Pro-angiogenic capacities of microvesicles produced by skin wound myofibroblasts
Wound healing is a very highly organized process where numerous cell types are tightly regulated to restore injured tissue. Myofibroblasts are cells that produce new extracellular matrix and contract wound edges. We previously reported that the human myofibroblasts isolated from normal wound (WMyos)...
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Published in | Angiogenesis (London) Vol. 20; no. 3; pp. 385 - 398 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
Dordrecht
Springer Netherlands
01.08.2017
Springer Nature B.V |
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Abstract | Wound healing is a very highly organized process where numerous cell types are tightly regulated to restore injured tissue. Myofibroblasts are cells that produce new extracellular matrix and contract wound edges. We previously reported that the human myofibroblasts isolated from normal wound (WMyos) produced microvesicles (MVs) in the presence of the serum. In this study, MVs were further characterized using a proteomic strategy and potential functions of the MVs were determined. MV proteins isolated from six WMyo populations were separated using two-dimensional differential gel electrophoresis. Highly conserved spots were selected and analyzed using mass spectrometry resulting in the identification of 381 different human proteins. Using the DAVID database, clusters of proteins involved in cell motion, apoptosis and adhesion, but also in extracellular matrix production (21 proteins, enrichment score: 3.32) and in blood vessel development/angiogenesis (19 proteins, enrichment score: 2.66) were identified. Another analysis using the functional enrichment analysis tool FunRich was consistent with these results. While the action of the myofibroblasts on extracellular matrix formation is well known, their angiogenic potential is less studied. To further characterize the angiogenic activity of the MVs, they were added to cultured microvascular endothelial cells to evaluate their influence on cell growth and migration using scratch test and capillary-like structure formation in Matrigel
®
. The addition of a MV-enriched preparation significantly increased endothelial cell growth, migration and capillary formation compared with controls. The release of microvesicles by the wound myofibroblasts brings new perspectives to the field of communication between cells during the normal healing process. |
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AbstractList | Wound healing is a very highly organized process where numerous cell types are tightly regulated to restore injured tissue. Myofibroblasts are cells that produce new extracellular matrix and contract wound edges. We previously reported that the human myofibroblasts isolated from normal wound (WMyos) produced microvesicles (MVs) in the presence of the serum. In this study, MVs were further characterized using a proteomic strategy and potential functions of the MVs were determined. MV proteins isolated from six WMyo populations were separated using two-dimensional differential gel electrophoresis. Highly conserved spots were selected and analyzed using mass spectrometry resulting in the identification of 381 different human proteins. Using the DAVID database, clusters of proteins involved in cell motion, apoptosis and adhesion, but also in extracellular matrix production (21 proteins, enrichment score: 3.32) and in blood vessel development/angiogenesis (19 proteins, enrichment score: 2.66) were identified. Another analysis using the functional enrichment analysis tool FunRich was consistent with these results. While the action of the myofibroblasts on extracellular matrix formation is well known, their angiogenic potential is less studied. To further characterize the angiogenic activity of the MVs, they were added to cultured microvascular endothelial cells to evaluate their influence on cell growth and migration using scratch test and capillary-like structure formation in Matrigel®. The addition of a MV-enriched preparation significantly increased endothelial cell growth, migration and capillary formation compared with controls. The release of microvesicles by the wound myofibroblasts brings new perspectives to the field of communication between cells during the normal healing process. Wound healing is a very highly organized process where numerous cell types are tightly regulated to restore injured tissue. Myofibroblasts are cells that produce new extracellular matrix and contract wound edges. We previously reported that the human myofibroblasts isolated from normal wound (WMyos) produced microvesicles (MVs) in the presence of the serum. In this study, MVs were further characterized using a proteomic strategy and potential functions of the MVs were determined. MV proteins isolated from six WMyo populations were separated using two-dimensional differential gel electrophoresis. Highly conserved spots were selected and analyzed using mass spectrometry resulting in the identification of 381 different human proteins. Using the DAVID database, clusters of proteins involved in cell motion, apoptosis and adhesion, but also in extracellular matrix production (21 proteins, enrichment score: 3.32) and in blood vessel development/angiogenesis (19 proteins, enrichment score: 2.66) were identified. Another analysis using the functional enrichment analysis tool FunRich was consistent with these results. While the action of the myofibroblasts on extracellular matrix formation is well known, their angiogenic potential is less studied. To further characterize the angiogenic activity of the MVs, they were added to cultured microvascular endothelial cells to evaluate their influence on cell growth and migration using scratch test and capillary-like structure formation in Matrigel . The addition of a MV-enriched preparation significantly increased endothelial cell growth, migration and capillary formation compared with controls. The release of microvesicles by the wound myofibroblasts brings new perspectives to the field of communication between cells during the normal healing process. Wound healing is a very highly organized process where numerous cell types are tightly regulated to restore injured