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The dipeptide prolyl-hydroxyproline promotes cellular homeostasis and lamellipodia-driven motility via active β1-integrin in adult tendon cells

Collagen-derived hydroxyproline (Hyp)-containing peptides have a variety of biological effects on cells. These bioactive collagen peptides are locally generated by the degradation of endogenous collagen in response to injury. However, no comprehensive study has yet explored the functional links betw...

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Autores principales: Ide, Kentaro, Takahashi, Sanai, Sakai, Keiko, Taga, Yuki, Ueno, Tomonori, Dickens, David, Jenkins, Rosalind, Falciani, Francesco, Sasaki, Takako, Ooi, Kazuhiro, Kawashiri, Shuichi, Mizuno, Kazunori, Hattori, Shunji, Sakai, Takao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Biochemistry and Molecular Biology 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8239475/
https://www.ncbi.nlm.nih.gov/pubmed/34029590
http://dx.doi.org/10.1016/j.jbc.2021.100819
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author Ide, Kentaro
Takahashi, Sanai
Sakai, Keiko
Taga, Yuki
Ueno, Tomonori
Dickens, David
Jenkins, Rosalind
Falciani, Francesco
Sasaki, Takako
Ooi, Kazuhiro
Kawashiri, Shuichi
Mizuno, Kazunori
Hattori, Shunji
Sakai, Takao
author_facet Ide, Kentaro
Takahashi, Sanai
Sakai, Keiko
Taga, Yuki
Ueno, Tomonori
Dickens, David
Jenkins, Rosalind
Falciani, Francesco
Sasaki, Takako
Ooi, Kazuhiro
Kawashiri, Shuichi
Mizuno, Kazunori
Hattori, Shunji
Sakai, Takao
author_sort Ide, Kentaro
collection PubMed
description Collagen-derived hydroxyproline (Hyp)-containing peptides have a variety of biological effects on cells. These bioactive collagen peptides are locally generated by the degradation of endogenous collagen in response to injury. However, no comprehensive study has yet explored the functional links between Hyp-containing peptides and cellular behavior. Here, we show that the dipeptide prolyl-4-hydroxyproline (Pro-Hyp) exhibits pronounced effects on mouse tendon cells. Pro-Hyp promotes differentiation/maturation of tendon cells with modulation of lineage-specific factors and induces significant chemotactic activity in vitro. In addition, Pro-Hyp has profound effects on cell proliferation, with significantly upregulated extracellular signal–regulated kinase phosphorylation and extracellular matrix production and increased type I collagen network organization. Using proteomics, we have predicted molecular transport, cellular assembly and organization, and cellular movement as potential linked-network pathways that could be altered in response to Pro-Hyp. Mechanistically, cells treated with Pro-Hyp demonstrate increased directional persistence and significantly increased directed motility and migration velocity. They are accompanied by elongated lamellipodial protrusions with increased levels of active β1-integrin–containing focal contacts, as well as reorganization of thicker peripheral F-actin fibrils. Pro-Hyp–mediated chemotactic activity is significantly reduced (p < 0.001) in cells treated with the mitogen-activated protein kinase kinase 1/2 inhibitor PD98059 or the α5β1-integrin antagonist ATN-161. Furthermore, ATN-161 significantly inhibits uptake of Pro-Hyp into adult tenocytes. Thus, our findings document the molecular basis of the functional benefits of the Pro-Hyp dipeptide in cellular behavior. These dynamic properties of collagen-derived Pro-Hyp dipeptide could lead the way to its application in translational medicine.
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spelling pubmed-82394752021-06-29 The dipeptide prolyl-hydroxyproline promotes cellular homeostasis and lamellipodia-driven motility via active β1-integrin in adult tendon cells Ide, Kentaro Takahashi, Sanai Sakai, Keiko Taga, Yuki Ueno, Tomonori Dickens, David Jenkins, Rosalind Falciani, Francesco Sasaki, Takako Ooi, Kazuhiro Kawashiri, Shuichi Mizuno, Kazunori Hattori, Shunji Sakai, Takao J Biol Chem Research Article Collagen-derived hydroxyproline (Hyp)-containing peptides have a variety of biological effects on cells. These bioactive collagen peptides are locally generated by the degradation of endogenous collagen in response to injury. However, no comprehensive study has yet explored the functional links between Hyp-containing peptides and cellular behavior. Here, we show that the dipeptide prolyl-4-hydroxyproline (Pro-Hyp) exhibits pronounced effects on mouse tendon cells. Pro-Hyp promotes differentiation/maturation of tendon cells with modulation of lineage-specific factors and induces significant chemotactic activity in vitro. In addition, Pro-Hyp has profound effects on cell proliferation, with significantly upregulated extracellular signal–regulated kinase phosphorylation and extracellular matrix production and increased type I collagen network organization. Using proteomics, we have predicted molecular transport, cellular assembly and organization, and cellular movement as potential linked-network pathways that could be altered in response to Pro-Hyp. Mechanistically, cells treated with Pro-Hyp demonstrate increased directional persistence and significantly increased directed motility and migration velocity. They are accompanied by elongated lamellipodial protrusions with increased levels of active β1-integrin–containing focal contacts, as well as reorganization of thicker peripheral F-actin fibrils. Pro-Hyp–mediated chemotactic activity is significantly reduced (p < 0.001) in cells treated with the mitogen-activated protein kinase kinase 1/2 inhibitor PD98059 or the α5β1-integrin antagonist ATN-161. Furthermore, ATN-161 significantly inhibits uptake of Pro-Hyp into adult tenocytes. Thus, our findings document the molecular basis of the functional benefits of the Pro-Hyp dipeptide in cellular behavior. These dynamic properties of collagen-derived Pro-Hyp dipeptide could lead the way to its application in translational medicine. American Society for Biochemistry and Molecular Biology 2021-05-23 /pmc/articles/PMC8239475/ /pubmed/34029590 http://dx.doi.org/10.1016/j.jbc.2021.100819 Text en © 2021 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Research Article
Ide, Kentaro
Takahashi, Sanai
Sakai, Keiko
Taga, Yuki
Ueno, Tomonori
Dickens, David
Jenkins, Rosalind
Falciani, Francesco
Sasaki, Takako
Ooi, Kazuhiro
Kawashiri, Shuichi
Mizuno, Kazunori
Hattori, Shunji
Sakai, Takao
The dipeptide prolyl-hydroxyproline promotes cellular homeostasis and lamellipodia-driven motility via active β1-integrin in adult tendon cells
title The dipeptide prolyl-hydroxyproline promotes cellular homeostasis and lamellipodia-driven motility via active β1-integrin in adult tendon cells
title_full The dipeptide prolyl-hydroxyproline promotes cellular homeostasis and lamellipodia-driven motility via active β1-integrin in adult tendon cells
title_fullStr The dipeptide prolyl-hydroxyproline promotes cellular homeostasis and lamellipodia-driven motility via active β1-integrin in adult tendon cells
title_full_unstemmed The dipeptide prolyl-hydroxyproline promotes cellular homeostasis and lamellipodia-driven motility via active β1-integrin in adult tendon cells
title_short The dipeptide prolyl-hydroxyproline promotes cellular homeostasis and lamellipodia-driven motility via active β1-integrin in adult tendon cells
title_sort dipeptide prolyl-hydroxyproline promotes cellular homeostasis and lamellipodia-driven motility via active β1-integrin in adult tendon cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8239475/
https://www.ncbi.nlm.nih.gov/pubmed/34029590
http://dx.doi.org/10.1016/j.jbc.2021.100819
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