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Cyclic Changes of Lymphatic and Venous Vessels in Human Endometrium

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Context: Cyclic changes of endometrial arteries are well established but possible cyclic changes of lymphatic and venous vessels have not been fully documented. There are no published morphological reports to support cyclic changes of endometrial lymphatic and venous vessels. Objective: Using cryosections of human endometrium, this study aimed to unveil possible cyclic changes of lymphatic and venous vessels. We previously reported cyclic changes of lymphatic vessels in human endometrium using D2-40. Design: A total of 16 cases representing menstrual, proliferative and mid and late secretary phase were studied. For Immunocytochemical staining, lymphatic vessel endothelial hyaluronan receptor 1 and von Willebr and factor were used for lymphatic and venous vessels, respectively. We used polyclonal LYVE-1 in this study, which revealed more lymphatic vessels than using D2-40. Results: Residual lymphatic and venous vessels were present in menstrual basalis. In Day 5 - 9 endometrium, there were sparse lymphatic vessels but were numerous growing venous vessels in thin proliferating functionalis. In Day 14 - 22 endometrium, there were scattered lymphatic vessels and numerous venous vessels in functionalis. In Day 25 - 26 endometrium, there were many dilated lymphatic vessels and numerous dilated, disintegrating venous vessels in upper functionalis than lower functionalis. Conclusion: The above findings support that lymphatic vessels are sparse but venous vessels are numerous in early proliferative functionalis. Lymphatic vessels grow from basalis to thin functionalis. In premenstrual phase, lymphatic vessels proliferate from lower to upper functionalis, and both lymphatic and venous vessels disintegrate for shedding by this immunocytochemical study using lymphatic and venous markers. Thus, all lymphatic, venous and arterial vessels undergo menstrual cyclic changes and shed for menstruation.
Cite this paper
Tomita, T. and Mah, K. (2014) Cyclic Changes of Lymphatic and Venous Vessels in Human Endometrium. Open Journal of Pathology, 4, 194-205. doi: 10.4236/ojpathology.2014.44025
 

