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Crosstalk between Hippo and TGFß: Subcellular Localization of YAP/TAZ/Smad Complexes.
Grannas, Karin; Arngården, Linda; Lönn, Peter; Mazurkiewicz, Magdalena; Blokzijl, Andries; Zieba, Agata; Söderberg, Ola.
  • Grannas K; Department of Immunology, Genetics and Pathology, Science for Life Laboratory, Uppsala University, 751 85 Uppsala, Sweden.
  • Arngården L; Department of Immunology, Genetics and Pathology, Science for Life Laboratory, Uppsala University, 751 85 Uppsala, Sweden.
  • Lönn P; Department of Immunology, Genetics and Pathology, Science for Life Laboratory, Uppsala University, 751 85 Uppsala, Sweden.
  • Mazurkiewicz M; Department of Oncology-Pathology, Karolinska University Hospital, 171 76 Stockholm, Sweden.
  • Blokzijl A; Department of Immunology, Genetics and Pathology, Science for Life Laboratory, Uppsala University, 751 85 Uppsala, Sweden.
  • Zieba A; Department of Immunology, Genetics and Pathology, Science for Life Laboratory, Uppsala University, 751 85 Uppsala, Sweden.
  • Söderberg O; Department of Immunology, Genetics and Pathology, Science for Life Laboratory, Uppsala University, 751 85 Uppsala, Sweden. Electronic address: Ola.Soderberg@igp.uu.se.
J Mol Biol ; 427(21): 3407-15, 2015 Oct 23.
Article en En | MEDLINE | ID: mdl-25937570
ABSTRACT
The Hippo pathway plays a crucial role in growth control, proliferation and tumor suppression. Activity of the signaling pathway is associated with cell density sensing and tissue organization. Furthermore, the Hippo pathway helps to coordinate cellular processes through crosstalk with growth-factor-mediated signaling pathways such as TGFß. Here we have examined the localization of interactions between proteins of the Hippo pathway (YAP/TAZ) and TGFß (Smad2/3) signaling pathway by using in situ proximity ligation assays. We investigated the formation of protein complexes between YAP/TAZ and Smad2/3 and examined how these interactions were affected by TGFß stimulation and cell density in HaCaT keratinocytes and in Smad4-deficient HT29 colon cancer cells. We demonstrate that TGFß induces formation of YAP/TAZ-Smad2/3 complexes in HaCaT cells. Under sparse cell conditions, the complexes were detected to a higher degree and were predominantly located in the nucleus, while under dense culture conditions, the complexes were fewer and mainly located in the cytoplasm. Surprisingly, we could not detect any YAP/TAZ-Smad2/3 complexes in HT29 cells. To examine if Smad4 deficiency was responsible for the absence of interactions, we treated HaCaT cells with siRNA targeting Smad4. However, we could still observe complex formation in the siRNA-treated cells, suggesting that Smad4 is not essential for the YAP-Smad2/3 interaction. In conclusion, this study shows localized, density-dependent formation of YAP/TAZ-Smad2/3 complexes in HaCaT cells and provides evidence supporting a crosstalk between the Hippo and the TGFß signaling pathways.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Fosfoproteínas / Factores de Transcripción / Transducción de Señal / Factor de Crecimiento Transformador beta / Proteínas Serina-Treonina Quinasas / Neoplasias del Colon / Proteínas Adaptadoras Transductoras de Señales / Proteínas Smad Reguladas por Receptores Límite: Humans Idioma: En Año: 2015 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Fosfoproteínas / Factores de Transcripción / Transducción de Señal / Factor de Crecimiento Transformador beta / Proteínas Serina-Treonina Quinasas / Neoplasias del Colon / Proteínas Adaptadoras Transductoras de Señales / Proteínas Smad Reguladas por Receptores Límite: Humans Idioma: En Año: 2015 Tipo del documento: Article