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Published on: May 23, 2014
Presence of immunoreactive corticotropin-releasing hormone in human endometrium
G Mastorakos1, C D Scopa, L C Kao
1Developmental Endocrinology Branch, National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland 20892, USA.
Insights
Corticotropin-releasing hormone (CRH) is present in the human endometrium, particularly in glandular cells. This finding suggests CRH may play a role in endometrial processes like repair and implantation.
Area of Science:
- Reproductive Endocrinology
- Immunology
- Cell Biology
Background:
- Immunoreactive corticotropin-releasing hormone (IrCRH) is produced locally in inflammatory conditions and by reproductive organs.
- CRH is secreted in vitro by human endometrial cells, suggesting a potential role in endometrial physiology.
Purpose of the Study:
- To investigate the presence and localization of CRH in the human endometrium in vivo.
- To explore the potential role of endometrial CRH in physiological processes.
Main Methods:
- Immunohistochemistry and extraction/radioimmunoassay (RIA) were used to detect IrCRH in endometrial biopsies from 33 women.
- Reverse-phase high-pressure liquid chromatography was employed to analyze the molecular properties of endometrial CRH.
Main Results:
- Intense IrCRH staining was observed in the cytoplasm of endometrial glandular cells across all menstrual cycle stages.
- IrCRH was also detected in decidualized stromal cells and local immune accessory cells.
- Endometrial CRH molecule characteristics were similar to rat/human CRH.
Conclusions:
- The presence of CRH in the human endometrium, especially glandular epithelium, supports its role in inflammatory-like endometrial processes.
- CRH may be involved in menstrual shedding, epithelial repair, and blastocyst implantation.
- CRH in decidualized stromal cells aligns with previous in vitro findings and placental CRH production.
Abstract:
Immunoreactive CRH (IrCRH) is produced locally in experimentally induced and spontaneous inflammation. Where it exerts autocrine or paracrine proinflammatory effects. In addition, CRH is secreted by the human placenta, rat Leydig cells, and rat and human ovaries, where it may participate in the inflammatory processes of ovulation and luteolysis, and/or the regulation of steroidogenesis. Finally, CRH is secreted in vitro by cultured human epithelial and decidualized stromal endometrial cells. To investigate the presence of CRH in human endometrium in vivo, we examined this tissue immunohistochemically and by extraction/RIA using a polyclonal, highly specific antirat/human CRH antibody. Endometrial biopsies from 33 women, aged 23-43 yr (median age, 33.5 yr), were performed by linear endometrial curettage for diagnostic purposes at different stages of the cycle. Intense IrCRH staining was localized in the cytoplasm of cells of the endometrial glands in all samples examined. IrCRH was also found in endometrial stromal cells exhibiting decidual reaction and in local immune accessory cells. The mobility of the endometrial IrCRH molecule was similar to that of r/hCRH in reverse phase high pressure liquid chromatography. The presence of CRH in the endometrium, and more specifically in the glandular epithelium during the proliferative and secretory phases of the menstrual cycle together with its known proinflammatory properties, suggest that this neuropeptide might participate in the inflammatory-like phenomena of endometrial physiology, such as menstrual shedding, surface epithelium repair, and/or implantation of the blastocyst. The presence of CRH in decidualized stromal cells is in accordance with its previously reported production by in vitro decidualized cultured endometrial stromal cells as well as by the placental decidua.
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