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轴突导向因子 1 促进肝癌细胞在 3D 细胞培养模型中的集体细胞迁移。

Netrin-1 promotes the collective cell migration of liver cancer cells in a 3D cell culture model.

机构信息

Department of Gastroenterology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, 1095# Jiefang Avenue, Wuhan, 430030, People's Republic of China.

出版信息

J Physiol Biochem. 2019 Nov;75(4):489-498. doi: 10.1007/s13105-019-00701-8. Epub 2019 Aug 12.

DOI:10.1007/s13105-019-00701-8
PMID:31407237
Abstract

Collective cell migration plays an important role in embryonic development, wound healing, and cancer metastasis. We aimed to investigate the expression, role, and mechanism of Netrin-1 in collective cell migration using a3D culture model. An immunohistochemical study showed that certain cells invaded surrounding tissue by collective migration and that Netrin-1 expression in these cells was increased, especially at the invasive front. In the 3D culture model, collective cell migration was clearly observed, as leader cells were followed by cells migrating along a canal. N-cadherin-mediated cell junctions were observed in collective cell migration, and Netrin-1 expression was elevated in these cells. Netrin-1 did not affect the expression of N-cadherin in 2D-cultured cells; however, in 3D culture, the overexpression of Netrin-1 increased N-cadherin and promoted the collective migration of Huh7 cells, while the knockdown of Netrin-1 decreased N-cadherin and inhibited collective migration in SK-Hep-1 cells. Interestingly, N-cadherin knockdown in Huh7 cells significantly diminished Netrin-1-promoted collective cell migration, while the overexpression of N-cadherin restored collective migration in Netrin-1-knockdown SK-Hep1 cells. These results suggest that Netrin-1 enhances N-cadherin junctions to promote liver cancer cell collective migration in 3D cell culture and may subsequently increase liver cancer metastasis.

摘要

细胞集体迁移在胚胎发育、伤口愈合和癌症转移中起着重要作用。我们旨在使用 3D 培养模型研究 Netrin-1 在细胞集体迁移中的表达、作用和机制。免疫组织化学研究表明,某些细胞通过集体迁移侵犯周围组织,这些细胞中的 Netrin-1 表达增加,尤其是在侵袭前沿。在 3D 培养模型中,明显观察到细胞集体迁移,先导细胞被沿着通道迁移的细胞跟随。在细胞集体迁移中观察到 N-钙粘蛋白介导的细胞连接,并且这些细胞中的 Netrin-1 表达增加。Netrin-1 不会影响 2D 培养细胞中 N-钙粘蛋白的表达;然而,在 3D 培养中,Netrin-1 的过表达增加了 N-钙粘蛋白并促进了 Huh7 细胞的集体迁移,而 Netrin-1 的敲低减少了 N-钙粘蛋白并抑制了 SK-Hep-1 细胞的集体迁移。有趣的是,Huh7 细胞中 N-钙粘蛋白的敲低显著减弱了 Netrin-1 促进的细胞集体迁移,而 Netrin-1 敲低的 SK-Hep1 细胞中 N-钙粘蛋白的过表达恢复了细胞集体迁移。这些结果表明,Netrin-1 增强了 N-钙粘蛋白连接,以促进 3D 细胞培养中的肝癌细胞集体迁移,并且可能随后增加肝癌转移。

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