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癌基因B细胞淋巴瘤6在胎盘滋养层细胞融合与分化过程中的作用。

Involvement of the oncogene B-cell lymphoma 6 in the fusion and differentiation process of trophoblastic cells of the placenta.

作者信息

Jasmer Britta, Muschol-Steinmetz Cornelia, Kreis Nina-Naomi, Friemel Alexandra, Kielland-Kaisen Ulrikke, Brüggmann Dörthe, Jennewein Lukas, Allert Roman, Solbach Christine, Yuan Juping, Louwen Frank

机构信息

Department of Gynecology and Obstetrics, School of Medicine, J. W. Goethe-University, Theodor-Stern-Kai 7, D-60590 Frankfurt, Germany.

出版信息

Oncotarget. 2017 Aug 24;8(65):108643-108654. doi: 10.18632/oncotarget.20586. eCollection 2017 Dec 12.

DOI:10.18632/oncotarget.20586
PMID:29312557
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5752470/
Abstract

The oncogene B-cell lymphoma 6 (BCL6) is associated with lymphomagenesis. Intriguingly, its expression is increased in preeclamptic placentas. Preeclampsia is one of the leading causes of maternal and perinatal mortality and morbidity. Preeclamptic placentas are characterized by various defects like deregulated differentiation and impaired fusion of trophoblasts. Its pathogenesis is however not totally understood. We show here that BCL6 is present throughout the cell fusion process in the fusogenic trophoblastic cell line BeWo. Suppression of BCL6 promotes trophoblast fusion, indicated by enhanced levels of fusion-related β-hCG, syncytin 1 and syncytin 2. Increased mRNA levels of these genes could also be observed in primary term cytotrophoblasts depleted of BCL6. Conversely, stable overexpression of BCL6 reduces the fusion capacity of BeWo cells. These data suggest that an accurately regulated expression of BCL6 is important for proper differentiation and successful syncytialization of trophoblasts. While deregulated BCL6 is linked to lymphomagenesis by blocking lymphocyte terminal differentiation, increased BCL6 in the placenta contributes to the development of preeclampsia by impairing trophoblast differentiation and fusion.

摘要

致癌基因B细胞淋巴瘤6(BCL6)与淋巴瘤的发生有关。有趣的是,其在子痫前期胎盘组织中的表达上调。子痫前期是孕产妇和围产儿死亡及发病的主要原因之一。子痫前期胎盘的特征是存在各种缺陷,如滋养层细胞分化失调和融合受损。然而,其发病机制尚未完全明确。我们在此研究表明,在具有融合能力的滋养层细胞系BeWo中,BCL6在整个细胞融合过程中均有表达。BCL6表达的抑制促进了滋养层细胞的融合,表现为融合相关的β - 人绒毛膜促性腺激素(β - hCG)、合胞素1和合胞素2水平升高。在BCL6缺失的足月原代细胞滋养层细胞中,也可观察到这些基因的mRNA水平升高。相反,BCL6的稳定过表达降低了BeWo细胞的融合能力。这些数据表明,BCL6的精确调控表达对于滋养层细胞的正常分化和成功合体化至关重要。虽然BCL6失调通过阻断淋巴细胞终末分化与淋巴瘤发生相关,但胎盘组织中BCL6表达增加通过损害滋养层细胞分化和融合,促使子痫前期的发生发展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d899/5752470/0e7129f7699d/oncotarget-08-108643-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d899/5752470/da26748ce54e/oncotarget-08-108643-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d899/5752470/1e820db35555/oncotarget-08-108643-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d899/5752470/55df869bd81d/oncotarget-08-108643-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d899/5752470/c191d6134655/oncotarget-08-108643-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d899/5752470/2e89549aaf40/oncotarget-08-108643-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d899/5752470/0e7129f7699d/oncotarget-08-108643-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d899/5752470/da26748ce54e/oncotarget-08-108643-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d899/5752470/1e820db35555/oncotarget-08-108643-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d899/5752470/55df869bd81d/oncotarget-08-108643-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d899/5752470/c191d6134655/oncotarget-08-108643-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d899/5752470/2e89549aaf40/oncotarget-08-108643-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d899/5752470/0e7129f7699d/oncotarget-08-108643-g006.jpg

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