The salivary peptide histatin‐1 promotes endothelial cell adhesion, migration, and angiogenesis

Saliva is a key factor that contributes to the high efficiency of wound healing in the oral mucosa. This is not only attributed to physical cues but also to the presence of specific peptides in the saliva, such as histatins. Histatin‐1 is a 38 aa antimicrobial peptide, highly enriched in human saliv...

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Veröffentlicht in:The FASEB journal 2017-11, Vol.31 (11), p.4946-4958
Hauptverfasser: Torres, Pedro, Díaz, Jorge, Arce, Maximiliano, Silva, Patricio, Mendoza, Pablo, Lois, Pablo, Molina‐Berríos, Alfredo, Owen, Gareth I., Palma, Verónica, Torres, Vicente A.
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container_end_page 4958
container_issue 11
container_start_page 4946
container_title The FASEB journal
container_volume 31
creator Torres, Pedro
Díaz, Jorge
Arce, Maximiliano
Silva, Patricio
Mendoza, Pablo
Lois, Pablo
Molina‐Berríos, Alfredo
Owen, Gareth I.
Palma, Verónica
Torres, Vicente A.
description Saliva is a key factor that contributes to the high efficiency of wound healing in the oral mucosa. This is not only attributed to physical cues but also to the presence of specific peptides in the saliva, such as histatins. Histatin‐1 is a 38 aa antimicrobial peptide, highly enriched in human saliva, which has been previously reported to promote the migration of oral keratinocytes and fibroblasts in vitro. However, the participation of histatin‐1 in other crucial events required for wound healing, such as angiogenesis, is unknown. Here we demonstrate that histatin‐1 promotes angiogenesis, as shown in vivo, using the chick chorioallantoic membrane model, and by an in vitro tube formation assay, using both human primary cultured endothelial cells (HUVECs) and the EA.hy926 cell line. Specifically, histatin‐1 promoted endothelial cell adhesion and spreading onto fibronectin, as well as endothelial cell migration in the wound closure and Boyden chamber assays. These actions required the activation of the Ras and Rab interactor 2 (RIN2)/Rab5/Rac1 signaling axis, as histatin‐1 increased the recruitment of RIN2, a Rab5–guanine nucleotide exchange factor (GEF) to early endosomes, leading to sequential Rab5/Rac1 activation. Accordingly, interfering with either Rab5 or Rac1 activities prevented histatin‐1‐dependent endothelial cell migration. Finally, by immunodepletion assays, we showed that salivary histatin‐1 is required for the promigratory effects of saliva on endothelial cells. In conclusion, we report that salivary histatin‐1 is a novel proangiogenic factor that may contribute to oral wound healing.—Torres, P., Díaz, J., Arce, M., Silva, P., Mendoza, P., Lois, P., Molina‐Berrios, A., Owen, G. I., Palma, V., Torres, V. A. The salivary peptide histatin‐1 promotes endothelial cell adhesion, migration, and angiogenesis. FASEB J. 31, 4946–4958 (2017). www.fasebj.org
doi_str_mv 10.1096/fj.201700085R
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This is not only attributed to physical cues but also to the presence of specific peptides in the saliva, such as histatins. Histatin‐1 is a 38 aa antimicrobial peptide, highly enriched in human saliva, which has been previously reported to promote the migration of oral keratinocytes and fibroblasts in vitro. However, the participation of histatin‐1 in other crucial events required for wound healing, such as angiogenesis, is unknown. Here we demonstrate that histatin‐1 promotes angiogenesis, as shown in vivo, using the chick chorioallantoic membrane model, and by an in vitro tube formation assay, using both human primary cultured endothelial cells (HUVECs) and the EA.hy926 cell line. Specifically, histatin‐1 promoted endothelial cell adhesion and spreading onto fibronectin, as well as endothelial cell migration in the wound closure and Boyden chamber assays. These actions required the activation of the Ras and Rab interactor 2 (RIN2)/Rab5/Rac1 signaling axis, as histatin‐1 increased the recruitment of RIN2, a Rab5–guanine nucleotide exchange factor (GEF) to early endosomes, leading to sequential Rab5/Rac1 activation. Accordingly, interfering with either Rab5 or Rac1 activities prevented histatin‐1‐dependent endothelial cell migration. Finally, by immunodepletion assays, we showed that salivary histatin‐1 is required for the promigratory effects of saliva on endothelial cells. In conclusion, we report that salivary histatin‐1 is a novel proangiogenic factor that may contribute to oral wound healing.—Torres, P., Díaz, J., Arce, M., Silva, P., Mendoza, P., Lois, P., Molina‐Berrios, A., Owen, G. I., Palma, V., Torres, V. A. The salivary peptide histatin‐1 promotes endothelial cell adhesion, migration, and angiogenesis. 