TY - JOUR
T1 - Phthalate monoesters affect membrane fluidity and cell-cell contacts in endometrial stromal adherent cell lines and spheroids
AU - Lavogina, Darja
AU - Kask, Keiu
AU - Kopanchuk, Sergei
AU - Visser, Nadja
AU - Laws, Mary
AU - Flaws, Jodi A.
AU - Kallak, Theodora Kunovac
AU - Olovsson, Matts
AU - Damdimopoulou, Pauliina
AU - Salumets, Andres
N1 - The work was supported by the Swedish Research Council for Environment, Agricultural Sciences and Spatial Planning (FORMAS, 2018-02280), The Family Planning foundation, Orion Research Foundation sr, the Estonian Research Council (grant no. PRG1076 and grant no. PSG608) and Horizon Europe (NESTOR, grant no. GA101120075).
PY - 2024/12
Y1 - 2024/12
N2 - Phthalate monoesters have been identified as endocrine disruptors in a variety of models, yet understanding of their exact mechanisms of action and molecular targets in cells remains incomplete. Here, we set to determine whether epidemiologically relevant mono(2-ethyl-5-hydroxyhexyl) phthalate (MEHHP) can affect biological processes by altering cell plasma membrane fluidity or formation of cell-cell contacts. As a model system, we chose endometrial stromal cell lines, one of which was previously used in a transcriptomic study with MEHHP or MEHHP-containing mixtures. A short-term exposure (1 h) of membrane preparations to endocrine disruptors was sufficient to induce changes in membrane fluidity/rigidity, whereas different mixtures showed different effects at various depths of the bilayer. A longer exposure (96 h) affected the ability of cells to form spheroids and highlighted issues with membrane integrity in loosely assembled spheroids. Finally, in spheroids assembled from T-HESC cells, MEHHP interfered with the formation of cell-cell contacts as indicated by the immunostaining of zonula occludens 1 protein. Overall, this study emphasized the need to consider plasma membrane, membrane-bound organelles, and secretory vesicles as possible biological targets of endocrine disruptors and offered an explanation for a multitude of endocrine disruptor roles documented earlier.
AB - Phthalate monoesters have been identified as endocrine disruptors in a variety of models, yet understanding of their exact mechanisms of action and molecular targets in cells remains incomplete. Here, we set to determine whether epidemiologically relevant mono(2-ethyl-5-hydroxyhexyl) phthalate (MEHHP) can affect biological processes by altering cell plasma membrane fluidity or formation of cell-cell contacts. As a model system, we chose endometrial stromal cell lines, one of which was previously used in a transcriptomic study with MEHHP or MEHHP-containing mixtures. A short-term exposure (1 h) of membrane preparations to endocrine disruptors was sufficient to induce changes in membrane fluidity/rigidity, whereas different mixtures showed different effects at various depths of the bilayer. A longer exposure (96 h) affected the ability of cells to form spheroids and highlighted issues with membrane integrity in loosely assembled spheroids. Finally, in spheroids assembled from T-HESC cells, MEHHP interfered with the formation of cell-cell contacts as indicated by the immunostaining of zonula occludens 1 protein. Overall, this study emphasized the need to consider plasma membrane, membrane-bound organelles, and secretory vesicles as possible biological targets of endocrine disruptors and offered an explanation for a multitude of endocrine disruptor roles documented earlier.
KW - Cell-cell contacts
KW - Endocrine disruptors
KW - Endometrial stromal cells
KW - Membrane fluidity
KW - Phthalate mixtures
KW - Spheroids
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U2 - 10.1016/j.reprotox.2024.108733
DO - 10.1016/j.reprotox.2024.108733
M3 - Article
C2 - 39396682
AN - SCOPUS:85206291457
SN - 0890-6238
VL - 130
JO - Reproductive Toxicology
JF - Reproductive Toxicology
M1 - 108733
ER -