Immunohistochemical Observation of Co-expression of E- and N-cadherins in Rat Organogenesis
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- Sakamoto Atsushi
- Division of Forensic Medicine, Center for Community Medicine, Jichi Medical University School of Medicine
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- Murata Kazumoto
- Division of Forensic Medicine, Center for Community Medicine, Jichi Medical University School of Medicine
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- Suzuki Hideto
- Division of Forensic Medicine, Center for Community Medicine, Jichi Medical University School of Medicine
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- Yatabe Megumi
- Division of Histology and Cell Biology, Department of Anatomy, Jichi Medical University School of Medicine
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- Kikuchi Motoshi
- Division of Histology and Cell Biology, Department of Anatomy, Jichi Medical University School of Medicine
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Cadherins are a family of transmembrane glycoproteins that mediate cell-to-cell adhesion. Isoforms, including E- and N-cadherin, have been identified and shown to regulate morphogenesis through homophilic binding. In the ontogeny, the expressions of E- and N-cadherin change spatiotemporally, and the changes in cadherin isoforms, called cadherin switching, impact the mechanical adhesion of cells. Furthermore, cadherin functions as a receptor that transfers information from outside to inside cells, and in terms of switching, it affects cell phenotypes. To observe the expression patterns of E- and N-cadherins during embryogenesis and to identify cells that transiently coexpress both cadherins, we employed a recently developed immunohistochemical double staining technique in rat fetuses. At embryonic day 9, embryonic ectodermal cells more dominantly expressed E-cadherin, while mesodermal cells more dominantly expressed N-cadherin. At embryonic day 10, the expression pattern of E-cadherin in the surface ectoderm and endoderm and that of N-cadherin in the neuroectoderm were established. After embryonic day 10, unique co-expression of E- and N-cadherin was observed in primordia, such as the bulbus cordis, otic pit, notochord, and Rathke’s pouch. In the present study, it was possible to visualize the expression patterns of E- and N-cadherin during early fetal development, which enabled us to morphologically clarify cadherin switching.<br>
収録刊行物
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- Acta Histochemica et Cytochemica
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Acta Histochemica et Cytochemica 41 (5), 143-147, 2008
日本組織細胞化学会
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詳細情報 詳細情報について
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- CRID
- 1390282679839044096
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- NII論文ID
- 130000070542
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- ISSN
- 13475800
- 00445991
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- 本文言語コード
- en
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- データソース種別
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- JaLC
- Crossref
- CiNii Articles
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- 抄録ライセンスフラグ
- 使用不可