tissue. Myofibroblasts are cells that produce new extracellular matrix and contract wound edges. We previously reported that the human myofibroblasts isolated from normal wound (WMyos) produced microvesicles (MVs) in the presence of the serum. In this study, MVs were further characterized using a proteomic strategy and potential functions of the MVs were determined. MV proteins isolated from six WMyo populations were separated using two-dimensional differential gel electrophoresis. Highly conserved spots were selected and analyzed using mass spectrometry resulting in the identification of 381 different human proteins. Using the DAVID database, clusters of proteins involved in cell motion, apoptosis and adhesion, but also in extracellular matrix production (21 proteins, enrichment score: 3.32) and in blood vessel development/angiogenesis (19 proteins, enrichment score: 2.66) were identified. Another analysis using the functional enrichment analysis tool FunRich was consistent with these results. While the action of the myofibroblasts on extracellular matrix formation is well known, their angiogenic potential is less studied. To further characterize the angiogenic activity of the MVs, they were added to cultured microvascular endothelial cells to evaluate their influence on cell growth and migration using scratch test and capillary-like structure formation in Matrigel ® . The addition of a MV-enriched preparation significantly increased endothelial cell growth, migration and capillary formation compared with controls. The release of microvesicles by the wound myofibroblasts brings new perspectives to the field of communication between cells during the normal healing process. Wound healing is a very highly organized process where numerous cell types are tightly regulated to restore injured tissue. Myofibroblasts are cells that produce new extracellular matrix and contract wound edges. We previously reported that the human myofibroblasts isolated from normal wound (WMyos) produced microvesicles (MVs) in the presence of the serum. In this study, MVs were further characterized using a proteomic strategy and potential functions of the MVs were determined. MV proteins isolated from six WMyo populations were separated using two-dimensional differential gel electrophoresis. Highly conserved spots were selected and analyzed using mass spectrometry resulting in the identification of 381 different human proteins. Using the DAVID database, clusters of proteins involved in cell motion, apoptosis and adhesion, but also in extracellular matrix production (21 proteins, enrichment score: 3.32) and in blood vessel development/angiogenesis (19 proteins, enrichment score: 2.66) were identified. Another analysis using the functional enrichment analysis tool FunRich was consistent with these results. While the action of the myofibroblasts on extracellular matrix formation is well known, their angiogenic potential is less studied. To further characterize the angiogenic activity of the MVs, they were added to cultured microvascular endothelial cells to evaluate their influence on cell growth and migration using scratch test and capillary-like structure formation in Matrigel. The addition of a MV-enriched preparation significantly increased endothelial cell growth, migration and capillary formation compared with controls. The release of microvesicles by the wound myofibroblasts brings new perspectives to the field of communication between cells during the normal healing process. |
Author | Merjaneh, Mays Ricard-Blum, Sylvie Langlois, Amélie Moulin, Véronique J. Larochelle, Sébastien Cloutier, Chanel Beaudoin |
Author_xml | – sequence: 1 givenname: Mays surname: Merjaneh fullname: Merjaneh, Mays organization: Centre de recherche en organogenese experimentale de l’Université Laval/LOEX, Centre de recherche du CHU de Quebec and Surgery Department, Faculty of Medicine, Universite Laval – sequence: 2 givenname: Amélie surname: Langlois fullname: Langlois, Amélie organization: Centre de recherche en organogenese experimentale de l’Université Laval/LOEX, Centre de recherche du CHU de Quebec and Surgery Department, Faculty of Medicine, Universite Laval – sequence: 3 givenname: Sébastien surname: Larochelle fullname: Larochelle, Sébastien organization: Centre de recherche en organogenese experimentale de l’Université Laval/LOEX, Centre de recherche du CHU de Quebec and Surgery Department, Faculty of Medicine, Universite Laval – sequence: 4 givenname: Chanel Beaudoin surname: Cloutier fullname: Cloutier, Chanel Beaudoin organization: CHU de Québec – sequence: 5 givenname: Sylvie surname: Ricard-Blum fullname: Ricard-Blum, Sylvie organization: Institut de Chimie et Biochimie Moléculaires et Supramoléculaires (ICBMS), UMR 5246 Université Lyon 1, CNRS, INSA Lyon, CPE Lyon – sequence: 6 givenname: Véronique J. surname: Moulin fullname: Moulin, Véronique J. email: veronique.moulin@fmed.ulaval.ca organization: Centre de recherche en organogenese experimentale de l’Université Laval/LOEX, Centre de recherche du CHU de Quebec and Surgery Department, Faculty of Medicine, Universite Laval |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/28391377$$D View this record in MEDLINE/PubMed |
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Keywords | Human Angiogenesis Myofibroblast Proteomic Healing Skin Microvesicle Endothelial cells |
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SubjectTerms | Adhesion Adult Angiogenesis Apoptosis Biomedical and Life Sciences Biomedicine Cancer Research Cardiology Cell Biology Cell growth Cell Movement Cell Proliferation Cell-Derived Microparticles - metabolism Clusters Electrophoresis Endothelial cells Endothelial Cells - pathology Enrichment Exosomes - metabolism Extracellular matrix Gel electrophoresis Gene Ontology Humans Mass spectrometry Mass spectroscopy Microvasculature Myofibroblasts - metabolism Neovascularization, Physiologic Oncology Ophthalmology Original Paper Populations Proteins Serum Skin Skin - blood supply Skin - pathology Spots Wound healing Wounds and Injuries - pathology Young Adult |
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Title | Pro-angiogenic capacities of microvesicles produced by skin wound myofibroblasts |
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