TY - JOUR
T1 - Intermedin/adrenomedullin 2 is associated with implantation and placentation via trophoblast invasion in human pregnancy
AU - Havemann, Dara
AU - Balakrishnan, Meena
AU - Borahay, Mostafa
AU - Theiler, Regan
AU - Jennings, Kristofer
AU - Endsley, Janice
AU - Phelps, John
AU - Hankins, Gary D.V.
AU - Yallampalli, Chandra
AU - Chauhan, Madhu
PY - 2013/2
Y1 - 2013/2
N2 - Rationale: Intermedin (IMD) is a novel peptide expressed in trophoblast cells inhumanplacentaand enhances the invasion, migration, and human leukocyte antigen class I, G (HLA-G) expression in first-trimester HTR-8SV/neo cells. Werecently reported that infusion of IMD antagonist in pregnant rats is detrimental to pregnancy outcome, resulting in impaired fetoplacental growth and deformed placental vasculature. Objective: This study was undertaken to assess expression of IMD and its involvement in human implantation and early placentation and assess whether its expression is altered in spontaneous abortion. Findings and Conclusions: Wedemonstrate for the first time that IMD is present in day 5 embryonic secretome; villous and decidual expression of IMD is higher at 6-8 weeks after a decline as gestation advances toward the second trimester; first-trimester spontaneous abortion is associated with a lower expression of IMD in serum, villi, and decidua; IMD stimulates the invasive capacity of first-trimester primary Extravillous cytotrophoblast cells; and IMD decreases elevated levels of tumor suppressor Kangia-1 in decidual explants from first-trimester spontaneous abortion. In conclusion, this study is the first to demonstrate a potential involvement of IMD in human embryo implantation and placental development via regulation of trophoblast invasion at the maternalfetal interface and suggests a physiological role for this novel peptide in establishment of human pregnancy.
AB - Rationale: Intermedin (IMD) is a novel peptide expressed in trophoblast cells inhumanplacentaand enhances the invasion, migration, and human leukocyte antigen class I, G (HLA-G) expression in first-trimester HTR-8SV/neo cells. Werecently reported that infusion of IMD antagonist in pregnant rats is detrimental to pregnancy outcome, resulting in impaired fetoplacental growth and deformed placental vasculature. Objective: This study was undertaken to assess expression of IMD and its involvement in human implantation and early placentation and assess whether its expression is altered in spontaneous abortion. Findings and Conclusions: Wedemonstrate for the first time that IMD is present in day 5 embryonic secretome; villous and decidual expression of IMD is higher at 6-8 weeks after a decline as gestation advances toward the second trimester; first-trimester spontaneous abortion is associated with a lower expression of IMD in serum, villi, and decidua; IMD stimulates the invasive capacity of first-trimester primary Extravillous cytotrophoblast cells; and IMD decreases elevated levels of tumor suppressor Kangia-1 in decidual explants from first-trimester spontaneous abortion. In conclusion, this study is the first to demonstrate a potential involvement of IMD in human embryo implantation and placental development via regulation of trophoblast invasion at the maternalfetal interface and suggests a physiological role for this novel peptide in establishment of human pregnancy.
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U2 - 10.1210/jc.2012-2172
DO - 10.1210/jc.2012-2172
M3 - Article
C2 - 23337723
AN - SCOPUS:84873622472
SN - 0021-972X
VL - 98
SP - 695
EP - 703
JO - Journal of Clinical Endocrinology and Metabolism
JF - Journal of Clinical Endocrinology and Metabolism
IS - 2
ER -