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Modulation of matrix metalloproteases by ciliary neurotrophic factor in human placental development
Ciliary neurotrophic factor (CNTF) is a pleiotropic cytokine that signals through a receptor complex containing a specific subunit, CNTF receptor α (CNTFRα). The two molecules are constitutively expressed in key structures for human placental growth and differentiation. The possible role of CNTF in...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer Berlin Heidelberg
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9525382/ https://www.ncbi.nlm.nih.gov/pubmed/35794391 http://dx.doi.org/10.1007/s00441-022-03658-1 |
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author | Tossetta, Giovanni Fantone, Sonia Busilacchi, Elena Marinelli Di Simone, Nicoletta Giannubilo, Stefano R. Scambia, Giovanni Giordano, Antonio Marzioni, Daniela |
author_facet | Tossetta, Giovanni Fantone, Sonia Busilacchi, Elena Marinelli Di Simone, Nicoletta Giannubilo, Stefano R. Scambia, Giovanni Giordano, Antonio Marzioni, Daniela |
author_sort | Tossetta, Giovanni |
collection | PubMed |
description | Ciliary neurotrophic factor (CNTF) is a pleiotropic cytokine that signals through a receptor complex containing a specific subunit, CNTF receptor α (CNTFRα). The two molecules are constitutively expressed in key structures for human placental growth and differentiation. The possible role of CNTF in enhancing cell proliferation and/or invasion during placental development and remodelling was investigated using HTR-8/SVneo and BeWo cells, taken respectively as cytotrophoblast and syncytiotrophoblast models. In both cell lines, treatment with human recombinant (hr) CNTF activated JAK2/STAT3 signalling and inhibited the ERK pathway. Interestingly, in HTR-8/SVneo cells, 50 ng hrCNTF induced significant downregulation of matrix metalloprotease (MMP)-1 and significant upregulation of MMP-9. Moreover, pharmacological inhibition of JAK2/STAT3 signalling by AG490 and curcumin resulted in MMP-9 downregulation; it activated the ERK signalling pathway and upregulated MMP-1 expression. Collectively, these data suggest a role for CNTF signalling in extravillous cytotrophoblast invasion through the modulation of specific MMPs. |
format | Online Article Text |
id | pubmed-9525382 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-95253822022-10-02 Modulation of matrix metalloproteases by ciliary neurotrophic factor in human placental development Tossetta, Giovanni Fantone, Sonia Busilacchi, Elena Marinelli Di Simone, Nicoletta Giannubilo, Stefano R. Scambia, Giovanni Giordano, Antonio Marzioni, Daniela Cell Tissue Res Regular Article Ciliary neurotrophic factor (CNTF) is a pleiotropic cytokine that signals through a receptor complex containing a specific subunit, CNTF receptor α (CNTFRα). The two molecules are constitutively expressed in key structures for human placental growth and differentiation. The possible role of CNTF in enhancing cell proliferation and/or invasion during placental development and remodelling was investigated using HTR-8/SVneo and BeWo cells, taken respectively as cytotrophoblast and syncytiotrophoblast models. In both cell lines, treatment with human recombinant (hr) CNTF activated JAK2/STAT3 signalling and inhibited the ERK pathway. Interestingly, in HTR-8/SVneo cells, 50 ng hrCNTF induced significant downregulation of matrix metalloprotease (MMP)-1 and significant upregulation of MMP-9. Moreover, pharmacological inhibition of JAK2/STAT3 signalling by AG490 and curcumin resulted in MMP-9 downregulation; it activated the ERK signalling pathway and upregulated MMP-1 expression. Collectively, these data suggest a role for CNTF signalling in extravillous cytotrophoblast invasion through the modulation of specific MMPs. Springer Berlin Heidelberg 2022-07-07 2022 /pmc/articles/PMC9525382/ /pubmed/35794391 http://dx.doi.org/10.1007/s00441-022-03658-1 Text en © The Author(s) 2022, corrected publication 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Regular Article Tossetta, Giovanni Fantone, Sonia Busilacchi, Elena Marinelli Di Simone, Nicoletta Giannubilo, Stefano R. Scambia, Giovanni Giordano, Antonio Marzioni, Daniela Modulation of matrix metalloproteases by ciliary neurotrophic factor in human placental development |
title | Modulation of matrix metalloproteases by ciliary neurotrophic factor in human placental development |
title_full | Modulation of matrix metalloproteases by ciliary neurotrophic factor in human placental development |
title_fullStr | Modulation of matrix metalloproteases by ciliary neurotrophic factor in human placental development |
title_full_unstemmed | Modulation of matrix metalloproteases by ciliary neurotrophic factor in human placental development |
title_short | Modulation of matrix metalloproteases by ciliary neurotrophic factor in human placental development |
title_sort | modulation of matrix metalloproteases by ciliary neurotrophic factor in human placental development |
topic | Regular Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9525382/ https://www.ncbi.nlm.nih.gov/pubmed/35794391 http://dx.doi.org/10.1007/s00441-022-03658-1 |
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