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细胞密度感应以细胞类型特异性的方式改变 TGF-β 信号,而不依赖 Hippo 通路的激活。

Cell density sensing alters TGF-β signaling in a cell-type-specific manner, independent from Hippo pathway activation.

机构信息

Institut Curie, Centre de Recherche, Team "TGF-β and Oncogenesis," Equipe Labellisée Ligue Contre le Cancer, 91400 Orsay, France; INSERM U1021, 91400 Orsay, France; CNRS UMR 3347, 91400 Orsay, France; Université Paris XI, 91400 Orsay, France.

Thoracic Disease Research Unit, Departments of Biochemistry/Molecular Biology and Medicine, Mayo Clinic Cancer Center, Rochester, MN 55905, USA.

出版信息

Dev Cell. 2015 Mar 9;32(5):640-51. doi: 10.1016/j.devcel.2015.01.011.

Abstract

Cell-cell contacts inhibit cell growth and proliferation in part by activating the Hippo pathway that drives the phosphorylation and nuclear exclusion of the transcriptional coactivators YAP and TAZ. Cell density and Hippo signaling have also been reported to block transforming growth factor β (TGF-β) responses, based on the ability of phospho-YAP/TAZ to sequester TGF-β-activated SMAD complexes in the cytoplasm. Herein, we provide evidence that epithelial cell polarization interferes with TGF-β signaling well upstream and independent of cytoplasmic YAP/TAZ. Rather, polarized basolateral presentation of TGF-β receptors I and II deprives apically delivered TGF-β of access to its receptors. Basolateral ligand delivery nonetheless remains entirely effective to induce TGF-β responses. These data demonstrate that cell-type-specific inhibition of TGF-β signaling by cell density is restricted to polarized epithelial cells and reflects the polarized distribution of TGF-β receptors, which thus affects SMAD activation irrespective of Hippo pathway activation.

摘要

细胞-细胞接触通过激活 Hippo 通路抑制细胞生长和增殖,该通路驱动转录共激活因子 YAP 和 TAZ 的磷酸化和核排斥。根据磷酸化 YAP/TAZ 将 TGF-β 激活的 SMAD 复合物隔离在细胞质中的能力,细胞密度和 Hippo 信号也被报道可阻断转化生长因子β (TGF-β) 反应。在此,我们提供的证据表明上皮细胞极化在上游和独立于细胞质 YAP/TAZ 干扰 TGF-β 信号。相反,TGF-β 受体 I 和 II 的极化基底外侧呈现剥夺了顶端递送至 TGF-β 的受体。基底外侧配体传递仍然完全有效以诱导 TGF-β 反应。这些数据表明,细胞密度对 TGF-β 信号的细胞类型特异性抑制仅限于极化上皮细胞,并反映了 TGF-β 受体的极化分布,这因此影响 SMAD 激活而不依赖于 Hippo 通路的激活。

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