The Involvement of Cell Adhesion Molecules, Tight Junctions, and Gap Junctions in Human Placentation
Placentation is a major determinant of the success of pregnancy. It is regulated by several factors such as cell adhesion molecules, tight junctions, and gap junctions. The cell adhesion molecules are integrins, cadherins, immunoglobulins, nectins, and selectins. The tight junctions are composed of...
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| Vydáno v: | Reproductive sciences (Thousand Oaks, Calif.) Ročník 28; číslo 2; s. 305 - 320 |
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| Médium: | Journal Article |
| Jazyk: | angličtina |
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Springer International Publishing
01.02.2021
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| ISSN: | 1933-7191, 1933-7205, 1933-7205 |
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| Abstract | Placentation is a major determinant of the success of pregnancy. It is regulated by several factors such as cell adhesion molecules, tight junctions, and gap junctions. The cell adhesion molecules are integrins, cadherins, immunoglobulins, nectins, and selectins. The tight junctions are composed of claudins, occludin, and junction adhesion molecule proteins while the gap junctions are composed of connexins of varying molecular weights. During placentation, some of these molecules regulate trophoblast proliferation, trophoblast fusion, trophoblast migration, trophoblast invasion, trophoblast-endothelium adhesion, glandular remodeling, and spiral artery remodeling. There is a dysregulated placental expression of some of these molecules during obstetric complications. We have, hereby, indicated the expression patterns of the subunits of each of these molecules in the various trophoblast subtypes and in the decidua, and have highlighted their involvement in physiological and pathological placentation. The available evidence points to the relevance of these molecules as distinguishing markers of the various trophoblast lineages and as potential therapeutic targets in the management of malplacentation-mediated diseases. |
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| AbstractList | Placentation is a major determinant of the success of pregnancy. It is regulated by several factors such as cell adhesion molecules, tight junctions, and gap junctions. The cell adhesion molecules are integrins, cadherins, immunoglobulins, nectins, and selectins. The tight junctions are composed of claudins, occludin, and junction adhesion molecule proteins while the gap junctions are composed of connexins of varying molecular weights. During placentation, some of these molecules regulate trophoblast proliferation, trophoblast fusion, trophoblast migration, trophoblast invasion, trophoblast-endothelium adhesion, glandular remodeling, and spiral artery remodeling. There is a dysregulated placental expression of some of these molecules during obstetric complications. We have, hereby, indicated the expression patterns of the subunits of each of these molecules in the various trophoblast subtypes and in the decidua, and have highlighted their involvement in physiological and pathological placentation. The available evidence points to the relevance of these molecules as distinguishing markers of the various trophoblast lineages and as potential therapeutic targets in the management of malplacentation-mediated diseases.Placentation is a major determinant of the success of pregnancy. It is regulated by several factors such as cell adhesion molecules, tight junctions, and gap junctions. The cell adhesion molecules are integrins, cadherins, immunoglobulins, nectins, and selectins. The tight junctions are composed of claudins, occludin, and junction adhesion molecule proteins while the gap junctions are composed of connexins of varying molecular weights. During placentation, some of these molecules regulate trophoblast proliferation, trophoblast fusion, trophoblast migration, trophoblast invasion, trophoblast-endothelium adhesion, glandular remodeling, and spiral artery remodeling. There is a dysregulated placental expression of some of these molecules during obstetric complications. We have, hereby, indicated the expression patterns of the subunits of each of these molecules in the various trophoblast subtypes and in the decidua, and have highlighted their involvement in physiological and pathological placentation. The available evidence points to the relevance of these molecules as distinguishing markers of the various trophoblast lineages and as potential therapeutic targets in the management of malplacentation-mediated diseases. Placentation is a major determinant of the success of pregnancy. It is regulated by several factors such as cell adhesion molecules, tight junctions, and gap junctions. The cell adhesion molecules are integrins, cadherins, immunoglobulins, nectins, and selectins. The tight junctions are composed of claudins, occludin, and junction adhesion molecule proteins while the gap junctions are composed of connexins of varying molecular weights. During placentation, some of these molecules regulate trophoblast proliferation, trophoblast fusion, trophoblast migration, trophoblast invasion, trophoblast-endothelium adhesion, glandular remodeling, and spiral artery remodeling. There is a dysregulated placental expression of some of these molecules during obstetric complications. We have, hereby, indicated the expression patterns of the subunits of each of these molecules in the various trophoblast subtypes and in the decidua, and have highlighted their involvement in physiological and pathological placentation. The available evidence points to the relevance of these molecules as distinguishing markers of the various trophoblast lineages and as potential therapeutic targets in the management of malplacentation-mediated diseases. |
| Author | Panhwar, Zulqarnain Wang, Ying-Xiong Czika, Armin Gorleku, Philip Narteh Ullah, Amin Adu-Gyamfi, Enoch Appiah Ding, Yu-Bin Ruan, Ling-Ling |
| Author_xml | – sequence: 1 givenname: Enoch Appiah orcidid: 0000-0002-0667-890X surname: Adu-Gyamfi fullname: Adu-Gyamfi, Enoch Appiah email: orkamanyame@gmail.com organization: Department of Reproductive Sciences, School of Basic Medicine, Chongqing Medical University, Joint International Research Laboratory of Reproduction & Development, Chongqing Medical University – sequence: 2 givenname: Armin surname: Czika fullname: Czika, Armin organization: Joint International Research Laboratory of Reproduction & Development, Chongqing Medical University – sequence: 3 givenname: Philip Narteh surname: Gorleku fullname: Gorleku, Philip Narteh organization: Department of Medical Imaging, School of Medical Sciences, University of Cape Coast – sequence: 4 givenname: Amin surname: Ullah fullname: Ullah, Amin organization: Joint International Research Laboratory of Reproduction & Development, Chongqing Medical University – sequence: 5 givenname: Zulqarnain surname: Panhwar fullname: Panhwar, Zulqarnain organization: Joint International Research Laboratory of Reproduction & Development, Chongqing Medical University – sequence: 6 givenname: Ling-Ling surname: Ruan fullname: Ruan, Ling-Ling organization: Joint International Research Laboratory of Reproduction & Development, Chongqing Medical University – sequence: 7 givenname: Yu-Bin surname: Ding fullname: Ding, Yu-Bin email: dingyb@cqmu.edu.cn organization: Department of Reproductive Sciences, School of Basic Medicine, Chongqing Medical University, Joint International Research Laboratory of Reproduction & Development, Chongqing Medical University – sequence: 8 givenname: Ying-Xiong surname: Wang fullname: Wang, Ying-Xiong email: 1600347366@qq.com organization: Department of Reproductive Sciences, School of Basic Medicine, Chongqing Medical University, Joint International Research Laboratory of Reproduction & Development, Chongqing Medical University |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/33146876$$D View this record in MEDLINE/PubMed |
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| Title | The Involvement of Cell Adhesion Molecules, Tight Junctions, and Gap Junctions in Human Placentation |
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