Spontaneous membranoproliferative glomerulonephritis in a young Crl:CD-1(ICR) mouse
Here, we reported a spontaneous case of membranoproliferative glomerulonephritis observed in a young ICR mouse. A 5-week-old female mouse was euthanized owing to abdominal swelling and increased body weight. At necropsy, generalized subcutaneous edema, and clear, colorless, non-viscous ascites were...
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Veröffentlicht in: | Journal of Toxicologic Pathology 2020, Vol.33(3), pp.177-181 |
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description | Here, we reported a spontaneous case of membranoproliferative glomerulonephritis observed in a young ICR mouse. A 5-week-old female mouse was euthanized owing to abdominal swelling and increased body weight. At necropsy, generalized subcutaneous edema, and clear, colorless, non-viscous ascites were observed. Histologically, the kidneys showed diffuse, bilateral glomerular lesions. The lesions were characterized by thickening and double contour of the basement membrane and an increase in mesangial cells and matrix, resulting in the narrowing of the capillary lumen. Additionally, eosinophilic hyaloid material accumulated in the subendothelial areas and Bowman’s space. The material was positive for periodic acid-Schiff, complement component C3, or immunoglobulin G, stained red by Masson’s trichrome, and stained blue by phosphotungstic acid-hematoxylin stain and was considered to be plasma due to glomerular leakage. The glomerular lesion was diagnosed as membranoproliferative glomerulonephritis, and an uncertain endothelial injury was suspected as the cause. |
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A 5-week-old female mouse was euthanized owing to abdominal swelling and increased body weight. At necropsy, generalized subcutaneous edema, and clear, colorless, non-viscous ascites were observed. Histologically, the kidneys showed diffuse, bilateral glomerular lesions. The lesions were characterized by thickening and double contour of the basement membrane and an increase in mesangial cells and matrix, resulting in the narrowing of the capillary lumen. Additionally, eosinophilic hyaloid material accumulated in the subendothelial areas and Bowman’s space. The material was positive for periodic acid-Schiff, complement component C3, or immunoglobulin G, stained red by Masson’s trichrome, and stained blue by phosphotungstic acid-hematoxylin stain and was considered to be plasma due to glomerular leakage. The glomerular lesion was diagnosed as membranoproliferative glomerulonephritis, and an uncertain endothelial injury was suspected as the cause.</description><identifier>ISSN: 0914-9198</identifier><identifier>EISSN: 1881-915X</identifier><identifier>EISSN: 1347-7404</identifier><identifier>DOI: 10.1293/tox.2019-0081</identifier><identifier>PMID: 32764843</identifier><language>eng</language><publisher>Tokyo: JAPANESE SOCIETY OF TOXICOLOGIC PATHOLOGY</publisher><subject>Ascites ; Body weight ; Case Report ; Complement component C3 ; CrlCD-1(ICR) mouse ; Edema ; Glomerulonephritis ; IgG antibody ; Immunoglobulin G ; Kidneys ; Lesions ; Leukocytes (eosinophilic) ; membranoproliferative glomerulonephritis ; Mesangial cells ; Necropsy ; spontaneous lesion ; Thickening</subject><ispartof>Journal of Toxicologic Pathology, 2020, Vol.33(3), pp.177-181</ispartof><rights>2020 The Japanese Society of Toxicologic Pathology</rights><rights>Copyright Japan Science and Technology Agency 2020</rights><rights>2020 The Japanese Society of Toxicologic Pathology 