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This is not only attributed to physical cues but also to the presence of specific peptides in the saliva, such as histatins. Histatin‐1 is a 38 aa antimicrobial peptide, highly enriched in human saliva, which has been previously reported to promote the migration of oral keratinocytes and fibroblasts in vitro. However, the participation of histatin‐1 in other crucial events required for wound healing, such as angiogenesis, is unknown. Here we demonstrate that histatin‐1 promotes angiogenesis, as shown in vivo, using the chick chorioallantoic membrane model, and by an in vitro tube formation assay, using both human primary cultured endothelial cells (HUVECs) and the EA.hy926 cell line. Specifically, histatin‐1 promoted endothelial cell adhesion and spreading onto fibronectin, as well as endothelial cell migration in the wound closure and Boyden chamber assays. These actions required the activation of the Ras and Rab interactor 2 (RIN2)/Rab5/Rac1 signaling axis, as histatin‐1 increased the recruitment of RIN2, a Rab5–guanine nucleotide exchange factor (GEF) to early endosomes, leading to sequential Rab5/Rac1 activation. Accordingly, interfering with either Rab5 or Rac1 activities prevented histatin‐1‐dependent endothelial cell migration. Finally, by immunodepletion assays, we showed that salivary histatin‐1 is required for the promigratory effects of saliva on endothelial cells. In conclusion, we report that salivary histatin‐1 is a novel proangiogenic factor that may contribute to oral wound healing.—Torres, P., Díaz, J., Arce, M., Silva, P., Mendoza, P., Lois, P., Molina‐Berrios, A., Owen, G. I., Palma, V., Torres, V. A. The salivary peptide histatin‐1 promotes endothelial cell adhesion, migration, and angiogenesis. 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Díaz, Jorge ; Arce, Maximiliano ; Silva, Patricio ; Mendoza, Pablo ; Lois, Pablo ; Molina‐Berríos, Alfredo ; Owen, Gareth I. ; Palma, Verónica ; Torres, Vicente A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c483R-4fe0502c3bdac182bc6371623565948aededc27abf6c4026c4d7d57a73a07a033</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Activation</topic><topic>Adhesion</topic><topic>Angiogenesis</topic><topic>Angiogenesis Inducing Agents - metabolism</topic><topic>Angiogenesis Inducing Agents - pharmacology</topic><topic>Assaying</topic><topic>Boyden chamber</topic><topic>Carrier Proteins - metabolism</topic><topic>Cell adhesion</topic><topic>Cell adhesion &amp; migration</topic><topic>Cell Adhesion - drug effects</topic><topic>Cell Line</topic><topic>Cell migration</topic><topic>Cell Movement - drug effects</topic><topic>Chorioallantoic membrane</topic><topic>Cues</topic><topic>Endosomes</topic><topic>Endothelial cells</topic><topic>Endothelial Cells - metabolism</topic><topic>Endothelial Cells - pathology</topic><topic>Fibroblasts</topic><topic>Fibronectin</topic><topic>GTPase</topic><topic>Guanine</topic><topic>Guanine nucleotide exchange factor</topic><topic>Guanine Nucleotide Exchange Factors - metabolism</topic><topic>Histatins - metabolism</topic><topic>Histatins - pharmacology</topic><topic>Humans</topic><topic>Keratinocytes</topic><topic>Mouth Mucosa - injuries</topic><topic>Mouth Mucosa - metabolism</topic><topic>Mouth Mucosa - pathology</topic><topic>Mucosa</topic><topic>Neovascularization, Physiologic - drug effects</topic><topic>Peptides</topic><topic>Rab5</topic><topic>rab5 GTP-Binding Proteins - metabolism</topic><topic>rac1 GTP-Binding Protein - metabolism</topic><topic>Rac1 protein</topic><topic>Recruitment</topic><topic>Saliva</topic><topic>Salivary Proteins and Peptides - metabolism</topic><topic>Salivary Proteins and Peptides - pharmacology</topic><topic>Signaling</topic><topic>Wound healing</topic><topic>Wound Healing - drug effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Torres, Pedro</creatorcontrib><creatorcontrib>Díaz, Jorge</creatorcontrib><creatorcontrib>Arce, Maximiliano</creatorcontrib><creatorcontrib>Silva, Patricio</creatorcontrib><creatorcontrib>Mendoza, Pablo</creatorcontrib><creatorcontrib>Lois, Pablo</creatorcontrib><creatorcontrib>Molina‐Berríos, Alfredo</creatorcontrib><creatorcontrib>Owen, Gareth I.</creatorcontrib><creatorcontrib>Palma, Verónica</creatorcontrib><creatorcontrib>Torres, Vicente A.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Animal Behavior Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Calcium &amp; 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subjects Activation
Adhesion
Angiogenesis
Angiogenesis Inducing Agents - metabolism
Angiogenesis Inducing Agents - pharmacology
Assaying
Boyden chamber
Carrier Proteins - metabolism
Cell adhesion
Cell adhesion & migration
Cell Adhesion - drug effects
Cell Line
Cell migration
Cell Movement - drug effects
Chorioallantoic membrane
Cues
Endosomes
Endothelial cells
Endothelial Cells - metabolism
Endothelial Cells - pathology
Fibroblasts
Fibronectin
GTPase
Guanine
Guanine nucleotide exchange factor
Guanine Nucleotide Exchange Factors - metabolism
Histatins - metabolism
Histatins - pharmacology
Humans
Keratinocytes
Mouth Mucosa - injuries
Mouth Mucosa - metabolism
Mouth Mucosa - pathology
Mucosa
Neovascularization, Physiologic - drug effects
Peptides
Rab5
rab5 GTP-Binding Proteins - metabolism
rac1 GTP-Binding Protein - metabolism
Rac1 protein
Recruitment
Saliva
Salivary Proteins and Peptides - metabolism
Salivary Proteins and Peptides - pharmacology
Signaling
Wound healing
Wound Healing - drug effects
title The salivary peptide histatin‐1 promotes endothelial cell adhesion, migration, and angiogenesis
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