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. 2024 May 7;65(6):100557. doi: 10.1016/j.jlr.2024.100557

Table 1.

Sphingolipids and sphingoid bases in Caco-2/TC7 cells and basolateral medium of cells incubated with deuterated sphingosine-enriched lipid micelles

Sphingolipids MM + SPH-d9
MM + SPH-d9 + C23:0
pmol/well
Cells
 SPH-d9 53.2 ± 2.7 58.2 ± 2.6
 S1P-d9 7.3 ± 0.3 5.4 ± 0.9
 d18:1 Cer-d9 2,850 ± 218 2,880 ± 125
 d18:1 SM-d9 1,039 ± 43 1,185 ± 108
Basolateral medium
 SPH-d9 ND ND
 S1P-d9 ND ND
 d18:1 Cer-d9 1,159 ± 62 1,228 ± 15
 d18:1 SM-d9 ND ND

Deuterated SPH (SPH-d9), deuterated S1P (S1P-d9), deuterated Cer (d18:1 Cer-d9), and deuterated SM (d18:1 SM-d9) in cells and basolateral medium of Caco-2/TC7 cells incubated for 16 h with MM enriched with SPH-d9 (MM + SPH-d9) or with SPH-d9 and C23:0 (MM + SPH-d9 + C23:0). MM preparation containing 75 nmol SPH-d9 was added in 1.5 ml apical medium. Data expressed as pmol/well, represent the mean ± SEM of one experiment realized in quadruplicate. No significant difference was observed between sphingolipids in (MM + SPH-d9) and (MM + SPH-d9 + C23:0) groups.

MM, mixed micelles; ND, not detectable; SPH, sphingosine; SPH-d9, deuterated sphingosine.