Fig. 4: Deciphering metabolic communication between organs.
From: Spatial isotope deep tracing deciphers inter-tissue metabolic crosstalk

a AFADESI-MS images of palmitic acid with a heatmap representing the signal intensity across organs (left) and images of palmitic acid M6 with a heatmap representing the ME across organs (right). Signal intensity is shown in ion counts. Bra, brain; Liv, liver; Kid, kidney; Hea, heart; Spleen, spl; Lun, lung; Pan, pancreas; BAT, brown adipose tissue; Int, intensity. b Schematic illustrating the incorporation of carbon from U-13C-glucose into palmitic acid. Light green circles denote 13C carbons, while white circles represent 12C carbons. CAR, carnitine; CoA, coenzyme A. c AFADESI-MS images of acetylcarnitine M2. Signal intensity is shown in ion counts. d Normalized labeling fraction of acetylcarnitine M2 across organs, as measured by LC‒MS. Data are presented as mean ± SD (n = 3 biological replicates). e Normalized labeling fraction of palmitoylcarnitine isotopologues in the BAT and brain. Data are presented as mean ± SD (n = 3 biological replicates). f Normalized labeling fraction of hexanoylcarnitine M2 in BAT, brain, heart and serum. Data are presented as mean ± SD (n = 3 biological replicates). g Labeling profile of palmitic acid in BAT, brain and serum. Data are presented as mean ± SD (n = 3 biological replicates). Source data are provided as a Source Data file. h Representative lipid profiles of TG (48:1) in BAT, brain, liver and serum. The color in the heatmap represents labeled fraction (LF) after logarithmic transformation. i Distinct labeling profile of representative lipids between the brain and liver. Lipids in the brain can incorporate more 13C carbons (up to M7), whereas lipids in the liver can only be labeled with M3, as measured by LC‒MS. j The potential 13C-carbon allocation of labeled TG (48:1). k Illustration of the proposed metabolic crosstalk model, created in BioRender. Li, X. (https://BioRender.com/plw7j67).