The content of the meibomian gland lipid exprimate is known, but littl
e is known about the phospholipids that comprise the glandular cells.
The purpose of the present study is to identify and quantitate the pho
spholipid complement of the meibomian gland cells that produce the lip
id secretion of meibomian oil and which is vital to tear film stabilit
y. Eyelids (n = 50) were excised from rabbits, and after surgical remo
val of surrounding tissues, the tarsal plates with and without express
ing meibomian oil were extracted and phospholipids of the plates quant
ified by P-31 nuclear magnetic resonance (NMR). Seventeen phospholipid
s were quantified from tarsal plates expressed of oil and tarsal plate
s containing meibomian oil: alkylacylphosphatidylcholine (AAPC), dihyd
rosphingomyelin (DHSM), dimethylphosphatidylethanolamine, diphosphatid
ylglycerol (cardiolipin), ethanolamine plasmalogen (EPLAS), lysoethano
lamine plasmalogen, lysophosphatidylcholine, lysophosphatidylethanolam
ine, lysophosphatidylserine, phosphatidic acid, phosphatidylcholine (P
C), phosphatidylethanolamine (PE), phosphatidylglycerol, phosphatidyli
nositol, phosphatidylserine, sphingomyelin (SM), sphingosylphosphorylc
holine. The six zwitterionic and neutral phospholipids, DHSM, EPLAS, P
E, SM, AAPC, and PC together comprise 79.5% of the total meibomian gla
nd phospholipid profile (in meibomian oil this value is 84.2%). The zw
itterionic and neutral phospholipids dominate meibomian gland phosphol
ipid profiles. Since the meibomian gland cells undergo holocrine secre
tion and form the meibomian gland secretion, such a composition is con
sistent with the hypothesis that a chemically stable lamellar surfacta
nt layer phospholipids bind non-polar meibomian oil to the aqueous lay
er of the tear film.