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Fractalkine receptor is expressed in mature ovarian teratomas and required for epidermal lineage differentiation

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posted on 2014-03-18, 00:00 authored by Lisa Rooper, Hilal Gurler, Andre A. Kajdacsy-Balla, Maria V. Barbolina
BACKGROUND: The goal of this study was to determine a predominant cell type expressing fractalkine receptor (CX3CR1) in mature ovarian teratomas and to establish functional significance of its expression in cell differentiation. METHODS: Specimens of ovarian teratoma and human fetal tissues were analyzed by immunohistochemistry for CX3CR1expression. Ovarian teratocarcinoma cell line PA-1 was used as a model for cell differentiation. RESULTS: We found that the majority of the specimens contained CX3CR1-positive cells of epidermal lineage. Skin keratinocytes in fetal tissues were also CX3CR1- positive. PA-1 cells with downregulated CX3CR1 failed to express a skin keratinocyte marker cytokeratin 14 when cultured on Matrigel in the presence of a morphogen, bone morphogenic protein 4 (BMP-4), as compared to those expressing scrambled shRNA. CONCLUSIONS: Here we demonstrate that CX3CR1 is expressed in both normally (fetal skin) and abnormally (ovarian teratoma) differentiated keratinocytes and is required for cell differentiation into epidermal lineage.

Funding

American Cancer Society, Illinois Division, grant #198484 (to MVB), NIH National Cancer Institute, grant #1R21CA160917 (to MVB), and Liz Tilberis Award from the Ovarian Cancer Research Fund (to MVB).

History

Publisher Statement

© 2013 Rooper et al.; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Publisher

BioMed Central

Language

  • en_US

issn

1757-2215

Issue date

2013-08-01

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