CRISPR/Cas9-mediated deletion of adipocyte genes associated with NAFLD alters adipocyte lipid handling and reduces steatosis in hepatocytes in vitro

Author:

Lopez-Yus Marta123,Frendo-Cumbo Scott4,del Moral-Bergos Raquel123,Garcia-Sobreviela Maria Pilar13,Bernal-Monterde Vanesa135,Rydén Mikael4,Lorente-Cebrian Silvia136,Arbones-Mainar Jose M.1237ORCID

Affiliation:

1. Adipocyte and Fat Biology Laboratory (AdipoFat), Translational Research Unit, University Hospital Miguel Servet, Zaragoza, Spain

2. Instituto Aragonés de Ciencias de la Salud (IACS), Zaragoza, Spain

3. Instituto de Investigación Sanitaria (IIS) Aragón, Zaragoza, Spain

4. Department of Medicine (H7), Karolinska Institutet, Karolinska University Hospital Huddinge, Huddinge, Sweden

5. Gastroenterology Department, Miguel Servet University Hospital, Zaragoza, Spain

6. Departamento de Farmacología, Fisiología y Medicina Legal y Forense, Universidad de Zaragoza, Instituto Agroalimentario de Aragón (IA2) (Universidad de Zaragoza-CITA), Zaragoza, Spain

7. CIBER Fisiopatología Obesidad y Nutrición (CIBERObn), Instituto Salud Carlos III, Madrid, Spain

Abstract

Clustered regularly interspaced short palindromic repeats (CRISPR)/Cas9 technology successfully edited genomic DNA of human adipose-derived mesenchymal stem cells (hADMSC). SOCS3, SIK1, and DUSP1 regulate adipocyte lipid handling. Silencing SOCS3, SIK1, and DUSP1 expression in hADMSC-derived adipocytes reduces hepatocyte lipid storage in vitro.

Funder

Spanish Ministry of Science

EC | European Research Council

European Molecular Biology Organization

Gobierno de Aragón

KI | Center for Innovative Medicine

Karolinska Institutet

Knut och Alice Wallenbergs Stiftelse

MEC | Instituto de Salud Carlos III

Novo Nordisk Foundation Center for Basic Metabolic Research

Stockholm läns landsting

Stockholms Läns Landsting

Svenska Diabetesstiftelsen

Universidad de Zaragoza

Vetenskapsrådet

Publisher

American Physiological Society

Subject

Cell Biology,Physiology

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