Abstract:CL (cardiolipin) is a major mitochondrial membrane phospholipid important for the regulation of mitochondrial function. We examined CL de novo biosynthesis and its resynthesis in isolated rat liver hepatocytes prepared 48 h subsequent to two-thirds PHx (partial hepatectomy). The pool size of CL and its de novo biosynthesis from [1,3-(3)H]glycerol were increased 3.3-fold (P<0.05) and 3.1-fold (P<0.05) respectively in hepatocytes prepared from PHx rats compared with sham-operated controls. The reason for the inc… Show more
“…These changes in lipid content resemble the results of Cascianelli et al [57], who showed an increased sphingomyelin and cholesterol content in nuclear microdomains of regenerated hepatocytes. Interestingly, increased hepatic cardiolipin synthesis, which is presumed to be under the control of transcription factors that regulate mitochondrial biogenesis [58], as well as the pool size of cardiolipin, increased during liver regeneration [59]. Although this study cannot explore the precise mechanisms of the effects observed, our results suggest that the changes in lipid content in the LM and nuclear fractions may be associated with an increase in the trophoblast proliferation rate.…”
Section: Mitochondria Is a Target Organelle Of Pesticide Toxicity Asmentioning
Blood cholinesterases and tissue carboxylesterases (CEs) are sensitive indicators of environmental organophosphate pesticides (OPs) exposure. The aim of this pilot study was to assess the impact of OP exposure on placental CE activity and lipid composition. We performed a study of 40 healthy women who live in agricultural farms. Samples were collected during the pulverization period (PP) and recess period (RP). The plasma cholinesterase and placental CE activity decreased in PP, suggesting that women were exposed to OPs and that these pesticides reached the placenta. The cardiolipin content increased and the phosphatidylethanolamine content decreased in the light mitochondrial fraction while total cholesterol and sphingomyelin increased in the nuclear fraction. These changes in lipid profiles suggest repair by hyperplasia of the cytotrophoblast. Decreased CE activity may have clinical and toxicological implications and thus entail potential risks to damage fetal growth and development.
“…These changes in lipid content resemble the results of Cascianelli et al [57], who showed an increased sphingomyelin and cholesterol content in nuclear microdomains of regenerated hepatocytes. Interestingly, increased hepatic cardiolipin synthesis, which is presumed to be under the control of transcription factors that regulate mitochondrial biogenesis [58], as well as the pool size of cardiolipin, increased during liver regeneration [59]. Although this study cannot explore the precise mechanisms of the effects observed, our results suggest that the changes in lipid content in the LM and nuclear fractions may be associated with an increase in the trophoblast proliferation rate.…”
Section: Mitochondria Is a Target Organelle Of Pesticide Toxicity Asmentioning
Blood cholinesterases and tissue carboxylesterases (CEs) are sensitive indicators of environmental organophosphate pesticides (OPs) exposure. The aim of this pilot study was to assess the impact of OP exposure on placental CE activity and lipid composition. We performed a study of 40 healthy women who live in agricultural farms. Samples were collected during the pulverization period (PP) and recess period (RP). The plasma cholinesterase and placental CE activity decreased in PP, suggesting that women were exposed to OPs and that these pesticides reached the placenta. The cardiolipin content increased and the phosphatidylethanolamine content decreased in the light mitochondrial fraction while total cholesterol and sphingomyelin increased in the nuclear fraction. These changes in lipid profiles suggest repair by hyperplasia of the cytotrophoblast. Decreased CE activity may have clinical and toxicological implications and thus entail potential risks to damage fetal growth and development.
“…33 Our analysis identified that among the proteins down-regulated in AH was a subset involved in the synthesis of cardiolipin (CL) (Table 2), a phospholipid that maintains mitochondria bioenergetics 34 during hepatocyte proliferation and liver regeneration. 35 Figure 7A summarizes the CL biosynthesis pathway and shows the primarily negative correlation between MELD score and enzymes in this pathway, including critical proteins 1acylglycerol-3-phosphate O-acyltransferase 2 (PLCB), protein tyrosine phosphatase mitochondrial 1 (PTPMT1), and hydroxyacyl-CoA dehydrogenase trifunctional complex subunit alpha (ECHA). 36 PLCB and PTPMT1 expression was slightly elevated from AH1 to AH2 but declined from AH2 to AH3 (PLCB being significant), whereas ECHA significantly declined from AH1 to AH3 (Figure 7B).…”
Section: Compromised Hepatic Cardiolipin Biosynthesis In Ac and Ahmentioning
“…Subcellular fractions were prepared as previously described [18,21] from murine liver, epidermal fat pad, or RAW 264.7 cells incubated plus or minus LPS. Cells were harvested using PBS and pipetted into test tubes.…”
Section: Preparation Of Subcellular Fractions and Assay Of Enzyme Actmentioning
We examined if lipopolysaccharide (LPS) treatment of mice affected cardiolipin (CL) synthesis. Mice were injected i.p. with LPS, the liver harvested, and CL synthase (CLS) enzyme activity and its mRNA expression examined. Treatment of mice with LPS resulted in a 55% decrease (p < 0.01) in mRNA expression of murine CLS compared to controls, but CLS enzyme activity was unaltered. The pool size of liver CL and other phospholipids were unaltered by LPS treatment. A similar effect was observed in murine epidermal fat pad and in vitro in RAW mouse macrophages and in human HepG2 cells. LPS treatment of HepG2 cells transiently expressing a histidine-tagged human cardiolipin synthase-1 (hCLS1) reduced hCLS1 mRNA and newly synthesized CLS activity indicating that LPS inhibits production of newly synthesized hCLS1 via reduction in hCLS1 mRNA. The results clearly indicate that CLS mRNA levels cannot be correlated with CLS enzyme activity nor CL content in the LPS model of inflammation.
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