Composition of the Stroma in the Human Endometrium and Endometriosis

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This study characterized human endometrial and endometriotic stromal cells, finding minimal differences between them and suggesting the eutopic endometrial stromal microenvironment does not contribute to endometriosis pathogenesis.

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The study analyzed stromal cell composition in human eutopic endometrium and in three types of endometriotic lesions (ovarian, peritoneal, and deep infiltrating) using immunohistochemistry markers for fibroblasts (CD90), myofibroblasts (α-smooth muscle actin), and mesenchymal stromal cells (CD10 and CD140b). Quantification showed that eutopic endometrium without endometriosis and endometriosis cases had highly similar proportions of CD140b- and CD10-positive stromal cells and CD90-positive cells, with only minor differences across lesion sites and a notable reduction of CD90-positive cells in endometriotic entities versus endometrium (most in ovarian lesions) alongside a moderate increase of α-smooth muscle actin-positive cells in ovarian lesions. The authors interpret these largely unchanged marker proportions as indicating that the stromal eutopic microenvironment does not contribute to endometriosis pathogenesis, although they limited comparisons to these marker-defined cell types. This paper is centrally about endometriosis — it examines whether endometrial and endometriotic stromal cell composition differs between ectopic disease types and eutopic endometrium.

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Abstract

To analyze whether the endometrial and endometriotic microenvironment is involved in the pathogenesis of endometriosis, we characterized the stromal composition. We used CD90 for fibroblasts, α-smooth muscle actin for myofibroblasts as well as CD10 and CD140b for mesenchymal stromal cells. Quantification of eutopic endometrial stroma of cases without endometriosis showed a high percentage of stromal cells positive for CD140b (80.7%) and CD10 (67.4%), a moderate number of CD90-positive cells (57.9%), and very few α-smooth muscle actin-positive cells (8.5%). These values are highly similar to cases with endometriosis showing only minor changes: CD140b (76.7%), CD10 (63%), CD90 (53.9%), and α-smooth muscle actin (6.9%). There are no significant differences in the composition of CD140b- and CD10-positive stromal cells between the eutopic endometrial stroma and the 3 different endometriotic entities (ovarian, peritoneal, and deep infiltrating endometriosis), except for a significant difference between CD10-positive stromal cells in peritoneal lesions compared to ovarian lesions. However, the percentage of CD90-positive stromal cells was reduced in the 3 different endometriotic entities compared to the endometrium, especially significant in the ovarian lesions. In contrast, the percentage of α-smooth muscle actin-positive cells in the ovary was moderately increased. Taken together, the marker signature of eutopic endometrial and endometriotic stromal cells resembles mostly mesenchymal stromal cells. Our results show clearly that the proportion of the different stromal cell types in the endometrium with or without endometriosis does not differ significantly, thus suggesting that the stromal eutopic endometrial microenvironment does not contribute to the pathogenesis of endometriosis.
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Abstract

To analyze whether the endometrial and endometriotic microenvironment is involved in the pathogenesis of endometriosis, we characterized the stromal composition. We used CD90 for fibroblasts, α-smooth muscle actin for myofibroblasts as well as CD10 and CD140b for mesenchymal stromal cells. Quantification of eutopic endometrial stroma of cases without endometriosis showed a high percentage of stromal cells positive for CD140b (80.7%) and CD10 (67.4%), a moderate number of CD90-positive cells (57.9%), and very few α-smooth muscle actin-positive cells (8.5%). These values are highly similar to cases with endometriosis showing only minor changes: CD140b (76.7%), CD10 (63%), CD90 (53.9%), and α-smooth muscle actin (6.9%). There are no significant differences in the composition of CD140b- and CD10-positive stromal cells between the eutopic endometrial stroma and the 3 different endometriotic entities (ovarian, peritoneal, and deep infiltrating endometriosis), except for a significant difference between CD10-positive stromal cells in peritoneal lesions compared to ovarian lesions. However, the percentage of CD90-positive stromal cells was reduced in the 3 different endometriotic entities compared to the endometrium, especially significant in the ovarian lesions. In contrast, the percentage of α-smooth muscle actin-positive cells in the ovary was moderately increased. Taken together, the marker signature of eutopic endometrial and endometriotic stromal cells resembles mostly mesenchymal stromal cells. Our results show clearly that the proportion of the different stromal cell types in the endometrium with or without endometriosis does not differ significantly, thus suggesting that the stromal eutopic endometrial micro-environment does not contribute to the pathogenesis of endometriosis. Similar content being viewed by others

References

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Sci. 25, 1106–1115 (2018). https://doi.org/10.1177/1933719117734319 Published: Version of record: Issue date: DOI: https://doi.org/10.1177/1933719117734319

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endometriosisdie_deep_infiltrating

MeSH descriptors

Endometriosis Endometrium Endometrium Stromal Cells Stromal Cells Adult Cells, Cultured Endometriosis Endometrium Female Fibroblasts Fibroblasts Humans Mesenchymal Stem Cells Mesenchymal Stem Cells Middle Aged Neprilysin Neprilysin Receptor, Platelet-Derived Growth Factor beta Receptor, Platelet-Derived Growth Factor beta

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