Přehled o publikaci
2024
Endocrine disruption of adipose physiology: Screening in SGBS cells
KUČERA, Jan; Zuzana CHALUPOVÁ; Martin WABITSCH a Julie DOBROVOLNÁZákladní údaje
Originální název
Endocrine disruption of adipose physiology: Screening in SGBS cells
Autoři
KUČERA, Jan; Zuzana CHALUPOVÁ; Martin WABITSCH a Julie DOBROVOLNÁ
Vydání
Journal of Applied Toxicology, HOBOKEN, WILEY, 2024, 0260-437X
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Stát vydavatele
Spojené státy
Utajení
není předmětem státního či obchodního tajemství
Odkazy
Označené pro přenos do RIV
Ano
Kód RIV
RIV/00216224:14310/24:00137604
Organizace
Přírodovědecká fakulta – Masarykova univerzita – Repozitář
UT WoS
EID Scopus
Klíčová slova anglicky
adipocyte; adipogenesis; endocrine disruptors; SGBS cells; Simpson Golabi Behmel Syndrome cell line
Návaznosti
825712, interní kód Repo. 857560, interní kód Repo. RECETOX RI II, velká výzkumná infrastruktura.
Změněno: 31. 7. 2025 00:50, RNDr. Daniel Jakubík
Anotace
V originále
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.