Immunohistochemical analysis of insulin-like growth factor-binding proteins -1, -2, and -3 in implantation sites of the mouse
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作者:
Damario, MA
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Cornell Univ Med Coll, Dept Obstet & Gynecol, Ctr Reprod Med & Infertil, New York, NY USACornell Univ Med Coll, Dept Obstet & Gynecol, Ctr Reprod Med & Infertil, New York, NY USA
Damario, MA
[1
]
Liu, HC
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Cornell Univ Med Coll, Dept Obstet & Gynecol, Ctr Reprod Med & Infertil, New York, NY USACornell Univ Med Coll, Dept Obstet & Gynecol, Ctr Reprod Med & Infertil, New York, NY USA
Liu, HC
[1
]
Mele, CA
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Cornell Univ Med Coll, Dept Obstet & Gynecol, Ctr Reprod Med & Infertil, New York, NY USACornell Univ Med Coll, Dept Obstet & Gynecol, Ctr Reprod Med & Infertil, New York, NY USA
Mele, CA
[1
]
Horenstein, MG
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Cornell Univ Med Coll, Dept Obstet & Gynecol, Ctr Reprod Med & Infertil, New York, NY USACornell Univ Med Coll, Dept Obstet & Gynecol, Ctr Reprod Med & Infertil, New York, NY USA
Horenstein, MG
[1
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Rosenwaks, Z
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Cornell Univ Med Coll, Dept Obstet & Gynecol, Ctr Reprod Med & Infertil, New York, NY USACornell Univ Med Coll, Dept Obstet & Gynecol, Ctr Reprod Med & Infertil, New York, NY USA
Rosenwaks, Z
[1
]
机构:
[1] Cornell Univ Med Coll, Dept Obstet & Gynecol, Ctr Reprod Med & Infertil, New York, NY USA
Purpose: Our purpose was to analyze potential interactions between the embryo and the maternal endometrial interface in vivo by analyzing immunolocalization of insulin-like growth factor-binding proteins (IGFBPs) -1, -2, and -3 in implantation sites of the mouse. Methods: Six-week-old B6D2F1 female mice underwent superovulation followed by mating and sacrifice at timed intervals. Formalin-fixed paraffin-embedded tissue was used for avidin-biotin immunocytochemical localization of IGFBPs utilizing standard methodology. Results: Immunostaining at 1.5 days post coitum revealed light staining in the epithelial glandular cells and faint staining in decidual stroma for both IGFBP-1 and IGFBP-2. At 7.5-10.5 days post coitum, there was moderate-dense immunostaining in the decidualized stromal cells at the implantation site for all three IGFBPs, whereas light immunostaining was seen in nonimplantation site decidua. Conclusions: Compartmentalization of immunostaining for IGFBP-1, -2, and -3 within decidualized stroma suggests that these proteins may be regulated by trophoblastic and/ or embryonic signals.