Expression of Allograft Inflammatory Factor-1 in Mouse Uterus and Poly (I:C)-induced Fetal Resorption
Problem: To investigate whether the allograft inflammatory factor‐1 (AIF‐1) is expressed and plays a role in the reproductive system. Method of study: AIF‐1 expression was examined in uteri of non‐pregnant and pregnant mice by Northern blot analysis, RT‐PCR and immunohistochemistry. Results: The exp...
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Published in | American journal of reproductive immunology (1989) Vol. 50; no. 1; pp. 104 - 112 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
Oxford, UK
Munksgaard International Publishers
01.07.2003
Blackwell |
Subjects | |
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Abstract | Problem: To investigate whether the allograft inflammatory factor‐1 (AIF‐1) is expressed and plays a role in the reproductive system.
Method of study: AIF‐1 expression was examined in uteri of non‐pregnant and pregnant mice by Northern blot analysis, RT‐PCR and immunohistochemistry.
Results: The expression of AIF‐1 varied during the estrous cycle with a peak at estrus. After the insemination, the expression of AIF‐1 mRNA diminished gradually and again increased in the pre‐implantation or implantation period in allogeneic or syngeneic pregnancy, respectively. Enhanced expressions of AIF‐1, tumor necrosis factor‐α (TNF‐α) and nitric oxide synthase 2 (NOS2) mRNA were observed in the embryos of resorption‐prone pregnancy injected with poly(I:C).
Conclusions: This study demonstrated for the first time that AIF‐1 was expressed in uterus. The expression level was associated with the population size of macrophage and varied during the estrous cycle and the pregnancy period. The augmented expression of AIF‐1 with concomitant expressions of TNF‐α and NOS2 mRNA in poly(I:C)‐injected mice suggests a correlation between AIF‐1 production and fetal resorption. |
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AbstractList | Problem: To investigate whether the allograft inflammatory factor‐1 (AIF‐1) is expressed and plays a role in the reproductive system.
Method of study: AIF‐1 expression was examined in uteri of non‐pregnant and pregnant mice by Northern blot analysis, RT‐PCR and immunohistochemistry.
Results: The expression of AIF‐1 varied during the estrous cycle with a peak at estrus. After the insemination, the expression of AIF‐1 mRNA diminished gradually and again increased in the pre‐implantation or implantation period in allogeneic or syngeneic pregnancy, respectively. Enhanced expressions of AIF‐1, tumor necrosis factor‐α (TNF‐α) and nitric oxide synthase 2 (NOS2) mRNA were observed in the embryos of resorption‐prone pregnancy injected with poly(I:C).
Conclusions: This study demonstrated for the first time that AIF‐1 was expressed in uterus. The expression level was associated with the population size of macrophage and varied during the estrous cycle and the pregnancy period. The augmented expression of AIF‐1 with concomitant expressions of TNF‐α and NOS2 mRNA in poly(I:C)‐injected mice suggests a correlation between AIF‐1 production and fetal resorption. To investigate whether the allograft inflammatory factor-1 (AIF-1) is expressed and plays a role in the reproductive system. AIF-1 expression was examined in uteri of non-pregnant and pregnant mice by Northern blot analysis, RT-PCR and immunohistochemistry. The expression of AIF-1 varied during the estrous cycle with a peak at estrus. After the insemination, the expression of AIF-1 mRNA diminished gradually and again increased in the pre-implantation or implantation period in allogeneic or syngeneic pregnancy, respectively. Enhanced expressions of AIF-1, tumor necrosis factor-alpha (TNF-alpha) and nitric oxide synthase 2 (NOS2) mRNA were observed in the embryos of resorption-prone pregnancy injected with poly(I:C). This study demonstrated for the first time that AIF-1 was expressed in uterus. The expression level was associated with the population size of macrophage and varied during the estrous cycle and the pregnancy period. The augmented expression of AIF-I with concomitant expressions of TNF-alpha and NOS2 mRNA in poly(I:C)-injected mice suggests a correlation between AIF-1 production and fetal resorption. Problem: To investigate whether the allograft inflammatory factor‐1 (AIF‐1) is expressed and plays a role in the reproductive system. Method of study: AIF‐1 expression was examined in uteri of non‐pregnant and pregnant mice by Northern blot analysis, RT‐PCR and immunohistochemistry. Results: The expression of AIF‐1 varied during the estrous cycle with a peak at estrus. After the insemination, the expression of AIF‐1 mRNA diminished gradually and again increased in the pre‐implantation or implantation period in allogeneic or syngeneic pregnancy, respectively. Enhanced expressions of AIF‐1, tumor necrosis factor‐ α (TNF‐ α ) and nitric oxide synthase 2 (NOS2) mRNA were observed in the embryos of resorption‐prone pregnancy injected with poly(I:C). Conclusions: This study demonstrated for the first time that AIF‐1 was expressed in uterus. The expression level was associated with the population size of macrophage and varied during the estrous cycle and the pregnancy period. The augmented expression of AIF‐1 with concomitant expressions of TNF‐ α and NOS2 mRNA in poly(I:C)‐injected mice suggests a correlation between AIF‐1 production and fetal resorption. |
