J 2024

Endocrine disruption of adipose physiology: Screening in SGBS cells

KUČERA, Jan; Zuzana CHALUPOVÁ; Martin WABITSCH and Julie DOBROVOLNÁ

Basic information

Original name

Endocrine disruption of adipose physiology: Screening in SGBS cells

Authors

KUČERA, Jan; Zuzana CHALUPOVÁ; Martin WABITSCH and Julie DOBROVOLNÁ

Edition

Journal of Applied Toxicology, HOBOKEN, WILEY, 2024, 0260-437X

Other information

Language

English

Type of outcome

Article in a journal

Country of publisher

United States of America

Confidentiality degree

is not subject to a state or trade secret

References:

Marked to be transferred to RIV

Yes

RIV identification code

RIV/00216224:14310/24:00137604

Organization

Přírodovědecká fakulta – Repository – Repository

EID Scopus

Keywords in English

adipocyte; adipogenesis; endocrine disruptors; SGBS cells; Simpson Golabi Behmel Syndrome cell line

Links

825712, interní kód Repo. 857560, interní kód Repo. RECETOX RI II, large research infrastructures.
Changed: 31/7/2025 00:50, RNDr. Daniel Jakubík

Abstract

In the original language

The increasing use of industrial chemicals has raised concerns regarding exposure to endocrine-disrupting chemicals (EDCs), which interfere with developmental, reproductive and metabolic processes. Of particular concern is their interaction with adipose tissue, a vital component of the endocrine system regulating metabolic and hormonal functions. The SGBS (Simpson Golabi Behmel Syndrome) cell line, a well-established human-relevant model for adipocyte research, closely mimics native adipocytes' properties. It responds to hormonal stimuli, undergoes adipogenesis and has been successfully used to study the impact of EDCs on adipose biology. In this study, we screened human exposure-relevant doses of various EDCs on the SGBS cell line to investigate their effects on viability, lipid accumulation and adipogenesis-related protein expression. Submicromolar doses were generally well tolerated; however, at higher doses, EDCs compromised cell viability, with cadmium chloride (CdCl2) showing the most pronounced effects. Intracellular lipid levels remained unaffected by EDCs, except for tributyltin (TBT), used as a positive control, which induced a significant increase. Analysis of adipogenesis-related protein expression revealed several effects, including downregulation of fatty acid-binding protein 4 (FABP4) by dibutyl phthalate, upregulation by CdCl2 and downregulation of perilipin 1 and FABP4 by perfluorooctanoic acid. Additionally, TBT induced dose-dependent upregulation of C/EBP alpha, perilipin 1 and FABP4 protein expression. These findings underscore the importance of employing appropriate models to study EDC-adipocyte interactions. Conclusions from this research could guide strategies to reduce the negative impacts of EDC exposure on adipose tissue.

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