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Merck

Estrogen Signaling Drives Ciliogenesis in Human Endometrial Organoids.

Endocrinology (2019-07-11)
Sandra Haider, Magdalena Gamperl, Thomas R Burkard, Victoria Kunihs, Ulrich Kaindl, Sini Junttila, Christian Fiala, Katy Schmidt, Sasha Mendjan, Martin Knöfler, Paulina A Latos
要旨

The human endometrium is the inner lining of the uterus consisting of stromal and epithelial (secretory and ciliated) cells. It undergoes a hormonally regulated monthly cycle of growth, differentiation, and desquamation. However, how these cyclic changes control the balance between secretory and ciliated cells remains unclear. Here, we established endometrial organoids to investigate the estrogen (E2)-driven control of cell fate decisions in human endometrial epithelium. We demonstrate that they preserve the structure, expression patterns, secretory properties, and E2 responsiveness of their tissue of origin. Next, we show that the induction of ciliated cells is orchestrated by the coordinated action of E2 and NOTCH signaling. Although E2 is the primary driver, inhibition of NOTCH signaling provides a permissive environment. However, inhibition of NOTCH alone is not sufficient to trigger ciliogenesis. Overall, we provide insights into endometrial biology and propose endometrial organoids as a robust and powerful model for studying ciliogenesis in vitro.

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Sigma-Aldrich
β-エストラジオール, BioReagent, powder, suitable for cell culture
Sigma-Aldrich
抗アセチル化チューブリン抗体、マウスモノクローナル マウス宿主抗体, clone 6-11B-1, purified from hybridoma cell culture
Sigma-Aldrich
Deshydroxy LY-411575, ≥98% (HPLC)