Mboat7 down-regulation by hyper-insulinemia induces fat accumulation in hepatocytes

Autor: Amalia Gastaldelli, Stefano Gatti, Miriam Longo, Stefano Romeo, Melania Gaggini, Paola Dongiovanni, Sara Badiali, Nicholas O. Davidson, Anna Ludovica Fracanzani, Guido Baselli, Serena Pelusi, Raffaela Rametta, Marica Meroni, Fabrizia Carli, Luca Valenti, Marco Maggioni
Rok vydání: 2019
Předmět:
Research paper
TGFβ
Transforming Growth Factor Beta

Intracellular Space
CRISPR
Clustered Regularly Interspaced Short Palindromic Repeats

hHEPS
Human Hepatocytes

Mice
0302 clinical medicine
LPIAT1
DAG
Diacylglycerol

i.p.
Intraperitoneal

media_common
Fatty Acids
General Medicine
3. Good health
030220 oncology & carcinogenesis
HOMA-IR
homeostasis Model Assessment of Insulin Resistance

MPO
morpholino

lcsh:Medicine (General)
medicine.medical_specialty
PE
Phosphatidyl-Ethanolamine

Nash
General Biochemistry
Genetics and Molecular Biology

03 medical and health sciences
TNFα
tumor Necrosis Factor Alpha

LDL
Low Density Lipoproteins

Hyperinsulinism
NAFLD
SD
Standard Diet

media_common.cataloged_instance
Humans
CPT1
Carnitine Palmitoyltransferase I

Phosphatidylinositol
Gene Silencing
European union
VLDL
Very Low Density Lipoprotein

lcsh:R
hHSC
Human Hepatic Stellate Cells

medicine.disease
Lipid Metabolism
OA
Oleic Acid

CI
Confidence Interval

Mboat7
Membrane bound O-acyltransferase domain containing 7

MCD
methionine choline deficient diet

030104 developmental biology
Endocrinology
chemistry
CDP
Cytidine-Diphosphate

FOXO1
Forkhead Box protein O1

NAFLD
nonalcoholic fatty liver disease

Steatohepatitis
BMI
Body Mass Index

CL
Cardiolipin

Acyltransferases
0301 basic medicine
Alcoholic liver disease
CXCL10
C-X-C Motif Chemokine 10

lcsh:Medicine
chemistry.chemical_compound
Non-alcoholic Fatty Liver Disease
IFG
Impaired Fasting Glucose

APOB
Apolipoprotein B

Nonalcoholic fatty liver disease
PIP
Phosphatidyl-Inositol-Phosphate

qRT-PCR
quantitative Real Time Polymerase Chain Reaction

Mice
Knockout

lcsh:R5-920
ORO
Oil Red O Staining

PI
Phosphatidylinositol

Fatty liver
TM6SF2
Transmembrane 6 Superfamily Member 2

Phospholipid
TAG
Triglycerides

NASH
Nonalcoholic Steatohepatitis

Lipogenesis
LPA
Lyso-Phosphatidic Acid

Signal Transduction
PS
Phosphatidyl-Serine

PA
Palmitic Acid

ALD
alcoholic liver disease

PC
Phosphatidylcholine

i.v.
Intravenous

FATP1
Fatty Acid Transport Protein 1

Models
Biological

Internal medicine
medicine
Animals
PPARα
Peroxisome Proliferator-Activated Receptor alpha

Obesity
G3P
Glyceraldehyde-3-Phosphate

SREBP1c
Sterol Regulatory Element-Binding Protein 1

HDL
High Density Lipoproteins

business.industry
PI3K
Phosphatidylinositol 3 Kinase

Membrane Proteins
NHEJ
Non-Homologues End Joining

PNPLA3
Patatin-like Phospholipase Domain-containing-3

MTTP
Microsomal Triglyceride Transfer Protein

LPIAT1
Lysophosphatidylinositol Acyltransferase 1

TMC4
Transmembrane Channel-Like 4

Disease Models
Animal

Gene Expression Regulation
Hepatocytes
FOXA2
Forkhead Box A2

mTOR
mammalian target of Rapamycin

Steatosis
Insulin Resistance
business
PG
Phosphatidyl-Glycerol

FABP1
Fatty Acid-Binding Protein 1
FAS
Fatty Acid Synthase

T2DM
Type 2 Diabetes Mellitus
Zdroj: EBioMedicine
EBioMedicine, Vol 52, Iss, Pp-(2020)
ISSN: 2352-3964
Popis: Background: Naturally occurring variation in Membrane-bound O-acyltransferase domain-containing 7 (MBOAT7), encoding for an enzyme involved in phosphatidylinositol acyl-chain remodelling, has been associated with fatty liver and hepatic disorders. Here, we examined the relationship between hepatic Mboat7 down-regulation and fat accumulation. Methods: Hepatic MBOAT7 expression was surveyed in 119 obese individuals and in experimental models. MBOAT7 was acutely silenced by antisense oligonucleotides in C57Bl/6 mice, and by CRISPR/Cas9 in HepG2 hepatocytes. Findings: In obese individuals, hepatic MBOAT7 mRNA decreased from normal liver to steatohepatitis, independently of diabetes, inflammation and MBOAT7 genotype. Hepatic MBOAT7 levels were reduced in murine models of fatty liver, and by hyper-insulinemia. In wild-type mice, Mboat7 was down-regulated by refeeding and insulin, concomitantly with insulin signalling activation. Acute hepatic Mboat7 silencing promoted hepatic steatosis in vivo and enhanced expression of fatty acid transporter Fatp1. MBOAT7 deletion in hepatocytes reduced the incorporation of arachidonic acid into phosphatidylinositol, consistently with decreased enzymatic activity, determining the accumulation of saturated triglycerides, enhanced lipogenesis and FATP1 expression, while FATP1 deletion rescued the phenotype. Interpretation: MBOAT7 down-regulation by hyper-insulinemia contributes to hepatic fat accumulation, impairing phosphatidylinositol remodelling and up-regulating FATP1. Funding: LV was supported by MyFirst Grant AIRC n.16888, Ricerca Finalizzata Ministero della Salute RF-2016–02,364,358, Ricerca corrente Fondazione IRCCS Ca’ Granda Ospedale Maggiore Policlinico; LV and AG received funding from the European Union Programme Horizon 2020 (No. 777,377) for the project LITMUS-“Liver Investigation: Testing Marker Utility in Steatohepatitis”. MM was supported by Fondazione Italiana per lo Studio del Fegato (AISF) ‘Mario Coppo’ fellowship. Keywords: LPIAT1, NAFLD, Nash, Nonalcoholic fatty liver disease, Steatohepatitis, Phospholipid, Phosphatidylinositol
Databáze: OpenAIRE