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Cadherin juxtamembrane region derived peptides inhibit TGFβ1 induced gene expression

Bioactive peptides in the juxtamembrane regions of proteins are involved in many signaling events. The juxtamembrane regions of cadherins were examined for the identification of bioactive regions. Several peptides spanning the cytoplasmic juxtamembrane regions of E- and N-cadherin were synthesized a...

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Autores principales: Stavropoulos, Ilias, Golla, Kalyan, Moran, Niamh, Martin, Finian, Shields, Denis C
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Landes Bioscience 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4201599/
https://www.ncbi.nlm.nih.gov/pubmed/25108297
http://dx.doi.org/10.4161/bioa.32143
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author Stavropoulos, Ilias
Golla, Kalyan
Moran, Niamh
Martin, Finian
Shields, Denis C
author_facet Stavropoulos, Ilias
Golla, Kalyan
Moran, Niamh
Martin, Finian
Shields, Denis C
author_sort Stavropoulos, Ilias
collection PubMed
description Bioactive peptides in the juxtamembrane regions of proteins are involved in many signaling events. The juxtamembrane regions of cadherins were examined for the identification of bioactive regions. Several peptides spanning the cytoplasmic juxtamembrane regions of E- and N-cadherin were synthesized and assessed for the ability to influence TGFβ responses in epithelial cells at the gene expression and protein levels. Peptides from regions closer to the membrane appeared more potent inhibitors of TGFβ signaling, blocking Smad3 phosphorylation. Thus inhibiting nuclear translocation of phosphorylated Smad complexes and subsequent transcriptional activation of TGFβ signal propagating genes. The peptides demonstrated a peptide-specific potential to inhibit other TGFβ superfamily members, such as BMP4.
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spelling pubmed-42015992015-05-01 Cadherin juxtamembrane region derived peptides inhibit TGFβ1 induced gene expression Stavropoulos, Ilias Golla, Kalyan Moran, Niamh Martin, Finian Shields, Denis C Bioarchitecture Research Paper Bioactive peptides in the juxtamembrane regions of proteins are involved in many signaling events. The juxtamembrane regions of cadherins were examined for the identification of bioactive regions. Several peptides spanning the cytoplasmic juxtamembrane regions of E- and N-cadherin were synthesized and assessed for the ability to influence TGFβ responses in epithelial cells at the gene expression and protein levels. Peptides from regions closer to the membrane appeared more potent inhibitors of TGFβ signaling, blocking Smad3 phosphorylation. Thus inhibiting nuclear translocation of phosphorylated Smad complexes and subsequent transcriptional activation of TGFβ signal propagating genes. The peptides demonstrated a peptide-specific potential to inhibit other TGFβ superfamily members, such as BMP4. Landes Bioscience 2014 2014-08-09 /pmc/articles/PMC4201599/ /pubmed/25108297 http://dx.doi.org/10.4161/bioa.32143 Text en Copyright © 2014 Landes Bioscience http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Research Paper
Stavropoulos, Ilias
Golla, Kalyan
Moran, Niamh
Martin, Finian
Shields, Denis C
Cadherin juxtamembrane region derived peptides inhibit TGFβ1 induced gene expression
title Cadherin juxtamembrane region derived peptides inhibit TGFβ1 induced gene expression
title_full Cadherin juxtamembrane region derived peptides inhibit TGFβ1 induced gene expression
title_fullStr Cadherin juxtamembrane region derived peptides inhibit TGFβ1 induced gene expression
title_full_unstemmed Cadherin juxtamembrane region derived peptides inhibit TGFβ1 induced gene expression
title_short Cadherin juxtamembrane region derived peptides inhibit TGFβ1 induced gene expression
title_sort cadherin juxtamembrane region derived peptides inhibit tgfβ1 induced gene expression
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4201599/
https://www.ncbi.nlm.nih.gov/pubmed/25108297
http://dx.doi.org/10.4161/bioa.32143
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