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Role of PAI-1 in hepatic steatosis and dyslipidemia
被引:43
|作者:
Levine, Joshua A.
[1
]
Oleaga, Carlota
[2
]
Eren, Mesut
[1
]
Amaral, Ansel P.
[1
]
Shang, Meng
[1
]
Lux, Elizabeth
[1
]
Khan, Sadiya S.
[1
]
Shah, Sanjiv J.
[1
]
Omura, Yasuhiro
[1
]
Pamir, Nathalie
[2
]
Hay, Joshua
[2
]
Barish, Grant
[1
,3
]
Miyata, Toshio
[4
]
Tavori, Hagai
[2
]
Fazio, Sergio
[2
]
Vaughan, Douglas E.
[1
]
机构:
[1] Northwestern Univ, Dept Med, Feinberg Sch Med, Arkes Pavil,Suite 2330,676 N St,Clair St, Chicago, IL 60611 USA
[2] Oregon Hlth & Sci Univ, Ctr Prevent Cardiol, Knight Cardiovasc Inst, Portland, OR 97201 USA
[3] Jesse Brown VA Med Ctr, Dept Med, Chicago, IL USA
[4] Tohoku Univ, Dept Mol Med & Therapy, United Ctr Adv Res & Translat Med, Grad Sch Med, Sendai, Miyagi, Japan
关键词:
PLASMINOGEN-ACTIVATOR INHIBITOR-1;
METABOLIC SYNDROME;
PCSK9;
OBESITY;
CHOLESTEROL;
DISEASE;
PROTECTS;
TM5441;
LDLR;
D O I:
10.1038/s41598-020-79948-x
中图分类号:
O [数理科学和化学];
P [天文学、地球科学];
Q [生物科学];
N [自然科学总论];
学科分类号:
07 ;
0710 ;
09 ;
摘要:
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.
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页数:13
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