Composition of the Stroma in the Human Endometrium and Endometriosis

• Published in: Reproductive sciences (Thousand Oaks, Calif.) Vol. 25; no. 7; pp. 1106 - 1115
• Main Authors: Konrad, Lutz, Kortum, Jessica, Nabham, Rai, Gronbach, Judith, Dietze, Raimund, Oehmke, Frank, Berkes, Eniko, Tinneberg, Hans-Rudolf
• Format: Journal Article
• Language: English
• Published: Los Angeles, CA SAGE Publications 01.07.2018; Springer International Publishing
• Subjects: Embryology; Medicine & Public Health; Obstetrics/Perinatology/Midwifery; Original Article; Reproductive Medicine; endometrium; endometriosis; stroma; CD90; CD10; CD140b
• ISSN: 1933-7191; 1933-7205
• DOI: 10.1177/1933719117734319

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.