Old) were collected for 72 h. for 72 h. The picture shows lipidupper lipid layers in the extraction samples. fecal samples. weeks old) have been collected The picture shows the upper the layers within the extraction tubes of fecal tubes of Quantification of (f) total fecalof (f) total fecal lipids and (g) fecal neutral sterols. (h,i) Cholesterol absorptionin chow diet-fed female mice Quantification lipids and (g) fecal neutral sterols. (h,i) Cholesterol absorption was measured was measured in chow dietfed four, ten weeks = four, ten a 4 h-fasting period, h-fasting gavaged with 200 gavaged with 200 corn [3 containing two (n =female mice (nold). Afterweeks old). Immediately after a 4mice have been period, mice were corn oil containing two ioilH]cholesterol i 200 cholesterol. Radioactivity was Radioactivity post-gavage in h plasma and (i) isolated tissues by liquid and [3H]cholesterol and 200 cholesterol. measured four h was measured four (h)post-gavage in (h) plasma and (i) isolated tissues by liquid scintillation counting. (j) Enterocyte mRNA expression of cholesterol transporters relative to Gapdh as scintillation counting. (j) Enterocyte mRNA expression of cholesterol transporters relative to Gapdh as reference gene reference gene (n = 5). Information represent 0.05 (),SD; p0.01 (), p p 0.001 (), p Student’s unpaired t-test. (n = five). Information represent signifies + SD; p indicates + p 0.05 (), 0.01 (). 0.001 (). Student’s unpaired t-test.3.3. LAL-KO Intestines Accumulate Lipids from the Systemic Circulation 3.3. LAL-KO Intestines Accumulate Lipids from the Systemic Circulation WTD-fed LAL-KO mice accumulate lipids predominantly in the duodenum and WTD-fed LAL-KO mice accumulate lipids predominantly inside the duodenum and jejunum, and the small intestine is markedly shorter in comparison to manage mice (Figure 3a). jejunum, as well as the little intestine is markedly shorter when compared with control mice (Figure 3a). We observed aa extreme intestinal accumulation neutral lipids in LAL-KO micemice (Figure observed serious intestinal accumulation of of neutral lipids in LAL-KO (Figure 3b,c). We 3b,c). Electron microscopy confirmed the of lipid-filledof lipid-filled lysosomes Electron microscopy confirmed the abundance abundance lysosomes predominantly predominantly in the (Figure 3d), which is constant with is consistent with prior within the lamina propria lamina propria (Figure 3d), which preceding reports describing reports models of LAL-D [12,42,43]. We have lately demonstrated the crucial part of in vivo describing in vivo models of LAL-D [12,42,43]. We’ve not too long ago demonstrated the important function of cytosolic lipases withinmetabolism of lipids derived from the basolateral cytosolic lipases within Toceranib Protocol enterocytes in the enterocytes in the metabolism of lipids derived from theside with the little intestine the tiny To figure out no matter if LAL-KO enterocytes (blood) basolateral (blood) side of [32,40]. intestine [32,40]. To establish whether LALKO enterocytes accumulate lipid species from the basolateral membrane of enterocytes,Cells 2021, ten,eight ofCells 2021, ten, x8 ofaccumulate lipid species in the basolateral membrane of enterocytes, we incorporated we incorporated [3H]oleate into an intralipid TNP-470 supplier emulsion, injected it intraperitoneally, and [3 H]oleate into an intralipid emulsion, injected it intraperitoneally, and measured the tracer 3 measured the tracer in diverse intestinal segments [32]. [3 H]oleate alternatively of cholesterol in unique intestinal segments [32]. The incorporation of your incorporation of [.
