The uPA/uPAR system in astrocytic wound healing
The repair of injured tissue is a highly complex process that involves cell proliferation, differentiation, and migration. Cell migration requires the dismantling of intercellular contacts in the injured zone and their subsequent reconstitution in the wounded area. Urokinase-type plasminogen activat...
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| Format: | Article |
| Language: | English |
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Wolters Kluwer Medknow Publications
2022-01-01
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| Series: | Neural Regeneration Research |
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| Online Access: | http://www.nrronline.org/article.asp?issn=1673-5374;year=2022;volume=17;issue=11;spage=2404;epage=2406;aulast=Yepes |
| _version_ | 1828334388469825536 |
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| author | Manuel Yepes |
| author_facet | Manuel Yepes |
| author_sort | Manuel Yepes |
| collection | DOAJ |
| description | The repair of injured tissue is a highly complex process that involves cell proliferation, differentiation, and migration. Cell migration requires the dismantling of intercellular contacts in the injured zone and their subsequent reconstitution in the wounded area. Urokinase-type plasminogen activator (uPA) is a serine proteinase found in multiple cell types including endothelial cells, smooth muscle cells, monocytes, and macrophages. A substantial body of experimental evidence with different cell types outside the central nervous system indicates that the binding of uPA to its receptor (uPAR) on the cell surface prompts cell migration by inducing plasmin-mediated degradation of the extracellular matrix. In contrast, although uPA and uPAR are abundantly found in astrocytes and uPA binding to uPAR triggers astrocytic activation, it is unknown if uPA also plays a role in astrocytic migration. Neuronal cadherin is a member of cell adhesion proteins pivotal for the formation of cell-cell contacts between astrocytes. More specifically, while the extracellular domain of neuronal cadherin interacts with the extracellular domain of neuronal cadherin in neighboring cells, its intracellular domain binds to β-catenin, which in turn links the complex to the actin cytoskeleton. Glycogen synthase kinase 3β is a serine-threonine kinase that prevents the cytoplasmic accumulation of β-catenin by inducing its phosphorylation at Ser33, Ser37, and Ser41, thus activating a sequence of events that lead to its proteasomal degradation. The data discussed in this perspective indicate that astrocytes release uPA following a mechanical injury, and that binding of this uPA to uPAR on the cell membrane induces the detachment of β-catenin from the intracellular domain of neuronal cadherin by triggering its extracellular signal-regulated kinase 1/2-mediated phosphorylation at Tyr650. Remarkably, this is followed by the cytoplasmic accumulation of β-catenin because uPA-induced extracellular signal-regulated kinase 1/2 activation also phosphorylates lipoprotein receptor-related protein 6 at Ser1490, which in turn, by recruiting glycogen synthase kinase 3β to its intracellular domain abrogates its effect on β-catenin. The cytoplasmic accumulation of β-catenin is followed by its nuclear translocation, where it induces the expression of uPAR, which is required for the migration of astrocytes from the injured edge into the wounded area. |
| first_indexed | 2024-04-13T21:32:21Z |
| format | Article |
| id | doaj.art-5e35b644a08b41578f03c9d628a707fc |
| institution | Directory Open Access Journal |
| issn | 1673-5374 |
| language | English |
| last_indexed | 2024-04-13T21:32:21Z |
| publishDate | 2022-01-01 |
| publisher | Wolters Kluwer Medknow Publications |
| record_format | Article |
| series | Neural Regeneration Research |
| spelling | doaj.art-5e35b644a08b41578f03c9d628a707fc2022-12-22T02:29:06ZengWolters Kluwer Medknow PublicationsNeural Regeneration Research1673-53742022-01-0117112404240610.4103/1673-5374.338991The uPA/uPAR system in astrocytic wound healingManuel YepesThe repair of injured tissue is a highly complex process that involves cell proliferation, differentiation, and migration. Cell migration requires the dismantling of intercellular contacts in the injured zone and their subsequent reconstitution in the wounded area. Urokinase-type plasminogen activator (uPA) is a serine proteinase found in multiple cell types including endothelial cells, smooth muscle cells, monocytes, and macrophages. A substantial body of experimental evidence with different cell types outside the central nervous system indicates that the binding of uPA to its receptor (uPAR) on the cell surface prompts cell migration by inducing plasmin-mediated degradation of the extracellular matrix. In contrast, although uPA and uPAR are abundantly found in astrocytes and uPA binding to uPAR triggers astrocytic activation, it is unknown if uPA also plays a role in astrocytic migration. Neuronal cadherin is a member of cell adhesion proteins pivotal for the formation of cell-cell contacts between astrocytes. More specifically, while the extracellular domain of neuronal cadherin interacts with the extracellular domain of neuronal cadherin in neighboring cells, its intracellular domain binds to β-catenin, which in turn links the complex to the actin cytoskeleton. Glycogen synthase kinase 3β is a serine-threonine kinase that prevents the cytoplasmic accumulation of β-catenin by inducing its phosphorylation at Ser33, Ser37, and Ser41, thus activating a sequence of events that lead to its proteasomal degradation. The data discussed in this perspective indicate that astrocytes release uPA following a mechanical injury, and that binding of this uPA to uPAR on the cell membrane induces the detachment of β-catenin from the intracellular domain of neuronal cadherin by triggering its extracellular signal-regulated kinase 1/2-mediated phosphorylation at Tyr650. Remarkably, this is followed by the cytoplasmic accumulation of β-catenin because uPA-induced extracellular signal-regulated kinase 1/2 activation also phosphorylates lipoprotein receptor-related protein 6 at Ser1490, which in turn, by recruiting glycogen synthase kinase 3β to its intracellular domain abrogates its effect on β-catenin. The cytoplasmic accumulation of β-catenin is followed by its nuclear translocation, where it induces the expression of uPAR, which is required for the migration of astrocytes from the injured edge into the wounded area.http://www.nrronline.org/article.asp?issn=1673-5374;year=2022;volume=17;issue=11;spage=2404;epage=2406;aulast=Yepesastrocytes; lipoprotein receptor-related protein 6; plasmin; urokinase receptor; urokinase-type plasminogen activator; wnt-β-catenin pathway; wound healing; β-catenin |
| spellingShingle | Manuel Yepes The uPA/uPAR system in astrocytic wound healing Neural Regeneration Research astrocytes; lipoprotein receptor-related protein 6; plasmin; urokinase receptor; urokinase-type plasminogen activator; wnt-β-catenin pathway; wound healing; β-catenin |
| title | The uPA/uPAR system in astrocytic wound healing |
| title_full | The uPA/uPAR system in astrocytic wound healing |
| title_fullStr | The uPA/uPAR system in astrocytic wound healing |
| title_full_unstemmed | The uPA/uPAR system in astrocytic wound healing |
| title_short | The uPA/uPAR system in astrocytic wound healing |
| title_sort | upa upar system in astrocytic wound healing |
| topic | astrocytes; lipoprotein receptor-related protein 6; plasmin; urokinase receptor; urokinase-type plasminogen activator; wnt-β-catenin pathway; wound healing; β-catenin |
| url | http://www.nrronline.org/article.asp?issn=1673-5374;year=2022;volume=17;issue=11;spage=2404;epage=2406;aulast=Yepes |
| work_keys_str_mv | AT manuelyepes theupauparsysteminastrocyticwoundhealing AT manuelyepes upauparsysteminastrocyticwoundhealing |