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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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. FASEB J. 31, 4946–4958 (2017). www.fasebj.org</description><subject>Activation</subject><subject>Adhesion</subject><subject>Angiogenesis</subject><subject>Angiogenesis Inducing Agents - metabolism</subject><subject>Angiogenesis Inducing Agents - pharmacology</subject><subject>Assaying</subject><subject>Boyden chamber</subject><subject>Carrier Proteins - metabolism</subject><subject>Cell adhesion</subject><subject>Cell adhesion & migration</subject><subject>Cell Adhesion - drug effects</subject><subject>Cell Line</subject><subject>Cell migration</subject><subject>Cell Movement - drug effects</subject><subject>Chorioallantoic membrane</subject><subject>Cues</subject><subject>Endosomes</subject><subject>Endothelial cells</subject><subject>Endothelial Cells - metabolism</subject><subject>Endothelial Cells - pathology</subject><subject>Fibroblasts</subject><subject>Fibronectin</subject><subject>GTPase</subject><subject>Guanine</subject><subject>Guanine nucleotide exchange factor</subject><subject>Guanine Nucleotide Exchange Factors - metabolism</subject><subject>Histatins - metabolism</subject><subject>Histatins - pharmacology</subject><subject>Humans</subject><subject>Keratinocytes</subject><subject>Mouth Mucosa - injuries</subject><subject>Mouth Mucosa - metabolism</subject><subject>Mouth Mucosa - pathology</subject><subject>Mucosa</subject><subject>Neovascularization, Physiologic - drug effects</subject><subject>Peptides</subject><subject>Rab5</subject><subject>rab5 GTP-Binding Proteins - metabolism</subject><subject>rac1 GTP-Binding Protein - metabolism</subject><subject>Rac1 protein</subject><subject>Recruitment</subject><subject>Saliva</subject><subject>Salivary Proteins and Peptides - metabolism</subject><subject>Salivary Proteins and Peptides - pharmacology</subject><subject>Signaling</subject><subject>Wound healing</subject><subject>Wound Healing - drug effects</subject><issn>0892-6638</issn><issn>1530-6860</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp90ElLw0AYBuBBFK3Vo1cJePFg6iyZJXjSYl0oCLWewzTzpZ2SpWYSpTd_gr_RX-KU1gUPHmaBeebl40XoiOAewbE4z-Y9ionEGCs-2kIdwhkOhRJ4G3WwimkoBFN7aN-5uTcEE7GL9qiSnHAqOkiPZxA4ndsXXS-DBSwaayCYWdfoxpYfb-8kWNRVUTXgAihN1cwgtzoPUsjzQJsZOFuVZ0Fhp7X_sLrq0vg1tdUUSv_qDtBOpnMHh5uzi54G1-P-bTh8uLnrXw7DNFJsFEYZYI5pyiZGp0TRSSqYJIIyLngcKQ0GTEqlnmQijTD1m5GGSy2ZxlJjxrrodJ3r531uwTVJYd1qTF1C1bqExDTisSCKe3ryh86rti79dF6piElJKPUqXKu0rpyrIUsWtS18TQnByar7JJsnP917f7xJbScFmG_9VbYHF2vwanNY_p-WDB6v6OD-V_wngyWRZw</recordid><startdate>201711</startdate><enddate>201711</enddate><creator>Torres, Pedro</creator><creator>Díaz, Jorge</creator><creator>Arce, Maximiliano</creator><creator>Silva, Patricio</creator><creator>Mendoza, Pablo</creator><creator>Lois, Pablo</creator><creator>Molina‐Berríos, Alfredo</creator><creator>Owen, Gareth I.</creator><creator>Palma, Verónica</creator><creator>Torres, Vicente A.</creator><general>Federation of American Societies for Experimental Biology</general><general>Federation of American Societies for Experimental Biology (FASEB)</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QG</scope><scope>7QL</scope><scope>7QO</scope><scope>7QP</scope><scope>7T5</scope><scope>7TK</scope><scope>7TM</scope><scope>7TO</scope><scope>7U7</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>201711</creationdate><title>The salivary peptide histatin‐1 promotes endothelial cell adhesion, migration, and angiogenesis</title><author>Torres, Pedro ; 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 & 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 & Calcified Tissue Abstracts</collection><collection>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>The FASEB journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Torres, Pedro</au><au>Díaz, Jorge</au><au>Arce, Maximiliano</au><au>Silva, Patricio</au><au>Mendoza, Pablo</au><au>Lois, Pablo</au><au>Molina‐Berríos, Alfredo</au><au>Owen, Gareth I.</au><au>Palma, Verónica</au><au>Torres, Vicente A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The salivary peptide histatin‐1 promotes endothelial cell adhesion, migration, and angiogenesis</atitle><jtitle>The FASEB journal</jtitle><addtitle>FASEB J</addtitle><date>2017-11</date><risdate>2017</risdate><volume>31</volume><issue>11</issue><spage>4946</spage><epage>4958</epage><pages>4946-4958</pages><issn>0892-6638</issn><eissn>1530-6860</eissn><abstract>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</abstract><cop>United States</cop><pub>Federation of American Societies for Experimental Biology</pub><pmid>28751526</pmid><doi>10.1096/fj.201700085R</doi><tpages>13</tpages></addata></record> |
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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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