Evidence for a Müllerian-inhibiting substance autocrine/paracrine system in adult human endometrium

• Published in: Fertility and sterility Vol. 91; no. 4; pp. 1195 - 1203
• Main Authors: Wang, Jeff, M.D, Dicken, Cary, M.D, Lustbader, Joyce W., Ph.D, Tortoriello, Drew V., M.D
• Format: Journal Article
• Language: English
• Published: New York, NY Elsevier Inc 01.04.2009; Elsevier
• Subjects: Adult; AMH; Anti-Mullerian Hormone - genetics; Anti-Mullerian Hormone - metabolism; Anti-Mullerian Hormone - pharmacology; Anti-Mullerian Hormone - physiology; Apoptosis - drug effects; Apoptosis - genetics; autocrine; Autocrine Communication - genetics; Autocrine Communication - physiology; Biological and medical sciences; Cell Proliferation - drug effects; Cell Survival - drug effects; Cell Survival - genetics; Cells, Cultured; endometrium; Endometrium - metabolism; Endometrium - physiology; Estradiol - pharmacology; Female; Gene Expression Profiling; Gynecology. Andrology. Obstetrics; Humans; Internal Medicine; Medical sciences; MIS; Obstetrics and Gynecology; paracrine; Paracrine Communication - genetics; Paracrine Communication - physiology; Progesterone - pharmacology; Receptors, Peptide - genetics; Receptors, Peptide - metabolism; Receptors, Transforming Growth Factor beta - genetics; Receptors, Transforming Growth Factor beta - metabolism; Recombinant Proteins - pharmacology; Transfection; endometrium; AMH; MIS; paracrine; autocrine; Human; Gynecology; Mullerian duct; Adult; Obstetrics; Endometrium
• ISSN: 0015-0282; 1556-5653
• DOI: 10.1016/j.fertnstert.2008.01.028

Objective To determine if adult human endometrium possesses an intact müllerian-inhibiting substance (MIS) signal transduction system and, if so, whether MIS can modulate endometrial cell viability. Design Adult human endometrial tissue was subjected to reverse transcription polymerase chain reaction (RT-PCR) analysis and immunohistochemistry. In addition, cultured human endometrial stromal cells were treated with recombinant MIS or transiently transfected with MIS and/or MIS type II receptor (MISRII) expression plasmids to assess for effects upon endometrial cell viability and apoptosis. The MIS in conditioned media was quantified by specific ELISA. Setting Academically affiliated medical center. Patient(s) Reproductive-age women undergoing routine infertility evaluation. Intervention(s) Endometrial sampling. Main Outcome Measure(s) Assessment of MIS gene transcription and protein translation in human endometrial tissue in vivo and in vitro. Result(s) 1) The RT-PCR revealed that adult human endometrium expresses the genes for MIS, MISRII, ALK3, and Smads 1 and 9. 2) Immunohistochemistry reveals that MIS and MISRII protein are expressed in human endometrium. 3) Immunocytochemistry of cultured human endometrial cells reveals that MIS and MISRII protein are primarily restricted to mitosing cells. 4) ELISA reveals that MIS is secreted by human endometrial cells in vitro and that this process is increased by sex steroids. 5) Increasing local MIS concentration in cultured human endometrial stromal cells either by exogenous administration or transient transfection significantly decreases cell viability and increases apoptosis. Conclusion(s) Adult human endometrium possesses a functional MIS signal transduction system which negatively regulates cellular viability.