leukemia cell line
Ee. Williams et al., Docosahexaenoic acid (DHA) alters the phospholipid molecular species composition of membranous vesicles exfoliated from the surface of a murine leukemia cell line, BBA-BIOMEMB, 1418(1), 1999, pp. 185-196
Previously, we presented evidence that the vesicles routinely exfoliated fr
om the surface of T27A tumor cells arise from vesicle-forming regions of th
e plasma membrane and possess a set of lateral microdomains distinct from t
hose of the plasma membrane as a whole. We also showed that docosahexaenoic
acid (DHA, or 22:6n-3), a fatty acyl chain known to alter microdomain stru
cture in model membranes, also alters the structure and composition of exfo
liated vesicles, implying a DHA-induced change in microdomain structure on
the cell surface. In this report we show that enrichment of the cells with
DHA reverses some of the characteristic differences in composition between
the parent plasma membrane and shed microdomain vesicles, but does not alte
r their phospholipid class composition. In untreated cells, DHA-containing
species were found to be a much greater proportion of the total phosphatidy
lethanolamine (PE) pool than the total phosphatidylcholine (PC) pool in bot
h the plasma membrane and the shed vesicles. After DHA treatment, the propo
rtion of DHA-containing species in the PE and PC pools of the plasma membra
ne were elevated, and unlike in untreated cells, their proportions were equ
al in the two pools. In the vesicles shed from DHA-loaded cells, the propor
tion of DHA-containing species of PE was the same as in the plasma membrane
. However, the proportion of DHA-containing species of PC in the vesicles (
0.089) was much lower than that found in the plasma membrane (0.194), and w
as relatively devoid of species with 16-carbon acyl components. These data
suggested that DHA-containing species of PC, particularly those having a 16
-carbon chain in the sn-1 position, were preferentially retained in the pla
sma membrane. The data can be interpreted as indicating that DHA induces a
restructuring of lateral microdomains on the surface of living cells simila
r to that predicted by its behavior in model membranes. (C) 1999 Elsevier S
cience B.V. All rights reserved.