CABLES1 expression is reduced in human subcutaneous adipose tissue in obesity and type 2 diabetes but may not directly impact adipocyte glucose and lipid metabolism

Adipocyte. 2023 Dec;12(1):2242997. doi: 10.1080/21623945.2023.2242997.

Abstract

Cdk5 and Abl enzyme substrate 1 (CABLES1) is a cell cycle regulator that has previously been identified as a candidate gene for obesity-related phenotypes, but little is known about its role in adipose tissue metabolism. In this study, we explore the role of CABLES1 in obesity and type 2 diabetes (T2D) in human subcutaneous adipose tissue (SAT). We performed gene expression analysis of SAT obtained from subjects with and without T2D, and from a second validation cohort consisting of subjects without T2D. We used CRISPR/Cas9 genome editing to perform CABLES1 loss-of-function studies in human primary preadipocytes and assessed them functionally after differentiation. CABLES1 gene expression in SAT was decreased in T2D by almost 25%, and inversely associated with insulin resistance markers and hyperglycaemia. mRNA levels were reduced with increasing BMI and negatively correlated with obesity markers. We found that adipocytes are likely the main CABLES1-expressing cell type in SAT, but CABLES1 depletion in adipocytes caused no phenotypical changes in regards to differentiation, glucose uptake, or expression of key genes of adipocyte function. These findings suggest that CABLES1 gene expression in SAT might be altered in obesity and T2D as a consequence of metabolic dysregulation rather than being a causal factor.

Keywords: CABLES1; adipocytes; adipose tissue; obesity; type 2 diabetes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipocytes / metabolism
  • Adipose Tissue / metabolism
  • Diabetes Mellitus, Type 2* / genetics
  • Diabetes Mellitus, Type 2* / metabolism
  • Glucose / metabolism
  • Humans
  • Lipid Metabolism* / genetics
  • Obesity / genetics
  • Obesity / metabolism
  • Subcutaneous Fat / metabolism

Substances

  • Glucose
  • CABLES1 protein, human

Grants and funding

This study was performed with the support of the Swedish Diabetes Foundation [DIA2021-661], the Swedish National Strategic Research Initiative EXODIAB (Excellence of Diabetes Research in Sweden), the Stiftelsen Familjen Ernfors Foundation, the P.O. Zetterlings stiftelse, the NovoNordisk Foundation [NNF20OC0063864], the Agnes and Mac Rudberg Foundation, the European Commission via the Marie Sklodowska Curie Innovative Training Network TREATMENT [H2020-MSCA-ITN-721236], AstraZeneca R&D, and the Uppsala University Hospital ALF grants.