Key result
Although LPL activity increases to high levels in mouse kidney after feeding, it appears to have a minor role for lipid uptake as no difference in chylomicron triglyceride uptake was found.
Why the study?
Lipoprotein lipase (LPL) activity is high in mouse kidney, but the reason remains poorly understood.
LPL activity in the mouse kidney is regulated by nutritional status and ANGPTL4, but it appears to play only a minor role in renal lipid uptake.
Does not support LPL as major driver of renal lipid uptake; leaves open its contribution to human kidney pathology.
Activity of lipoprotein lipase (LPL) is high in mouse kidney, but the reason is poorly understood. The aim was to characterize localization, regulation, and function of LPL in kidney of C57BL/6J mice. We found LPL mainly in proximal tubules, localized inside the tubular epithelial cells, under all conditions studied. In fed mice, some LPL colocalized with the endothelial markers CD31 and GPIHBP1 and could be removed by perfusion with heparin, indicating a vascular location. The role of angiopoietin-like protein 4 (ANGPTL4) for nutritional modulation of LPL activity was studied in wild-type and Angptl4−/−mice. In Angptl4−/−mice, kidney LPL activity remained high in fasted animals, indicating that ANGPTL4 is involved in suppression of LPL activity on fasting, like in adipose tissue. The amount of ANGPTL4 protein in kidney was low, and the protein appeared smaller in size, compared with ANGPTL4 in heart and adipose tissue. To study the influence of obesity, mice were challenged with high-fat diet for 22 wk, and LPL was studied after an overnight fast compared with fasted mice given food for 3 h. High-fat diet caused blunting of the normal adaptation of LPL activity to feeding/fasting in adipose tissue, but in kidneys this adaptation was lost only in male mice. LPL activity increases to high levels in mouse kidney after feeding, but as no difference in uptake of chylomicron triglycerides in kidneys is found between fasted and fed states, our data confirm that LPL appears to have a minor role for lipid uptake in this organ.
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Nyrén et al. (2019) studied this question. High-fat diet and nutritional modulation (fasting/feeding) vs. Normal diet / fasted state was evaluated on LPL activity and chylomicron triglyceride uptake in kidney. Although LPL activity increases to high levels in mouse kidney after feeding, it appears to have a minor role for lipid uptake as no difference in chylomicron triglyceride uptake was found.
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