Cargando…

Approaches in Hydroxytyrosol Supplementation on Epithelial—Mesenchymal Transition in TGFβ1-Induced Human Respiratory Epithelial Cells

Hydroxytyrosol (HT) is an olive polyphenol with anti-inflammatory and antioxidant properties. This study aimed to investigate the effect of HT treatment on epithelial–mesenchymal transition (EMT) in primary human respiratory epithelial cells (RECs) isolated from human nasal turbinate. HT dose–respon...

Descripción completa

Detalles Bibliográficos
Autores principales: Razali, Rabiatul Adawiyah, Yazid, Muhammad Dain, Saim, Aminuddin, Idrus, Ruszymah Bt Hj, Lokanathan, Yogeswaran
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9967984/
https://www.ncbi.nlm.nih.gov/pubmed/36835384
http://dx.doi.org/10.3390/ijms24043974
_version_ 1784897401598771200
author Razali, Rabiatul Adawiyah
Yazid, Muhammad Dain
Saim, Aminuddin
Idrus, Ruszymah Bt Hj
Lokanathan, Yogeswaran
author_facet Razali, Rabiatul Adawiyah
Yazid, Muhammad Dain
Saim, Aminuddin
Idrus, Ruszymah Bt Hj
Lokanathan, Yogeswaran
author_sort Razali, Rabiatul Adawiyah
collection PubMed
description Hydroxytyrosol (HT) is an olive polyphenol with anti-inflammatory and antioxidant properties. This study aimed to investigate the effect of HT treatment on epithelial–mesenchymal transition (EMT) in primary human respiratory epithelial cells (RECs) isolated from human nasal turbinate. HT dose–response study and growth kinetic study on RECs was performed. Several approaches on HT treatment and TGFβ1 induction with varying durations and methods was studied. RECs morphology and migration ability were evaluated. Vimentin and E-cadherin immunofluorescence staining and Western blotting [E-cadherin, vimentin, SNAIL/SLUG, AKT, phosphorylated (p)AKT, SMAD2/3 and pSMAD2/3] were performed after 72-h treatment. In silico analysis (molecular docking) of HT was performed to evaluate the potential of HT to bind with the TGFβ receptor. The viability of the HT-treated RECs was concentration-dependent, where the median effective concentration (EC(50)) was 19.04 μg/mL. Testing of the effects of 1 and 10 µg/mL HT revealed that HT suppressed expression of the protein markers vimentin and SNAIL/SLUG while preserving E-cadherin protein expression. Supplementation with HT protected against SMAD and AKT pathway activation in the TGFβ1-induced RECs. Furthermore, HT demonstrated the potential to bind with ALK5 (a TGFβ receptor component) in comparison to oleuropein. TGFβ1-induced EMT in RECs and HT exerted a positive effect in modulating the effects of EMT.
format Online
Article
Text
id pubmed-9967984
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-99679842023-02-27 Approaches in Hydroxytyrosol Supplementation on Epithelial—Mesenchymal Transition in TGFβ1-Induced Human Respiratory Epithelial Cells Razali, Rabiatul Adawiyah Yazid, Muhammad Dain Saim, Aminuddin Idrus, Ruszymah Bt Hj Lokanathan, Yogeswaran Int J Mol Sci Article Hydroxytyrosol (HT) is an olive polyphenol with anti-inflammatory and antioxidant properties. This study aimed to investigate the effect of HT treatment on epithelial–mesenchymal transition (EMT) in primary human respiratory epithelial cells (RECs) isolated from human nasal turbinate. HT dose–response study and growth kinetic study on RECs was performed. Several approaches on HT treatment and TGFβ1 induction with varying durations and methods was studied. RECs morphology and migration ability were evaluated. Vimentin and E-cadherin immunofluorescence staining and Western blotting [E-cadherin, vimentin, SNAIL/SLUG, AKT, phosphorylated (p)AKT, SMAD2/3 and pSMAD2/3] were performed after 72-h treatment. In silico analysis (molecular docking) of HT was performed to evaluate the potential of HT to bind with the TGFβ receptor. The viability of the HT-treated RECs was concentration-dependent, where the median effective concentration (EC(50)) was 19.04 μg/mL. Testing of the effects of 1 and 10 µg/mL HT revealed that HT suppressed expression of the protein markers vimentin and SNAIL/SLUG while preserving E-cadherin protein expression. Supplementation with HT protected against SMAD and AKT pathway activation in the TGFβ1-induced RECs. Furthermore, HT demonstrated the potential to bind with ALK5 (a TGFβ receptor component) in comparison to oleuropein. TGFβ1-induced EMT in RECs and HT exerted a positive effect in modulating the effects of EMT. MDPI 2023-02-16 /pmc/articles/PMC9967984/ /pubmed/36835384 http://dx.doi.org/10.3390/ijms24043974 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Razali, Rabiatul Adawiyah
Yazid, Muhammad Dain
Saim, Aminuddin
Idrus, Ruszymah Bt Hj
Lokanathan, Yogeswaran
Approaches in Hydroxytyrosol Supplementation on Epithelial—Mesenchymal Transition in TGFβ1-Induced Human Respiratory Epithelial Cells
title Approaches in Hydroxytyrosol Supplementation on Epithelial—Mesenchymal Transition in TGFβ1-Induced Human Respiratory Epithelial Cells
title_full Approaches in Hydroxytyrosol Supplementation on Epithelial—Mesenchymal Transition in TGFβ1-Induced Human Respiratory Epithelial Cells
title_fullStr Approaches in Hydroxytyrosol Supplementation on Epithelial—Mesenchymal Transition in TGFβ1-Induced Human Respiratory Epithelial Cells
title_full_unstemmed Approaches in Hydroxytyrosol Supplementation on Epithelial—Mesenchymal Transition in TGFβ1-Induced Human Respiratory Epithelial Cells
title_short Approaches in Hydroxytyrosol Supplementation on Epithelial—Mesenchymal Transition in TGFβ1-Induced Human Respiratory Epithelial Cells
title_sort approaches in hydroxytyrosol supplementation on epithelial—mesenchymal transition in tgfβ1-induced human respiratory epithelial cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9967984/
https://www.ncbi.nlm.nih.gov/pubmed/36835384
http://dx.doi.org/10.3390/ijms24043974
work_keys_str_mv AT razalirabiatuladawiyah approachesinhydroxytyrosolsupplementationonepithelialmesenchymaltransitionintgfb1inducedhumanrespiratoryepithelialcells
AT yazidmuhammaddain approachesinhydroxytyrosolsupplementationonepithelialmesenchymaltransitionintgfb1inducedhumanrespiratoryepithelialcells
AT saimaminuddin approachesinhydroxytyrosolsupplementationonepithelialmesenchymaltransitionintgfb1inducedhumanrespiratoryepithelialcells
AT idrusruszymahbthj approachesinhydroxytyrosolsupplementationonepithelialmesenchymaltransitionintgfb1inducedhumanrespiratoryepithelialcells
AT lokanathanyogeswaran approachesinhydroxytyrosolsupplementationonepithelialmesenchymaltransitionintgfb1inducedhumanrespiratoryepithelialcells