TABLE 1.
Simulated parameters representing the contributions of TAG biosynthesis pathways and the selectivity of reacylation manifest in mouse organs
Sample | K1 | K2 | K3 | k1 | k2 | k3 | γ |
Skeletal muscle | 0 | 1.000 | 0 | 0.11 ± 0.09 | 0.05 ± 0.05 | 0.01 ± 0.01 | 0.977 ± 0.007 |
Heart | 0.145 ± 0.033 | 0.825 ± 0.043 | 0.030 ± 0.014 | 0.01 ± 0.01 | 0 | 0 | 0.960 ± 0.015 |
Liver | 0.493 ± 0.031 | 0.507 ± 0.031 | 0 | 0.47 ± 0.15 | 0.23 ± 0.05 | 0 | 0.943 ± 0.007 |
The determined TAG levels of mouse skeletal muscle, heart, and liver by MDMS-SL (supplementary Table I) were simulated with the TAG biosynthesis pathways as illustrated in Fig. 1. The parameters of K1, K2, and K3 represent the contributions of individual pathways (i.e., PA-, MAG-, and PI-DAG pathways, respectively) to the TAG pools. The parameters of k1, k2, and k3 represent the degrees of acyltransferase selectivity to the different fatty acyl chains at the sn-1, 2, and 3 positions of TAG species, respectively (see text for details).