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Expression dynamics of Crry at the implantation sites in normal pregnancy and response against miscarriage induction
In mammals, immune tolerance against fetal tissue has been established for normal pregnancy progression. It is known that Crry regulates complemental activity to prevent injury of the mouse embryo and extra-embryonic tissue. This study aimed to examine the expression appearance and normal localizati...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Japanese Society of Veterinary Science
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9887214/ https://www.ncbi.nlm.nih.gov/pubmed/36450590 http://dx.doi.org/10.1292/jvms.22-0286 |
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author | KUNIYOSHI, Nobue HANADA, Saki ANDO, Reina YUSTINASARI, Lita Rakhma KURATOMI, Maria KAGAWA, Seizaburo IMAI, Hiroyuki KUSAKABE, Ken Takeshi |
author_facet | KUNIYOSHI, Nobue HANADA, Saki ANDO, Reina YUSTINASARI, Lita Rakhma KURATOMI, Maria KAGAWA, Seizaburo IMAI, Hiroyuki KUSAKABE, Ken Takeshi |
author_sort | KUNIYOSHI, Nobue |
collection | PubMed |
description | In mammals, immune tolerance against fetal tissue has been established for normal pregnancy progression. It is known that Crry regulates complemental activity to prevent injury of the mouse embryo and extra-embryonic tissue. This study aimed to examine the expression appearance and normal localization sites of Crry in the mouse placenta. Also, the emergency responses of Crry were verified at the time of experimental miscarriage induction. Moreover, we investigated an existing similar protein of Crry in animal placentas other than mice. Crry expression level showed a peak at day 8.5 of pregnancy. Trophoblast giant cells and decidual cells indicated a positive reaction to anti-Crry antibody. After treatments of interferon-γ, Crry expression was increased significantly in the survived implantation sites as compared with the controls. However, there was no significant difference in the miscarriage-initiated sites. It disclosed that Crry distributes from the early to middle periods of the placentas and involves complement regulation at the extraembryonic tissue and decidua basalis. Crry also showed an ability to respond to risk against external initiation for urgent miscarriage. Finally, we found anti-mouse Crry antibody-bound proteins in the placenta of many animals. It suggests a potency of Crry to make an environment of immune tolerance in many types of mammal placentas. |
format | Online Article Text |
id | pubmed-9887214 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Japanese Society of Veterinary Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-98872142023-02-02 Expression dynamics of Crry at the implantation sites in normal pregnancy and response against miscarriage induction KUNIYOSHI, Nobue HANADA, Saki ANDO, Reina YUSTINASARI, Lita Rakhma KURATOMI, Maria KAGAWA, Seizaburo IMAI, Hiroyuki KUSAKABE, Ken Takeshi J Vet Med Sci Anatomy In mammals, immune tolerance against fetal tissue has been established for normal pregnancy progression. It is known that Crry regulates complemental activity to prevent injury of the mouse embryo and extra-embryonic tissue. This study aimed to examine the expression appearance and normal localization sites of Crry in the mouse placenta. Also, the emergency responses of Crry were verified at the time of experimental miscarriage induction. Moreover, we investigated an existing similar protein of Crry in animal placentas other than mice. Crry expression level showed a peak at day 8.5 of pregnancy. Trophoblast giant cells and decidual cells indicated a positive reaction to anti-Crry antibody. After treatments of interferon-γ, Crry expression was increased significantly in the survived implantation sites as compared with the controls. However, there was no significant difference in the miscarriage-initiated sites. It disclosed that Crry distributes from the early to middle periods of the placentas and involves complement regulation at the extraembryonic tissue and decidua basalis. Crry also showed an ability to respond to risk against external initiation for urgent miscarriage. Finally, we found anti-mouse Crry antibody-bound proteins in the placenta of many animals. It suggests a potency of Crry to make an environment of immune tolerance in many types of mammal placentas. The Japanese Society of Veterinary Science 2022-11-29 2023-01 /pmc/articles/PMC9887214/ /pubmed/36450590 http://dx.doi.org/10.1292/jvms.22-0286 Text en ©2023 The Japanese Society of Veterinary Science https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (by-nc-nd) License. (CC-BY-NC-ND 4.0: https://creativecommons.org/licenses/by-nc-nd/4.0/) |
spellingShingle | Anatomy KUNIYOSHI, Nobue HANADA, Saki ANDO, Reina YUSTINASARI, Lita Rakhma KURATOMI, Maria KAGAWA, Seizaburo IMAI, Hiroyuki KUSAKABE, Ken Takeshi Expression dynamics of Crry at the implantation sites in normal pregnancy and response against miscarriage induction |
title | Expression dynamics of Crry at the implantation sites in normal pregnancy and response against miscarriage induction |
title_full | Expression dynamics of Crry at the implantation sites in normal pregnancy and response against miscarriage induction |
title_fullStr | Expression dynamics of Crry at the implantation sites in normal pregnancy and response against miscarriage induction |
title_full_unstemmed | Expression dynamics of Crry at the implantation sites in normal pregnancy and response against miscarriage induction |
title_short | Expression dynamics of Crry at the implantation sites in normal pregnancy and response against miscarriage induction |
title_sort | expression dynamics of crry at the implantation sites in normal pregnancy and response against miscarriage induction |
topic | Anatomy |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9887214/ https://www.ncbi.nlm.nih.gov/pubmed/36450590 http://dx.doi.org/10.1292/jvms.22-0286 |
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