Combined application of geranylgeranylacetone and amelogenin promotes angiogenesis and wound healing in human periodontal ligament cells

Amelogenin directly binds to glucose‐regulated protein 78 (Grp78). Cell migration activity is expected to increase when human periodontal ligament cells (hPDLCs) overexpressing Grp78 are treated with amelogenin. Geranylgeranylacetone (GGA) is a drug that induces the expression of heat shock protein...

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Veröffentlicht in:Journal of cellular biochemistry 2021-07, Vol.122 (7), p.716-730
Hauptverfasser: Yamato, Hiroaki, Sanui, Terukazu, Yotsumoto, Karen, Nakao, Yuki, Watanabe, Yukari, Hayashi, Chikako, Aihara, Ryosuke, Iwashita, Misaki, Tanaka, Urara, Taketomi, Takaharu, Fukuda, Takao, Nishimura, Fusanori
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container_issue 7
container_start_page 716
container_title Journal of cellular biochemistry
container_volume 122
creator Yamato, Hiroaki
Sanui, Terukazu
Yotsumoto, Karen
Nakao, Yuki
Watanabe, Yukari
Hayashi, Chikako
Aihara, Ryosuke
Iwashita, Misaki
Tanaka, Urara
Taketomi, Takaharu
Fukuda, Takao
Nishimura, Fusanori
description Amelogenin directly binds to glucose‐regulated protein 78 (Grp78). Cell migration activity is expected to increase when human periodontal ligament cells (hPDLCs) overexpressing Grp78 are treated with amelogenin. Geranylgeranylacetone (GGA) is a drug that induces the expression of heat shock protein and is routinely used to treat gastric ulcers. Here, we investigated the changes in the properties and behavior of hPDLCs in response to treatment with GGA and the synergistic effects of amelogenin stimulation in hPDLCs pretreated with GGA for the establishment of a novel periodontal tissue regenerative therapy. We observed that GGA treatment increased Grp78 protein expression in hPDLCs and enhanced cell migration. Microarray analysis demonstrated that increased Grp78 expression triggered the production of angiopoietin‐like 4 and amphiregulin, which are involved in the enhancement of angiogenesis and subsequent wound healing via the activation of hypoxia‐inducible factor 1α and peroxisome proliferator‐activated receptors as well as the phosphorylation of cAMP response element‐binding protein and protein kinase A. Moreover, the addition of recombinant murine amelogenin (rM180) further accelerated hPDLC migration and tube formation of human umbilical vein endothelial cells due to the upregulation of interleukin‐8 (IL‐8), monocyte chemotactic protein 1, and IL‐6, which are also known as angiogenesis‐inducing factors. These findings suggest that the application of GGA to gingival tissue and alveolar bone damaged by periodontal disease would facilitate the wound healing process by inducing periodontal ligament cells to migrate to the root surface and release cytokines involved in tissue repair. Additionally, supplementation with amelogenin synergistically enhanced the migratory capacity of these cells while actively promoting angiogenesis. Therefore, the combined application of GGA and amelogenin may establish a suitable environment for periodontal wound healing and further drive the development of novel therapeutics for periodontal tissue regeneration. Our study demonstrated that geranylgeranylacetone (GGA) increases glucose‐regulated protein 78 (Grp78) expression and enhances the migration of human periodontal ligament cells (hPDLCs). Also, this increased Grp78 expression triggers the production of Angptl4 and Areg, which are involved in angiogenesis and wound healing, via the activation of hypoxia‐inducible factor 1α (HIF‐1α) and peroxisome proliferator‐activated
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Cell migration activity is expected to increase when human periodontal ligament cells (hPDLCs) overexpressing Grp78 are treated with amelogenin. Geranylgeranylacetone (GGA) is a drug that induces the expression of heat shock protein and is routinely used to treat gastric ulcers. Here, we investigated the changes in the properties and behavior of hPDLCs in response to treatment with GGA and the synergistic effects of amelogenin stimulation in hPDLCs pretreated with GGA for the establishment of a novel periodontal tissue regenerative therapy. We observed that GGA treatment increased Grp78 protein expression in hPDLCs and enhanced cell migration. Microarray analysis demonstrated that increased Grp78 expression triggered the production of angiopoietin‐like 4 and amphiregulin, which are involved in the enhancement of angiogenesis and subsequent wound healing via the activation of hypoxia‐inducible factor 1α and peroxisome proliferator‐activated receptors as well as the phosphorylation of cAMP response element‐binding protein and protein kinase A. Moreover, the addition of recombinant murine amelogenin (rM180) further accelerated hPDLC migration and tube formation of human umbilical vein endothelial cells due to the upregulation of interleukin‐8 (IL‐8), monocyte chemotactic protein 1, and IL‐6, which are also known as angiogenesis‐inducing factors. These findings suggest that the application of GGA to gingival tissue and alveolar bone damaged by periodontal disease would facilitate the wound healing process by inducing periodontal ligament cells to migrate to the root surface and release cytokines involved in tissue repair. Additionally, supplementation with amelogenin synergistically enhanced the migratory capacity of these cells while actively promoting angiogenesis. Therefore, the combined application of GGA and amelogenin may establish a suitable environment for periodontal wound healing and further drive the development of novel therapeutics for periodontal tissue regeneration. Our study demonstrated that geranylgeranylacetone (GGA) increases glucose‐regulated protein 78 (Grp78) expression and enhances the migration of human periodontal ligament cells (hPDLCs). Also, this increased Grp78 expression triggers the production of Angptl4 and Areg, which are involved in angiogenesis and wound healing, via the activation of hypoxia‐inducible factor 1α (HIF‐1α) and peroxisome proliferator‐activated receptor δ (PPARδ) and the phosphorylation of CREB and PKA. 