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Biology of Reproduction 60, 428-434 (1999)
©Copyright 1999 Society for the Study of Reproduction, Inc.

Expression of Cell Adhesion Molecules in Murine Placentas and a Placental Cell Line1

Jeffery A. Bowena, and Joan S. Hunt2,a

a Department of Anatomy and Cell Biology, University of Kansas Medical Center, Kansas City, Kansas 66160-7400

Integrins and vascular cell adhesion molecule-1 (VCAM-1) are required for normal placental development. In this study, integrin subunits {alpha}4, {alpha}v, ß1, and ß3, and VCAM-1 were investigated for expression in uteroplacental units (gestation day [g.d.] 6 and 8) and placentas (g.d. 10, 12, 14, 16, and 18) of Swiss-Webster mice. All subunits and VCAM-1 mRNA (identified by reverse transcriptase polymerase chain reaction [RT-PCR]) and protein (detected by immunofluorescence) were present in all tissues throughout gestation. VCAM-1 was expressed strongly in the ectoplacental cone and trophoblast giant cells, {alpha}4 was expressed strongly by trophoblast giant cells and moderately by spongiotrophoblast and labyrinthine trophoblast, and {alpha}v was expressed more strongly in the spongiotrophoblast than in the labyrinthine zone. The ß1 was more strongly expressed in the labyrinthine than the spongiotrophoblast zone, while ß3 and VCAM-1 were essentially equal in the two zones. Trophoblast-like SM9–1 cells were positive for all of the adhesion molecules when tested by RT-PCR and immunocytochemistry. Adhesion molecule expression in SM9–1 cells was consistent with expression in the labyrinthine zone. Collectively, the results of this study demonstrate that murine placentas contain mRNA and protein for {alpha}4, {alpha}v, ß1, ß3, and VCAM-1, and that expression is cell-specific. These results and the identification of an adhesion molecule-expressing trophoblastic cell line should facilitate future studies on the function of adhesion molecules in placental development.

1 This work was supported by grants from the National Institutes of Health to J.S.H. (HD29156), the Kansas Mental Retardation Research Center (HD02528), and the Kansas P30 Center for Reproductive Sciences (HD33994). J.A.B. was supported in part by a Reproductive Biology Training Grant (HD07455) and a Fellowship from the Lalor Foundation.

2 Correspondence: Joan S. Hunt, Department of Anatomy and Cell Biology, University of Kansas Medical Center, 3901 Rainbow Blvd., Kansas City, KS 66160–7400. FAX: 913 588 2710; jhunt{at}kumc.edu




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