The essential fatty acid 22:6(n-3) is a minor component of the Western diet
, but a major fatty acid in human testis and semen. In mature spermatozoa,
the physical and fusogenic properties of the plasma membrane are probably i
nfluenced by its particular fatty acid composition. In this study, the synt
hesis of 22:6(n-3) and 22:5(n-6) was investigated in isolated human testicu
lar cells. [1-C-14]20:4(n-6), [1-C-14]20:5(n-3), [1-C-14]22:4(n-6) and [1-C
-14]22:5(n-3) were incubated in a 'crude' cell suspension (consisting of a
mixture of the cells in the seminiferous tubule), and in fractionated pachy
tene spermatocytes and round spermatids. The esterification of fatty acids
in lipid and phospholipid classes and the fatty acid chain elongation and d
esaturation were measured. The crude cell suspension metabolized the fatty
acids more actively than did the fractionated germ cell suspension, indicat
ing that types of cell other than the germ cells are important for fatty ac
id elongation and desaturation and thus the production of 22:6(n-3). This f
inding is in agreement with previous results in rats that indicated that th
e Sertoli cells are the most important type of cell for the metabolism of e
ssential fatty acids in the testis. Some [1-C-14]20:5(n-3) was elongated to
[C-14]22:5(n-3) in the fractionated germ cells, but very little was elonga
ted further to [C-14]24:5(n-3), possibly restricting the formation of [C-14
]22:6(n-3). In the fractionated germ cells, the fatty acid substrates were
recovered primarily in the phospholipid fraction, indicating an incorporati
on in the membranes, whereas in the crude cells, more substrates were ester
ified in the triacylglycerol fraction. In the phospholipids, more radioacti
vity was recovered in phosphatidylcholine than in phosphatidylethanolamine
and more radioactivity was recovered in phosphatidylethanolamine than in ph
osphatidylinositol or phosphatidylserine.