[1] Buga, G.A.B. (2007) The Normal Menstrual Cycle. In: Kruger, T.F. and Batha, M.H., Eds., Clinical Gynecology, 3rd Edition, Juta & Co., Cape Town, 73-87.
[2] Mutter, G.L. and Frenczy, A. (2002) Anatomy and Histology of the Uterine Corpus. In: Kurman, R.J., Ed., Blaunstein’s Pathology of the Female Genital Tract, 5th Edition, Springer, New York, 383-419.
[3] Lumsden, M.A., McGavigean, J. (2002) Menstruation and Menstrual Disorder. In: Gynecology, Elsevier, Philadelphia, 459-476.
[4] Tomita, T. (2007) Immunocytochemical Localization of Lymphatic and Venous Vesselsincolonic Polyps and Adenomas. Digestive Diseases and Sciences, 53, 1880-1885. http://dx.doi.org/10.1007/s10620-007-0078-9
[5] Tomita, T. (2009) LYVE-1 Immunocytochemical Staining for Gastrointestinal Carcinoids. Pathology, 41, 248-253. http://dx.doi.org/10.1080/00313020902756253
[6] Koukoulakis, M., Giatromanolaki, A., Sivridis, E., et al. (2005) LYVE-1 Immunohistochemical Assessment of Lymphangiogenesis in Endometrial and Lung Cancer. Journal of Clinical Pathology, 58, 202-206. http://dx.doi.org/10.1136/jcp.2004.019174
[7] Red-Horse, K., Rivera, J., Shatz, A., Zhou, Y., Winn, V., et al. (2006) Cytotrophoblast Induction of Arterial Apoptosis and Lymphangiogenesis in an in Vitro Model of Human Placentation. Journal of Clinical Investigation, 116, 2643-2652. http://dx.doi.org/10.1172/JCI27306.
[8] Blackwell, P. and Fraser, I. (1981) Superficial Lymphatics in the Functionalis Zone of Normal Human Endometrium. Microvascular Research, 21, 142-152. http://dx.doi.org/10.1016/0026-2862(81)90027-3
[9] Uchino, S., Ishikawa, S., Okuno, M., Nakamura, Y. and Imura, A. (1987) Methods of Detection of Lymphatics and Their Changes with Oesterous Cycle. International Angiology, 6, 271-278.
[10] Garling, J.E. and Rogers, P.A.W. (2012) The Endometrial Lymphatic Vasculature: Function and Dysfunction. Reviews in Endocrine and Metabolic Disorders, 13, 265-275.
http://dx.doi.org/10.1007/s11154-012-9224-6
[11] Rogers, P.A.W., Donoghue, J.F. and Girling, J.E. (2008) Endometrial Lymphangiogenesis. Placenta, 22, 48-54. http://dx.doi.org/10.1016/j.placenta.2007.09.009
[12] Rogers, P.A.W., Donoghue, J.F., Walter, L.M., et al. (2009) Endometrial Angiogenesis, Vascular Maturation and Lymphangiogenesis. Reproductive Sciences, 16, 147-151.
http://dx.doi.org/10.1177/1933719108325509
[13] Brenner, R.M., Slayden, O.D., Rodgers, W.H., et al. (2003) Immunocytochemical Assessment of Mitotic Activity with an Antibody to Phosphorylated Histone H3 in the Macaque and Human Endometrium. Human Reproduction, 18, 1185-1193. http://dx.doi.org/10.1093/humrep/deg255
[14] Nayak, N.R., Critchley, H.O.D., Slayden, O.D., Menrad, A., Schwalisz, K., Baird, D.T. and Brenner, R.M. (2000) Progesterone Withdrawal Up-Regulates Vascular Endothelial Growth Factor Receptor Type 2 in the Superficial Zone Stroma of the Human and Macaque Endometrium. The Journal of Clinical Endocrinology and Metabolism, 85, 3443-3452.
[15] Slayden, O.D., Nayak, N.R., Burton, K.A., Chwalisz, K., Cameron, S.T., Critchley, H.O.D., Baird, D.T. and Brenner, R.M. (2001) Progesterone Antagonists Increase Androgen Receptor Expression in the Rhesus Macaque and Human Endometrium. The Journal of Clinical Endocrinology and Metabolism, 86, 2668-2679.
[16] Tomita, T. (2014) Cyclic Changes of Lymphaticvessels in Human Endometrium. Open Journal of Pathology, 4, 5-12. http://dx.doi.org/10.4236/ojpathology.2014.41002
[17] Slayden, O.D., Koji, T. and Brenner, R.M. (1995) Microwave Stabilization Enhances Immunocytochemical Detection of Estrogen Receptor in Frozen Sections of Macaque Oviduct. Endocrinology, 136, 4012-4021.
[18] Tomita, T., Mah, K., Cao, W.G., Brenner, R.M., et al. (2006) Cyclic Changes in Endometrial Lymphatics. Journal of the Society for Gynecologic Investigation, 13, 81A. (Abstract)
[19] Rogers, P.A. (1996) Structure and Function of Endometrial Blood Vessels. Human Reproduction, 2, 57-62. http://dx.doi.org/10.4236/ojpathology.2014.41002
[20] Benerg, S., Ni, J., Wang, S.X., Clasper, S., Su, J., et al. (1999) Lyve-1, a New Homologue of the CD 44 Glycoprotein, Is a Lymph Specific Receptor for Hyaluronan. The Journal of Cell Biology, 144, 789-801. http://dx.doi.org/10.1083/jcb.144.4.789
[21] Jackson, D.J. (2003) The Lymphatics Revisited: New Prospective from the Hyaluronan Receptor LYVE-1. Trends in Cardiovascular Medicine, 13, 1-7. http://dx.doi.org/10.1016/S1050-1738(02)00189-5
[22] Jackson, D.G. (2009) Immunological Features of Hyaluronan and Its Receptors in the Lymphatics. Immunological Reviews, 230, 216-231. http://dx.doi.org/10.1111/j.1600-065X.2009.00803.x
[23] Marks, A., Sutherland, D.R., Bailey, D., Iglesias, J., Law, J., et al. (1999) Characterization and Distribution of an Oncofetal Antigen (M2A Antigen) Expressed on Testicular Germ Cell Tumors. British Journal of Cancer, 80, 569-578. http://dx.doi.org/10.1038/sj.bjc.6690393
[24] Franke, F.E., Pauls, K., Marks, S., Bergmann, M., et al. (2002) Differentiation Markers of Sertoli Cells and Germ Cells in Fetal and Early Postnatal Human Testis. Anatomy and Embryology, 209, 169-177.
[25] Kahn, H.J. and Marks, A. (2002) A New Monoclonal Antibody, D2-40, for Detection of Lymphatic Invasion of Primary Tumors. Laboratory Investigation, 82, 1255-1257.
http://dx.doi.org/10.1097/01.LAB.0000028824.03032.AB
[26] Rogers, P.A.W., Donoghue, J.F., Walter, L.M. and Girling, J.E. (2009) Endometrial Angiogenesis, Vascular Maturation and Lymphangiogenesis. Reproductive Sciences, 16, 147-151.
http://dx.doi.org/10.1177/1933719108325509
[27] Uyeki, M. (1991) Histologic Study of Endometriosis and Examination of Lymph Drainage in and from Uterus. American Journal of Obstetrics & Gynecology, 165, 201-209. http://dx.doi.org/10.1016/0002-9378(91)90252-M
[28] Fraser, I.S. and Peek, M.J. (1992) Effects of Exogenous Hormonesones on Endometrialcapillaries. In: Alexander, N.J. and d’Arcangues, C., Eds., Steroid Hormones and Uterine Bleeding, AAAS Press, Washington DC, 67-79.
[29] Donoghue, J.F., McGavigan, C.J., Lederman, F.L., Cann, L.M., Fu, L., et al. (2012) Dilated Thin-Walled Blood and Lymphatic Vessels in Human Endometrium: A Potential Role for VEGF-D in Progestin-Induced Break-Through Bleeding. PLos ONE, 7, e30916.
http://dx.doi.org/10.1371/journal.pone.0030916
[30] Frenczy, A., Bertrand, G. and Gelfand, M.M. (1979) Proliferation Kinetics of Human Endometrium during the Normal Menstrual Cycle. American Journal of Obstetrics & Gynecology, 133, 859-869.
[31] Ramsey, E.M. (1982) Vascular Anatomy. In: Wynn, R.M., Ed., Biology of the Uterus, 2nd Edition, Plenum Press, New York, 59-76.        eww141023lx

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