Author | Shimada, Shigeki Yamada, Hideto Iwabuchi, Kazuya Minakami, Hisanori Watano, Keiko Onoé, Kazunori Shimizu, Hidemi |
Author_xml | – sequence: 1 givenname: Shigeki surname: Shimada fullname: Shimada, Shigeki organization: Division of Immunobiology, Research Section of Pathophysiology, Institute for Genetic Medicine, Hokkaido University, Sapporo, Japan – sequence: 2 givenname: Kazuya surname: Iwabuchi fullname: Iwabuchi, Kazuya organization: Division of Immunobiology, Research Section of Pathophysiology, Institute for Genetic Medicine, Hokkaido University, Sapporo, Japan – sequence: 3 givenname: Keiko surname: Watano fullname: Watano, Keiko organization: Division of Immunobiology, Research Section of Pathophysiology, Institute for Genetic Medicine, Hokkaido University, Sapporo, Japan – sequence: 4 givenname: Hidemi surname: Shimizu fullname: Shimizu, Hidemi organization: Department of Anatomy, Hokkaido University Graduate School of Medicine, Sapporo, Japan – sequence: 5 givenname: Hideto surname: Yamada fullname: Yamada, Hideto organization: Department of Obstetrics, Hokkaido University Graduate School of Medicine, Sapporo, Japan – sequence: 6 givenname: Hisanori surname: Minakami fullname: Minakami, Hisanori organization: Department of Obstetrics, Hokkaido University Graduate School of Medicine, Sapporo, Japan – sequence: 7 givenname: Kazunori surname: Onoé fullname: Onoé, Kazunori organization: Division of Immunobiology, Research Section of Pathophysiology, Institute for Genetic Medicine, Hokkaido University, Sapporo, Japan |
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Keywords | Enzyme Rodentia Homograft Resorption Gene expression Nitric-oxide synthase Pregnancy Vertebrata Mammalia Mouse Uterus AIF-1 fetal resorption Female genital system Female Fetus Oxidoreductases Estrous cycle Tumor necrosis factor α |
Language | English |
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References_xml | – volume: 182 start-page: 1143 year: 1995 end-page: 1151 article-title: Early embryo loss is associated with local production of nitric oxide by decidual mononuclear cells publication-title: J Exp Med – volume: 158 start-page: 4886 year: 1997 end-page: 4892 article-title: Early embryo loss is associated with the prior expression of macrophage activation markers in the decidua publication-title: J Immunol – volume: 104 start-page: 307 year: 2001 end-page: 316 article-title: Allograft inflammatory factor‐1 augments production of interleukin‐6, ‐10 and ‐12 by a mouse macrophage line publication-title: Immunology – volume: 12 start-page: 64 year: 2000 end-page: 76 article-title: Reactive oxygen and reactive nitrogen intermediates in innate and specific immunity publication-title: Curr Opin Immunol – year: 1968 – volume: 228 start-page: 29 year: 1996 end-page: 37 article-title: cDNA cloning of human allograft inflammatory factor‐1: tissue distribution, cytokine induction, and mRNA expression in injured rat carotid arteries publication-title: Biochem Biophys Res Commun – volume: 95 start-page: 2954 year: 1995 end-page: 2962 article-title: Cloning and characterization of allograft inflammatory factor‐1: a novel macrophage factor identified in rat cardiac allografts with chronic rejection publication-title: J Clin Invest – volume: 52 start-page: 106 year: 1980 end-page: 118 article-title: Impairment of host‐versus‐graft reaction in pregnant mice. 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Snippet | Problem: To investigate whether the allograft inflammatory factor‐1 (AIF‐1) is expressed and plays a role in the reproductive system.
Method of study: AIF‐1... To investigate whether the allograft inflammatory factor-1 (AIF-1) is expressed and plays a role in the reproductive system. AIF-1 expression was examined in... Problem: To investigate whether the allograft inflammatory factor‐1 (AIF‐1) is expressed and plays a role in the reproductive system. Method of study: AIF‐1... |
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SubjectTerms | AIF-1 Animals Biological and medical sciences Blotting, Northern Calcium-Binding Proteins - analysis Calcium-Binding Proteins - genetics Embryo, Mammalian - chemistry Epithelial Cells - chemistry Estrous Cycle Female fetal resorption Fetal Resorption - chemically induced Fetal Resorption - genetics Fetal Resorption - metabolism Fundamental and applied biological sciences. Psychology Gene Expression Regulation - drug effects Immunohistochemistry - methods Interferon-gamma - genetics Macrophages - chemistry Macrophages - cytology Macrophages - metabolism Male Mammalian female genital system Mice Mice, Inbred BALB C Mice, Inbred C57BL Mice, Inbred CBA Mice, Inbred DBA Microfilament Proteins Morphology. Physiology Placenta - chemistry Poly I-C - pharmacology Pregnancy RNA, Messenger - genetics RNA, Messenger - metabolism Tumor Necrosis Factor-alpha - genetics Uterus - chemistry Uterus - metabolism Vertebrates: reproduction |
Title | Expression of Allograft Inflammatory Factor-1 in Mouse Uterus and Poly (I:C)-induced Fetal Resorption |
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