Novel three dimensional human endocervix cultures respond to 28-day hormone treatment.

The endocervix has both anatomical and biological functions that participate in the delicate balance between tolerance necessary for conception and protection from pathogens. Our goal was to develop a robust 3-dimensional (3D) endocervix model that was a reliable representation of the in vivo tissues and to identify the physiological responses to changing levels of steroid hormones during a 28-day time period. Human endocervical cells were grown on polystyrene scaffolds, and the morphologic and hormonal responses of cultured cells were assessed in response to fluctuating levels of estradiol (E2) or progesterone (P4). Morphologically, the 3D cultures were composed of a mixed population of cells, including epithelial and stromal cells. Treatment with E2 and P4 (d 28) increased cell growth and proliferation as compared with no treatment control. Cells expressed estrogen receptor and P4 receptor and produced both neutral and acidic mucins, including Mucin 16. In addition, a 45-plex Luminex assay identified numerous factors secreted and regulated by hormones. Specifically, IL-1β and leukemia inhibitory factor significantly decreased in the presence of E2 and P4 as compared with the no hormone control at day 26. Cotreatment with RU486 (mifepristone) attenuated the inhibition of IL-1β and leukemia inhibitory factor secretion. In summary, a robust, novel 3D endocervical culture was developed, and physiologic responses to the menstrual cycle mimic of E2 and P4 levels for a period of 28 days were identified.

[1]  J. Williams,et al.  Intratracheal injection of LPS and cytokines. V. LPS induces expression of LIF and LIF inhibits acute inflammation. , 1994, The American journal of physiology.

[2]  S. Przyborski,et al.  Alvetex®: polystyrene scaffold technology for routine three dimensional cell culture. , 2011, Methods in molecular biology.

[3]  M. Cohen,et al.  The impact of the ovulatory cycle on cytokine production: evaluation of systemic, cervicovaginal, and salivary compartments. , 2000, Journal of interferon & cytokine research : the official journal of the International Society for Interferon and Cytokine Research.

[4]  P. Sluss,et al.  Age-related analysis of inhibin A, inhibin B, and activin a relative to the intercycle monotropic follicle-stimulating hormone rise in normal ovulatory women. , 2004, The Journal of clinical endocrinology and metabolism.

[5]  Dong-bao Chen,et al.  Implantation: Leukaemia inhibitory factor in human endometrium during the menstrual cycle: cellular origin and action on production of glandular epithelial cell prostaglandin in vitro , 1995 .

[6]  I. Gipson,et al.  Variation in the amount of T antigen and N-acetyllactosamine oligosaccharides in human cervical mucus secretions with the menstrual cycle. , 2002, The Journal of clinical endocrinology and metabolism.

[7]  W. Stolz,et al.  Regulated expression of cytokines in human endometrium throughout the menstrual cycle: dysregulation in habitual abortion. , 2000, Molecular human reproduction.

[8]  A. Gettie,et al.  Sex Hormones Selectively Impact the Endocervical Mucosal Microenvironment: Implications for HIV Transmission , 2014, PloS one.

[9]  E. Dimitriadis,et al.  Leukemia Inhibitory Factor Enhances Endometrial Stromal Cell Decidualization in Humans and Mice , 2011, PloS one.

[10]  G. Hughes,et al.  Cutting Edge: Progesterone Regulates IFN-α Production by Plasmacytoid Dendritic Cells1 , 2008, The Journal of Immunology.

[11]  A. Quayle,et al.  ORIGINAL ARTICLE: Quantification and Comparison of Toll‐Like Receptor Expression and Responsiveness in Primary and Immortalized Human Female Lower Genital Tract Epithelia , 2008, American journal of reproductive immunology.

[12]  J. Fahey,et al.  A new strategy to understand how HIV infects women: identification of a window of vulnerability during the menstrual cycle. , 2008, AIDS.

[13]  J. Pollard,et al.  Leukemia inhibitory factor (LIF) and LIF receptor expression in human endometrium suggests a potential autocrine/paracrine function in regulating embryo implantation. , 1996, Proceedings of the National Academy of Sciences of the United States of America.

[14]  S. Yen,et al.  Hormonal dynamics at midcycle: a reevaluation. , 1983, The Journal of clinical endocrinology and metabolism.

[15]  G. Hansson,et al.  Large Scale Identification of Proteins, Mucins, and Their O-Glycosylation in the Endocervical Mucus during the Menstrual Cycle*S , 2007, Molecular & Cellular Proteomics.

[16]  T. Chew,et al.  Myosin light chain kinase mediates transcellular intravasation of breast cancer cells through the underlying endothelial cells: a three-dimensional FRET study , 2010, Journal of Cell Science.

[17]  S. Wallenstein,et al.  PRO 2000 elicits a decline in genital tract immune mediators without compromising intrinsic antimicrobial activity , 2007, AIDS.

[18]  R. Ritter,et al.  Comparison of Mucin Levels at the Ocular Surface of Postmenopausal Women With and Without a History of Dry Eye , 2011, Cornea.

[19]  M. Tsujimoto,et al.  Increased interleukin-1 and interleukin-1 receptor antagonist levels in cervical mucus in the ovulatory phase in comparison with the follicular phase. , 1997, Gynecologic and obstetric investigation.

[20]  G. Buirski,et al.  Increased levels of leukemia inhibitory factor in synovial fluid from patients with rheumatoid arthritis and other inflammatory arthritides. , 1993, Arthritis and rheumatism.

[21]  J. Mestecky,et al.  Mucosal immunity in the female reproductive tract: correlation of immunoglobulins, cytokines, and reproductive hormones in human cervical mucus around the time of ovulation. , 1998, AIDS research and human retroviruses.

[22]  H. Miyaura,et al.  Direct and Indirect Inhibition of Th1 Development by Progesterone and Glucocorticoids1 , 2002, The Journal of Immunology.

[23]  J. Baeten,et al.  Use of hormonal contraceptives and risk of HIV-1 transmission : a prospective cohort study , 2011 .

[24]  J. Sinden,et al.  The effects of microRNAs on human neural stem cell differentiation in two- and three-dimensional cultures , 2014, Stem Cell Research & Therapy.

[25]  W. Okulicz,et al.  Differential gene regulation by estrogen and progesterone in the primate endometrium , 1995, Molecular and Cellular Endocrinology.

[26]  Maria Bokhari,et al.  Culture of HepG2 liver cells on three dimensional polystyrene scaffolds enhances cell structure and function during toxicological challenge , 2007, Journal of anatomy.

[27]  M. Piccinni T‐cell Cytokines in Pregnancy , 2002, American journal of reproductive immunology.

[28]  I. Gipson Mucins of the human endocervix. , 2001, Frontiers in bioscience : a journal and virtual library.