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C L Hedberg

Publications and source records attributed to C L Hedberg.

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The nonpolar lipids of pig epidermis.

Epidermis was removed from several sites on the intact bodies of each of seven pigs and the lipids were extracted and analyzed by thin-layer chromatography. The principal nonpolar components were cholesterol, free fatty acids and cholesteryl esters. Small and variable amounts of paraffin hydrocarbons, triglycerides, and an unidentified lipid were noted. In a series of time-course experiments, epidermal lipids were labeled by intradermal injection of [1-14C] acetate at varying times up to 21 days before removal of the epidermis. The hydrocarbons never acquired radioactivity, while the triglycerides retained label only for about 1 day after injection. Squalene and lanosterol retained considerable radioactivity for up to 12 h after labeling. Radioactivity appeared in free fatty acids and cholesteryl esters 2-3 days after labeling and began to decline after 21 days. Epidermis from uninjected sites did not acquire significant radioactivity. From these results it was concluded that cholesterol, cholesteryl esters and free fatty acids are synthesized locally in the epidermis and remain until lost by desquamation. Triglycerides are also synthesized but do not persist into the stratum corneum, so the small amounts found there may be environmental contaminants. Alkanes are not synthesized, and are most probably derived from petroleum waxes.

Animals↗

The time course of lipid biosynthesis in pig epidermis.

In order to examine the time course of lipid metabolism in the epidermis, pairs of sites on each of two pigs were given seven intradermal injections of 10 microCi of [1-14C]-acetate at 1, 3, 6, 12, 24, 36, and 48 h before the animals were killed. A second time course was obtained with two other pigs at 1 h and 3.5, 7, 10.5, 14, 17.5, and 21 d after labeling. The epidermis over each injection site was recovered, and the lipids were extracted and analyzed by thin-layer chromatography and by autoradiography. Virtually all of the radioactivity in aliphatic chains was found first in phospholipids and was then transferred to glucosylceramides, and then into ceramides, between 1 and 7 d after labeling. Labeling of free fatty acids showed a similar time course. Most of the radioactivity acquired by acylglucosylceramide was transferred to hydroxyceramide, bound to the corneocyte envelope, between 2 and 10 d after labeling. The hydroxyacid and sphingosine moieties of the hydroxy-ceramide had equal specific activity. The results indicate that the aliphatic lipids of the stratum corneum are synthesized de novo in the epidermis via phospholipids. Cholesterol, however, was synthesized directly from acetate within hours of labeling, and its esters acquired label 3 to 7 d later.

Acetates↗