Involvement of endoplasmic reticulum stress in regulation of endometrial stromal cell invasiveness: possible role in pathogenesis of endometriosis

Choi J, JongYeob Choi, Jo M, MinWha Jo, Eunyoung Lee, Lee E, Dong‐Yun Lee, Lee DY, Dong-Yun Lee, DooSeok Choi, Choi D
Molecular human reproduction · 2019 · vol. 25(3) , pp. 101–110 · doi:10.1093/molehr/gaz002 · PMID:30657961 · W2911072271
Lab / animal OA: bronze CC0 ⤵ 14 in-corpus citations
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Endoplasmic reticulum stress reduces normal endometrial stromal cell invasiveness via the AKT/mTOR pathway, but this response is impaired in endometriotic cells, leading to increased invasiveness.

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Abstract

Endoplasmic reticulum (ER) stress is known to reduce invasiveness in some cancer cells by inhibiting the AKT/mTOR pathway. A previous study from our laboratory suggested that ER stress is promoted by progesterone in human endometrial cells, which suggests that progesterone may inhibit endometrial cell invasiveness by up-regulating ER stress. Therefore, aberrant ER stress in response to progesterone may contribute to the altered invasiveness found in endometriotic tissues. To test this hypothesis, we elucidate whether ER stress is involved in regulation of human endometrial cell invasiveness through the AKT/mTOR pathway and if this involvement is associated with altered invasiveness in endometriotic cells. Specifically, we sought to determine the effects of ER stress on AKT/mTOR pathway by evaluating ER stress-mediated CHOP/TRIB3 signaling, a negative regulator of AKT. We found that ER stress marker GRP78 expression increased with CHOP and TRIB3 expression in normal endometrial stromal cells (NESCs) treated with tunicamycin, and this increase was accompanied by decreased AKT and mTOR activity and cellular invasiveness. Similarly, progesterone increased GRP78, CHOP and TRIB3 expression in NESCs. Subsequently, inhibition of AKT and mTOR activity decreased cellular invasiveness. This progesterone-induced decrease in cellular invasiveness was reversed by inhibition of ER stress. In contrast, progesterone did not change CHOP, TRIB3, AKT, mTOR or invasiveness in endometriotic cyst stromal cells. In contrast to normal endometrium, endometriotic tissues showed no changes in CHOP, TRIB3 and invasion-related proteins (MMP2 and MMP9) expression throughout the menstrual cycle. Taken together, our findings indicate that abnormal ER stress response to progesterone increased endometriotic stromal cell invasiveness via the AKT/mTOR pathway.

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Condition tags

endometriosis

MeSH descriptors

Endometriosis Endoplasmic Reticulum Stress Stromal Cells Blotting, Western Blotting, Western Cell Cycle Proteins Cell Cycle Proteins Cell Cycle Proteins Cell Cycle Proteins Endometriosis Endometriosis Endometriosis Endoplasmic Reticulum Chaperone BiP Endoplasmic Reticulum Chaperone BiP Endoplasmic Reticulum Stress Endoplasmic Reticulum Stress Endoplasmic Reticulum Stress Female Female Humans

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Papers in the corpus that this work cites (lower rings, blue) and that cite this one (upper rings, green). Dot size scales with the paper's in-corpus citation count — bigger dot = more influential within the endo/adeno field. Click a dot to open that paper. Outer rings show 2-hop neighbours — papers reached through the immediate citers/citees. [ collapse to 1-hop ]

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