| Literature DB >> 33432099 |
Joshua A Levine1, Carlota Oleaga2, Mesut Eren1, Ansel P Amaral1, Meng Shang1, Elizabeth Lux1, Sadiya S Khan1, Sanjiv J Shah1, Yasuhiro Omura1, Nathalie Pamir2, Joshua Hay2, Grant Barish1,3, Toshio Miyata4, Hagai Tavori2, Sergio Fazio2, Douglas E Vaughan5.
Abstract
Plasminogen activator inhibitor 1 (PAI-1) is a functional biomarker of the metabolic syndrome. Previous studies have demonstrated that PAI-1 is a mechanistic contributor to several elements of the syndrome, including obesity, hypertension and insulin resistance. Here we show that PAI-1 is also a critical regulator of hepatic lipid metabolism. RNA sequencing revealed that PAI-1 directly regulates the transcriptional expression of numerous genes involved in mammalian lipid homeostasis, including PCSK9 and FGF21. Pharmacologic or genetic reductions in plasma PAI-1 activity ameliorates hyperlipidemia in vivo. These experimental findings are complemented with the observation that genetic deficiency of PAI-1 is associated with reduced plasma PCSK9 levels in humans. Taken together, our findings identify PAI-1 as a novel contributor to mammalian lipid metabolism and provides a fundamental mechanistic insight into the pathogenesis of one of the most pervasive medical problems worldwide.Entities:
Year: 2021 PMID: 33432099 PMCID: PMC7801442 DOI: 10.1038/s41598-020-79948-x
Source DB: PubMed Journal: Sci Rep ISSN: 2045-2322 Impact factor: 4.379