2020</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c608t-4e7da4c1badaa97ea39c6a8df7581f2ef2cf5dafe98e988f4b4e02b717999e373</citedby><cites>FETCH-LOGICAL-c608t-4e7da4c1badaa97ea39c6a8df7581f2ef2cf5dafe98e988f4b4e02b717999e373</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7396734/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7396734/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,1881,4014,27914,27915,27916,53782,53784</link.rule.ids></links><search><creatorcontrib>Tochitani, Tomoaki</creatorcontrib><creatorcontrib>Kouchi, Mami</creatorcontrib><creatorcontrib>Fuji, Yuta</creatorcontrib><creatorcontrib>Yoshino, Yuka</creatorcontrib><creatorcontrib>Matsumoto, Izumi</creatorcontrib><creatorcontrib>Sumitomo Dainippon Pharma Co</creatorcontrib><creatorcontrib>Preclinical Research Unit</creatorcontrib><creatorcontrib>Ltd</creatorcontrib><title>Spontaneous membranoproliferative glomerulonephritis in a young Crl:CD-1(ICR) mouse</title><title>Journal of Toxicologic Pathology</title><addtitle>J Toxicol Pathol</addtitle><description>Here, we reported a spontaneous case of membranoproliferative glomerulonephritis observed in a young ICR mouse. A 5-week-old female mouse was euthanized owing to abdominal swelling and increased body weight. At necropsy, generalized subcutaneous edema, and clear, colorless, non-viscous ascites were observed. Histologically, the kidneys showed diffuse, bilateral glomerular lesions. The lesions were characterized by thickening and double contour of the basement membrane and an increase in mesangial cells and matrix, resulting in the narrowing of the capillary lumen. Additionally, eosinophilic hyaloid material accumulated in the subendothelial areas and Bowman’s space. The material was positive for periodic acid-Schiff, complement component C3, or immunoglobulin G, stained red by Masson’s trichrome, and stained blue by phosphotungstic acid-hematoxylin stain and was considered to be plasma due to glomerular leakage. The glomerular lesion was diagnosed as membranoproliferative glomerulonephritis, and an uncertain endothelial injury was suspected as the cause.</description><subject>Ascites</subject><subject>Body weight</subject><subject>Case Report</subject><subject>Complement component C3</subject><subject>CrlCD-1(ICR) mouse</subject><subject>Edema</subject><subject>Glomerulonephritis</subject><subject>IgG antibody</subject><subject>Immunoglobulin G</subject><subject>Kidneys</subject><subject>Lesions</subject><subject>Leukocytes (eosinophilic)</subject><subject>membranoproliferative glomerulonephritis</subject><subject>Mesangial cells</subject><subject>Necropsy</subject><subject>spontaneous lesion</subject><subject>Thickening</subject><issn>0914-9198</issn><issn>1881-915X</issn><issn>1347-7404</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNpVkd2L1DAUxYMo7uzqo-8FX_Shaz6aJvFBkLquCwuCq-BbuG1vZzK0SU3Txf3vzTjLiBDuDdxzfyfkEPKK0UvGjXiXwu9LTpkpKdXsCdkwrVlpmPz5lGyoYVW-G31GzpdlTylXVIrn5ExwVVe6EhtydzcHn8BjWJdiwqmN4MMcw-gGjJDcPRbbMUwY1zF4nHfRJbcUzhdQPITVb4smju-bTyV7c9N8e1tMGYMvyLMBxgVfPvYL8uPz1ffmS3n79fqm-XhbdjXVqaxQ9VB1rIUewCgEYboadD8oqdnAceDdIHsY0Oh89FC1FVLeKqaMMSiUuCAfjtx5bSfsO_Qpwmjn6CaIDzaAs_9PvNvZbbi3SphaiSoDXj8CYvi14pLsPqzR5zdbXnEjpaZSZlV5VHUxLEvE4eTAqD1kYHMG9pCBPWSQ9ddHfXZ2HeR_G53Hf-i-F3lhhrzCaV4RgorcpKVMqVwyQqqaSZ5JzZG0XxJs8eQLMbluxL--QlhxKCf_07TbQbToxR_ixqlp</recordid><startdate>2020</startdate><enddate>2020</enddate><creator>Tochitani, Tomoaki</creator><creator>Kouchi, Mami</creator><creator>Fuji, Yuta</creator><creator>Yoshino, Yuka</creator><creator>Matsumoto, Izumi</creator><general>JAPANESE SOCIETY OF TOXICOLOGIC PATHOLOGY</general><general>The Japanese Society of Toxicologic Pathology</general><general>Japan Science and Technology Agency</general><general>Japanese Society of Toxicologic Pathology</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7U7</scope><scope>C1K</scope><scope>5PM</scope></search><sort><creationdate>2020</creationdate><title>Spontaneous