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About:
Establishment of a transgenic mouse model with liver-specific expression of secretory immunoglobulin D
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covidontheweb.inria.fr
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Type:
Academic Article
research paper
schema:ScholarlyArticle
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type
Academic Article
research paper
schema:ScholarlyArticle
isDefinedBy
Covid-on-the-Web dataset
has title
Establishment of a transgenic mouse model with liver-specific expression of secretory immunoglobulin D
Creator
Wang, Ping
Dai, Yunping
Wang, Meili
Zheng, Min
Chen, X
Bowen, Yan
Cheng, Xueqian
Huang, Tan
Kemian, Gou
Wang, Xifeng
Yi, Sun
Zhiguo, Wei
Source
Medline; PMC
abstract
Mutation of mevalonate kinase (MVK) is thought to account for most cases of hyperimmunoglobulinemia D syndrome (HIDS) with recurrent fever. However, its mechanism and the relationship between elevated serum immunoglobulin D (IgD) and the clinical features of HIDS are unclear. In this study, we generated by fusion PCR a vector to express high levels of chimeric secretory IgD (csIgD) specifically in the liver. We then generated seven founder lines of transgenic mice by co-microinjection, and verified them using genomic PCR and Southern blotting. We detected the expression of csIgD by reverse transcription PCR, quantitative PCR, western blotting, and enzyme-linked immunosorbent assays. We demonstrated that csIgD could be specifically and stably expressed in the liver. We used flow cytometry to show that overexpression of csIgD in the bone marrow and spleen cells had no effect on B cell development. Morphologic and anatomical observation of the transgenic mice revealed skin damage, hepatosplenomegaly, and nephromegaly in some transgenic mice; in these mice, pathological sections showed high levels of cell necrosis and protein-like sediments in the liver, spleen, and kidney. We demonstrated that the genomic insertion sites of the transgenes did not disrupt the MVK gene on mouse chromosome 5. This transgenic mouse will be useful to explore the pathogenesis of HIDS.
has issue date
2012-04-14
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bibo:doi
10.1007/s11427-012-4301-3
bibo:pmid
22527518
has license
cc-by
sha1sum (hex)
c3cca3d66fd6ef068573a246a76360a9e574cad1
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https://doi.org/10.1007/s11427-012-4301-3
resource representing a document's title
Establishment of a transgenic mouse model with liver-specific expression of secretory immunoglobulin D
has PubMed Central identifier
PMC7089205
has PubMed identifier
22527518
schema:publication
Sci China Life Sci
resource representing a document's body
covid:c3cca3d66fd6ef068573a246a76360a9e574cad1#body_text
is
schema:about
of
named entity 'MVK'
named entity 'MVK'
named entity 'generated'
named entity 'overexpression'
named entity 'mechanism'
named entity 'liver'
named entity 'sediments'
named entity 'necrosis'
named entity 'IgD'
named entity 'generated'
named entity 'enzyme-linked immunosorbent assays'
named entity 'LINES'
named entity 'DETECTED'
named entity 'INSERTION'
named entity 'MVK GENE'
named entity 'CASES'
named entity 'TRANSGENES'
named entity 'ELEVATED'
named entity 'SKIN DAMAGE'
named entity 'DEMONSTRATED'
named entity 'REVERSE TRANSCRIPTION PCR'
named entity 'FUSION'
named entity 'CELLS'
named entity 'VECTOR'
named entity 'COULD BE'
named entity 'LIKE'
named entity 'TO EXPRESS'
named entity 'IMMUNOGLOBULIN D'
named entity 'CLINICAL FEATURES'
named entity 'THESE'
named entity 'MICE'
named entity 'MICROINJECTION'
named entity 'ANATOMICAL'
named entity 'PATHOLOGICAL'
named entity 'REVEALED'
named entity 'HYPERIMMUNOGLOBULINEMIA D SYNDROME'
named entity 'B CELL DEVELOPMENT'
named entity 'RELATIONSHIP'
named entity 'MEVALONATE KINASE'
named entity 'SEVEN'
named entity 'PCR'
named entity 'USED'
named entity 'KIDNEY'
named entity 'MUTATION'
named entity 'SOUTHERN BLOTTING'
named entity 'PROTEIN'
named entity 'EXPRESSED'
named entity 'UNCLEAR'
named entity 'SERUM IMMUNOGLOBULIN'
named entity 'ENZYME-LINKED IMMUNOSORBENT ASSAYS'
named entity 'OVEREXPRESSION'
named entity 'FOUNDER'
named entity 'DID'
named entity 'USEFUL'
named entity 'VERIFIED'
named entity 'LIVER'
named entity 'EXPRESSION'
named entity 'HIDS'
named entity 'MECHANISM'
named entity 'SECRETORY'
named entity 'GENERATED'
named entity 'PATHOGENESIS'
named entity 'QUANTITATIVE PCR'
named entity 'TRANSGENIC MOUSE'
named entity 'MOUSE MODEL'
named entity 'IMMUNOGLOBULIN D'
named entity 'ESTABLISHMENT'
named entity 'USING'
named entity 'EXPRESSION'
named entity 'CHINA'
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