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Cell migration activity is expected to increase when human periodontal ligament cells (hPDLCs) overexpressing Grp78 are treated with amelogenin. Geranylgeranylacetone (GGA) is a drug that induces the expression of heat shock protein and is routinely used to treat gastric ulcers. Here, we investigated the changes in the properties and behavior of hPDLCs in response to treatment with GGA and the synergistic effects of amelogenin stimulation in hPDLCs pretreated with GGA for the establishment of a novel periodontal tissue regenerative therapy. We observed that GGA treatment increased Grp78 protein expression in hPDLCs and enhanced cell migration. Microarray analysis demonstrated that increased Grp78 expression triggered the production of angiopoietin‐like 4 and amphiregulin, which are involved in the enhancement of angiogenesis and subsequent wound healing via the activation of hypoxia‐inducible factor 1α and peroxisome proliferator‐activated receptors as well as the phosphorylation of cAMP response element‐binding protein and protein kinase A. Moreover, the addition of recombinant murine amelogenin (rM180) further accelerated hPDLC migration and tube formation of human umbilical vein endothelial cells due to the upregulation of interleukin‐8 (IL‐8), monocyte chemotactic protein 1, and IL‐6, which are also known as angiogenesis‐inducing factors. These findings suggest that the application of GGA to gingival tissue and alveolar bone damaged by periodontal disease would facilitate the wound healing process by inducing periodontal ligament cells to migrate to the root surface and release cytokines involved in tissue repair. Additionally, supplementation with amelogenin synergistically enhanced the migratory capacity of these cells while actively promoting angiogenesis. Therefore, the combined application of GGA and amelogenin may establish a suitable environment for periodontal wound healing and further drive the development of novel therapeutics for periodontal tissue regeneration. Our study demonstrated that geranylgeranylacetone (GGA) increases glucose‐regulated protein 78 (Grp78) expression and enhances the migration of human periodontal ligament cells (hPDLCs). Also, this increased Grp78 expression triggers the production of Angptl4 and Areg, which are involved in angiogenesis and wound healing, via the activation of hypoxia‐inducible factor 1α (HIF‐1α) and peroxisome proliferator‐activated receptor δ (PPARδ) and the phosphorylation of CREB and PKA. 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Cell migration activity is expected to increase when human periodontal ligament cells (hPDLCs) overexpressing Grp78 are treated with amelogenin. Geranylgeranylacetone (GGA) is a drug that induces the expression of heat shock protein and is routinely used to treat gastric ulcers. Here, we investigated the changes in the properties and behavior of hPDLCs in response to treatment with GGA and the synergistic effects of amelogenin stimulation in hPDLCs pretreated with GGA for the establishment of a novel periodontal tissue regenerative therapy. We observed that GGA treatment increased Grp78 protein expression in hPDLCs and enhanced cell migration. Microarray analysis demonstrated that increased Grp78 expression triggered the production of angiopoietin‐like 4 and amphiregulin, which are involved in the enhancement of angiogenesis and subsequent wound healing via the activation of hypoxia‐inducible factor 1α and peroxisome proliferator‐activated receptors as well as the phosphorylation of cAMP response element‐binding protein and protein kinase A. Moreover, the addition of recombinant murine amelogenin (rM180) further accelerated hPDLC migration and tube formation of human umbilical vein endothelial cells due to the upregulation of interleukin‐8 (IL‐8), monocyte chemotactic protein 1, and IL‐6, which are also known as angiogenesis‐inducing factors. These findings suggest that the application of GGA to gingival tissue and alveolar bone damaged by periodontal disease would facilitate the wound healing process by inducing periodontal ligament cells to migrate to the root surface and release cytokines involved in tissue repair. Additionally, supplementation with amelogenin synergistically enhanced the migratory capacity of these cells while actively promoting angiogenesis. Therefore, the combined application of GGA and amelogenin may establish a suitable environment for periodontal wound healing and further drive the development of novel therapeutics for periodontal tissue regeneration. Our study demonstrated that geranylgeranylacetone (GGA) increases glucose‐regulated protein 78 (Grp78) expression and enhances the migration of human periodontal ligament cells (hPDLCs). Also, this increased Grp78 expression triggers the production of Angptl4 and Areg, which are involved in angiogenesis and wound healing, via the activation of hypoxia‐inducible factor 1α (HIF‐1α) and peroxisome proliferator‐activated receptor δ (PPARδ) and the phosphorylation of CREB and PKA. 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subjects Alveolar bone
Amelogenin
Amphiregulin
Angiogenesis
Angiopoietin
Bone healing
Cell adhesion & migration
Cytokines
Drug development
Endothelial cells
geranylgeranylacetone
GRP78 protein
Heat shock proteins
Hypoxia
Interleukins
Kinases
Leukocyte migration
Ligaments
migration
Monocyte chemoattractant protein 1
Monocytes
Periodontal disease
Periodontal diseases
Periodontal ligament
periodontal ligament cells
Phosphorylation
Protein kinase A
Proteins
Regeneration
Supplements
Synergistic effect
Tissue engineering
Tissues
Ulcers
Umbilical vein
Wound healing
title Combined application of geranylgeranylacetone and amelogenin promotes angiogenesis and wound healing in human periodontal ligament cells
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