membranoproliferative glomerulonephritis in a young Crl:CD-1(ICR) mouse</title><author>Tochitani, Tomoaki ; Kouchi, Mami ; Fuji, Yuta ; Yoshino, Yuka ; Matsumoto, Izumi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c608t-4e7da4c1badaa97ea39c6a8df7581f2ef2cf5dafe98e988f4b4e02b717999e373</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Ascites</topic><topic>Body weight</topic><topic>Case Report</topic><topic>Complement component C3</topic><topic>CrlCD-1(ICR) mouse</topic><topic>Edema</topic><topic>Glomerulonephritis</topic><topic>IgG antibody</topic><topic>Immunoglobulin G</topic><topic>Kidneys</topic><topic>Lesions</topic><topic>Leukocytes (eosinophilic)</topic><topic>membranoproliferative glomerulonephritis</topic><topic>Mesangial cells</topic><topic>Necropsy</topic><topic>spontaneous lesion</topic><topic>Thickening</topic><toplevel>online_resources</toplevel><creatorcontrib>Tochitani, Tomoaki</creatorcontrib><creatorcontrib>Kouchi, Mami</creatorcontrib><creatorcontrib>Fuji, Yuta</creatorcontrib><creatorcontrib>Yoshino, Yuka</creatorcontrib><creatorcontrib>Matsumoto, Izumi</creatorcontrib><creatorcontrib>Sumitomo Dainippon Pharma Co</creatorcontrib><creatorcontrib>Preclinical Research Unit</creatorcontrib><creatorcontrib>Ltd</creatorcontrib><collection>CrossRef</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of Toxicologic Pathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tochitani, Tomoaki</au><au>Kouchi, Mami</au><au>Fuji, Yuta</au><au>Yoshino, Yuka</au><au>Matsumoto, Izumi</au><aucorp>Sumitomo Dainippon Pharma Co</aucorp><aucorp>Preclinical Research Unit</aucorp><aucorp>Ltd</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Spontaneous membranoproliferative glomerulonephritis in a young Crl:CD-1(ICR) mouse</atitle><jtitle>Journal of Toxicologic Pathology</jtitle><addtitle>J Toxicol Pathol</addtitle><date>2020</date><risdate>2020</risdate><volume>33</volume><issue>3</issue><spage>177</spage><epage>181</epage><pages>177-181</pages><issn>0914-9198</issn><eissn>1881-915X</eissn><eissn>1347-7404</eissn><abstract>Here, we reported a spontaneous case of membranoproliferative glomerulonephritis observed in a young ICR mouse. A 5-week-old female mouse was euthanized owing to abdominal swelling and increased body weight. At necropsy, generalized subcutaneous edema, and clear, colorless, non-viscous ascites were observed. Histologically, the kidneys showed diffuse, bilateral glomerular lesions. The lesions were characterized by thickening and double contour of the basement membrane and an increase in mesangial cells and matrix, resulting in the narrowing of the capillary lumen. Additionally, eosinophilic hyaloid material accumulated in the subendothelial areas and Bowman’s space. The material was positive for periodic acid-Schiff, complement component C3, or immunoglobulin G, stained red by Masson’s trichrome, and stained blue by phosphotungstic acid-hematoxylin stain and was considered to be plasma due to glomerular leakage. The glomerular lesion was diagnosed as membranoproliferative glomerulonephritis, and an uncertain endothelial injury was suspected as the cause.</abstract><cop>Tokyo</cop><pub>JAPANESE SOCIETY OF TOXICOLOGIC PATHOLOGY</pub><pmid>32764843</pmid><doi>10.1293/tox.2019-0081</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Ascites Body weight Case Report Complement component C3 CrlCD-1(ICR) mouse Edema Glomerulonephritis IgG antibody Immunoglobulin G Kidneys Lesions Leukocytes (eosinophilic) membranoproliferative glomerulonephritis Mesangial cells Necropsy spontaneous lesion Thickening |
title | Spontaneous membranoproliferative glomerulonephritis in a young Crl:CD-1(ICR) mouse |
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