Transcription Factor CCAAT Enhancer-binding Protein β (C/EBPβ) Regulates the Formation of a Unique Extracellular Matrix That Controls Uterine Stromal Differentiation and Embryo Implantation

被引:22
|
作者
Ramathal, Cyril [2 ,4 ]
Wang, Wei [1 ,4 ]
Hunt, Elizabeth [1 ,4 ]
Bagchi, Indrani C. [3 ,4 ]
Bagchi, Milan K. [1 ,4 ]
机构
[1] Univ Illinois, Dept Mol & Integrat Physiol, Urbana, IL 61801 USA
[2] Univ Illinois, Dept Cell & Dev Biol, Urbana, IL 61801 USA
[3] Univ Illinois, Dept Comparat Biosci, Urbana, IL 61801 USA
[4] Univ Illinois, Ctr Res Reprod & Infertil, Urbana, IL 61801 USA
基金
美国国家卫生研究院;
关键词
BASEMENT-MEMBRANES; CELL-PROLIFERATION; TROPHOBLAST CELLS; MESSENGER-RNA; IN-VITRO; LAMININ; MOUSE; DECIDUALIZATION; EXPRESSION; LOCALIZATION;
D O I
10.1074/jbc.M110.191759
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
During implantation, the uterine stromal cells undergo terminal differentiation into decidual cells, which support the proper progression of maternal-embryo interactions to successful establishment of pregnancy. The decidual cells synthesize extracellular matrix (ECM) components, such as laminins and collagens, which assemble into a unique basal lamina-like network that surrounds these cells. The functional significance of this matrix during implantation is unknown. We previously showed that the transcription factor CCAAT enhancer-binding protein beta (C/EBP beta) critically regulates decidualization in the mouse. We now provide evidence that C/EBP beta directly controls the Lamc1 gene, which encodes a predominant laminin constituent of the ECM produced by the decidual cells. Suppression of Lamc1 expression in mouse primary endometrial stromal cells prevented the assembly of this ECM and impaired stromal differentiation. Attenuation of expression of integrin beta 1, a major constituent of the integrin receptors targeted by decidual laminins, also inhibited this differentiation process. Disruption of laminin-integrin interactions led to impaired activation of the focal adhesion kinase, an integrin-mediated regulator of cytoskeletal remodeling during decidualization. To further analyze the role of the decidual ECM in modulating maternal-embryo interactions, we monitored trophoblast invasion into differentiating uterine stromal monolayers, using a co-culture system. Silencing of stromal Lamc1 expression, which prevented formation of the basal lamina-like matrix, resulted in marked reduction in trophoblast outgrowth. Collectively, our findings identified C/EBP beta as a critical regulator of the unique ECM that controls decidual cell architecture and differentiation, and it provided new insights into the mechanisms by which the uterine stromal microenvironment controls the progression of embryo implantation.
引用
收藏
页码:19860 / 19871
页数:12
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