2008
DOI: 10.1016/j.metabol.2008.07.023
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Phosphatidylinositol acts through mitogen-activated protein kinase to stimulate hepatic apolipoprotein A-I secretion

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Cited by 9 publications
(17 citation statements)
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“…42 In contrast, apoA-I reuptake and degradation appears centrally important to HDL secretion and LA-phospholipid stimulants of HDL secretion appear to primarily act through this route. [25][26][27] Much as niacin, these lipids do not increase apoA-I gene transcription but instead appear to impact the secretory process by regulating the retroendocytic degradation of apoA-I (Figure 11). 26 HDL retroendocytic pathways appear to involve several cell surface HDL binding proteins.…”
Section: Discussionmentioning
confidence: 99%
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“…42 In contrast, apoA-I reuptake and degradation appears centrally important to HDL secretion and LA-phospholipid stimulants of HDL secretion appear to primarily act through this route. [25][26][27] Much as niacin, these lipids do not increase apoA-I gene transcription but instead appear to impact the secretory process by regulating the retroendocytic degradation of apoA-I (Figure 11). 26 HDL retroendocytic pathways appear to involve several cell surface HDL binding proteins.…”
Section: Discussionmentioning
confidence: 99%
“…[25][26][27] Much as niacin, these lipids do not increase apoA-I gene transcription but instead appear to impact the secretory process by regulating the retroendocytic degradation of apoA-I (Figure 11). 26 HDL retroendocytic pathways appear to involve several cell surface HDL binding proteins. A number of candidate HDL receptors have been identified in hepatocyte membranes, but the proteins shown to play the most active role in interactions with apoA-I are SR-BI and ABCA1.…”
Section: Discussionmentioning
confidence: 99%
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